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Project Manager Biotech Jobs in Manchester, NH (NOW HIRING)

In collaboration with validation management, the engineer provides guidance to internal project ... Technical understanding of pharmaceutical/biotechnology unit operations. * Ability to evaluate ...

In collaboration with validation management, the engineer provides guidance to internal project ... Technical understanding of pharmaceutical/biotechnology unit operations. * Ability to evaluate ...

Director, Validation

Bedford, NH · On-site

$120 - $160/hr

... or Biotechnology industry, required. * Sound industry knowledge of pharmaceutical and medical ... Strong experience with project and people management, particularly for large validation projects or ...

... scope projects with site and regional impact - Build and execute productivity plans through ... biotech, electronics, energy, instrumentation, machinery, defense/aerospace, medical, cosmetics ...

... the biotechnology, medical device or pharmaceutical industry. * Strong understanding of technical project management, Good Engineering Practices, reliability, and Lean Principles * GMP and non-GMP ...

... the biotechnology, medical device or pharmaceutical industry. * Strong understanding of technical project management, Good Engineering Practices, reliability, and Lean Principles * GMP and non-GMP ...

... the biotechnology, medical device or pharmaceutical industry. * Strong understanding of technical project management, Good Engineering Practices, reliability, and Lean Principles * GMP and non-GMP ...

Showing results 21-40

Project Manager Biotech information

See Manchester, NH salary details

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$74

How much do project manager biotech jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for project manager biotech in Manchester, NH is $45.10, according to ZipRecruiter salary data. Most workers in this role earn between $39.13 and $49.47 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

What are popular job titles related to Project Manager Biotech jobs in Manchester, NH?

For Project Manager Biotech jobs in Manchester, NH, the most frequently searched job titles are:

What job categories do people searching Project Manager Biotech jobs in Manchester, NH look for?

The top searched job categories for Project Manager Biotech jobs in Manchester, NH are:

What cities near Manchester, NH are hiring for Project Manager Biotech jobs?

Cities near Manchester, NH with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Manchester, NH as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $93,812 per year, or $45.1 per hour.

Associate Director, Research & Development

Advanced Regenerative Manufacturing Institute Inc

Manchester, NH • On-site

Full-time

Re-posted 5 days ago


Job description

Overview
The Advanced Regenerative Manufacturing Institute (ARMl)IBioFabUSA is a Member-based non-profit, member-driven, public-private partnership with a mission to advance the bioeconomy and transform the future of human health. ARMI provides technical and wrap-around commercialization services to companies seeking to advance technologies that will contribute to this impact.
The Impact That You Will Make
ARMI is seeking an independent, self-starter with experience overseeing diverse research teams including analytical and early-stage process development focused on advancing cell therapies. The successful candidate will be responsible for oversight of R&D activities, management of personnel to ensure milestones and timelines are met, and collaboration with leadership to develop study plans and hypotheses. This individual will lead a team of scientists and lab technicians to develop early phase manufacturing processes and analytical assays as part of grant programs, for internal transfer, or in collaboration with external parties. This role requires particularly strong attention to detail, a deep understanding of analytical tests, extensive experience with stem cell biology, and the ability to think outside the box to solve problems creatively and proactively. The ideal candidate will have experience with hPSCs, cell and tissue engineering, flow cytometry, RNASeq, assay development, ELNs, SOP drafting, root-cause analysis, and other documentation.
Your Role
Leadership and Oversight
  • Lead daily R&D operations/tasks.
  • Ensure team compliance with GLP and safety standards.
  • Coach team members on root-cause analysis, documentation, and CAPA.
  • Collaborate with cross-functional teams including Quality, Facilities, and Project Management.
  • Manage multiple projects simultaneously and confidentially while meeting critical timelines and deliverables.
  • Work with management to develop robust, well controlled, hypothesis driven research.
  • Support internal tech transfer and client interactions as needed.
  • Manage external communications on projects as needed.

Process Execution & Documentation
  • Conduct technology transfers within ARMI's facility.
  • Draft and review/approve accurate SOPs, technical documentation, ELN entries, and detailed reports as needed.
  • Monitor research progress through experimental design and data analysis.
  • Troubleshoot issues, perform root cause analysis, and implement corrective actions.

Instrumentation & Maintenance
  • Collaborate with Operations, service engineers, and vendors for process equipment, calibration, preventative maintenance, optimization, and upgrades.
  • Ensure proper training of laboratory personnel on process and safety procedures.

Your Skills and Experiences
Education & Experience
  • Biotechnology, Biology, Biochemistry, or related life science degree. PhD with 4-6 years of experience in human stem cell biology, tissue engineering, and/or analytical assay development.
  • Familiarity with phase appropriate GMP and relevant FDA regulations and requirements.
  • Demonstrated experience leading teams and cross-functional interactions.

Technical Skills
  • Extensive cell biology experience
  • Experience with process equipment including a variety of cell culture technologies from flasks to stirred tank reactors, counterflow and continuous centrifugation, etc.
  • Experience with ELN, data analysis software (e.g., GraphPad, JMP), and statistical methods (e.g. ANOVA).
  • Familiarity with RNASeq or other sequencing modalities and flow cytometry
  • Familiarity with Phase appropriate application of regulations
  • Familiarity with project management tools and techniques

Professional Qualities
  • Commitment to quality, scientific integrity, and company mission
  • Strong analytical and proactive problem-solving skills with a strong attention to detail
  • Excellent written and verbal communication abilities
  • Ability to work independently and manage competing priorities
  • Team-oriented mindset with collaborative cross-functional approach

Working Conditions
  • BSL2 and cleanroom laboratory environment with exposure to biologics, chemical reagents, and analytical instruments
  • Overtime, weekend, and holiday coverage may be required
  • Occasional overtime may be required to meet project deadlines
  • Some travel may be required for conferences, training, or client meetings

By applying, I understand that any offer of employment is contingent upon the successful completion of a background check, in accordance with applicable laws.