290 Manufacturing jobs in Newburyport
Manufacturing Technician
Posted 11 days ago
Job Viewed
Job Description
Job Description
Are you looking for a unique opportunity to be a part of something great? Want to join a 20,000-member team that works on the technology that powers the world around us? Looking for an atmosphere of trust, empowerment, respect, , and communication? How about an opportunity to own a piece of a multi-billion dollar (with a B!) global organization? We offer all that and more at Microchip Technology, Inc.
People come to work at Microchip because we help design the technology that runs the world. They stay because our culture supports their growth and stability. They are challenged and driven by an incredible array of products and solutions with unlimited career potential. Microchip's nationally-recognized Leadership Passage Programs support career growth where we proudly enroll over a thousand people annually. We take pride in our commitment to employee development, values-based decision making, and strong sense of community, driven by our Vision, Mission, and 11 Guiding Values; we affectionately refer to it as the Aggregate System and it's won us countless awards for and workplace excellence.
Our company is built by dedicated team players who love to challenge the status quo; we did not achieve record revenue and over 30 years of quarterly profitability without a great team dedicated to empowering innovation. People like you.
Visit our careers page to see what exciting opportunities and company perks await!
Job Description:
- Perform mechanical and electrical assembly of components, modules, and systems.
- Follow established procedures for assembly, test, and repair tasks.
- Incorporate engineering changes and upgrades, including rework of field-returned units.
- Assemble printed circuit boards (PCBAs) using through-hole and surface mount techniques.
- Conduct top-level system integration of PCBAs, modules, subassemblies, and housings.
- Perform soldering, wiring/cabling, connector installation, bonding, and de-soldering of components.
- Apply UV-curable epoxies and conformal coatings, including masking and coating of boards.
- Operate reflow soldering equipment and process ovens for curing, cleaning, and coating.
- Perform related tasks and other duties as assigned to support production goals and team objectives.
Requirements/Qualifications:
Required Qualifications:
- 2-5 years of experience in electronics or mechanical assembly and testing with a proven track record.
- Ability to multi-task and stay organized in a fast-paced, high-volume production environment.
- Comfortable working with cross-functional teams.
- Detail-oriented, especially when handling documentation and paperwork.
Qualifications:
- Experience in a related field, particularly with high-precision timing and test measurements.
- J-STD-001 Certification
- J-STD-001 Space Addendum Certification
Schedule:
- M-F, 7am-3:30pm (some flexibility)
Benefits:
To reflect and honor how essential our team is, they have access to all the following benefits:
- 2 weeks of Vacation AND 1 week of Personal (60-day waiting period to use)
- 40 hours of sick time (90-day waiting period to use)
- 10 Paid Holidays
- Quarterly Bonuses
- Restricted Stock Units & Employee Stock Purchase Plans
- Medical, Dental, Vision, and Legal Benefits on Day 1
- 401k & Company Match
- Tuition Reimbursement
U.S. Export Controls Requirements: This job requires access to technology, materials, software or hardware that is controlled by the export laws of the United States. Candidates are required to provide proof of either US citizenship, Permanent US or classification as a protected individual as defined in 8 USC 1324b (a) (3).
Travel Time:
No Travel
Physical Attributes:
Carrying, Crouching, Feeling, Foot Controls, Handling, Hearing, Kneeling, Lifting, Noise and/or vibration, Other, Pulling, Pushing, Reaching, Seeing, Talking, Works Alone, Works Around Others
Physical Requirements:
Carry 15lbs,Sit 40%, standing 40%, walking 20% able to lift 15lbs
Microchip Technology Inc is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to , , , , , religion, , , protected Veteran status, , or any other characteristic protected by law.
For more information on applicable equal employment regulations, please refer to the Know Your Rights: Workplace Discrimination is Illegal Poster.
To all recruitment agencies : Microchip Technology Inc. does not accept unsolicited agency resumes. Please do not forward resumes to our recruiting team or other Microchip employees. Microchip is not responsible for any fees related to unsolicited resumes.
Manufacturing Technician
Posted 25 days ago
Job Viewed
Job Description
Manufacturing Technician
Responsible for supporting the Design, Quality, Manufacturing Engineering, and the Materials Organization in the development & assembly of new and existing products. Manufacturing technician will be responsible for a wide array of assembly responsibilities for a diverse set of aerospace sensors.
How you will do it
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Actively participates in the development, implementation and application of processes (assembly and test) for mechanical, electromechanical, and electronic instruments
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Interface directly with Design, Quality, and Manufacturing Engineering assisting with the development and documentation of new product, associated processes, fixtures, tooling and equipment.
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Capable to build qualification and first build products from sketches and detailed work instruction documentation. Performs manufacturing operations as required by verbal instruction, engineering drawings, manufacturing or quality documents and other standards.
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Proactively support opportunities to improve new and existing manufacturing process, fixtures, tooling and equipment. Support may be in the form of suggestions and/or active participation with engineering teams focused on process improvement and Operational Excellence initiatives utilizing formal tools such as six sigma, lean manufacturing, 5S, Kaizen and others.
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Legacy product and production runs. Perform all manufacturing tasks (fabrication, assembly and test) required to support on-going production at this site.
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Support product transitions. Support the preparation of product, equipment, fixtures, tooling, related documentation and processes for transitions to other AMETEK manufacturing sites.
Preferred Skills/Qualifications
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High School Diploma
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5-7 years experience in a manufacturing setting
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Ability to read, interpret, and understand requirements specified on engineering drawings, sketches, manufacturing instructions, characteristic cards, routings, pick-lists, packing specifications, customer instructions and other means to communicate operational requirements
Due to contractrats with the United States Government, Candidates must be a US citizen or Green Card holder.
Why work at AMETEK?
-
Competitive Compensation & Holiday Pay
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Great Health Benefits, and 401(k) plans
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Paid Time Off (PTO) per year, amount depending on level
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Less red tape - we have an environment that supports the entrepreneurial spirit
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Fun & challenging culture while still providing work/life balance for our employees
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Fast growth opportunities and quicker career development for the right candidate
Mentors to help you grow both personally and professionally.
Compensation
Employee Type: Hourly
Salary Minimum: $40,000
Salary Maximum: $5,000
Incentive: No
Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location.
For more information on AMETEK's competitive benefits, please click here.
AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over 7.0 billion.
AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers' most complex challenges. We employ 21,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK (NYSE:AME) is a component of the S&P 500. Visit for more information.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call .
Nearest Major Market: Boston
Manufacturing Engineer
Posted 15 days ago
Job Viewed
Job Description
Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins.
**Job Description**
**Job Summary:**
Work as a member of the manufacturing engineering team on complex projects; design, simulate, and implement molding machinery and processes; construct equipment and fixtures, and analyze production processes to assess automation's best applications. Work with multi-disciplinary team to setup, qualify, and maintain a new molding-based production line. Work to document and improve our molding processes. Experience with Encapsulation molding, transfer molding, compression molding, and/or potting preferred.
**Detailed Description:**
+ Developing and maintaining clear and accurate documentation of molding equipment or processes
+ Assists in the procurement and installation of equipment and all other duties assigned
+ Works closely with production and engineering by communicating and facilitating recommendations and design changes as applicable
+ Perform any special assignment in or outside the department when requested
+ Determine problem resolutions and implement improvements
+ Evaluate manufacturing processes and workflows to identify opportunities for improvement
+ Developing and implementing cost-saving measures and quality control systems
+ Ensuring Manufacturing processes and equipment comply with safety standards
+ Participate in cross-functional meetings to ensure collaboration
**Education and Experience:**
+ BS in Electrical Engineering, Mechanical Engineering, Manufacturing Engineering a must
+ Minimum of 2 years hands on practical experience supporting and designing molds and molding systems
+ Minimum of 2 years hands on practical experience in a production and/or assembly environment
+ Equipment trouble shooting skills - you will often need to debug or trouble shoot an existing system
+ Communication skills- will need to be able to explain novel and complex ideas to stakeholders of all levels and within multidisciplinary teams.
+ Problem Solving and creative thinking
+ Flexibility and Adaptability
+ Must have knowledge and experience in Lean and/or Sigma
+ Desired knowledge of Project Management, Risk Assessment, and Design of Experiments
#DGO
Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions.
Teledyne is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other characteristic or non-merit based factor made unlawful by federal, state, or local laws.
You may not realize it, but Teledyne enables many of the products and services you use every day **.**
Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
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.
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.
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GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
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.
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.