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Biotech Operations Jobs in California (NOW HIRING)

PSC Biotech

Quality Engineer

Pomona, CA · On-site

$110K - $120K/yr

The Experience With operations spanning the globe and featuring a multi-cultural team, PSC Biotech is passionate about bringing the best and brightest together in an effort to form something truly ...

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Biotech Operations information

See California salary details

$11

$25

$52

How much do biotech operations jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for biotech operations in California is $25.90, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $29.90 per hour, depending on experience, location, and employer.

What is biotech operations?

Biotech operations refer to the management and coordination of processes involved in developing, manufacturing, and distributing biotechnology products. This includes overseeing laboratory research, quality control, regulatory compliance, production scaling, and supply chain logistics. Professionals in biotech operations ensure that products such as pharmaceuticals, vaccines, or genetically engineered organisms are produced safely, efficiently, and in compliance with industry standards. Their work is critical in bringing scientific discoveries from the lab to market and ultimately to patients or consumers.

What are the key skills and qualifications needed to thrive in biotech operations, and why are they important?

Thriving in Biotech Operations requires a solid background in life sciences or engineering, experience with regulatory compliance, and a relevant degree such as a B.S. or M.S. in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), quality management systems (QMS), and certifications like Six Sigma or GMP training are highly valuable. Excellent problem-solving abilities, attention to detail, and strong collaboration skills help individuals excel and adapt in dynamic environments. These competencies are essential for ensuring operational efficiency, regulatory adherence, and successful product development in the biotech industry.

What are some common challenges faced in biotech operations, and how can new team members effectively navigate them?

Biotech Operations professionals often encounter challenges such as stringent regulatory compliance, maintaining production timelines, and managing cross-functional communication between research, quality, and manufacturing teams. New team members can navigate these challenges by proactively seeking mentorship, staying organized with project management tools, and maintaining open communication channels with colleagues in related departments. Embracing a mindset of continuous learning and adaptability is also crucial, as processes and technologies in biotech are constantly evolving.

What is the difference between Biotech Operations vs Laboratory Technician?

AspectBiotech OperationsLaboratory Technician
Required CredentialsBachelor's degree in biotech, biology, or related field; sometimes certifications in GMP or quality assuranceAssociate's or bachelor's degree in biology, chemistry, or related field; lab safety certifications often preferred
Work EnvironmentManufacturing facilities, quality control labs, production linesResearch labs, clinical labs, testing facilities
Employer & Industry UsageBiotech companies, pharmaceutical manufacturers, biotech startupsResearch institutions, hospitals, biotech and pharma labs

Biotech Operations roles focus on managing production processes, quality assurance, and ensuring compliance in manufacturing settings. Laboratory Technicians primarily perform experiments, testing, and data collection in research or clinical labs. While both roles require scientific knowledge, Biotech Operations emphasizes process management and compliance, whereas Laboratory Technicians focus on hands-on lab work and data analysis.

What are popular job titles related to Biotech Operations jobs in California?

For Biotech Operations jobs in California, the most frequently searched job titles are:

What job categories do people searching Biotech Operations jobs in California look for?

The top searched job categories for Biotech Operations jobs in California are:

What cities in California are hiring for Biotech Operations jobs?

Cities in California with the most Biotech Operations job openings:

Biotech Operations jobs near you
Infographic showing various Biotech Operations job openings in California as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $53,874 per year, or $25.9 per hour.

Associate Director, Clinical Operations

San Francisco, CA

Vir Biotechnology
Biotechnology Research and Development • 51 - 200 employees
Learn more about Vir Biotechnologyexternal

$176K - $246K/yr

Full-time

Medical, Retirement, PTO

Re-posted 12 days ago

Job description

THE OPPORTUNITY

Vir Bio is looking for an Associate Director, Clinical Operations, responsible for independently leading global and complex clinical trials. You will lead the Study Management Team, oversee clinical vendors and CRO(s) and is accountable for ensuring the successful execution and conduct of clinical trial(s).  In this role, you will be directly managing a large complex early phase oncology study. Activities will include vendor selection and management, protocol and study document development, feasibility/study start-up, maintenance, and closure.  You will serve in a leadership role within Clinical Operations and may lead/participate on SOP development working groups and initiatives, manage direct reports, and provide stakeholder management for cross functional teams within clinical development.

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

WHAT YOU'LL DO
  • Provide strategic input and leadership in study set-up and execution of highly complex oncology clinical trials. May support multiple trials
  •  Establish and continuously monitor study timelines and budgets, promptly escalating significant risks or changes, as appropriate
  • Develop and manage study contracts, budgets and timelines
  • Author/review core study documents including protocol and Informed Consent Forms
  • Manage CRO, central lab, systems vendors, and ancillary vendors to ensure on target deliverables
  • Develop study plans and relevant study document templates for study teams
  • Able to support regulatory strategy and assess trial/program impact and RFIs from multiple countries
  • May lead RFP process, budget development, and study forecast/planning including timelines
  • May perform sponsor oversight site visits
  • Manages oversight of clinical monitoring activities including monitoring trip report review and the overall site management ensuring compliance with Good Clinical Practices (GCP) and applicable regulations and tracking of site performance metrics
  • Reviews monitoring trip reports and track resolution of all action items
  • Manage team with direct reports within therapeutic area
  • Clinical Operations lead on cross functional project teams and alliance teams
WHO YOU ARE AND WHAT YOU BRING
  • Bachelor of Science degree is required, preferably in the life sciences
  • 10+ years of clinical development experience in the biotech/pharmaceutical industry
  • Extensive experience working on oncology clinical studies
  • Experience in managing and leading clinical studies both in early phase through late stage of development
  • Experience in leading all stages of clinical trials including start up, maintenance and closeout
  • Thorough understanding of FDA, EMEA, and ROW ICH and GCP guidelines, as well as thorough understanding of cross-functional clinical processes including and not limited to data management, biostatistics, medical monitoring, drug safety, regulatory affairs
  • Experience with regulatory compliance audits and inspections
  • Experience directing and leading in a complex team environment
  • Ability to function at a high level when leading a group or managing staff, but ability to manage day-to-day details when needed
  • Flexibility to travel domestically and internationally
#LI-AS1
#LI-Onsite
WHO WE ARE AND WHAT WE OFFER

The expected salary range for this position is $176,500 to $246,500 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.

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