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Biotech Operations Manager Jobs in Bothell, WA (NOW HIRING)

Our client is an innovative clinical-stage biotechnology company advancing next-generation ... You will also help us build our clinical operational infrastructure and teams. Travel Requirement:

Our client is an innovative clinical-stage biotechnology company advancing next-generation ... You will also help us build our clinical operational infrastructure and teams. Travel Requirement:

Our client is an innovative clinical-stage biotechnology company advancing next-generation ... You will also help us build our clinical operational infrastructure and teams. Travel Requirement:

... through biotechnology. Work Location: Redmond, WA Reports to: Sr. Production Manager, Product ... Provide operational leadership to production team, including training, coaching, and team members ...

Production Lead- LNP

Redmond, WA · On-site

$70K - $85K/yr

... through biotechnology. Work Location: Redmond, WA Reports to: Sr. Production Manager, Product ... Provide operational leadership to production team, including training, coaching, and team members ...

LNP Lab Technician

Redmond, WA · On-site

$55K - $65K/yr

HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence ... Inventory Management: Keep track of inventory using our management system, and proactively order ...

HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence ... Inventory Management: Keep track of inventory using our management system, and proactively order ...

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Biotech Operations Manager information

See Bothell, WA salary details

$34.7K

$70.9K

$132.5K

How much do biotech operations manager jobs pay per year?

As of Jun 21, 2026, the average yearly pay for biotech operations manager in Bothell, WA is $70,937.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,800.00 and $86,600.00 per year, depending on experience, location, and employer.

What are some common challenges faced by Biotech Operations Managers, and how can they be addressed?

Biotech Operations Managers often face challenges such as maintaining regulatory compliance, managing cross-functional teams, and ensuring smooth production processes. These challenges can be addressed by staying updated on industry regulations, fostering clear communication between departments, and implementing robust quality control systems. Additionally, leveraging project management tools and continuous process improvement strategies can help streamline operations and minimize risks.

What is the difference between Biotech Operations Manager vs Biotech Laboratory Supervisor?

AspectBiotech Operations ManagerBiotech Laboratory Supervisor
CredentialsBachelor's or Master's in Life Sciences, Business, or related fields; experience in biotech operationsBachelor's or Master's in Life Sciences; laboratory management experience; relevant certifications often preferred
Work EnvironmentOversees multiple departments, manages projects, and ensures compliance across operationsManages daily lab activities, supervises lab staff, and maintains lab safety and procedures
Employer & Industry UsageUsed in biotech companies for operational oversightCommon in research labs, biotech firms, and pharmaceutical companies for lab management

The Biotech Operations Manager focuses on overseeing overall biotech operations, including project management and compliance, while the Biotech Laboratory Supervisor concentrates on managing daily lab activities and staff. Both roles require relevant scientific credentials, but their scope and responsibilities differ significantly.

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

To thrive as a Biotech Operations Manager, you need a solid background in life sciences, business management, and regulatory compliance, often supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and project management tools is typically required, along with certifications like Six Sigma or PMP being advantageous. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for managing teams and cross-functional projects. These skills ensure efficient operations, regulatory adherence, and successful product delivery in the highly regulated biotech industry.

What does a Biotech Operations Manager do?

A Biotech Operations Manager is responsible for overseeing the daily operations of biotechnology facilities, ensuring that production processes run efficiently and comply with industry regulations. They manage teams, coordinate schedules, oversee supply chains, and implement quality control measures. Additionally, they work closely with research and development, regulatory, and quality assurance teams to ensure products meet all safety and efficacy standards. Their role is crucial in maintaining productivity, safety, and compliance in a biotech organization.
What are popular job titles related to Biotech Operations Manager jobs in Bothell, WA? For Biotech Operations Manager jobs in Bothell, WA, the most frequently searched job titles are:
What job categories do people searching Biotech Operations Manager jobs in Bothell, WA look for? The top searched job categories for Biotech Operations Manager jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Biotech Operations Manager jobs? Cities near Bothell, WA with the most Biotech Operations Manager job openings:
Infographic showing various Biotech Operations Manager job openings in Bothell, WA as of June 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $70,937 per year, or $34.1 per hour.

Clinical Trial Manager

NWRPros

Bellevue, WA • On-site

Other

Posted 19 days ago


Job description

Our client is an innovative clinical-stage biotechnology company advancing next-generation therapeutics through proprietary localized, extended-release drug delivery technology. Their platform is designed to precisely target treatment to specific tissues, with the potential to enhance safety, tolerability, efficacy, and duration of effect while reducing systemic exposure and side effects often associated with conventional delivery methods. The company is currently progressing programs in pain and inflammatory gastrointestinal disease, with broader future applications across oncology, infectious disease, and other areas of significant unmet medical need. This is an exciting opportunity to join a science-driven organization focused on transforming how established and novel therapies are delivered to patients.
Scope:
As our client's Clinical Trial Manager (CTM) you will be primarily responsible for the operational management and oversight of clinical studies. You will also help us build our clinical operational infrastructure and teams.
Travel Requirement: Must be willing to travel domestically and internationally (approximately 20%), as needed
Primary Responsibilities:
  • Ensuring studies are carried out according to the study protocol, SOPs, and ICH/GCP guidelines/regulations and study specific manuals and procedures
  • Independently developing the trial's timelines, budgets, key deliverables, and risk/mitigation strategies
  • Leading the development of trial materials (e.g., protocol, informed consent forms, case report forms (CRF), CRF completion guidelines, monitoring guidelines, site initiation visit materials, site tools and worksheets, product administration guidelines)
  • Planning and leading study team meetings
  • Managing, mentoring, and training clinical operational staff
  • Leading the identification and engagement of CROs and other third-party study vendors
  • Managing and improving performance of third party vendors and field CRAs to ensure compliance with study protocol and consistency with scope of work; identify areas of concern and escalate as appropriate
  • Identifying, selecting, and monitoring performance of investigational sites; ensuring accurate and timely site visit reports
  • Developing and maintaining good working relationships with investigators and study staff
  • Negotiating and managing the budgets and payments for investigative sites
  • Tracking and ensuring optimization of site startup activities and activation, subject enrollment, data collection, and study closeout
  • Ensuring completeness and accuracy of Trial Master File
  • Managing investigational product release packages and investigational product accountability
  • Performing clinical data review of data listings and summary tables, including query generation
  • Other duties as assigned

Job Qualifications and Requirements:
  • Bachelor's degree or equivalent in life sciences
  • At least 6 years of clinical operations experience in the pharmaceutical industry with significant knowledge of GCP/ICH guidelines and the clinical development process
  • At least 1 year of experience managing industry sponsored pharmaceutical clinical trials as a sponsor employee
  • Ability to plan, organize and conduct clinical trials with minimum oversight
  • Experience leading, managing, or mentoring clinical operational staff and cross-functional teams
  • Significant experience managing CROs and other vendors and assessing performance and finances (e.g., invoice review, change order management, and budget reforecasting)
  • Strong interpersonal, communication (written and verbal), and organizational skills
  • Able to motivate a team to work effectively
  • Able to solve problems under pressure