1

Gmp Production Manager Jobs in Rochester, NH (NOW HIRING)

Ensure that the manufacturing facility is in a continuous state of readiness for production and GMP ... Skills • Able to manage multiple cross-functional teams simultaneously. • Ability to work inter ...

Manager, Operations

Portsmouth, NH · On-site

$105K - $120K/yr

Review production metrics daily and identify trends requiring corrective or preventive action. * Ensure compliance with ISO, FDA, GMP, safety, and quality system requirements * Manage labor ...

Manager, Operations

Portsmouth, NH · On-site

$105K - $120K/yr

Review production metrics daily and identify trends requiring corrective or preventive action. * Ensure compliance with ISO, FDA, GMP, safety, and quality system requirements * Manage labor ...

Manager, Operations

Portsmouth, NH · On-site

$105K - $120K/yr

Review production metrics daily and identify trends requiring corrective or preventive action ... Ensure compliance with ISO, FDA, GMP, safety, and quality system requirementsManage labor ...

Independently make routine GMP-related decisions and collaborate with senior staff or management on ... Awareness of product clearance and line clearance requirements during manufacturing operations.

Independently make routine GMP-related decisions and collaborate with senior staff or management on ... Awareness of product clearance and line clearance requirements during manufacturing operations.

Independently make routine GMP-related decisions and collaborate with senior staff or management on ... Awareness of product clearance and line clearance requirements during manufacturing operations.

... GMP-regulated environment. * Ensure laboratory activities support manufacturing schedules, product ... Strong performance management skills, including coaching, mentoring, and accountability.

... GMP-regulated environment. * Ensure laboratory activities support manufacturing schedules, product ... Strong performance management skills, including coaching, mentoring, and accountability.

... Manager. * Participate in Tier meetings or shift handoffs as needed to communicate quality ... Identify recurring product quality concerns, documentation gaps, GMP observations, or process ...

next page

Showing results 1-20

Gmp Production Manager information

See Rochester, NH salary details

$28.9K

$69.4K

$111.6K

How much do gmp production manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for gmp production manager in Rochester, NH is $69,364.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,800.00 and $78,800.00 per year, depending on experience, location, and employer.

What is a GMP Production manager?

GMP Production Managers are professionals responsible for overseeing manufacturing processes in facilities that follow Good Manufacturing Practice (GMP) regulations. They ensure that all production activities comply with strict quality and safety standards set by regulatory agencies, such as the FDA or EMA. Their duties include supervising staff, managing production schedules, and ensuring documentation is accurate and complete. GMP Production Managers play a critical role in maintaining product quality, minimizing risks of contamination, and ensuring that products meet all legal and regulatory requirements.

What are the key skills and qualifications needed to thrive as a GMP Production manager?

To thrive as a GMP Production Manager, you need expertise in Good Manufacturing Practices (GMP), process optimization, and a background in life sciences or engineering, often supported by a relevant degree and industry experience. Familiarity with quality management systems (QMS), regulatory compliance software, and certifications like Six Sigma or Lean are highly valuable. Strong leadership, problem-solving, and communication skills are essential for managing teams and ensuring cross-departmental collaboration. These skills and qualifications are crucial for maintaining product quality, regulatory compliance, and operational efficiency in a regulated manufacturing environment.

What are some common challenges faced by GMP Production managers, and how can they be addressed?

GMP Production Managers often face challenges such as ensuring strict regulatory compliance, managing complex documentation, and maintaining consistent product quality. These challenges can be addressed by fostering a culture of quality, providing regular training for staff on GMP standards, and implementing robust quality management systems. Additionally, proactive communication with cross-functional teams, such as quality assurance and regulatory affairs, helps to anticipate and resolve issues quickly, supporting smooth production operations.

What is the difference between Gmp Production Manager vs Gmp Quality Assurance Manager?

AspectGmp Production ManagerGmp Quality Assurance Manager
Primary FocusOverseeing manufacturing processes to ensure compliance with GMP standardsEnsuring products meet quality and safety standards through audits and testing
Required CredentialsTypically requires a degree in life sciences or engineering, GMP trainingSimilar credentials, often with additional QA certifications
Work EnvironmentManufacturing facilities, production linesLaboratories, quality control departments
Industry UsagePharmaceutical, biotech, and medical device manufacturingSame industries, focusing on quality assurance processes

While both roles require GMP knowledge and related credentials, the Gmp Production Manager focuses on managing manufacturing operations, whereas the Gmp Quality Assurance Manager emphasizes maintaining product quality through testing and audits. Both roles are essential in GMP-regulated industries and often collaborate closely to ensure compliance and product safety.

Is a Gmp Production Manager a hard job?

A GMP Production Manager is responsible for overseeing manufacturing processes in regulated environments, which requires strong attention to detail, compliance knowledge, and leadership skills. The role can be demanding due to strict quality standards, regulatory requirements, and the need for effective coordination across teams, often involving shift work and certification requirements. Overall, it is considered a challenging but essential position in pharmaceutical and biotech industries.

What cities near Rochester, NH are hiring for Gmp Production Manager jobs?

Cities near Rochester, NH with the most Gmp Production Manager job openings:

Infographic showing various Gmp Production Manager job openings in Rochester, NH as of August 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $69,364 per year, or $33.3 per hour.

Senior Production Support, Biotechnologist

Portsmouth, NH • On-site

Lonza
Biotechnology Research and Development • 10K+ employees

Full-time

Medical, Dental, Vision, PTO

Re-posted 28 days ago


Key responsibilities

  • Lead the technical coordination, staging, and movement of process-critical materials, consumables, and equipment to ensure continuous supply for production.

  • Support production activities by maintaining suite readiness, managing material flow, and directly assisting manufacturing teams during full-scale campaigns.

  • Author, review, and execute GMP documentation to ensure compliance with GDP standards.


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz


Job description

Senior Production Support, Biotechnologist - Large Scale Allogenic Manufacturing

Location: Portsmouth, NH, USA.

Schedule: Monday - Friday, 8:00 AM - 5:00 PM (Standard Business Hours). Note: Flexibility to adjust schedules to support shifting campaign timelines or floor demands may be required.

We are seeking a proactive and highly organized technical professional to join our team in Portsmouth, NH, as a Production Support Biotechnologist II. This specialized role is designed for a candidate with a traditional cGMP biomanufacturing background who wants to focus on the operational staging, material lifecycle management, and equipment readiness that makes production possible. Operating under general supervision, you will ensure that the production suites have a flawless, continuous supply of materials-including single-use bioreactors, specialized raw materials, and processing consumables. While your primary mandate is logistical readiness and material flow, you will maintain the technical baseline necessary to jump onto the manufacturing floor and support production operations directly when campaigns reach full-scale execution.

What will you get?

  • An agile career and dynamic working culture

  • An inclusive and ethical workplace

  • Compensation programs that recognize high performance

  • Medical, dental and vision insurance, as well as PTO and more

  • Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you'll do:

  • Material & Equipment Staging: Lead the technical coordination, staging, and movement of all process-critical materials, consumables, and equipment (including single-use bioreactor assemblies and hardware) to prevent floor delays.

  • Re-usable Parts Management: Facilitate management of reusable parts include use of the parts washer and autoclave where applicable.

  • Weigh & Dispense: Support production of media and buffers by weighing components to be used in media/buffer formulation.

  • Suite Readiness & On-Time Delivery: Support the development and execution of robust suite readiness checklists, ensuring manufacturing teams are fully set up for flawless campaign execution.

  • Cross-Functional Procurement Tracking: Partner with internal supply chain and materials specialists to track purchase requisitions, manage BOM inventories, and monitor deliveries against strict project metrics.

  • Technical Transfer Operational Support: Provide crucial operational and material-flow support during tech transfer milestones, including facility water runs, particle runs, and engineering runs.

  • Documentation Compliance: Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work Instructions (WIs), and material tracking sheets-ensuring total GDP compliance.

  • Direct Manufacturing Assistance: Maintain processing proficiency across core unit operations (e.g., cell growth, harvest, or fill/finish) to seamlessly jump in and directly assist manufacturing teams on the floor as production demand dictates.

  • Quality & EHS Alignment: Manage daily tasks in strict compliance with site safety objectives and cGMP guidelines, actively participating in room clearance, facility sanitization, and the resolution of material-related deviations.

What we're looking for:

  • Experience: 5+ years of experience within a cGMP biological manufacturing or regulated clinical laboratory environment is required.

  • Technical Background: Background identical to a standard manufacturing associate, including an understanding of aseptic techniques, hygienic processing concepts, and basic microbiology principles.

  • Skills: Excellent proactive communication, strong computer literacy, and superior organizational skills required to coordinate complex material requirements across multiple internal departments.

  • Adaptability: Ability to think quickly, draw accurate conclusions, and thrive under the dynamic, shifting priorities of an active pharmaceutical manufacturing asset.

  • Education: High School Diploma or equivalent is required. A Bachelor's Degree in a life sciences discipline (Biology, Biotechnology, Biochemistry, etc.) is strongly preferred.

  • Physical Requirements: Ability to sit, stand, walk the production floor for extended periods, comfortably handle continuous cleanroom gowning protocols, and occasionally lift up to 50 lbs.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.


What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Lonza logo

About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US