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

High Liner Foods

QA Technician

Portsmouth, NH · On-site

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

Tailored Management

QC Analyst 3

Portsmouth, NH

$65.69/hr

... production by contributing to the completion of technical transfer activities. Applies job skills ... Potential previous use of GMP Quality Systems such as TrackWise, LIMS Key Requirements:

Lonza

Biotechnologist Level 2

Portsmouth, NH · On-site

... GMP-regulated environment supporting both clinical and commercial operations. What you will get ... Perform manufacturing operations within cell therapy production areas while maintaining safety ...

Lonza

Biotechnologist Level 2

Portsmouth, NH · On-site

... GMP-regulated environment supporting both clinical and commercial operations. What you will get ... Perform manufacturing operations within cell therapy production areas while maintaining safety ...

TekWissen LLC

Manufacturing Associate

Portsmouth, NH · On-site

$20 - $26/hr

Complete production documentation in written and electronic systems following GMP and GDP standards ... Manage routine administrative tasks, including email communication. * Perform other duties as ...

Lonza

Biotechnologist Level 2

Portsmouth, NH

... GMP-regulated environment supporting both clinical and commercial operations. What you will get ... Perform manufacturing operations within cell therapy production areas while maintaining safety ...

Lonza

Biotechnologist II-Day Shift

Portsmouth, NH · On-site

... GMP-regulated environment supporting both clinical and commercial operations. What you will get ... Perform manufacturing operations within cell therapy production areas while maintaining safety ...

Kellton Tech

QC Analyst III - Portsmouth, NH

Portsmouth, NH · On-site

$35 - $40/hr

In this role, you will act as a key member of the Quality Control department, supporting production ... Quality Systems & Documentation Write and manage Quality Records, including Deviations, CAPAs, and ...

TekWissen LLC

QC Analyst III

Portsmouth, NH · On-site

$25 - $30/hr

TekWissen group is a workforce management provider throughout the USA and many other countries in ... It supports every stage of drug development, from early research to commercial production, and ...

Lonza

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

... final product samples to ensure the safety and quality of drug products. You will perform ... GMP and data integrity standards * Use laboratory systems and software to record and manage data

Lonza

QC Analyst II-Microbial Control

Portsmouth, NH · On-site

$24.50 - $32.75/hr

... final product samples to ensure the safety and quality of drug products. You will perform ... GMP and data integrity standards * Use laboratory systems and software to record and manage data

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All JobsGmp Production JobsGmp Production Manager JobsGmp Production Manager Jobs in Rochester, NH

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:

Gmp Production Manager jobs near you
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.

QA Technician

Portsmouth, NH • On-site

High Liner Foods
Manufacturing • 1 - 5K employees
Learn more about High Liner Foodsexternal

Full-time

Re-posted 18 days ago

Job description

Responsibilities:
  • Verify employee adherence to safe work practices, GMPs, and food safety expectations; promptly communicate unsafe or non-compliant conditions to QA and Operations leadership.
  • Perform assigned quality, food safety, GMP, prerequisite program, and HACCP verification activities according to established procedures and frequencies.
  • Confirm product specifications are signed off by Line Leads and Line Supervisors prior to lines being started.

  • Complete audit, in-process, pre-operational, finished product, and other quality records accurately and on time; ensure required corrections are completed according to cGMP and documentation standards, escalate gaps as appropriate, and maintain records so they are filed, accessible, and archived as required.

  • Conduct product evaluations in accordance with 50CFR.

  • Identify out-of-specification, potentially non-conforming, or questionable products and materials; place product on hold and/or escalate to QA leadership according to site procedures and support timely disposition decisions.

  • Complete daily sanitation and pre-op inspections, using visual and analytical methods such as ATP and protein swabs.

  • Complete daily sensory and organoleptic evaluations and ensure findings are documented clearly, accurately, and escalated when results do not meet expectations.
  • Support R&D trials, plant trials, and first productions by completing assigned quality checks, documenting observations, verifying product and process requirements, and escalating food safety or quality concerns in real time.
  • Provide real-time feedback to manufacturing employees and leaders regarding housekeeping, GMP adherence, product handling, and audit-ready behaviors.

  • Ensure scales and thermometers being used by the manufacturing team are calibrated and function as intended.
  • Update pre-operational findings tracking sheet each day and report findings to QA Supervisor/Manager.

  • Participate in Tier meetings or shift handoffs as needed to communicate quality observations, open issues, holds, trial observations, and follow-up needs.
  • Perform other quality, food safety, sanitation verification, documentation, trial support, and plant support duties as assigned.

Continuous Improvement:
  • Identify recurring product quality concerns, documentation gaps, GMP observations, or process opportunities and communicate them to QA leadership and cross-functional partners.
  • Participate in continuous improvement, corrective action, and problem-solving activities as assigned by providing accurate floor observations and practical input.
  • Support product and process improvement efforts that improve made-right-first-time performance, reduce repeat defects, strengthen audit performance, and reduce customer and consumer complaints.

General:
  • Quarantine or place non-conforming materials on hold according to site procedures, maintain hold identification and documentation, and support QA leadership with investigation and disposition follow-up.
  • Support preparation for and execution of GFSI, customer, regulatory, internal, and GMP audits by maintaining accurate records, following procedures, and supporting timely corrective actions.
  • Provide practical feedback on quality and food safety procedures, job aids, training materials, and forms to improve usability and daily execution.
  • Assist with training and onboarding new Quality Assurance Technicians by demonstrating proper inspection, verification, documentation, escalation, and GMP practices.
  • Maintain the lab and quality workspace in a clean, organized, audit-ready condition and ensure required consumable supplies are available.

Qualifications:
  • High School diploma or GED
  • Associates degree or above preferred, but not required

  • HACCP certification preferred; must be able to complete required HACCP, GMP, food safety, and role-specific training.
  • Strong basic math, measurement, documentation, and practical problem-identification
  • Reliable, detail-oriented, and able to use sound judgment, urgency, and professionalism when completing routine checks or escalating issues.
  • 3+ years prior experience in quality assurance, food handling, food processing, sanitation, laboratory, or manufacturing preferred.
  • Knowledge of GMPs, sanitation requirements, HACCP, allergen control, foreign material prevention, and food safety programs preferred.
  • Demonstrated ability to read, write, and communicate clearly in English, including accurate completion of quality and food safety records.
  • Ability to communicate quality and food safety expectations in a respectful, clear, and effective manner with hourly employees, leads, supervisors, and QA leadership.

  • Must be available for overtime as needed
  • Ability to flex schedule to support business needs.

Working conditions
  • Must work in -44° to 90° Fahrenheit/ -42° to 32° Celsius for short durations.

Plant environment with loud noise, food grade dusts and odors, moving and vibrating
  • machinery, heaving equipment, powered industrial trucks heights, traffic, anhydrous ammonia, oil, electricity.
  • Potentially wet, humid, and icy environment
  • Ability to lift and move cases of product, up to 50lbs

Physical requirements/Allergens
  • Work with allergen containing food materials: Fish, shellfish, tree nuts (including coconut), eggs, wheat, soy, dairy and other sensitizing agents.
  • Standing and walking for long periods on production floor or in laboratory environment.
  • Sitting for computer work, preparation of documents, reports, research and investigations.

Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
AAP/EEO Statement
High Liner Foods (USA), Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, High Liner Foods (USA), Inc. complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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