204 Manufacturing jobs in Haverhill

**Job Title: Manufacturing Associate**
**Job Description**
The Manufacturing Associate plays a crucial role in the manufacturing department, performing a variety of mechanical and labor functions within a dynamic manufacturing environment. This position involves setting up and operating various manufacturing equipment such as drills, hand power tools, and test equipment.
**Responsibilities**
+ Set up and operate various manufacturing equipment, including drills and hand power tools.
+ Perform visual quality inspections of parts.
+ Work with paints, adhesives, solvents, and primers.
+ Follow written work instructions and standard operating procedures.
+ Collaborate effectively with the engineering team.
**Essential Skills**
+ Experience in manufacturing using hand tools.
+ Comfortable working in a team environment.
**Additional Skills & Qualifications**
+ High School Diploma (HSD) or General Educational Development (GED).
**Why Work Here?**
Join a company that offers room for growth and the opportunity to work with military products. Experience a supportive work environment where collaboration and professional development are valued.
**Work Environment**
The role is based on the 1st shift, from 6:00 AM to 2:30 PM, offering a structured work schedule in a manufacturing setting. Employees are expected to adhere to safety protocols while handling paints, adhesives, solvents, and primers.
**Job Type & Location**
This is a Permanent position based out of Hudson, New Hampshire.
**Pay and Benefits**
The pay range for this position is $42120.00 - $46280.00/yr.
health dental vision 401k
**Workplace Type**
This is a fully onsite position in Hudson,NH.
**Application Deadline**
This position is anticipated to close on Aug 14, 2025.
**About Aerotek:**
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

**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._

**Description:** You will be a Manufacturing Engineer, responsible for overseeing the production of microwave hybrids, including the design of assembly techniques and materials. Our team is dedicated to delivering high-quality products, and we're looking for a skilled and experienced engineer like you to join our team.
**What You Will Be Doing**
As a Manufacturing Engineer, you will have a deep understanding of all assembly techniques and materials used to produce microwave hybrids, including substrate and die epoxy attach, wire bonding, and other processes.
Your responsibilities will include:
- Understand and apply your experience with J-STD-001 solder assembly, conductive epoxy attach of substrates and semiconductor die, gold wedge and ball-bonding, and seal / hermeticity testing.
- Design the sequence of operations and specify procedures for the fabrication of tooling and other functions that affect product performance.
- Inspect performance of machinery, equipment, and tools to verify their efficiency.
- Investigate hardware failures and initiate corrective action of problems and deficiencies to ensure product quality.
- Ensure processes and procedures are in compliance with regulations.
**Why Join Us**
As a Manufacturing Engineer, you will be part of a team that is dedicated to delivering innovative solutions that make a real difference in global security. You'll work in a dynamic and fast-paced environment, with a team of professionals who share your passion for excellence and precision. If you're looking for a challenging and rewarding role that will help you grow professionally, we encourage you to apply.
We are committed to supporting your work-life balance and overall well-being, offering flexible scheduling options. Learn more about Lockheed Martin's comprehensive benefits package here.
**Further Information About This Opportunity:**
This position is in Chelmsford. Discover more about our Chelmsford, Massachusetts location.
MUST BE A U.S. CITIZEN - This position is located at a facility that requires special access. The selected candidate must be able to obtain a secret clearance. A company-sponsored interim secret is required to start.
**Basic Qualifications:**
- Bachelor's degree from an accredited college in Engineering, Microelectronics, Manufacturing, or related discipline.
- Candidate must have an outstanding work ethic, excellent teaming skills, and ability to multi-task with multiple projects and job tasks.
- Candidate must be self-motivated, customer-focused, proactive, and able to professionally support and quickly adapt to changes in program or customer requirements.
- Candidate must have good verbal and written communication skills as well as excellent interpersonal skills and the ability to interact effectively with management, customers and peers.
- Candidate must be proficient in Microsoft Office applications, particularly Outlook, Excel, Word and PowerPoint.
- Ability to obtain and maintain a Secret level security clearance, which requires U.S. citizenship.
**Desired Skills:**
- Microwave Hybrid manufacturing experience.
- Design of Experiment experience.
- Automated epoxy dispense & component placement or automated wire bonding equipment.
- Lean/Six Sigma certification and/or J-STD-001 certification.
- Knowledge of MRSI, Palomar, Hesse Mechatronics, Delvotec equipment is beneficial.
- Defense industry experience is a plus.
- Experience with Creo, SolidWorks, or CATIA is a plus.
**Security Clearance Statement:** This position requires a government security clearance, you must be a US Citizen for consideration.
**Clearance Level:** Secret
**Other Important Information You Should Know**
**Expression of Interest:** By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match. Should this match be identified you may be contacted for this and future openings.
**Ability to Work Remotely:** Onsite Full-time: The work associated with this position will be performed onsite at a designated Lockheed Martin facility.
**Work Schedules:** Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees. Schedules range from standard 40 hours over a five day work week while others may be condensed. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits.
**Schedule for this Position:** 4x10 hour day, 3 days off per week
**Lockheed Martin is an equal opportunity employer. Qualified candidates will be considered without regard to legally protected characteristics.**
**The application window will close in 90 days; applicants are encouraged to apply within 5 - 30 days of the requisition posting date in order to receive optimal consideration.**
At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work.
With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility.
If this sounds like a culture you connect with, you're invited to apply for this role. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs , and apply for roles that align with your qualifications.
**Experience Level:** Experienced Professional
**Business Unit:** MISSILES AND FIRE CONTROL
**Relocation Available:** Possible
**Career Area:** Manufacturing
**Type:** Full-Time
**Shift:** First

GMP Manufacturing Supervisor - Nights

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.

What we’re looking for:

• 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.

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 Supervisor - Nights

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.

What we’re looking for:

• 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.

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.

GMP Manufacturing Supervisor - Nights

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.

What we’re looking for:

• 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.