275 Manufacturing jobs in Lawrence

Adecco is assisting a local client recruiting for Manufacturing Technician opportunities in Tewksbury, MA. This is an excellent opportunity to join a winning culture and get your foot in the door with a company that values innovation, teamwork, and precision in manufacturing operations. If Manufacturing Technician sounds like something you would be interested in, and you meet the qualifications listed below, apply now!
**Responsibilities for a Manufacturing Technician include but are not limited to:**
- Assemble and perform basic functional testing on a variety of electrical and mechanical parts and sub-assemblies following detailed work instructions.
- Participate as an active member of the production cell by supporting inventory control and equipment management.
- Rework and reassemble units based on written or verbal instructions for failure analysis or product development activities.
- Utilize computers to input, track, and process production data accurately.
**Candidates for Manufacturing Technician must meet the following requirements to be considered:**
- Minimum of 1 year of experience in a manufacturing, operations, production, or lab environment.
- High school diploma or equivalent required.
- Strong attention to detail and ability to follow written work instructions.
- Basic computer literacy; familiarity with Microsoft Suite preferred.
- Soldering experience and knowledge of Lean Manufacturing principles a plus.
**What's in this Manufacturing Technician position for you?**
- Pay: $24.00 per hour
- Shift **:** Monday - Friday, flexible start times (6:00am-2:30pm, 6:30am-3:00pm, or 7:00am-3:30pm EST)
- Weekly paycheck
- Dedicated Onboarding Specialist & Recruiter
- Access to Adecco's Aspire Academy with thousands of free upskilling courses
This Manufacturing Technician position is being recruited for by one of our Centralized Delivery Team and not your local Branch. For instant consideration for this **Manufacturing Technician** position and other opportunities with Adecco in **Tewksbury, MA** , apply today!
**Pay Details:** $24.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

**Manufacturing Technician (Day Shift)**
**Position Summary:**
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The Boston-area facility is Catalent's global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest Good Manufacturing Practices (CGMP) unit of its kind for DPI in North America.
Catalent Pharma Solutions in Boston is hiring a Manufacturing Technician. The Manufacturing Technician assists in the performance of routine operations for the GMP production of pharmaceutical products. This individual operates in accordance with environmental, health, safety, and cGMP guidelines. The Manufacturing Technician executes production activities under direct supervision for the Spray Drying of Active Pharmaceutical Ingredients.
**This is a full-time, on-site, hourly role. Work schedule will be a 7-day rotating 12-hour schedule from 6:00 a.m. to 6:00 p.m. Week 1 will be 48 hours over 4 days, and week two will be 36 hours over 3 days (often referred to as a Pitman Schedule). Overtime and Holiday pay will be included.**
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.**
**The Role:**
+ Performs Clean-In-Place, Clean-Out-of-Place, and equipment decontamination as required
+ Operates and monitors manufacturing equipment for the production of clinical and commercial pharmaceutical products
+ Assists in the execution of routine and complex production processes
+ Completes GMP documentation in legible and organized fashion
+ Receives and distributes supplies in the manufacturing area
+ All other duties as assigned
**The Candidate:**
+ A High School Diploma or equivalent is required. Biotechnology Certificate or Associate's Degree is highly desired
+ Must have at least one (1) year of prior work history, preferably in a Manufacturing Environment
+ Working knowledge of Good Documentation and Good Manufacturing Practices preferred
+ Must be proficient in Microsoft Office Suite
+ Physical requirements: Individual may be required to sit, stand, walk regularly, use hands regularly, and occasionally lift up to 50 pounds
**Why you should join Catalent:**
+ Defined career path and annual performance review and feedback process
+ Diverse, inclusive culture
+ Positive working environment focusing on continually improving processes to remain innovative
+ Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
+ 152 Hours + 8 paid holidays
+ Several Employee Resource Groups focusing on D&I
+ Dynamic, fast-paced work environment
+ Community engagement and green initiatives
+ Generous 401K match
+ Company match on donations to organizations
+ Medical, dental and vision benefits effective day one of employment
+ Tuition Reimbursement - Let us help you finish your degree or start a new degree!
+ WellHub program to promote overall physical wellness
+ Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

General Atomics (GA), and its affiliated companies, is one of the world's leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies.
General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS' expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide.
**DUTIES AND RESPONSIBILITIES**
+ Capable of Hands On Assembly and Test of Opto-Mechanical systems.
+ Function as a Process Engineer to document all process procedures for Optical-Mechanical assemblies.
+ Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub- assemblies, and final assemblies.
+ Conducts tests throughout all stages of production to determine control over applicable variables and troubleshooting and resolving manufacturing problems of moderate scope and complexity.
+ Support efforts to set-up and maintain the following testing capabilities: Vibration, EMI, Thermal and TVAC chambers, or other pieces of test equipment.
+ Works with Cryogenic, High-Vacuum or High-Pressure Systems, or their subcomponents. Provide technical expertise on thermal vacuum systems
+ Capable of Hands-On Vibration, EMI and Thermal Vacuum Test of Opto-Mechanical systems and Optical Payloads.
+ Develop solutions to problems that occur including assisting in the design of specialized components.
+ Fabricates assemblies and fixtures to optical specifications in a machine shop maintaining quality assurance and documentation.
+ Diagnoses and corrects operational problems or trouble sources in equipment or tests.
+ Collaborates with product design engineering on technical specifications that will best utilize equipment and manufacturing techniques.
+ Interface with all engineering disciplines from start to finish of products to keep on schedule and on cost.
+ Ensures that production processes and procedures are in compliance with regulations.
+ Maintains records and reporting systems for coordination of manufacturing operations.
+ Maintains strict confidentiality of sensitive information.
+ Performs other duties as assigned.
+ Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company.
+ Expected to work in a safe manner in accordance with established operating procedures and practices.
+ Other duties as needed.
We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply.51434
**Job Qualifications:**
+ Typically requires a bachelors in engineering or a related technical field as well as five or more years of manufacturing engineering experience. May substitute equivalent experience in lieu of education.
+ Must have a general understanding of manufacturing engineering concepts, principles, and theory with technical experience demonstrating the application of those concepts while ensuring safety and regulatory compliance.
+ Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment and organize work assignments to meet established timetables.
+ Good communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team.
+ Must be able to work extended hours as required.
+ Ability to obtain and maintain secret level clearance is desired.
**Salary:** $81,080 - $141,650 **Travel Percentage Required** 0 - 25 **Relocation Assistance Provided** Not Provided **US Citizenship Required?** Yes **Clearance Required?** Desired **Clearance Level** Mid-Level (3-7 years) **Workstyle** Onsite
General Atomics is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity/Affirmative Action Employer and will consider all qualified applicants for employment without regard to race, color, religion, religious creed, ancestry, gender, pregnancy, sex, sexual orientation, transitioning status, gender identity, gender expression, national origin, age, genetic information, military and veteran status, marital status, medical condition, mental disability, physical disability, or any other basis protected by local, state, or federal law. EEO is the law. We also prohibit compensation discrimination under all applicable laws. To learn more visit Notices.pdf. U.S. Citizenship is required for certain positions.

**Manufacturing Associate (Night Shift)**
**Position Summary:**
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
The Boston-area facility is Catalent's global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest Good Manufacturing Practices (CGMP) unit of its kind for DPI in North America.
Catalent Pharma Solutions in Boston is hiring a Manufacturing Associate. The Manufacturing Associate performs routine and complex operations for the GMP production of pharmaceutical products. This individual operates in accordance with environmental, health, safety, and cGMP guidelines. This individual is responsible for the hands-on execution of production activities as they relate to spray drying operations of manufactured products.
**This is a full-time, on-site, hourly role. Work schedule will be a 7-day rotating 12-hour schedule from 6:00 p.m. to 6:00 a.m. Week 1 will be 48 hours over 4 days, and week two will be 36 hours over 3 days (often referred to as a Pitman Schedule). Overtime and Holiday pay will be included.**
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.**
**The Role:**
+ Performs Clean-In-Place, Clean-Out-of-Place, and equipment sanitization
+ Operates and monitors manufacturing equipment for the production of clinical and commercial pharmaceutical products under minimal supervision
+ Executes routine and complex production processes
+ Troubleshoots manufacturing equipment in conjunction with supporting functional groups to resolve issues and optimize process; Performs inspection of equipment and documents; Receives and distributes supplies in the manufacturing area
+ Provides feedback to manager on recommendations for procedural and process improvements
+ Utilizes process knowledge to influence positive change during the review and revision of Standard Operating Procedures (SOPs)
+ Participates in continuous improvement activities and projects as needed
+ All other duties as assigned
**The Candidate:**
+ A high school diploma or equivalent combined with five (5) years of experience, OR a Biotechnology Certificate or Associate's Degree in science related field combined with three (3) years of experience is required. A Bachelor's Degree in Physical or Chemical Sciences (life sciences) or related Engineering field, and one (1) year of experience is preferred
+ Experience with operating automated manufacturing control systems is preferred
+ Experience utilizing parts washers and autoclaves for the preparation of manufacturing and/or laboratory equipment
+ Critical understanding of the importance of documentation and data traceability
+ Extensive familiarity with executing Standard Operating Procedures in a manufacturing or assembling environment, preferably in the pharmaceutical industry
+ Must have experience with Microsoft Office Suite. Strong working knowledge of Good Documentation and current Good Manufacturing Practices
+ Demonstrated ability to perform product and/or process investigations preferred
+ Physical requirements: Individual may be required to sit, stand, walk regularly, use hands regularly, and occasionally lift up to 50 pounds
**Why you should join Catalent:**
+ Defined career path and annual performance review and feedback process
+ Diverse, inclusive culture
+ Positive working environment focusing on continually improving processes to remain innovative
+ Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
+ 152 Hours + 8 paid holidays
+ Several Employee Resource Groups focusing on D&I
+ Dynamic, fast-paced work environment
+ Community engagement and green initiatives
+ Generous 401K match
+ Company match on donations to organizations
+ Medical, dental and vision benefits effective day one of employment
+ Tuition Reimbursement - Let us help you finish your degree or start a new degree!
+ WellHub program to promote overall physical wellness
+ Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

Job Title: Manufacturing Engineer Job Description
As a Manufacturing Engineer, you will play a crucial role in ensuring adherence to safety and quality requirements, including compliance with Quality Management Systems, Environmental Management Systems, FDA regulations, and other regulatory standards. You will be responsible for creating and implementing lean processes in a cellular environment, utilizing methods such as CNC turning and milling, laser etching, welding, polishing, cleaning, assembly, and inspection. Additionally, you will define, produce, and implement documents like standard work and process work instructions.
Responsibilities
+ Identify, develop, justify, and execute detailed project plans for engineering work with minimal supervision.
+ Launch new products effectively in a contract manufacturing environment.
+ Investigate, develop, and implement new process technologies.
+ Communicate complex issues successfully with customers and internal team members.
+ Create, review, and approve engineering drawings, equipment layouts, change orders, and specifications.
+ Develop tooling, fixtures, and equipment used in manufacturing to optimize productivity and cost.
+ Own and manage CAPAs pertaining to areas of responsibility.
+ Collaborate with development, programmers, machinists, and suppliers to evaluate designs for manufacturability and cost reduction.
+ Create and execute validation protocols, processes, and material evaluations.
Essential Skills
+ Strong background in CNC operations.
+ Experience in project management.
+ Medical device industry experience is highly preferred.
+ Experience specific to metals machining can supersede a degree.
+ Expertise in manufacturing processes and machining.
+ Design skills.
Additional Skills & Qualifications
+ 7+ years of applicable engineering experience.
+ Lean or Six Sigma certification preferred.
+ Strong problem-solving skills.
+ Ability to provide solid rationale and justification for process improvement change requests.
+ Lean manufacturing and new product development or launch support experience is highly desirable.
+ Understanding of metals machining, processing, and polishing is strongly preferred.
+ Ability to work in a team environment.
+ Strong written and oral communication skills.
Work Environment
The work environment is a combination of office and manufacturing floor settings. This role requires engagement with cutting-edge technology in the growing Medtech world.
Job Type & Location
This is a Contract position based out of Hudson, New Hampshire.
Pay and Benefits
The pay range for this position is $40.00 - $70.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Hudson,NH.
Application Deadline
This position is anticipated to close on Oct 24, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

**Engineer, Manufacturing**
**Position Summary**
This key role will be reporting to the Engineering Manager and will have the responsibility and authority to develop, introduce and improve highly capable manufacturing processes to produce components for medical instruments and aerospace applications. Scope includes but will not be limited to machining, moulding assembly, finishing and packaging operations.
**Principle Responsibilities**
+ Develops and implements optimized, highly capable, and cost-effective manufacturing processes and inspection methods, in accordance with product specifications and quality standards.
+ Recommends and implements improvements to production processes, assembly methods and controls by utilizing Lean Manufacturing and Six Sigma tools.
+ Collaborates with Quality Engineering for product tooling, gauging and fixtures design to ensure production methods are robust in support to achieving zero defects, reducing cost of poor quality and implement standard work.
+ Supports creation of PFMEAs and control plans.
+ Estimates resource requirements, production times, and relative costs to provide data for operational decision-making.
+ Documents and qualifies manufacturing and inspection methods.
+ Assists with justifications for capital expenditures.
+ Works closely with manufacturing departments to develop, coordinate, and implement technical training for employees.
+ Provides engineering support to the production department to troubleshoot and resolve technical problems to ensure On Time Delivery to customers as well as improving productivity.
+ Leads Root Cause Analysis for non-conformances and Corrective Actions (CAPA).
+ Leads IQ/OQ/PQ and other process validations activities.
+ Leads projects for Lean Initiatives.
+ Performs other related duties as assigned.
**Qualification Requirements**
**Credentials/Experience:**
+ Bachelor's degree in industrial engineering, or related Engineering field or Manufacturing
+ Minimum 3 years' experience in a manufacturing machining environment preferably in sheet metal fabrication or plastic environment as well as assembly using state-of-art manufacturing processes including cellular manufacturing and Demand Flow Technology or equivalent combination of education and experience.
**Knowledge, Skills, and Abilities:**
+ Demonstrated engineering experience in a high precision machine shop and/or assembly environment.
+ Experience in medical devices manufacturing is highly preferred.
+ Experience and demonstrated proficiency in the use of Mastercam, SolidWorks, CREO/ProE or other CAD/CAM software.
+ Knowledge of blueprint reading, and GD&T required.
+ Ability to develop CNC programs desired.
+ Secondary process experience (welding, polishing, electro-polish, passivation, assembly) desired.
+ Experience in fixture design and tooling selection.
+ Strong statistical analysis background preferred.
+ Highly knowledgeable of lean techniques and six sigma tools with a Green Belt certification being a plus.
+ Technical skills in manufacturing processes and methods including flow, layout, and production equipment required.
+ Effective at planning, prioritizing, and organizing own work and activities.
+ Experience with quality control systems and documentation.
+ Excellent communication skills and self-motivated.
+ Team player with entrepreneurial attitude.
+ Problem solving and root cause analysis experience.
**Other Requirements**
**Work Environment**
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
**Physical Requirements**
While performing the duties of this job, the employee could be required to stand.  The employee could frequently be required to walk; use hand to finger, handle, or feel; reach with hands and arms and talk or hear. The employee could be required to sit; climb or balance and stoop, kneel, crouch, or crawl.   The employee could occasionally lift and or move up to 50 pounds. Specific vision abilities required by the job could include close vision, distance vision, peripheral vision, and ability to adjust focus. 
**Travel Requirements**
N/A
**Americans with Disabilities Act (ADA):** Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
_The statements herein are intended to describe the general nature and level of work being performed by employees and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the Company._

Job Description

Job Description

At Parallel Fluidics, we are building infrastructure to power the next generation of life science tools. In this role, you will work with the manufacturing team to fabricate microfluidic devices using our custom-built equipment, CNC machining centers, and inspection systems. Operators play a key role in the success of our rapidly evolving manufacturing projects. Please apply if you are excited to join a fast-paced environment at a seed-stage startup.

Responsibilities :

• Fabricate microfluidic devices using the Parallel manufacturing process

• Operate CNC machining centers

• Operate custom automation equipment

• Inspect devices against specifications

• Track progress and present results during fabrication team meetings

• Record detailed notes of observations during fabrication

Qualifications

• Hands-on assembly and fabrication skills

• Experience operating manufacturing equipment

• Attention to detail

• Excellent communication skills

We value diversity of all kinds and are committed to building a diverse and inclusive workplace where we learn from each other. We are an equal-opportunity employer and welcome people of all different backgrounds, experiences, and perspectives.

The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.

Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.

What you’ll get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Compensation programs that recognize high performance.

• Medical, dental and vision insurance.

The full list of our global benefits can be also found on .

What you’ll do:

• Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.

• Lead and develop the manufacturing team to meet business needs and career goals.

• Support the timely and complete delivery of clinical and commercial materials.

• Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.

• Maintain manufacturing areas to the highest cleanliness and 6S standards.

• Support technology transfer activities and ensure timely goal achievement.

• Establish methods and procedures for attaining specific goals.

What we’re looking for:

• BS degree preferred significant experience may be considered in lieu of degree.

• Minimum 5 years related experience with a degree or 8 years without.

• Proven experience in biological GMP manufacturing operations.

• Strong leadership and team development skills.

• Ability to coordinate complex projects and ensure timely delivery.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.

Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.

What you’ll get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Compensation programs that recognize high performance.

• Medical, dental and vision insurance.

The full list of our global benefits can be also found on .

What you’ll do:

• Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.

• Lead and develop the manufacturing team to meet business needs and career goals.

• Support the timely and complete delivery of clinical and commercial materials.

• Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.

• Maintain manufacturing areas to the highest cleanliness and 6S standards.

• Support technology transfer activities and ensure timely goal achievement.

• Establish methods and procedures for attaining specific goals.

What we’re looking for:

• BS degree preferred significant experience may be considered in lieu of degree.

• Minimum 5 years related experience with a degree or 8 years without.

• Proven experience in biological GMP manufacturing operations.

• Strong leadership and team development skills.

• Ability to coordinate complex projects and ensure timely delivery.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.