ZipRecruiter

Log In

1

Manager Biotherapeutics Jobs (NOW HIRING)

Iovance Biotherapeutics

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor ... Management skills and operational capabilities * Ability to perform under pressure and meet ...

next page

Showing results 1-20

All JobsManager Biotherapeutics Jobs

Manager Biotherapeutics information

See salary details

$23K

$61.4K

$102.5K

How much do manager biotherapeutics jobs pay per year?

As of Jun 15, 2026, the average yearly pay for manager biotherapeutics in the United States is $61,351.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,000.00 per year, depending on experience, location, and employer.

What are Manager Biotherapeutics?

A Manager Biotherapeutics is a professional responsible for overseeing teams and projects involved in the research, development, and production of biotherapeutic products such as monoclonal antibodies, vaccines, and cellular therapies. They coordinate scientific activities, manage budgets, ensure compliance with regulatory standards, and facilitate collaboration between cross-functional teams. Their role is crucial in advancing new biologic medicines from research to market while maintaining quality, safety, and efficiency throughout the process.

What are the key skills and qualifications needed to thrive as a Manager Biotherapeutics, and why are they important?

To thrive as a Manager Biotherapeutics, you need a solid background in life sciences or biotechnology, leadership experience, and expertise in drug development processes. Familiarity with laboratory information management systems (LIMS), regulatory compliance tools, and project management software is typically required, along with relevant certifications such as PMP or advanced degrees (e.g., Ph.D., MSc). Strong interpersonal, organizational, and problem-solving skills help foster effective team collaboration and drive project success. These skills and qualifications are essential for ensuring regulatory adherence, optimizing research outcomes, and leading teams in the fast-paced biotherapeutics sector.

How does a Manager Biotherapeutics typically collaborate with cross-functional teams during the drug development process?

A Manager Biotherapeutics works closely with multidisciplinary teams, including research scientists, regulatory affairs, clinical operations, and manufacturing. They coordinate project timelines, ensure alignment on objectives, and facilitate communication between departments to drive biotherapeutic programs forward. Regular meetings, detailed project tracking, and problem-solving sessions are common, and the role often requires balancing scientific rigor with business priorities. This collaborative approach is essential for successful development and timely delivery of biotherapeutic products.
More about Manager Biotherapeutics jobs
What cities are hiring for Manager Biotherapeutics jobs? Cities with the most Manager Biotherapeutics job openings:
What are the most commonly searched types of Biotherapeutics jobs? The most popular types of Biotherapeutics jobs are:
What states have the most Manager Biotherapeutics jobs? States with the most job openings for Manager Biotherapeutics jobs include:
What job categories do people searching Manager Biotherapeutics jobs look for? The top searched job categories for Manager Biotherapeutics jobs are:
Manager Biotherapeutics jobs near you
Infographic showing various Manager Biotherapeutics job openings in the United States as of June 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $61,351 per year, or $29.5 per hour.

QA Manager, Qualified Treatment Center Oversight

Genetix Biotherapeutics

Somerville, MA • On-site

$115K - $140K/yr

Full-time

Medical, Life, Retirement

Posted 13 days ago

Job description

About Genetix Biotherapeutics
At Genetix Biotherapeutics every role has meaning, every team member is respected, and every day is a chance to make a difference. When you join Genetix, you're not just landing a new role, you become part of a company that's pursuing curative gene therapies to give patients and their families more days. We are doers, thinkers and collaborators who embrace and live by our values:
Our innovation is rooted in the diversity of our teams and results are achieved through cooperation and the integration of multiple viewpoints. This is personal and we approach every challenge with radical care.
SUMMARY
The Quality Assurance Manager, Qualified Treatment Centers will provide QA oversight for onboarding and routine operations at QTCs supporting Genetix's commercial gene therapies. Additionally, the incumbent in this highly visible role will support building scalable QA processes as Genetix continues to grow, creating energized, efficient, and effective teams internally collaborating with Apheresis Operations, Global Supply Chain (Patient Supply) and Quality Compliance. Day to day responsibilities include establishing and maintaining Quality Agreements with QTCs, primary QA oversight of change controls managing QTC onboarding, QA approval and resolution of QTC-related quality documentation. In addition, support for quality system record management related to collecting and transporting apheresis products and the quality oversight of QTC use of Genetix traceability systems.
This is a full-time hybrid position (3 days a week) in our Somerville - Assembly Row, Massachusetts office.
RESPONSIBILITIES
  • Ensuring compliance with quality expectations and industry guidelines in the areas of Good Tissue Practices (GTP), Good Manufacturing Practice (GMP) and Good Documentation Practice (GDocP) for apheresis products and Genetix QTCs
  • Building relationships with QA partners at QTCs, ensuring quality issues are tracked and resolved in a timely manner and working across the internal Genetix functional network in providing quality oversight of our QTC external partnerships
  • Ensuring an appropriate, consistent, and harmonized quality approach is standard across all QTCs through Quality Agreement initiation, review, execution, and maintenance
  • Tracking and trending quality system event generation at QTCs, providing periodic updates to management
  • Reviewing and approving documents including apheresis collection records, policies and procedures, deviations, investigations, and partner CAPA action plans
  • Reviewing and approving internal deviations, CAPA, and Change Control, performing Failure Mode and Effect Analyses, root cause analyses, and CAPA effectiveness check as required
  • Developing, monitoring and improving Quality processes which are scalable and sustainable to meet the organization's growing needs while supporting the development, implementation, and revision of corporate quality systems
  • Assisting with internal and external Quality Audits
  • Fostering a Quality mindset throughout the company by ensuring consistent, risk-based and innovative thought processes are employed to advise and make decisions)

QUALIFICATIONS
  • BS/BA and a minimum of 7+ years working experience in cell therapy (or applicable) environment. Experience in a hospital setting preferred
  • Knowledge of FACT accreditation requirements and their application for collection of apheresis and/or cell therapy lab preferred
  • Strong knowledge of GTP regulations and guidance documents
  • Experience with quality agreements
  • Demonstrated leadership within cross-functional teams with identifying areas of improvement, then participating in the design and delivery of improvements
  • Technical understanding of biopharmaceutical production, with experience in cell and gene therapy a plus.

Additional Information
The pay transparency range provided below is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. This role is eligible for an annual bonus and long-term incentive. Actual base salary pay will be based on several factors, including but not limited to experience, skills, relevant education/qualifications, external market, internal equity, and other job-related factors permitted by law.
Genetix's total rewards package also provides employees with a comprehensive and competitive benefits suite to support a variety of employee needs. These benefits include comprehensive health, life and disability insurance, employer-matched 401(k) plan, lifestyle spending account, flexible time-off + paid holidays and winter holiday period, tuition reimbursement & loan repayment assistance, paid parental leave, paid onsite parking, commuter subsidy, and much more.
Pay Transparency
$115,000-$140,000 USD
Genetix is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics.

Apply