ZipRecruiter

Log In

1

Biotechnology Management Jobs (NOW HIRING)

Global Channel Management, Inc.

BIOTECH

Sanford, NC · On-site

$20/hr

Our account managers and recruiters have over a decade of experience in various verticals. GCM ... BA/BS Tech/Bus/Industry/Science with minimum 2 years direct regulated manufacturing pharma/biotech ...

next page

Showing results 1-20

All JobsBiotechnology Management Jobs

Biotechnology Management information

See salary details

$24K

$75.4K

$161.5K

How much do biotechnology management jobs pay per year?

As of Jun 20, 2026, the average yearly pay for biotechnology management in the United States is $75,444.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $99,500.00 per year, depending on experience, location, and employer.

What careers can you do with biotechnology?

Biotechnology management professionals can pursue careers in research and development, quality assurance, regulatory affairs, clinical trials management, and biotech project management. These roles often require knowledge of laboratory techniques, regulatory standards, and project coordination. Careers in biotech also include positions in sales, marketing, and business development within biotech companies.

What is the highest paying job in biotechnology?

The highest paying jobs in biotechnology are typically executive roles such as Chief Scientific Officer or Vice President of R&D, which can offer salaries exceeding $200,000 annually. These positions require advanced degrees, extensive industry experience, and strong leadership skills, often overseeing research strategies and company direction.

What are the key skills and qualifications needed to thrive in the Biotechnology Management position, and why are they important?

To thrive in Biotechnology Management, you need a strong background in life sciences or biotechnology, combined with business management skills such as project planning, budgeting, and regulatory understanding, typically supported by an advanced degree (e.g., MBA, MSc, or PhD). Familiarity with laboratory information management systems (LIMS), compliance standards like GMP, and project management tools is highly beneficial. Outstanding leadership, cross-functional communication, and problem-solving abilities set top performers apart in this field. These competencies are essential for successfully bridging scientific innovation and business objectives while ensuring regulatory compliance and team performance.

What does a biotech manager do?

A biotech manager oversees research and development projects, manages teams, and ensures compliance with regulatory standards in biotechnology companies. They coordinate activities between scientists, engineers, and stakeholders, often utilizing project management tools and requiring knowledge of biotech regulations and industry practices.

What are some typical challenges faced by professionals in Biotechnology Management roles?

Professionals in Biotechnology Management often navigate complex challenges such as balancing scientific research priorities with business objectives, ensuring compliance with stringent regulatory standards, and managing multidisciplinary project teams. They may also face tight timelines for product development and commercialization, requiring excellent organizational and decision-making skills. Building effective communication between scientists, executives, and external partners is key to driving successful outcomes. Embracing these challenges can lead to significant professional growth and positively impact both team and organizational success.

What is a Biotechnology Management job?

A Biotechnology Management job involves overseeing the development, commercialization, and regulatory aspects of biotech products and processes. Professionals in this role bridge the gap between science and business, managing research projects, securing funding, ensuring regulatory compliance, and leading teams. They work in pharmaceuticals, healthcare, agriculture, and environmental sectors, among others. Strong knowledge of both biotechnology and business strategy is essential for success in this field.

What are 5 careers in biotechnology?

Five common careers in biotechnology include biotechnologist, research scientist, quality control analyst, clinical research associate, and bioprocess engineer. These roles often require knowledge of laboratory techniques, data analysis, and sometimes advanced degrees or certifications. They are typically found in pharmaceutical, agricultural, and healthcare industries.
More about Biotechnology Management jobs
What cities are hiring for Biotechnology Management jobs? Cities with the most Biotechnology Management job openings:
What states have the most Biotechnology Management jobs? States with the most job openings for Biotechnology Management jobs include:
What job categories do people searching Biotechnology Management jobs look for? The top searched job categories for Biotechnology Management jobs are:
Biotechnology Management jobs near you
Senior Manager, Quality Control

Senior Manager, Quality Control

Vir Biotechnology

San Francisco, CA

$142K - $199K/yr

Other

Medical, Retirement, PTO

Posted 22 days ago

Job description

THE OPPORTUNITY

The Senior Manager, Technical Operations Quality Control, is responsible for executing and operationalizing QC strategy across assigned programs and external testing partners (e.g., CDMOs/CTLs) from Phase 1 through commercialization. This role ensures the timely and compliant delivery of QC activities, including release and stability testing, method lifecycle management, and vendor oversight. 

The Senior Manager partners cross-functionally with Quality, Technical Operations, Regulatory, and Analytical Development to deliver program milestones, maintain inspection readiness, and support global regulatory submissions. This individual contributes to the development of QC strategy and drives continuous improvement in QC processes, systems, and external network performance. 

This role is located in our San Francisco headquarters with an expectation of 3 days per week in office.

WHAT YOU'LL DO
  • Execute and operationalize QC strategy for assigned programs and external testing networks in alignment with QC and Quality organization strategy.  
  • Lead QC activities across the product lifecycle (Phase 1 through commercial) for designated programs, ensuring effective implementation of phase-appropriate control strategies.  
  • Support development and refinement of QC strategies, including methods, specifications, and testing approaches, in collaboration with Analytical Development and QC leadership.  
  • Drive consistent execution and harmonization of QC methods, specifications, and practices across programs and external partners.  
  •  Identify, assess, and escalate risks to QC performance, supply continuity, and compliance, and implement mitigation plans with cross-functional stakeholders. 
  • Represent QC on program teams and sub-teams, ensuring alignment of analytical deliverables, timelines, and QC readiness for key CMC milestones. 
  • Manage day-to-day execution of QC operations to ensure timely, compliant testing for clinical and commercial programs.  
  • Coordinate and oversee release and stability testing (including CDMOs/CTLs), including review of analytical data, batch records, and supporting documentation; support CoA generation.  
  • Lead execution of QC GMP processes (deviations, OOS/OOT, change controls, investigations) in collaboration with QA.  
  • Coordinate QC documentation and logistics at external labs, including sampling plans, shipments, and reagent/inventory management.  
  • Manage vendor performance and execution, including CTL/CDMO oversight and routine operational interactions.  
  • Execute method lifecycle activities (qualification, transfer, validation, implementation, and monitoring) across internal and external labs.  
WHO YOU ARE AND WHAT YOU BRING
  • BA/BS with 10 + years experience, MA/MS/MBA with 8+ years experience in Biochemistry, Chemistry, Biology, Virology, Chemical Engineering or a related discipline is preferred
  • Technical expertise in a wide range of analytical methods for release and stability testing of monoclonal antibodies
  • Strong scientific background in Quality Control and/or assay development in biotech industry with strong knowledge of cGMP/ICH/FDA/EMA regulations
  • Expertise with analytical test method optimization, validation, and transfer as well as working with contract organizations 
#LI-AS1
#LI-Onsite
 
WHO WE ARE AND WHAT WE OFFER

The expected salary range for this position is $142,500 to $199,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person's experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.

Apply