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Manager Program Biotech Jobs in Seattle, WA (NOW HIRING)

GenScript/ProBio

LNP Lab Technician

Redmond, WA · On-site

$55K - $65K/yr

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... Inventory Management: Keep track of inventory using our management system, and proactively order ...

AST

Product Manager

Tacoma, WA · On-site

Monitor the pharma/biotech landscape, including market trends, emerging technologies, and ... Direct complex development programs, maintaining full accountability for budget adherence and ...

Echodyne Corp

Facilities Manager

Kirkland, WA

Develop preventive, predictive, and reliability-centered maintenance programs. * Drive operational ... semiconductor, electronics, biotechnology, or similarly complex technical environments.

Systimmune

Executive Director, Finance

Redmond, WA · On-site

$200K - $270K/yr

Manage alliance finance responsibilities for partnered clinical programs, ensuring consistent ... Required Qualifications and Behaviors : * 12+ years of progressive finance experience in biotech ...

BioLife Solutions

Senior Manager Facilities

Bothell, WA · On-site

$124.94 - $181.16/hr

Experience: 7‑10 years of biotech or GMP industry experience in program management. * Experience: 5+ years of people management and development. * Experience: 5+ years of facilities and/or ...

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All JobsProgram Biotech JobsManager Program Biotech JobsManager Program Biotech Jobs in Seattle, WA

Manager Program Biotech information

See Seattle, WA salary details

$43.8K

$122.3K

$178.7K

How much do manager program biotech jobs pay per year?

As of Aug 20, 2026, the average yearly pay for manager program biotech in Seattle, WA is $122,293.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,500.00 and $150,800.00 per year, depending on experience, location, and employer.

What does a manager program biotech do?

A Manager Program Biotech oversees and coordinates biotechnology projects within an organization. They are responsible for planning, executing, and monitoring projects to ensure they meet scientific, regulatory, and business objectives. This role involves leading cross-functional teams, managing budgets and timelines, and communicating progress to stakeholders. Managers in this position often work closely with research scientists, regulatory affairs, and business development teams to bring biotech products from concept to market.

What are the key skills and qualifications needed to thrive as a manager program biotech?

To thrive as a Manager Program Biotech, you need a strong background in life sciences, project management experience, and typically an advanced degree such as an MS or PhD in biotechnology or a related field. Familiarity with project management software, regulatory compliance systems, and knowledge of drug development processes are essential. Outstanding leadership, communication, and problem-solving skills set exceptional candidates apart in this role. These competencies ensure effective coordination of complex projects, regulatory adherence, and successful cross-functional team management in a rapidly evolving industry.

What are some typical challenges faced by a manager program biotech, and how can they be addressed?

A Manager Program in biotech often encounters challenges such as coordinating multidisciplinary teams, managing complex project timelines, and navigating shifting regulatory requirements. Effective communication and proactive risk management are crucial to address these issues. Building strong relationships with stakeholders and fostering a collaborative team environment can also help ensure project milestones are met while maintaining compliance with industry standards.

What is the difference between Manager Program Biotech vs Project Coordinator Biotech?

AspectManager Program BiotechProject Coordinator Biotech
Required CredentialsBachelor's/Master's in Life Sciences, Project Management certification often preferredBachelor's in Life Sciences or related field, PMP or similar certification beneficial
Work EnvironmentOversees multiple projects, manages teams, strategic planningSupports project teams, coordinates activities, tracks project progress
Employer & Industry UsageBiotech companies, pharmaceutical firms, research organizationsBiotech firms, research labs, clinical trial organizations

The Manager Program Biotech typically holds a higher level of responsibility, overseeing multiple projects and managing teams, whereas the Project Coordinator Biotech focuses on supporting project execution and coordination. Both roles require similar educational backgrounds and certifications, but differ in scope and leadership responsibilities.

Manager Program Biotech jobs near you
Infographic showing various Manager Program Biotech job openings in Seattle, WA as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $122,293 per year, or $58.8 per hour.

LNP Lab Technician

GenScript/ProBio

Redmond, WA • On-site

$55K - $65K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 9 days ago

Job description

About GenScript
Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
Job Description:
Are you ready to join a dynamic and innovative team on the cutting edge of biotechnology? We are looking for a skilled individual to play a crucial role in our mission. As a key member of our team, you will have the opportunity to work on exciting projects involving the encapsulation and purification of mRNA and genetic payloads, ensuring the highest quality standards throughout the entire process.
Key Responsibilities:
  • Advanced Payload Encapsulation: Expertly encapsulate a range of genetic payloads, including mRNA, Circular RNA, and sgRNA, within a diverse array of lipids.
  • Precise Purification and Concentration: Follow LNP downstream processing SOP to perform LNP purification and concentrating. Related technical skill include but not limit to ultrafiltration, TFF, sterile filtration, and FPLC methods.
  • Performing complicate antibody decorated LNP process and related purification process following SOP guidance
  • In process QC for LNP size, zeta, PDI, encapsulation efficiency measure and others, make sure following good documentation rule and take care for details
  • Nanoparticle Quality Assurance: Conduct quality checks on particle size and zeta potential to ensure the highest standards of quality and performance.
  • Final Product Preparation: Prepare the final product for shipment, including filtering, aliquot filling, and affixing labels to shipping tubes.
  • Standard Operating Procedures (S.O.P.) Compliance: Strictly adhere to production S.O.P.s to maintain consistency, quality to validated processes.
  • Thorough Documentation: Maintain comprehensive records accordance to ISO 9001 of all processes and materials used in the production.
  • Inventory Management: Keep track of inventory using our management system, and proactively order materials as needed for production.
  • High Throughput and Accuracy: Quickly and accurately perform tasks in high repetition.

If you are looking for a challenging and rewarding opportunity to make a meaningful impact in the biotechnology field, we encourage you to apply and be part of our innovative team. Your expertise and dedication will contribute to groundbreaking advancements in science and technology.
Qualifications:
  • Educational Background: Possess a Bachelor's degree in Chemical Engineering, Biology, or a related field in Chemistry.
  • Relevant Experience: Prior experience working with mRNA or Lipid Nanoparticles (LNP) is a definite plus.
  • Technical Proficiency: Experience with techniques such as PCR, HPLC, or enzymatic reactions is highly desired.
  • Team Collaboration: The ability to work effectively as part of a small cross-disciplinary team is essential to achieve both short-term and long-term goals.
  • Adaptability: Experience in a fast-paced, high-demand environment is highly desirable.
  • Effective Communication: The capability to communicate with peers and managers in a polite and concise manner is a valuable asset.

Benefit:
  • Medical Insurance/ Vision Insurance/ Dental Insurance
  • 401(k) & Retirement Savings Plan (RSP)
  • Short Term Disability Insurance
  • New Child Leave
  • Paid Time Off
  • Paid Company Holidays per year
  • Paid Sick Days (earned based on hours worked)
  • Compassionate Leave
  • Jury Duty Leave
  • Float day
  • Personal days

Perks:
  • Free colleague meals during shift
  • Onsite massages Charis
  • Onsite gyms

Compensation:
Salary range: $55,000 - $65,000 total compensation, including bonus, depending on experience and qualifications.
Benefits:
Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

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