191 Manufacturing jobs in Amesbury
Manufacturing Operator
Posted 3 days ago
Job Viewed
Job Description
**Job Title:** Manufacturing Operator
**Location:** Lee
**Pay Range:**
**Shift: 1st**
**What's the Job?**
+ Operate and monitor manufacturing equipment to ensure optimal performance.
+ Perform quality checks on products to maintain high standards.
+ Assist in troubleshooting equipment issues and perform minor repairs.
+ Maintain a clean and organized work environment.
+ Collaborate with team members to improve production processes.
**What's Needed?**
+ High school diploma or equivalent.
+ Previous experience in a manufacturing or production environment preferred.
+ Ability to follow safety protocols and procedures.
+ Strong communication skills and ability to work in a team.
+ Willingness to learn and adapt to new technologies.
**What's in it for me?**
+ Opportunity to work in a fast-paced and rewarding environment.
+ Gain valuable experience in the manufacturing sector.
+ Be part of a supportive and collaborative team.
+ Potential for career growth and advancement.
+ Engage in continuous training and development opportunities.
**Upon completion of waiting period associates are eligible for:**
+ Medical and Prescription Drug Plans
+ Dental Plan
+ Supplemental Life Insurance
+ Short Term Disability Insurance
+ 401(k)
If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!
**About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells**
_ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands -_ **_Manpower, Experis, Talent Solutions, and Jefferson Wells_** _-_ creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.
Manufacturing Engineer
Posted 18 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, program, simulate, and test automated machinery and processes; construct equipment and fixtures, and analyze production processes to assess automation's best use; perform regular maintenance on automation equipment, troubleshooting, repairs, and calibration. Experienced in Automated Electromechanical / Mechatronic equipment in the manufacturing environment including, working with state-of-the-art automation, hands on experience working with various types of automation utilizing robotics, pneumatic, servos, plc's
**Detailed Description**
+ Developing and maintaining clear and accurate documentation of automation equipment or processes
+ Assists in the procurement and installation of equipment and all other duties as assigned.
+ Works closely with production and engineering by communicating and facilitating recommendations and design changes as applicable.
+ Designs fixtures and tooling; evaluates processes for increased through put and trouble shoots issues on products and processes.
+ 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 meet capability and capacity requirements.
+ Researching and developing new processes, new equipment, and new products introduction (NPI).
+ 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
+ Minimum of 2 years hands on practical experience supporting and designing automated systems
+ Minimum of 2 years hands on practical experience in a production and/or assembly environment
+ Excellent computer skills - particularly in programming and software development. Many aspects of the role of an Automation Engineer require the use of a computer
+ Equipment troubleshooting skills - as you will often need to debug or troubleshoot 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. Written communication skills will also be needed for record keeping and documentation.
+ Problem-solving and creative thinking - will be required to troubleshoot problems as they arise and find effective solutions
+ Flexibility & Adaptability - must be able to keep up with latest techniques and technologies as they develop
+ Must have knowledge and experience in Lean and/or Six 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
Open to relocation
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.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
Open to relocation
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.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
Open to relocation
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.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
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.
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.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
Open to relocation
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.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
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.
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.