158 Manufacturing jobs in Leominster

**Job Title: Manufacturing Engineer**
**Location** : Hudson, NH - Onsite
**Duration:** 6 months with possible extensions.
**Shift Schedule:** 9-80 Schedule - 1 st Shift
**Active Security Clearance is required**
**Position Summary:**
+ As a Manufacturing Engineer in the Defense and Aerospace industry, your primary responsibility will be to develop and improve manufacturing processes and systems to ensure the efficient and cost-effective production of defense and aerospace products.
+ You will collaborate with cross-functional teams, including design engineers, production personnel, and quality assurance, to optimize manufacturing operations and drive continuous improvement initiatives.
+ Your expertise will contribute to the development and delivery of high-quality, reliable, and technologically advanced products for defense and aerospace applications.
**Key Responsibilities:**
+ **Process Development:** Design and develop manufacturing processes, procedures, and work instructions to meet product specifications and quality standards. Identify and implement improvements to enhance efficiency, productivity, and safety.
+ **Production Optimization:** Collaborate with design engineers to ensure producibility and manufacturability of new products. Analyze production data, identify bottlenecks, and implement corrective actions to optimize production flow and reduce cycle times.
+ **Equipment Selection and Integration:** Evaluate manufacturing equipment and technologies, recommend suitable options, and oversee their integration into production lines. Ensure equipment meets industry standards, safety regulations, and customer requirements.
+ **Continuous Improvement:** Lead and participate in Lean Manufacturing and Six Sigma initiatives. Identify areas for improvement, implement process enhancements, and drive cost reduction, waste elimination, and quality improvement efforts.
+ **Quality Assurance:** Collaborate with the quality team to establish and maintain quality control procedures, including inspection and testing methods. Resolve production-related quality issues and implement preventive measures to ensure compliance with industry and customer specifications.
+ **Supply Chain Coordination:** Collaborate with suppliers to ensure timely availability of materials, components, and equipment. Evaluate supplier capabilities and performance to support production schedules and quality requirements.
+ **Documentation and Reporting:** Prepare and maintain accurate documentation, including process specifications, standard operating procedures, and engineering change orders. Generate reports on key performance indicators, production metrics, and improvement initiatives.
+ **Safety and Compliance:** Ensure compliance with safety regulations and industry standards. Identify potential hazards and implement measures to mitigate risks and promote a safe working environment.
**Qualifications and Skills:**
+ Bachelor's degree in manufacturing engineering, Industrial Engineering, Mechanical Engineering, or a related field. Advanced degrees may be preferred.
+ Previous experience in manufacturing engineering roles, preferably in the defense or aerospace industry.
+ Strong knowledge of manufacturing processes, equipment, and technologies, including CNC machining, additive manufacturing, assembly, and testing.
+ Familiarity with industry standards and regulations, such as AS9100, ITAR, and NADCAP.
+ Proficiency in CAD/CAM software for process development and optimization.
+ Experience with Lean Manufacturing, Six Sigma, or other continuous improvement methodologies.
+ Excellent problem-solving skills and the ability to analyze and interpret complex data.
+ Strong communication and collaboration skills to work effectively with cross-functional teams.
+ Attention to detail, with a focus on quality and reliability.
+ Ability to work in a fast-paced, dynamic environment and adapt to changing priorities and deadlines.
**Why Join Us?**
**Professional Development:** Gain hands-on experience with cutting-edge industry standards.
**Collaborative Environment:** Work with a supportive team committed to high-quality outcomes.
**Impactful Work:** Ensure our products meet rigorous quality and regulatory standards.
**Apply today to take the next step in your career!**
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Engineering?
Your engineering skills are in demand, but how do you find the right fit? Easy. At Kelly Engineering, our team creates expert talent solutions to solve the world's most critical challenges. We connect you with leading organizations where you can collaborate on innovative projects, work with cutting-edge technologies and accelerate your growth. Whether you prefer the variety and flexibility of short-term projects or are looking for a long-term opportunity, we're here to guide you to the next step in your engineering career.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

**Job Title:** Manufacturing Associate
**Location:** Framingham, MA
**Hours:** This is a 12-hour, Night-time (7:00 pm-7:00 am), rotating position
**About the Job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
8 NYA is an integrated, continuous, biomanufacturing facility (ICBF). The facility is operated by upstream, downstream and support services groups which support a 24/7 large-scale therapeutic protein manufacturing facility housing multiple products.
This is a 12-hour, Night-time (7pm-7am), rotating position in a flexible, single-use technology, large scale cGMP biologics facility. Initial job responsibilities will include leading a team responsible for a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations.
The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
**Main Responsibilities**
+ Maintains a safe working environment and reporting of incidents/accidents to Manufacturing management.
+ Effectively demonstrates understanding of GMPs and how they apply to specific responsibilities.
+ Follows verbal and written procedures in operating production and equipment and performing processing steps; accurately completes appropriate production documentation.
+ Maintains cleanliness and orderliness in process area.
+ Ensures production area is stocked with supplies.
+ Performs batch record review, EWI (Electronic Work Instruction) revisions, and work order generation.
+ Interacts with other support functions such as Quality Assurance, Quality Control, Manufacturing Engineering, MSAT, Validation, etc.
+ Utilizes manufacturing knowledge to improve process operations and affect positive change.
+ Demonstrates ability to troubleshoot basic mechanical operations.
+ Effectively utilizes Microsoft Office applications.
+ Mentors less experienced operators.
+ Fulfills the role of Team Lead in the absence of the Sr. Manufacturing Associate.
+ Escalates production floor issues related to personnel, safety, procedures, materials, process, equipment, automation, utilities, and/or information systems to Manufacturing management and/or appropriate functional area(s).
+ Performs in process analytical testing.
+ Demonstrates general knowledge of automation systems (INFOR, MES, ERP, DeltaV).
+ Demonstrates general knowledge and practice of aseptic techniques.
**Additional Responsibilities**
+ Cross train manufacturing personnel
**Continuous Improvement**
+ Contributes to continual improvement of all manufacturing documentation (SOP's, EWI's, MBR's, OJT's) to ensure they are current, accurate, and clear.
+ Supports plant floor continuous improvement initiatives.
*Key Responsibilities may differ among employees with the same job title and may change over time, in accordance with business needs.
**About You**
**Basic Qualifications**
+ High School diploma/GED with 3-5 years of experience in a cGXP environment, or a Bachelor's degree with 1-3 years of experience.
+ Must have prior experience in cGMP manufacturing operations.
**Preferred Qualifications**
+ Bachelor's degree with 2-4 years of experience in bulk biologics GMP manufacturing.
+ Effectively uses process automation systems to operate production processes (i.e. Delta V).
+ Familiarity with deviation management systems (i.e. Veeva).
**Special Working Conditions**
+ Ability to lift up to 50 lbs.
+ Ability to stand on average 10 hours per shift.
+ Ability to gown and gain entry to manufacturing areas.
+ Ability to work a twelve-hour rotating shift and every other weekend, including holidays as scheduled.
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SG
#LI-GZ
#LI-Onsite
#vhd
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
_North America Applicants Only_
The salary range for this position is:
$26.32 - $35.09
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK ( .
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**Job Title:** Manufacturing Associate
**Location:** Framingham, MA
**Hours:** This is a 12-hour, Night-time (7:00 pm-7:00 am), rotating position
**About the Job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
8 NYA is an integrated, continuous, biomanufacturing facility (ICBF). The facility is operated by upstream, downstream and support services groups which support a 24/7 large-scale therapeutic protein manufacturing facility housing multiple products.
This is a 12-hour, Night-time (7pm-7am), rotating position in a flexible, single-use technology, large scale cGMP biologics facility. Initial job responsibilities will include leading a team responsible for a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations.
The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
**Main Responsibilities**
+ Maintains a safe working environment and reporting of incidents/accidents to Manufacturing management.
+ Effectively demonstrates understanding of GMPs and how they apply to specific responsibilities.
+ Follows verbal and written procedures in operating production and equipment and performing processing steps; accurately completes appropriate production documentation.
+ Maintains cleanliness and orderliness in process area.
+ Ensures production area is stocked with supplies.
+ Performs batch record review, EWI (Electronic Work Instruction) revisions, and work order generation.
+ Interacts with other support functions such as Quality Assurance, Quality Control, Manufacturing Engineering, MSAT, Validation, etc.
+ Utilizes manufacturing knowledge to improve process operations and affect positive change.
+ Demonstrates ability to troubleshoot basic mechanical operations.
+ Effectively utilizes Microsoft Office applications.
+ Mentors less experienced operators.
+ Fulfills the role of Team Lead in the absence of the Sr. Manufacturing Associate.
+ Escalates production floor issues related to personnel, safety, procedures, materials, process, equipment, automation, utilities, and/or information systems to Manufacturing management and/or appropriate functional area(s).
+ Performs in process analytical testing.
+ Demonstrates general knowledge of automation systems (INFOR, MES, ERP, DeltaV).
+ Demonstrates general knowledge and practice of aseptic techniques.
**Additional Responsibilities**
+ Cross train manufacturing personnel
**Continuous Improvement**
+ Contributes to continual improvement of all manufacturing documentation (SOP's, EWI's, MBR's, OJT's) to ensure they are current, accurate, and clear.
+ Supports plant floor continuous improvement initiatives.
*Key Responsibilities may differ among employees with the same job title and may change over time, in accordance with business needs.
**About You**
**Basic Qualifications**
+ High School diploma/GED with 3-5 years of experience in a cGXP environment, or a Bachelor's degree with 1-3 years of experience.
+ Must have prior experience in cGMP manufacturing operations.
**Preferred Qualifications**
+ Bachelor's degree with 2-4 years of experience in bulk biologics GMP manufacturing.
+ Effectively uses process automation systems to operate production processes (i.e. Delta V).
+ Familiarity with deviation management systems (i.e. Veeva).
**Special Working Conditions**
+ Ability to lift up to 50 lbs.
+ Ability to stand on average 10 hours per shift.
+ Ability to gown and gain entry to manufacturing areas.
+ Ability to work a twelve-hour rotating shift and every other weekend, including holidays as scheduled.
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SG
#LI-GZ
#LI-Onsite
#vhd
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
_North America Applicants Only_
The salary range for this position is:
$26.32 - $35.09
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK ( .
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**Job Title:** Manufacturing Associate
**Location** : Framingham, MA
**Day Shift:** 12 Hour Rotation: 6:45 am - 6:45 pm
**About the Job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
This is a 12-hour, rotating position in a flexible, single-use technology, large scale cGMP biologics facility. Initial job responsibilities will include leading a team responsible for a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations.
The Manufacturing Associate will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
**Main Responsibilities**
+ Maintains a safe working environment and reporting of incidents/accidents to Manufacturing management.
+ Effectively demonstrates understanding of GMPs and how they apply to specific responsibilities.
+ Follows verbal and written procedures in operating production and equipment and performing processing steps; accurately completes appropriate production documentation.
+ Maintains cleanliness and orderliness in process area.
+ Ensures production area is stocked with supplies.
+ Performs batch record review, EWI (Electronic Work Instruction) revisions, and work order generation.
+ Interacts with other support functions such as Quality Assurance, Quality Control, Manufacturing Engineering, MSIT, Validation, etc.
+ Utilizes manufacturing knowledge to improve process operations and affect positive change.
+ Demonstrates ability to troubleshoot basic mechanical operations.
+ Effectively utilizes Microsoft Office applications.
+ Mentors less experienced operators.
+ Fulfills the role of Team Lead in the absence of the Manufacturing Sr. Associate.
+ Escalates production floor issues related to personnel, safety, procedures, materials, process, equipment, automation, utilities, and/or information systems to Manufacturing management and/or appropriate functional area(s).
+ Performs in process analytical testing.
+ Demonstrates general knowledge of automation systems (INFOR, MES, ERP, Delta V).
+ Demonstrates general knowledge and practice of aseptic techniques.
+ Cross train manufacturing personnel
+ Supports plant floor continuous improvement initiatives.
Key Responsibilities may differ among employees with the same job title and may change over time, in accordance with business needs.
**About You**
**Basic Qualifications:**
**High School diploma/GED with 3-5 years of experience in a cGXP environment, or a Bachelor's degree with 1-3 years of experience.**
**Must have prior experience in cGMP manufacturing operations.**
**Preferred Qualifications:**
**Effectively uses process automation systems to operate production processes (i.e. Delta V).**
**Familiarity with deviation management systems (i.e. Phenix).**
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SG
#LI-GZ
#LI-Onsite
#vhd
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
_North America Applicants Only_
The salary range for this position is:
$26.32 - $39.48
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK ( .
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (

**POSITION SUMMARY:** The Manufacturing Engineer will primarily be responsible for coordinating the launch of new products/projects from prototype to production and striving to continuously improve our manufacturing processes to maximize quality, productivity, and cost. The ideal candidate possesses superior problem-solving skills, is detail- and process-oriented, and demonstrates excellent collaboration skills in team situations. Key deliverables for the position are to drive improvements and sustainment of the metrics established for Safety, Quality, Delivery, and Cost on both sustaining product and new opportunities. **KEY RESPONSIBILITIES:** + Design and develop manufacturing processes including production flow, assembly methods, and production equipment, documents processes via work instructions and trains team to standards. + Support the manufacturing team in resolving issues identified during production. + Act as customer advocate when addressing quality issues by utilizing problem solving techniques to drive to root cause / corrective action for any escapes. + Establish control plans/charts to monitor part and process performance and utilize data to drive priorities and improvements in manufacturing. + Design, develop, and qualify various tools, machinery and equipment for recommended manufacturing methods. Procure tooling for production as needed. + Develop and implement process improvements related to cycle time reduction, cost reduction, and other activities by reducing/eliminating non-value-added activities. + Provide feedback to engineering on new designs with a focus on ensuring Design for Manufacturability and Design for Reliability. + Participate in design review and review/approve part drawings from engineering. + Lead the implementation and sustainment of the various DBS tools to drive quality, delivery, and cost improvements on both sustaining and new production cells. + Support the Engineering Change Order (ECO) system from generation through implementation. + Develop poka-yoke and fixturing strategies to be used in reducing process variation in assembly processes. + Design tooling/fixturing and establish process flow that enables the safest possible working environment. + Establish part criticality levels based on design intent and correlation to system performance. + Establish part and system traceability requirements and support record maintenance. + Perform first article inspections/qualification of internally machined and supplied parts as needed. + Implement AQL-driven sampling plans and methods to ensure part compliance and drive supplier accountability. + Design and test product packaging in accordance with ISTA standards. QUALIFICATIONS: Critical Success Factors: + Exceptional creativity and ability to trystorm. + Superior organization and problem-solving skills. + Outstanding teamwork and collaboration skills. + Proven bias towards action. + Strong analytical skills: ability to collect, organize, analyze and disseminate information with attention to detail and accuracy. + Strong reporting skills; ability to present data in a variety of formats and to a variety of audiences, including staff and executives. + Demonstrated ability to communicate clearly to all functions within the organization. + Strong proponent of continuous improvement and organizational change. + Proven ability to develop and write technical documentation. **Required Skills/Experience:** + Demonstrated knowledge of manufacturing, engineering, and/or quality tools and techniques, including: FMEA, Design for Manufacturability (DfM), Statistical Process Control, and variation reduction. + Kaizen and/or Lean Manufacturing experience. + SolidWorks and/or ProE drawing and modeling proficiency. + Proficient with mechanical inspection using hand tools, calipers, force gauges, etc. **Desired Skills/Experience:** + Experience in machining and/or precision mechanical assembly. + Workign knowledge of CMM inspection equipment. + Basic familiarity with ISO:9001 standard. + Understanding of regulatory requirements related to RoHS and REACH. + Proficiency utilizing Microsoft Office. **Education:** + Bachelor of Science degree in Mechanical Engineering or related technical field. **TRAVEL:** <5% of overnight travel required for the position. Key Relationships: + Director of Operations + Project Managers + Design Engineers + Quality Team + Production Team + Supply Chain Team #LI-PW1 **Ralliant Corporation Overview** Ralliant, originally part of Fortive, now stands as a bold, independent public company driving innovation at the forefront of precision technology. With a global footprint and a legacy of excellence, we empower engineers to bring next-generation breakthroughs to life - faster, smarter, and more reliably. Our high-performance instruments, sensors, and subsystems fuel mission-critical advancements across industries, enabling real-world impact where it matters most. At Ralliant we're building the future, together with those driven to push boundaries, solve complex problems, and leave a lasting mark on the world. We Are an Equal Opportunity Employer Ralliant Corporation and all Ralliant Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Ralliant and all Ralliant Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at **About Dover Motion** Dover Motion, Inc. is a subsidiary of Ralliant Corporation and we are revolutionizing the way things move. We partner with life science and diagnostics leaders around the world to co-create lifesaving technologies in healthcare that millions rely on every day. Our stages and electronic motion control bring quantum leaps in throughput, precision, efficiency, and reliability for microscopy and factory automation applications. Dover Motion's relationship with Ralliant allows its employees access to competitive benefits, extensive training, and exciting development opportunities. To learn more about any of the above, please visit

**Position Title** **Position Report to** **Date**
**Manufacturing Engineer 1** Focus Factory Manager 5/8/2025
**Supervises** **Travel Frequency (%)** **Location**
Manufacturing Engineering Technician 10% Boxborough
**Purpose of Position:**
Gems Setra is looking to add a critical new employee who possesses superior problem-solving skills, is detail and process-oriented, and demonstrates excellent collaboration skills to join their team as a Manufacturing Engineer. The Manufacturing Engineer will primarily be responsible for resolving issues that occur in the manufacturing lines, coordinating the launch of new products/projects from prototype to production and support achievement of manufacturing targets in Safety, Quality, Delivery and Productivity through daily management and continuous improvement initiatives. This position will develop, design, and lead complex engineering projects relating to manufacturing process development.
**Essential Functions** :
+ Design, develop and document manufacturing processes including production flow, assembly methods, and production equipment.
+ Use structured problem-solving techniques to investigate and countermeasure process and product failures, equipment failures, and quality issues, identify root cause and implement solutions
+ Design and develop tooling, fixtures, automation and testing equipment by applying knowledge of product design and manufacturing processes, product performance specifications, process acceptance criteria, and product /system testing.
+ Develop and implement process improvements related to cycle time reduction, capacity increase, cost reduction, and other activities by reducing/eliminating non-value-added activities.
+ Participate in new product design review and review/approve part drawings from engineering and support the transition of new products from Design Engineering to manufacturing.
+ Facilitate the implementation and sustainment of the various FBS tools to drive quality, reliability, delivery, and cost improvements on both sustaining and new production cells.
+ Act as customer advocate when addressing quality issues by utilizing problem solving techniques to drive to root cause / corrective action for any escapes.
+ Support the Engineering Change Order (ECO) system from generation through implementation.
+ Develop poka-yoke and fixturing strategies to be used in reducing process variation in assembly processes.
+ Perform first article inspections/qualification of internally machined and supplied parts as needed.
+ Leads, Facilitates and applies lean manufacturing tools such as Standard Work, 5S and VRK to solve production problems
**Critical Success Factors:**
+ Solid understanding of manufacturing processes, tools, and technologies.
+ Exceptional creativity and ability to try new ideas on the spot.
+ Customer Focus
+ Superior organization and problem-solving skills.
+ Outstanding teamwork and collaboration skills.
+ Proven bias towards action.
+ Strong analytical skills; ability to collect, organize, analyze and disseminate information with attention to detail and accuracy.
+ Strong reporting skills; ability to present data in a variety of formats and to a variety of audiences, including staff and executives.
+ Demonstrated ability to communicate clearly to all functions within the organization.
+ Strong proponent of continuous improvement and organizational change.
+ Proven ability to develop and write technical documentation.
+ Lead and execute completion of capital expenditure projects.
+ Provide training to team members on new and updated processes to ensure proper implementation and adherence.
+ Ability to own multiple projects simultaneously.
**Education & Experience Required:**
+ Bachelor of Science or equivalent in Mechanical Engineering, Electrical Engineering, or related technical field required.
+ Professional experience of 1+ years creating solutions in a Manufacturing environment and/or with continuous improvement tools, can include internships and co-ops
+ Demonstrated knowledge of manufacturing engineering, and/or quality tools and techniques, including: FMEA, Design for Manufacturability (DFM), Statistical Process Control, and variation reduction.
+ SolidWorks and/or ProE drawing and modeling/drafting.
+ knowledge with mechanical inspection using hand tools, calipers, Micrometers, etc.
+ Proficiency in Microsoft Office.
**Desired Skills:**
+ Experience in machining and/or precision mechanical assembly.
+ Working knowledge of Semiconductor, Fiber Optics, transducers and/or cleanroom environment.
+ Basic familiarity with ISO:9001 standards.
+ Understanding of regulatory requirements related to RoHS and REACH.
+ Knowledge of Copy Exactly process control.
+ Lean manufacturing experience
**PHYSICAL DEMANDS / ENVIRONMENT** **-**
The work environment characteristics described here are representative of those that associates encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is frequently required to reach with hands and arms. The employee is frequently required to stand/or sit, squat, turn/twist, reach, use hands to: finger, handle, feel or operate objects, tools or controls, and computer keyboards.
The employee must occasionally lift, carry, push or pull up to 30 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
While performing the duties of this job, the employee may be subjected to moving mechanical parts, electrical currents, vibrations, fumes, odors, dusts, gases, chemicals, oils, extreme temperatures and workspace restrictions.
The noise level in the work environment is occasionally loud.
Employees will be **required** to wear the proper Personal Protective Equipment (PPE), which **may** include eye, hearing and respiratory protection, protective smock, steel toe shoes, gloves, hard hats, or face shields. Contact lenses **may not** be allowed in some areas.
The associate must also be willing and able to travel by all forms of transportation.
The duties listed in job descriptions are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related or a logical assignment to the position. The job description does not constitute an employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change.
_The purpose of this description is to assist in ADA compliance and is not intended for other purposes._
#LI-PW1
**Ralliant Corporation Overview**
Ralliant, originally part of Fortive, now stands as a bold, independent public company driving innovation at the forefront of precision technology. With a global footprint and a legacy of excellence, we empower engineers to bring next-generation breakthroughs to life - faster, smarter, and more reliably. Our high-performance instruments, sensors, and subsystems fuel mission-critical advancements across industries, enabling real-world impact where it matters most. At Ralliant we're building the future, together with those driven to push boundaries, solve complex problems, and leave a lasting mark on the world.
We Are an Equal Opportunity Employer
Ralliant Corporation and all Ralliant Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Ralliant and all Ralliant Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at
**About Gems Setra**
Gems Setra is a leading global supplier of sensing and monitoring technologies, operating within the Precision Technologies platform of Fortive Corporation. Through our comprehensive portfolio of premium sensing products, we deliver solutions to customer problems and challenges. As two Fortive businesses merged in 2022, Gems Setra's vision is to connect our customers to their environment to create a safer, healthier, more sustainable world. Gems Sensors product offerings include a range of products that encompass liquid level, flow, and pressure sensors, miniature solenoid valves, proximity switches, and integrated fluid management solutions. The Setra Systems product line offers an extensive selection of high-quality sensing instruments for humidity, current, vacuum, energy, and pressure measurements. At the heart of our combined company's mission lies a shared dedication between Gems Sensors and Setra Systems to deliver high-quality sensing solutions, backed by reliable customer support on a global scale. As a part of Fortive, we embrace a culture of innovation, driving progress and empowering advancements in the industries and customers we serve.
We Are an Equal Opportunity Employer. Fortive Corporation and all Fortive Companies are proud to be equal opportunity employers. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity or expression, or other characteristics protected by law. Fortive and all Fortive Companies are also committed to providing reasonable accommodations for applicants with disabilities. Individuals who need a reasonable accommodation because of a disability for any part of the employment application process, please contact us at
**Pay Range**
The salary range for this position in local currency is 65100.00 - 120900.00

Job ID: 702311BR
Date posted: Aug. 21, 2025

Description: You will be a Manufacturing Planner for our team, responsible for developing and maintaining a comprehensive production schedule for Chelmsford programs. Chelmsford Operations facility is a leading hub for innovation in microelectronics, supporting critical aerospace and defense programs. Located in Chelmsford, Massachusetts, we are dedicated to producing advanced technology solutions that safeguard national security and advance the industry

What You Will Be Doing
As a Manufacturing Planner with our Buy Planning team, you'll be responsible for developing and maintaining a comprehensive production schedule for Chelmsford programs that align with customer requirements, production capacity, and resource availability. You'll join a select group of individuals who are responsible for providing support to numerous Chelmsford programs. You must be a self-starter, possess strong interpersonal skills, and have the ability to lead projects from conception to closure. You will work closely with Global Supply Chain (GSC) and Make Planners to ensure that deliveries meet program needs. You will be responsible for coordinating interdepartmental activities with quality assurance, manufacturing, purchasing, engineering, inventory control, traffic, contracts, administration, etc.

Your responsibilities will include:
• Performing Buy planning activities associated with Manufacturing Resource Planning (MRP) transactions
• Performing one or more multiple manufacturing activities within various manufacturing functions. Maintaining production system integrity to drive inventory optimization to minimize cost
• Expediting and optimizing material flow through the supply chain to meet customer requirements. Coordinating with Supply Chain Stakeholders including Procurement and Operations Management to determine appropriate time-phased plan for procured parts and executing processes to ensure deliverables meet production schedule requirements
• Supporting cross functional planning and management teams providing daily status updates, as required
• Maintaining MRP parameters including lead times and lot sizes and coordinating with Engineering and Change Board Rep to make the associated changes to the BOM
• Tracking and managing sub-contract POs
• Analyzing production data to identify trends, opportunities for improvement, and potential bottlenecks in the production process
• Developing solutions to complex problems which require the regular use of ingenuity and innovation and ensuring solutions are consistent with organization objectives

Why Join Us
We're looking for a highly motivated and organized Manufacturing Planner to join our team. As a key member of our Buy Planning team, you will have the opportunity to work in a fast-paced and dynamic environment, collaborate with cross-functional teams, and contribute to the success of our operations. If you're a self-starter with strong interpersonal skills and a passion for manufacturing planning, we encourage you to apply.

We are committed to supporting your work-life balance and overall well-being, offering flexible scheduling options. Learn more about Lockheed Martin's comprehensive benefits package here.

Further Information About This Opportunity:
This position is located in Chelmsford. Discover more about our Chelmsford, Massachusetts location.

MUST BE A U.S. CITIZEN - This position is located at a facility that requires special access. The selected candidate must be able to obtain a secret clearance. A company-sponsored interim secret is required to start.
Basic Qualifications:
• Completed Bachelor's degree from an accredited college/university
• 5+ years in a production operations environment
• Strong knowledge of Production Planning & Control principles, processes, and tools
• Strong working knowledge and experience in inventory management, scheduling, and production control
• Experience with ERP/MRP (SAP, Oracle, etc.)
• Ability to obtain and maintain a Secret clearance, which requires U.S. citizenship
Desired Skills:
• Experience in an electrical assembly and integration facility
• Inventory Control and material handling knowledge, including familiarity with material requirements and Dock/Receiving/Warehouse/Shipping areas
• Experience communicating with peers, leadership, and internal customers effectively on multiple platforms (face-to-face, virtually, email, Teams, etc.)
• Demonstrated ability to work well in both a team environment and alone
• Demonstrated analytical, problem-solving, and ability to manage various tasks under time-sensitive constraints
• Demonstrated ability to ensure data integrity and consistency
• Understanding of MRP and Manufacturing Execution Systems
• Working knowledge of SAP and Apriso WM
• Ability to understand engineering drawings and parts lists
• Green Belt trained/certified
Security Clearance Statement: This position requires a government security clearance, you must be a US Citizen for consideration.
Clearance Level: Secret
Other Important Information You Should Know
Expression of Interest: By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings.
Ability to Work Remotely: Part-time Remote Telework: The employee selected for this position will work part of their work schedule remotely and part of their work schedule at a designated Lockheed Martin facility. The specific weekly schedule will be discussed during the hiring process.
Work Schedules: Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits.
Schedule for this Position: 4x10 hour day, 3 days off per week
Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics.
The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration.
At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work.

With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility.

If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs, and apply for roles that align with your qualifications.
Experience Level: Experienced Professional
Business Unit: MISSILES AND FIRE CONTROL
Relocation Available: Possible
Career Area: Manufacturing
Type: Full-Time
Shift: First

Job ID: 702311BR
Date posted: Aug. 21, 2025

Description: You will be a Manufacturing Planner for our team, responsible for developing and maintaining a comprehensive production schedule for Chelmsford programs. Chelmsford Operations facility is a leading hub for innovation in microelectronics, supporting critical aerospace and defense programs. Located in Chelmsford, Massachusetts, we are dedicated to producing advanced technology solutions that safeguard national security and advance the industry

What You Will Be Doing
As a Manufacturing Planner with our Buy Planning team, you'll be responsible for developing and maintaining a comprehensive production schedule for Chelmsford programs that align with customer requirements, production capacity, and resource availability. You'll join a select group of individuals who are responsible for providing support to numerous Chelmsford programs. You must be a self-starter, possess strong interpersonal skills, and have the ability to lead projects from conception to closure. You will work closely with Global Supply Chain (GSC) and Make Planners to ensure that deliveries meet program needs. You will be responsible for coordinating interdepartmental activities with quality assurance, manufacturing, purchasing, engineering, inventory control, traffic, contracts, administration, etc.

Your responsibilities will include:
• Performing Buy planning activities associated with Manufacturing Resource Planning (MRP) transactions
• Performing one or more multiple manufacturing activities within various manufacturing functions. Maintaining production system integrity to drive inventory optimization to minimize cost
• Expediting and optimizing material flow through the supply chain to meet customer requirements. Coordinating with Supply Chain Stakeholders including Procurement and Operations Management to determine appropriate time-phased plan for procured parts and executing processes to ensure deliverables meet production schedule requirements
• Supporting cross functional planning and management teams providing daily status updates, as required
• Maintaining MRP parameters including lead times and lot sizes and coordinating with Engineering and Change Board Rep to make the associated changes to the BOM
• Tracking and managing sub-contract POs
• Analyzing production data to identify trends, opportunities for improvement, and potential bottlenecks in the production process
• Developing solutions to complex problems which require the regular use of ingenuity and innovation and ensuring solutions are consistent with organization objectives

Why Join Us
We're looking for a highly motivated and organized Manufacturing Planner to join our team. As a key member of our Buy Planning team, you will have the opportunity to work in a fast-paced and dynamic environment, collaborate with cross-functional teams, and contribute to the success of our operations. If you're a self-starter with strong interpersonal skills and a passion for manufacturing planning, we encourage you to apply.

We are committed to supporting your work-life balance and overall well-being, offering flexible scheduling options. Learn more about Lockheed Martin's comprehensive benefits package here.

Further Information About This Opportunity:
This position is located in Chelmsford. Discover more about our Chelmsford, Massachusetts location.

MUST BE A U.S. CITIZEN - This position is located at a facility that requires special access. The selected candidate must be able to obtain a secret clearance. A company-sponsored interim secret is required to start.
Basic Qualifications:
• Completed Bachelor's degree from an accredited college/university
• 5+ years in a production operations environment
• Strong knowledge of Production Planning & Control principles, processes, and tools
• Strong working knowledge and experience in inventory management, scheduling, and production control
• Experience with ERP/MRP (SAP, Oracle, etc.)
• Ability to obtain and maintain a Secret clearance, which requires U.S. citizenship
Desired Skills:
• Experience in an electrical assembly and integration facility
• Inventory Control and material handling knowledge, including familiarity with material requirements and Dock/Receiving/Warehouse/Shipping areas
• Experience communicating with peers, leadership, and internal customers effectively on multiple platforms (face-to-face, virtually, email, Teams, etc.)
• Demonstrated ability to work well in both a team environment and alone
• Demonstrated analytical, problem-solving, and ability to manage various tasks under time-sensitive constraints
• Demonstrated ability to ensure data integrity and consistency
• Understanding of MRP and Manufacturing Execution Systems
• Working knowledge of SAP and Apriso WM
• Ability to understand engineering drawings and parts lists
• Green Belt trained/certified
Security Clearance Statement: This position requires a government security clearance, you must be a US Citizen for consideration.
Clearance Level: Secret
Other Important Information You Should Know
Expression of Interest: By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings.
Ability to Work Remotely: Part-time Remote Telework: The employee selected for this position will work part of their work schedule remotely and part of their work schedule at a designated Lockheed Martin facility. The specific weekly schedule will be discussed during the hiring process.
Work Schedules: Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits.
Schedule for this Position: 4x10 hour day, 3 days off per week
Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics.
The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration.
At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work.

With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility.

If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs, and apply for roles that align with your qualifications.
Experience Level: Experienced Professional
Business Unit: MISSILES AND FIRE CONTROL
Relocation Available: Possible
Career Area: Manufacturing
Type: Full-Time
Shift: First

Description:You will be a Manufacturing Planner for our team, responsible for developing and maintaining a comprehensive production schedule for Chelmsford programs. Chelmsford Operations facility is a leading hub for innovation in microelectronics, supporting critical aerospace and defense programs. Located in Chelmsford, Massachusetts, we are dedicated to producing advanced technology solutions that safeguard national security and advance the industry

What You Will Be Doing

As a Manufacturing Planner with our Buy Planning team, you'll be responsible for developing and maintaining a comprehensive production schedule for Chelmsford programs that align with customer requirements, production capacity, and resource availability. You'll join a select group of individuals who are responsible for providing support to numerous Chelmsford programs. You must be a self-starter, possess strong interpersonal skills, and have the ability to lead projects from conception to closure. You will work closely with Global Supply Chain (GSC) and Make Planners to ensure that deliveries meet program needs. You will be responsible for coordinating interdepartmental activities with quality assurance, manufacturing, purchasing, engineering, inventory control, traffic, contracts, administration, etc.

Your responsibilities will include:

* Performing Buy planning activities associated with Manufacturing Resource Planning (MRP) transactions
* Performing one or more multiple manufacturing activities within various manufacturing functions. Maintaining production system integrity to drive inventory optimization to minimize cost
* Expediting and optimizing material flow through the supply chain to meet customer requirements. Coordinating with Supply Chain Stakeholders including Procurement and Operations Management to determine appropriate time-phased plan for procured parts and executing processes to ensure deliverables meet production schedule requirements
* Supporting cross functional planning and management teams providing daily status updates, as required
* Maintaining MRP parameters including lead times and lot sizes and coordinating with Engineering and Change Board Rep to make the associated changes to the BOM
* Tracking and managing sub-contract POs
* Analyzing production data to identify trends, opportunities for improvement, and potential bottlenecks in the production process
* Developing solutions to complex problems which require the regular use of ingenuity and innovation and ensuring solutions are consistent with organization objectives

Why Join Us

We're looking for a highly motivated and organized Manufacturing Planner to join our team. As a key member of our Buy Planning team, you will have the opportunity to work in a fast-paced and dynamic environment, collaborate with cross-functional teams, and contribute to the success of our operations. If you're a self-starter with strong interpersonal skills and a passion for manufacturing planning, we encourage you to apply.

We are committed to supporting your work-life balance and overall well-being, offering flexible scheduling options. Learn more about Lockheed Martin's comprehensive benefits package here.

Further Information About This Opportunity:

This position is located in Chelmsford. Discover more about our Chelmsford, Massachusetts location.

MUST BE A U.S. CITIZEN - This position is located at a facility that requires special access. The selected candidate must be able to obtain a secret clearance. A company-sponsored interim secret is required to start.

Basic Qualifications:

* Completed Bachelor's degree from an accredited college/university
* 5+ years in a production operations environment
* Strong knowledge of Production Planning & Control principles, processes, and tools
* Strong working knowledge and experience in inventory management, scheduling, and production control
* Experience with ERP/MRP (SAP, Oracle, etc.)
* Ability to obtain and maintain a Secret clearance, which requires U.S. citizenship

Desired Skills:

* Experience in an electrical assembly and integration facility
* Inventory Control and material handling knowledge, including familiarity with material requirements and Dock/Receiving/Warehouse/Shipping areas
* Experience communicating with peers, leadership, and internal customers effectively on multiple platforms (face-to-face, virtually, email, Teams, etc.)
* Demonstrated ability to work well in both a team environment and alone
* Demonstrated analytical, problem-solving, and ability to manage various tasks under time-sensitive constraints
* Demonstrated ability to ensure data integrity and consistency
* Understanding of MRP and Manufacturing Execution Systems
* Working knowledge of SAP and Apriso WM
* Ability to understand engineering drawings and parts lists
* Green Belt trained/certified

Security Clearance Statement: This position requires a government security clearance, you must be a US Citizen for consideration.

Clearance Level: Secret

Other Important Information You Should Know

Expression of Interest: By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings.

Ability to Work Remotely: Part-time Remote Telework: The employee selected for this position will work part of their work schedule remotely and part of their work schedule at a designated Lockheed Martin facility. The specific weekly schedule will be discussed during the hiring process.

Work Schedules: Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits.

Schedule for this Position: 4x10 hour day, 3 days off per week

Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics.

The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration.

At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work.

With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility.

If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs, and apply for roles that align with your qualifications.

Experience Level: Experienced Professional

Business Unit: MISSILES AND FIRE CONTROL

Relocation Available: Possible

Career Area: Manufacturing

Type: Full-Time

Shift: First