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

Xaira Therapeutics

Contracts Manager

Seattle, WA · On-site

$101K - $135K/yr

Maintain and optimize the Contract Lifecycle Management (CLM) platform, including system ... Prior in-house experience as a member of a legal department in a biotech company or drafting and ...

Aurion Biotech Inc.

Clinical Study Manager

Seattle, WA · On-site

$95K - $113K/yr

... stage biotechnology company dedicated to restoring vision to millions of patients through ... Support procurement activities for clinical operations including vendor contracts, purchase orders

Aurion Biotech Inc.

Quality Coordinator

Seattle, WA · On-site

$72K - $79K/yr

Senior Manager, Quality Control SALARY RANGE: $72,000 to $79,000 ABOUT THE POSITION The Quality ... ABOUT AURION BIOTECH With offices in Seattle, Boston, and Tokyo, Aurion Biotech is a clinical-stage ...

AGC Biologics

Project Manager

Bothell, WA

$94K - $129K/yr

Financial acumen, including experience managing budgets, contracts, and invoicing processes ... Bachelor's degree in Life Sciences, Chemistry, Biotechnology, Engineering, or a related field. * 3 ...

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Biotech Contract Manager information

See Seattle, WA salary details

$46.7K

$120.7K

$158.2K

How much do biotech contract manager jobs pay per year?

As of Aug 23, 2026, the average yearly pay for biotech contract manager in Seattle, WA is $120,670.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,300.00 and $135,400.00 per year, depending on experience, location, and employer.

What is a biotech contract manager?

A Biotech Contract Manager oversees contracts related to biotechnology partnerships, vendors, research agreements, and regulatory compliance. They negotiate terms, ensure adherence to legal and industry standards, and mitigate risks for their organization. Their role requires collaboration with legal teams, procurement, and scientific departments to support business objectives. Effective contract management helps biotech companies streamline operations, maintain compliance, and optimize financial and operational outcomes.

What are the typical day-to-day responsibilities of a biotech contract manager?

As a Biotech Contract Manager, your daily tasks often include drafting, reviewing, and negotiating a variety of contracts such as research agreements, vendor contracts, and licensing deals. You will regularly collaborate with legal, procurement, research, and finance teams to ensure terms align with company goals and regulatory requirements. Managing timelines, tracking key deliverables, and monitoring compliance throughout the contract lifecycle are also core parts of the role. This position requires balancing multiple priorities and maintaining strong communication with both internal teams and external partners to support the company’s scientific and commercial objectives.

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

A Biotech Contract Manager should possess a strong background in contract law, negotiation, and life sciences, often supported by a bachelor's or master's degree in a related field and relevant experience in biotech or pharmaceutical contract management. Familiarity with contract management software, compliance platforms (such as Icertis or DocuSign), and regulatory guidelines like FDA and GxP is highly beneficial. Superior attention to detail, analytical thinking, and excellent interpersonal and communication skills set outstanding professionals apart in this role. These capabilities ensure accurate and efficient contract execution, risk mitigation, and effective collaboration with internal and external stakeholders in a highly regulated industry.

What are popular job titles related to Biotech Contract Manager jobs in Seattle, WA?

For Biotech Contract Manager jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Biotech Contract Manager jobs in Seattle, WA look for?

The top searched job categories for Biotech Contract Manager jobs in Seattle, WA are:

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Cities near Seattle, WA with the most Biotech Contract Manager job openings:

Biotech Contract Manager jobs near you
Infographic showing various Biotech Contract Manager job openings in Seattle, WA as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $120,670 per year, or $58 per hour.

Contract: Manager, CMC Stability Management and Analysis

Immunome, Inc.

Bothell, WA • On-site

$99K - $133K/yr

Full-time

Re-posted 23 days ago

Job description

Position Overview

Immunome is seeking an experienced Contract: Manager, CMC Stability Management and Analysis to oversee execution of outsourced stability programs. This contract role will be responsible for maintaining stability pull schedules, data review, and vendor oversight activities across mAb intermediate, drug substance, and drug product. 

The successful consultant will bring practical expertise in GMP stability operations, biologics and large-molecule stability requirements, understanding of ADC stability indicating assays and outsourced laboratory management. This position requires a hands-on program manager who can translate technical and regulatory expectations into actionable plans, manage timelines and risks across external partners, and ensure stability deliverables are met. 

Responsibilities

Study Execution and Operational Oversight 

  • Review stability protocols for long-term and accelerated studies. 
  • Create and maintain stability plans, master schedules, pull calendars, and study trackers across multiple development programs. 
  • Oversee execution of stability studies and ensure timely sample pulls, testing initiation, data delivery, and escalation of schedule or quality risks. 

Data Review, Trending, and Technical Assessment 

  • Review stability data for completeness, accuracy, data integrity, trend behavior, specification compliance, and consistency with expected product quality attributes. 
  • Support evaluation of OOS/OOT results and atypical trends. 
  • Prepare stability summaries, trend reports, shelf-life assessments, retest/expiry recommendations, and technical risk assessments to support program decision-making. 

Qualifications

  • Bachelor's or advanced degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Chemical Engineering, or a related field. 
  • 8+ years of experience in stability, QC, Analytical Development, CMC, or technical operations within the biotechnology or biopharmaceutical industry, or equivalent. 
  • Demonstrated experience managing GMP stability programs for biologics, monoclonal antibodies, fusion proteins, or other large molecules; ADC experience preferred. 
  • Hands-on experience with stability data review, trending, shelf-life assessment. 
  • Prior experience managing external CTLs, CDMOs, CROs, or stability storage vendors supporting regulated studies. 
  • Working knowledge of GMP requirements, data integrity expectations, ICH stability guidance, and regulatory expectations for biologics stability studies. 
  • Contract or consultant experience in a matrixed biotech environment preferred. 

Knowledge and Skills

  • In-depth understanding of biologics stability program management, including drug substance and drug product stability, retest/expiry dating, storage condition justification, and ongoing stability commitments. 
  • Working knowledge of ICH Q1A(R2), Q1B, Q1D, Q1E, Q5C, relevant FDA/EMA expectations, and phase-appropriate application of stability requirements. 
  • Strong understanding of biologics product quality attributes. 
  • Familiarity with analytical technologies used in biologics stability testing, including HPLC/UPLC, SEC, CE-SDS/cIEF/icIEF, ELISA, binding and potency assays. 
  • Strong project management skills with the ability to manage detailed schedules, multiple vendors, cross-functional dependencies, and competing program priorities. 
  • Ability to interpret stability trends, identify risks, escalate issues appropriately, and drive practical solutions in collaboration with technical and quality stakeholders. 
  • Excellent documentation, communication, and stakeholder management skills. 
  • Comfort with ambiguity and dynamic timelines; ability to operate independently and drive execution with limited supervision. 

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