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Biotech Product Manager Jobs in Raleigh, NC (NOW HIRING)

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Excellent communication, stakeholder management, and cross-functional collaboration skills.

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Change Control * Deviation Management * Thorough understanding of cGMP regulations, FDA ...

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Change Control * Deviation Management * Thorough understanding of cGMP regulations, FDA ...

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Biotech Product Manager information

See Raleigh, NC salary details

$50.1K

$155K

$191.5K

How much do biotech product manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for biotech product manager in Raleigh, NC is $154,954.00, according to ZipRecruiter salary data. Most workers in this role earn between $137,100.00 and $191,500.00 per year, depending on experience, location, and employer.

What is a biotech product manager?

A Biotech Product Manager oversees the development, commercialization, and lifecycle management of biotechnology products. They work at the intersection of science, business, and marketing to ensure a product meets customer needs and regulatory requirements. Responsibilities include market analysis, product strategy, cross-functional team coordination, and communication with stakeholders. They collaborate with R&D, regulatory, sales, and marketing teams to drive product success. Strong scientific knowledge and business acumen are essential for this role.

What does a biotech product manager do?

A typical workweek for a Biotech Product Manager involves a blend of strategic planning, cross-functional meetings, market analysis, and project oversight. You'll regularly collaborate with R&D, regulatory affairs, sales, and marketing teams to ensure product milestones are met and align with business objectives. Time is often spent developing go-to-market strategies, gathering customer feedback, and addressing product or market challenges. This dynamic environment provides opportunities to influence product direction and drive impactful results in an exciting and innovative industry.

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

A successful Biotech Product Manager typically possesses a background in life sciences or a related field, strong project management abilities, and an understanding of product lifecycle management. Familiarity with technical tools such as CRM platforms, regulatory compliance software, and data analytics tools, as well as relevant certifications like PMP or an MBA, are commonly advantageous. Superior communication, leadership, and problem-solving skills help drive cross-functional collaboration and adapt to fast-changing markets. These skills ensure the effective development, launch, and optimization of biotech products in alignment with market and regulatory demands.

What are popular job titles related to Biotech Product Manager jobs in Raleigh, NC?

For Biotech Product Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Biotech Product Manager jobs in Raleigh, NC look for?

The top searched job categories for Biotech Product Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Biotech Product Manager jobs?

Cities near Raleigh, NC with the most Biotech Product Manager job openings:

Infographic showing various Biotech Product Manager job openings in Raleigh, NC as of September 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 54% In-person, and 46% Remote job distribution, with an average salary of $154,954 per year, or $74.5 per hour.

Manufacturing Programs Senior Manager: New Product Introduction (NPI)

Holly Springs, NC • On-site

$150 - $200/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 21 days ago


Job description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

Manufacturing Programs Senior Manager: New Product Introduction (NPI) Live

Let’s do this. Let’s change the world. In this vital role you will communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance Manufacturing plant and Process Development scientific groups. As part of ANC’s Manufacturing Support team, this position is responsible for ensuring new products are successfully introduced into ANC’s biologics manufacturing facility. It is a highly visible role across the site with the core responsibility of driving cross-functional deliverables supporting the tech transfers into the facility. This role will also offer the opportunity to propose, participate, and lead team improvement initiatives to drive improved productivity and scheduling accuracy.

What you will do

Responsibilities:

  • New Product Introduction (NPI) subject matter expert coordinating with Manufacturing, Process Development, Supply Chain, Planning, Facilities and Engineering, Quality, and other teams to introduce new Drug Substance products and/or advanced technologies into the plant using project management tools.
  • Rapid problem-solving capabilities to help the team resolve technical challenges.
  • Leading a team of NPI manufacturing specialists while building a culture that helps staff thrive.
  • Technical expert who leads or participates in projects, ensuring that production documents are accurate and up to date.
  • Support Manufacturing in troubleshooting, problem-solving and RCAs. Support CAPA development to prevent error recurrence.
  • Champions Lean Transformation and OE initiatives, facilitates the drive towards continuous improvement in the plant, and tracks progress on a plant level.
What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The manufacturing professional we seek has a biologics DS manufacturing background with strong cross-functional project management and communication skills as well as the below qualifications.

Basic Qualifications:
  • Doctorate degree and 2 years of biotechnology operations experience
  • Master’s degree in chemistry, biology or engineering & 6 years of biotechnology operations experience or
  • Bachelor’s degree and 8 years of biotechnology operations experience or
  • Associate’s degree & 10 years of biotechnology operations experience or
  • High school diploma / GED & 12 years of biotechnology operations experience
  • AND In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above
Preferred Qualifications:
  • Degree in Chemical Engineering, Industrial Engineering, Biology, or Biochemistry.
  • Excellent cross-functional project management, meeting facilitation, and technical writing skills.
  • Experience in GMP manufacturing operations.
  • Strong technical knowledge of drug substance processing in Cell Culture or Purification (chromatography, filtration, buffer compounding) and a broad understanding of related disciplinary areas in bioprocessing.
  • Ability to organize, analyze and interpret technical data through trend analysis, forecasting, modeling, etc.
  • Ability to effectively communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writing forms.
  • Ability to coach, mentor and/or cross train colleagues within core technical areas.
  • Background in lean manufacturing methodologies and operational excellence.
What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The annual base salary range for this opportunity in the U.S. is provided below.

In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan.
  • Stock-based long-term incentives.
  • Award-winning time-off plans and bi-annual company-wide shutdowns.
  • Flexible work models, including remote work arrangements, where possible.

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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