Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
... management of disease, and give back to our communities through philanthropy and volunteerism. We ... The Sr. Director HSE is responsible for the productivity and development of the HSE employees ...
... management of disease, and give back to our communities through philanthropy and volunteerism. We ... The Sr. Director HSE is responsible for the productivity and development of the HSE employees ...
Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
Facilitate management of reusable parts include use of the parts washer and autoclave where ... Author, review, and execute GMP documentation-including Standard Operating Procedures (SOPs), Work ...
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 ...
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 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 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 ...
... production footprint. * Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... Whatwe'relooking for: * Experience: 10+ years of direct, job-related experience in GMP ...
... production footprint. * Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... Whatwe'relooking for: * Experience: 10+ years of direct, job-related experience in GMP ...
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 ...
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.
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.
... production footprint. * Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... Experience: 10+ years of direct, job-related experience in GMP manufacturing and extensive early ...
... production footprint. * Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... Experience: 10+ years of direct, job-related experience in GMP manufacturing and extensive early ...
... production footprint. Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... What we're looking for: Experience: 10+ years of direct, job-related experience in GMP ...
... production footprint. Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... What we're looking for: Experience: 10+ years of direct, job-related experience in GMP ...
... production footprint. * Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... Experience: 10+ years of direct, job-related experience in GMP manufacturing and extensive early ...
... production footprint. * Budget & Schedule Governance: Manage, forecast, and reconcile the $25M USD ... Experience: 10+ years of direct, job-related experience in GMP manufacturing and extensive early ...
QC Supervisor (Day Shift)
Portsmouth, NH · On-site
... GMP-regulated environment. * Ensure laboratory activities support manufacturing schedules, product ... Strong performance management skills, including coaching, mentoring, and accountability.
QC Supervisor (Day Shift)
Portsmouth, NH · On-site
... GMP-regulated environment. * Ensure laboratory activities support manufacturing schedules, product ... Strong performance management skills, including coaching, mentoring, and accountability.
QC Supervisor (Day Shift)
Portsmouth, NH · On-site
... GMP-regulated environment. * Ensure laboratory activities support manufacturing schedules, product ... Strong performance management skills, including coaching, mentoring, and accountability.
QC Supervisor (Day Shift)
Portsmouth, NH · On-site
... GMP-regulated environment. * Ensure laboratory activities support manufacturing schedules, product ... Strong performance management skills, including coaching, mentoring, and accountability.
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 ...
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 ...
Gmp Production Manager information
See Rochester, NH salary details
$28.9K - $36.4K
2% of jobs
$36.4K - $43.9K
6% of jobs
$43.9K - $51.4K
11% of jobs
$54.9K is the 25th percentile. Wages below this are outliers.
$51.4K - $58.9K
13% of jobs
The median wage is $66K / yr.
$58.9K - $66.5K
19% of jobs
$66.5K - $74K
19% of jobs
$76.8K is the 75th percentile. Wages above this are outliers.
$74K - $81.5K
13% of jobs
$81.5K - $89K
7% of jobs
$89K - $96.5K
4% of jobs
$96.5K - $104.1K
3% of jobs
$104.1K - $111.6K
2% of jobs
$28.9K
$69.4K
$111.6K
How much do gmp production manager jobs pay per year?
What is a GMP Production manager?
What are the key skills and qualifications needed to thrive as a GMP Production manager?
What are some common challenges faced by GMP Production managers, and how can they be addressed?
What is the difference between Gmp Production Manager vs Gmp Quality Assurance Manager?
| Aspect | Gmp Production Manager | Gmp Quality Assurance Manager |
|---|---|---|
| Primary Focus | Overseeing manufacturing processes to ensure compliance with GMP standards | Ensuring products meet quality and safety standards through audits and testing |
| Required Credentials | Typically requires a degree in life sciences or engineering, GMP training | Similar credentials, often with additional QA certifications |
| Work Environment | Manufacturing facilities, production lines | Laboratories, quality control departments |
| Industry Usage | Pharmaceutical, biotech, and medical device manufacturing | Same 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?
What cities near Rochester, NH are hiring for Gmp Production Manager jobs?
Cities near Rochester, NH with the most Gmp Production Manager job openings:

Senior Production Support, Biotechnologist
Portsmouth, NH • On-site
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
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.
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