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:
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:
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:
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:
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GMP Documentation - QC
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$48.25/hr
... biotechnology manufacturing environment. This position is responsible for creating, maintaining, and updating raw-material specifications using a Document Management System (DMS) and Management ...
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Be Seen First
GMP Documentation - QC
Portsmouth, NH · On-site
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Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new ...
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Portsmouth, NH · On-site
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The Data Entry Specialist will play a key role in supporting *'s local and global manufacturing ... High School Diploma or Equivalent 0 3 years of experience in the biotech industry or with data ...
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Principal will lead front end design programming for pharmaceutical and biotechnology manufacturing facilities requiring site survey, space programming and equipment evaluation/selection, economic ...
Principal will lead front end design programming for pharmaceutical and biotechnology manufacturing facilities requiring site survey, space programming and equipment evaluation/selection, economic ...
Principal will lead front end design programming for pharmaceutical and biotechnology manufacturing facilities requiring site survey, space programming and equipment evaluation/selection, economic ...
Principal will lead front end design programming for pharmaceutical and biotechnology manufacturing facilities requiring site survey, space programming and equipment evaluation/selection, economic ...
Biotechnologist I-Night Shift
Portsmouth, NH · On-site
$14 - $17.25/hr
Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs ... Experience (A Plus): Prior experience in a GMP, biotech, or pharmaceutical environment is ...
Biotechnologist I-Night Shift
Portsmouth, NH · On-site
$14 - $17.25/hr
Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs ... Experience (A Plus): Prior experience in a GMP, biotech, or pharmaceutical environment is ...
Biotechnologist I-Night Shift
$14 - $17.25/hr
Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs ... Experience (A Plus): Prior experience in a GMP, biotech, or pharmaceutical environment is ...
Biotechnologist I-Night Shift
$14 - $17.25/hr
Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs ... Experience (A Plus): Prior experience in a GMP, biotech, or pharmaceutical environment is ...
Biotechnology manufacturing background is preferred * Knowledge of cGMP and regulations * Project Management Experience: Presentation, Customer Liaison, Meeting facilitation * Demonstrates ...
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Biotechnology manufacturing background is preferred * Knowledge of cGMP and regulations * Project Management Experience: Presentation, Customer Liaison, Meeting facilitation * Demonstrates ...
Biotechnologist I-Night Shift
Portsmouth, NH · On-site
$14 - $17.25/hr
Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs ... Experience (A Plus): Prior experience in a GMP, biotech, or pharmaceutical environment is ...
Biotechnologist I-Night Shift
Portsmouth, NH · On-site
$14 - $17.25/hr
Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs ... Experience (A Plus): Prior experience in a GMP, biotech, or pharmaceutical environment is ...
Biotechnologist I
Portsmouth, NH · On-site
Job Title: Manufacturing Associate I Location: Portsmouth, NH, (On-site) As a Manufacturing Associate I, you will help produce life-saving therapeutic proteins in a regulated manufacturing ...
Biotechnologist I
Portsmouth, NH · On-site
Job Title: Manufacturing Associate I Location: Portsmouth, NH, (On-site) As a Manufacturing Associate I, you will help produce life-saving therapeutic proteins in a regulated manufacturing ...
Biotechnologist I
Portsmouth, NH · On-site
Job Title: Manufacturing Associate I Location: Portsmouth, NH, (On-site) As a Manufacturing Associate I, you will help produce life-saving therapeutic proteins in a regulated manufacturing ...
Biotechnologist I
Portsmouth, NH · On-site
Job Title: Manufacturing Associate I Location: Portsmouth, NH, (On-site) As a Manufacturing Associate I, you will help produce life-saving therapeutic proteins in a regulated manufacturing ...
The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures ...
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The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures ...
Bachelor's degree in life sciences discipline or equivalent experience * 2-4 years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding ...
Bachelor's degree in life sciences discipline or equivalent experience * 2-4 years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding ...
Bachelor's degree in life sciences discipline or equivalent experience * 2-4 years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding ...
Bachelor's degree in life sciences discipline or equivalent experience * 2-4 years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding ...
Biotechnologist Associate Location: Portsmouth, NH (Onsite) Duration: 12 months contract with ... Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions.
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Biotechnologist Associate Location: Portsmouth, NH (Onsite) Duration: 12 months contract with ... Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions.
Bachelor's degree in life sciences discipline or equivalent experience * 8+ years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding of ...
Bachelor's degree in life sciences discipline or equivalent experience * 8+ years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding of ...
Bachelor's degree in life sciences discipline or equivalent experience * 8+ years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding of ...
Bachelor's degree in life sciences discipline or equivalent experience * 8+ years of experience in a cGMP-regulated pharmaceutical or biotechnology manufacturing environment * Strong understanding of ...
Senior Validation Engineer
Portsmouth, NH · On-site
$35 - $45/hr
Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new ...
Quick apply
Senior Validation Engineer
Portsmouth, NH · On-site
$35 - $45/hr
Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new ...
Biotech Manufacturing information
See Rochester, NH salary details
$12 - $13.88
5% of jobs
$13.88 - $15.76
17% of jobs
$15.99 is the 25th percentile. Wages below this are outliers.
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24% of jobs
The median wage is $18.03 / hr.
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$11
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How much do biotech manufacturing jobs pay per hour?
What is biotech manufacturing?
What are the key skills and qualifications needed to thrive in biotech manufacturing?
What are some common challenges faced in biotech manufacturing, and how can new team members prepare for them?
What is the difference between Biotech Manufacturing vs Biotech Quality Control?
| Aspect | Biotech Manufacturing | Biotech Quality Control |
|---|---|---|
| Credentials | Typically requires a degree in biotech, biology, or chemistry | Similar credentials, often with additional certifications in quality assurance |
| Work Environment | Production floors, laboratories, cleanrooms | Laboratories, testing facilities, quality assurance labs |
| Employer & Industry Usage | Manufacturing plants, biotech companies, pharmaceutical firms | Quality assurance departments within biotech and pharma companies |
| Common Search & Comparison | Biotech Manufacturing vs Biotech Quality Control |
Biotech Manufacturing focuses on producing biotech products, involving process development and production. Biotech Quality Control emphasizes testing and ensuring product quality, often working closely with manufacturing but with a focus on compliance and standards.
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Full-time
Medical, Dental, Vision, PTO
Re-posted 5 days ago
Lonza rating
8.3
Based on 42 frontline employees who took The Breakroom Quiz
25th of 86 rated pharmaceutical
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
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