Biotech & Pharma Jobs in New Hampshire with Green Card Sponsorship
New Hampshire's biotech and pharma sector, anchored by companies like Lonza in Portsmouth and BAE Systems' biopharma divisions, offers Green Card sponsorship opportunities for skilled international workers. The Manchester and Nashua corridors host research, manufacturing, and regulatory roles where employers routinely support permanent residency through EB-2 and EB-3 pathways.
See All Biotech & Pharma JobsOverview
Showing 5 of 164+ Biotech & Pharma Green Card Sponsorship Jobs in New Hampshire jobs


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?


Have you applied for this role?
See all 164+ Biotech & Pharma Green Card Sponsorship Jobs in New Hampshire jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Biotech & Pharma Green Card Sponsorship Jobs in New Hampshire roles.
Get Access To All Jobs
Computer Systems Validation (Analytical) Supervisor
Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
As the Computer Computer Systems Validation (CSV) Supervisor you will lead a team of professionals to deliver validation projects on schedule while ensuring strict adherence to Quality and Data Integrity standards. You will collaborate with Operations Technology (OT), Engineering, and Quality Assurance to support site goals, enhance compliance, and drive on-time, right-first-time performance.
What you will get:
- Competitive salary and comprehensive benefits package.
- Opportunities for career development and advancement.
- Supportive and collaborative team environment.
- Access to cutting-edge technology and tools.
- Commitment to employee well-being and safety.
- Inclusive workplace culture.
- Recognition and reward for your contributions.
Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:
- Provide technical support for the design, operation, and troubleshooting of analytical equipment across departments.
- Lead the planning and execution of equipment-related IQ/OQ/PQ validation plans and process improvements.
- Manage Quality Management System (TW) records, review EDMS documents, and lead risk assessments and change controls.
- Identify quality concerns, engage stakeholders, and drive issues to final resolution.
- Coach and develop staff through performance reviews, career planning, and consistent 1:1 meetings.
- Handle administrative duties, including daily meetings, task assignment, and hiring/onboarding activities.
- Partner with CSV, OT, and other validation teams to ensure site-wide consistency and compliance.
What we are looking for:
- Bachelor’s degree of Science/Engineering is required.
- 5-10 years’ of Computer Systems Validation experience – Manufacturing and QC systems.
- Advanced knowledge of manufacturing operations, Validation principles (process, equipment, systems), and Data Integrity.
- Hands-on experience managing deviations, change controls, and CAPAs within systems like TrackWise.
- Proven ability to lead medium-to-large projects, drive planning/controlling, and utilize tools like RCA, FMEA, and VSM.
- Strong verbal/written communication skills and effective leadership in fostering cross-functional, customer-focused collaboration.
- Expert knowledge of GMP/Safety standards and proficiency in MS Office (Project, Excel, Word, PowerPoint).
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.

Computer Systems Validation (Analytical) Supervisor
Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
As the Computer Computer Systems Validation (CSV) Supervisor you will lead a team of professionals to deliver validation projects on schedule while ensuring strict adherence to Quality and Data Integrity standards. You will collaborate with Operations Technology (OT), Engineering, and Quality Assurance to support site goals, enhance compliance, and drive on-time, right-first-time performance.
What you will get:
- Competitive salary and comprehensive benefits package.
- Opportunities for career development and advancement.
- Supportive and collaborative team environment.
- Access to cutting-edge technology and tools.
- Commitment to employee well-being and safety.
- Inclusive workplace culture.
- Recognition and reward for your contributions.
Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:
- Provide technical support for the design, operation, and troubleshooting of analytical equipment across departments.
- Lead the planning and execution of equipment-related IQ/OQ/PQ validation plans and process improvements.
- Manage Quality Management System (TW) records, review EDMS documents, and lead risk assessments and change controls.
- Identify quality concerns, engage stakeholders, and drive issues to final resolution.
- Coach and develop staff through performance reviews, career planning, and consistent 1:1 meetings.
- Handle administrative duties, including daily meetings, task assignment, and hiring/onboarding activities.
- Partner with CSV, OT, and other validation teams to ensure site-wide consistency and compliance.
What we are looking for:
- Bachelor’s degree of Science/Engineering is required.
- 5-10 years’ of Computer Systems Validation experience – Manufacturing and QC systems.
- Advanced knowledge of manufacturing operations, Validation principles (process, equipment, systems), and Data Integrity.
- Hands-on experience managing deviations, change controls, and CAPAs within systems like TrackWise.
- Proven ability to lead medium-to-large projects, drive planning/controlling, and utilize tools like RCA, FMEA, and VSM.
- Strong verbal/written communication skills and effective leadership in fostering cross-functional, customer-focused collaboration.
- Expert knowledge of GMP/Safety standards and proficiency in MS Office (Project, Excel, Word, PowerPoint).
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.
Job Roles in Biotech & Pharma in New Hampshire
See all 164+ Biotech & Pharma New Hampshire jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Biotech & Pharma New Hampshire roles.
Get Access To All JobsFrequently Asked Questions
Which biotech & pharma companies sponsor Green Card visas in New Hampshire?
Several established employers in New Hampshire have a documented history of sponsoring Green Card petitions for biotech and pharma professionals. Lonza's Portsmouth biologics manufacturing facility, Dartmouth Health's research divisions, and contract development and manufacturing organizations (CDMOs) operating in the Nashua area have filed PERM labor certifications for roles in process development, quality assurance, and regulatory affairs. Sponsorship patterns vary by company size, role type, and current headcount needs.
Which cities in New Hampshire have the most biotech & pharma Green Card sponsorship jobs?
Portsmouth and Nashua concentrate the largest share of biotech and pharma employment in New Hampshire, driven by biomanufacturing facilities and pharma service companies. Manchester, as the state's largest city, also hosts life sciences employers with regulatory and clinical operations. The Lebanon area, near Dartmouth-Hitchcock Medical Center, supports research-oriented roles that may qualify for EB-2 sponsorship, particularly for candidates with advanced degrees.
What types of biotech & pharma roles typically qualify for Green Card sponsorship in New Hampshire?
Roles requiring specialized education and skills are most commonly sponsored. These include bioprocess engineers, analytical chemists, quality control scientists, regulatory affairs specialists, clinical research associates, and bioinformatics professionals. Positions demanding a bachelor's degree or higher in a specific scientific discipline typically qualify under EB-3, while roles requiring a master's or Ph.D., or those demonstrating exceptional merit, may qualify under EB-2 or EB-2 NIW pathways.
How do I find biotech & pharma Green Card sponsorship jobs in New Hampshire?
Migrate Mate lists biotech and pharma positions in New Hampshire where employers have indicated willingness to sponsor Green Card visas. You can filter specifically by Green Card sponsorship and the biotechnology and pharmaceuticals industry to surface relevant openings in cities like Portsmouth, Nashua, and Manchester. Reviewing employer PERM filing history through DOL disclosure data can also help you identify which New Hampshire companies have sponsored international workers in similar roles.
Are there state-specific considerations for Green Card sponsorship in New Hampshire's biotech & pharma industry?
New Hampshire does not have a dedicated state immigration program, so Green Card sponsorship in biotech and pharma follows standard federal PERM labor certification and I-140 petition processes. However, the state's proximity to Boston's life sciences ecosystem means some employers operate across both markets, which can influence where PERM applications are filed and which prevailing wage determinations apply. Candidates should confirm that the sponsoring entity is the specific New Hampshire-based subsidiary or facility.
What is the prevailing wage for Green Card biotech & pharma jobs in New Hampshire?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.
See which biotech & pharma employers are hiring and sponsoring visas in New Hampshire right now.
Search Biotech & Pharma Jobs in New Hampshire