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Biotech Government Contract Jobs (NOW HIRING)

Kymanox

(Contract) Engineer, PD&C

Boston, MA · On-site

The Kymanox Product Development & Commercialization team is seeking a (Contract) Combination ... small biotech/pharma/med device companies and familiarity with government and private sector ...

New England Lab

Regional Operations Manager

Durham, NC · On-site

... biotech, government, industrial, and medical research facilities in the Carolinas, Mid-Atlantic ... contracts, schedules, cost control, changes, delivery, installation, and closeout. You will ...

Regeneron Pharmaceuticals

... Government Agency (PGA) requirements impacting import and export compliance for biotech products ... You have proven contract drafting skills and the ability to work in a fast-paced, dynamic ...

New England Lab

Regional Operations Manager

Durham, NC · On-site

... biotech, government, industrial, and medical research facilities in the Carolinas, Mid-Atlantic ... Manage cost control, contract status, and profitability by coordinating with accounting and ...

Danaher

Senior Contract Manager

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... S. government contracts (e.g., EPC, construction, or capital equipment agreements) with values ...

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Biotech Government Contract information

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$15

$36

$54

How much do biotech government contract jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for biotech government contract in the United States is $36.34, according to ZipRecruiter salary data. Most workers in this role earn between $26.44 and $43.75 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in a Biotech Government Contract role, and why are they important?

To thrive in a Biotech Government Contract role, you typically need a background in biotechnology or life sciences, experience with regulatory compliance, and familiarity with federal contracting procedures. Knowledge of contract management systems, government procurement tools, and certifications like Certified Federal Contracts Manager (CFCM) are highly valued. Strong analytical thinking, attention to detail, and effective communication skills help manage complex requirements and foster successful stakeholder relationships. These skills ensure compliance, efficient project execution, and the ability to navigate the unique demands of government-funded biotech initiatives.

What are some common challenges faced when managing biotech government contracts, and how can job seekers prepare for them?

Biotech government contract roles often involve navigating complex regulatory requirements, strict reporting deadlines, and the need for meticulous documentation. Job seekers should be prepared to coordinate closely with cross-functional teams—including scientists, legal advisors, and financial analysts—to ensure compliance and successful project delivery. Familiarity with government procurement processes, such as FAR (Federal Acquisition Regulation) guidelines, and strong organizational skills are highly beneficial. Proactively seeking training in contract management and regulatory affairs can help you excel in this dynamic environment.

What is a Biotech Government Contract?

A Biotech Government Contract is a formal agreement between a biotechnology company and a government agency for the provision of products, research, or services in the field of biotechnology. These contracts can cover areas such as pharmaceuticals, medical devices, diagnostics, or research and development projects that address public needs or national interests. The government typically issues requests for proposals (RFPs), and biotech companies bid to fulfill these specifications. Successful contracts can provide crucial funding and foster innovation, but often require strict compliance with regulations and reporting standards.
What cities are hiring for Biotech Government Contract jobs? Cities with the most Biotech Government Contract job openings:
What are the most commonly searched types of Biotech Government jobs? The most popular types of Biotech Government jobs are:
What states have the most Biotech Government Contract jobs? States with the most job openings for Biotech Government Contract jobs include:
What job categories do people searching Biotech Government Contract jobs look for? The top searched job categories for Biotech Government Contract jobs are:
Biotech Government Contract jobs near you
Infographic showing various Biotech Government Contract job openings in the United States as of June 2026, with employment types broken down into 6% Full Time, 16% Part Time, 3% Temporary, and 75% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $75,585 per year, or $36.3 per hour.
(Contract) Engineer, PD&C

(Contract) Engineer, PD&C

Kymanox

Boston, MA • On-site

Contractor

Posted 15 days ago

Job description

Description
Is Kymanox the right fit for you?
You want to make a difference and have an impact...
You enjoy having an influence in your day-to-day work...
You are motivated by working alongside a team filled with
subject matter experts who will help you learn and grow...
You wake up every day and do what you do
because patients deserve better.
If this sounds like you, you've come to the right place.
The Kymanox Product Development & Commercialization team is seeking a (Contract) Combination Product Engineer or Scientist with a strong technical and/or operations background in the pharmaceutical, biotechnology, diagnostics, or medical device industries. Ideal candidates will build on their proven past performance supporting complex product development or life cycle management programs involving drug-device combination products, Class 1/2/3 medical devices, and/or in vitro diagnostics.
This position is hybrid with an average of 3 days of week at a client site.
Job Description:
Utilizes technical expertise and project management skills to support client development projects in the medical device and combination product space.
Basic responsibilities include:
  • Writing technical documentation with minimal direction.
  • Conducting laboratory testing and data analysis.
  • Representing Kymanox and work product in client-facing meetings.
  • Basic project management (i.e., meeting minutes, schedules, correspondence)

Projects may include any of the following technical areas:
  • Creating technical documentation supporting product development efforts, including design and development files and technical files.
  • Technology evaluation, due diligence, and selection.
  • CMO due diligence, evaluation, and client representation.
  • Regulatory submission authorship.
  • Conducting testing activities, including combination product and medical device design verification and human factors testing.
  • Statistical analysis of development and production data.

Aptitude and Skill Set:
  • Versatile and adaptable technical skills
  • Positive attitude, and welcomes new challenges
  • Flexible to be present at client sites and sometimes travel
  • Able to execute activities with minimal supervision, manages time wisely
  • Strong professional presence and presentation skills
  • Extremely detail-orientated and highly organized
  • Excellent written and oral English communication skills
  • Comfortable providing feedback and influencing internal and external stakeholders
  • Emotionally stable and can navigate challenging clients and situations
  • Seasoned soft skills - high EQ and team player
  • Ability to work effectively with remote team members
  • Tackle problems proactively
  • A mindset of innovation and creativity
  • Computer and IT savvy
  • Thrive in a fast-paced, growing, and dynamic work environment
  • Expertly solicit and utilize subject matter expert input
  • Value and understand quality
  • Uncompromised honesty and integrity

Educational Background:
Minimum bachelor's degree in natural sciences (Chemistry, Biology, or similar) or engineering (Chemical, Biomedical, or Mechanical Engineering), or related technical discipline from an accredited institution. Early career master's and Ph.D. level candidates encouraged to apply. Industry certificates in project management (e.g., PMP, CAPM), six-sigma, quality, or regulatory affairs preferred but not required.
Experience:
  • 2-5 years of experience (including advanced degrees) in product development and/or manufacturing in the combination product, medical device, pharmaceutical, biotechnology, and/or diagnostic sectors is required.
  • Demonstrated contributions to complex, multi-disciplinary development programs, pharmaceutical (drug product) development, in vitro diagnostic development, clinical development, or electromechanical systems development is desirable.
  • Experience working at startup companies or small biotech/pharma/med device companies and familiarity with government and private sector funding mechanisms is highly favorable.

Region:
Boston, MA
Travel:
Travel may be necessary to support client work. Periodic visits (e.g. 1-2 visits per year) to Kymanox office(s) are required.
Compensation:
Hourly rate is commensurate with experience, qualifications, and other intangibles evident during the interview process - as well as market conditions.
About Kymanox:
Join Kymanox - a life sciences professional services company dedicated to life sciences who has successfully delivered over 4000 projects across 20+ countries. Become a member of a dynamic, fulfilling team that helps a broad range of life science products get to market more quickly, more affordably, and with the highest quality and safety standards possible in today's biotechnology, pharmaceutical, medical device, and combination product industries. With a reputation of providing unparalleled professional services and our highly collaborative team of engineering, compliance, and project management experts, Kymanox provides an outstanding opportunity for learning and career advancement. Kymanox encourages team members, especially new graduates, and young professionals, to work on a variety of projects to gain increased learnings in Kymanox's service offerings and the life science industry as a whole.
Kymanox is looking for motivated individuals who want to solve problems in the life science industries while doing the work they love and helping get modern medicines that enhance and save patient lives to market. Kymanox provides professional services related to engineering, compliance, and project management. We service clients ranging from Fortune 100 companies to virtual start-up companies. The company was founded in 2004 and has been growing steadily since its inception. Our corporate HQ is based in Research Triangle Park, NC, and we have offices in Boston, Chicago, Philadelphia, and New Jersey.
To learn more about our company, please visit our website: Life Science Solutions Kymanox
Kymanox is an equal-opportunity employer and works diligently to protect the rights of job seekers by following all local, state, and federal laws as well as best Human Resource (HR) practices in the Life Science industry.

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