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Cmc Project Manager Jobs in Redmond, WA (NOW HIRING)

Senior Project Manager

Redmond, WA · On-site

$100 - $160/hr

We are seeking a Senior Project Manager, R&D to support cross‑functional planning and execution ... Ensure alignment across Research, Nonclinical, CMC, Regulatory, Clinical, Biomarker/Translational ...

Senior Project Manager

Redmond, WA · On-site

$60K - $85K/yr

We are seeking a Senior Project Manager, R&D to support cross-functional planning and execution for ... Ensure alignment across Research, Nonclinical, CMC, Regulatory, Clinical, Biomarker/Translational ...

Senior Project Manager

Redmond, WA · On-site

$60K - $85K/yr

We are seeking a Senior Project Manager, R&D to support cross-functional planning and execution for ... Ensure alignment across Research, Nonclinical, CMC, Regulatory, Clinical, Biomarker/Translational ...

Project Manager

Bothell, WA · On-site

$94K - $129K/yr

Lead CMC development, technology transfer, and GMP manufacturing programs from project initiation ... Manage project financials and contractual commitments, including Project Change Orders. * Provide ...

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Showing results 1-20

Cmc Project Manager information

See Redmond, WA salary details

$50.4K

$117.6K

$189.8K

How much do cmc project manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for cmc project manager in Redmond, WA is $117,624.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,000.00 and $143,900.00 per year, depending on experience, location, and employer.

What is a CMC Project Manager?

A CMC (Chemistry, Manufacturing, and Controls) Project Manager oversees the development, manufacturing, and regulatory aspects of pharmaceutical products. They coordinate cross-functional teams, manage timelines, and ensure compliance with regulatory requirements. Their role is critical in guiding drug development from early stages to commercialization while maintaining quality and efficiency.

What are the typical responsibilities of a CMC Project Manager in a pharmaceutical company?

A CMC Project Manager is responsible for coordinating cross-functional teams to ensure successful delivery of project milestones related to product development, manufacturing, and regulatory submissions. Their daily tasks often include developing project timelines, managing risk assessments, overseeing documentation, and facilitating communication between technical, regulatory, and quality departments. They play a pivotal role in preparing CMC sections for regulatory filings, supporting process optimization, and troubleshooting manufacturing challenges. This position requires excellent multitasking abilities and close collaboration with internal stakeholders and external partners throughout the product lifecycle.

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

A CMC Project Manager needs strong expertise in Chemistry, Manufacturing, and Controls (CMC) processes, project management certifications (such as PMP), and a background in pharmaceutical or biotech industries. Familiarity with regulatory submission systems, quality management software, and documentation tools is highly valued. Exceptional organizational skills, problem-solving ability, and effective cross-functional communication help candidates excel in this role. These capabilities are critical for ensuring project milestones are met, regulatory requirements are satisfied, and product development remains on track.

What job categories do people searching Cmc Project Manager jobs in Redmond, WA look for?

The top searched job categories for Cmc Project Manager jobs in Redmond, WA are:

What cities near Redmond, WA are hiring for Cmc Project Manager jobs?

Cities near Redmond, WA with the most Cmc Project Manager job openings:

Infographic showing various Cmc Project Manager job openings in Redmond, WA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $117,624 per year, or $56.5 per hour.

Senior Project Manager

Systimmune

Redmond, WA • On-site

$100 - $160/hr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 29 days ago


Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using established drug development platforms, focusing on bi‑specific, multi‑specific antibodies, and antibody‑drug conjugates (ADCs). With multiple assets in various stages of clinical trials for solid tumor and hematologic indications, SystImmune also maintains a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND‑enabling stages.

We are seeking a Senior Project Manager, R&D to support cross‑functional planning and execution for oncology biologics programs from early discovery through IND‑enabling activities and IND submission. This role will partner closely with Research, Translational Sciences, Nonclinical, Regulatory, Clinical Pharmacology, and external partners to drive an integrated development strategy, stage‑appropriate planning, risk management, and operational execution.

Key Responsibilities
  • Lead cross‑functional project planning and execution for oncology biologics programs spanning target/lead discovery, candidate selection, IND‑enabling studies, CMC development, and IND submission.
  • Build, maintain, and drive integrated project plans, timelines, milestones, scenarios, and critical path analyses across multiple functional areas.
  • Partner with program leaders and functional heads to define development strategy, key objectives, deliverables, governance milestones, and resource assumptions.
  • Facilitate cross‑functional team meetings, sub‑team meetings, and governance reviews; document decisions, action items, risks, and next steps.
  • Identify interdependencies, operational risks, and potential bottlenecks early; drive mitigation plans and upscale issues appropriately.
  • Ensure alignment across Research, Nonclinical, CMC, Regulatory, Clinical, Biomarker/Translational, Quality, and partner organizations.
  • Drive program team preparedness for major stage gates, including candidate nomination, development candidate selection, IND‑enabling study initiation, and IND submission.
  • Support budget planning, resource tracking, and external partner/CRO coordination as needed.
  • Develop concise, decision‑oriented communications for senior leadership, governance bodies, and key stakeholders.
  • Track progress against program goals and proactively highlight deviations, trade‑offs, and decision needs.
  • Promote disciplined program management practices, clear accountability, and efficient team operations.
  • Contribute to portfolio planning and cross‑program prioritization discussions where appropriate.
  • Help apply and improve R&D project management tools, templates, dashboards, and best practices.
  • Drive scalable adoption of AI‑enabled and digital program management practices, including automation, dashboards, AI‑assisted synthesis, standardized workflows, and data‑driven reporting while ensuring human oversight, data integrity, and compliance.
Required Qualifications
  • Bachelor’s degree in life sciences, biomedical sciences, chemistry, engineering, or related field.
  • 8+ years of relevant experience in biotech, biopharma, or related life sciences industry.
  • 5+ years of project or program management experience supporting drug discovery and/or development programs.
  • Demonstrated experience managing biologics programs in oncology or closely related therapeutic areas.
  • Strong understanding of drug development from discovery through IND, including: discovery research and candidate selection, IND‑enabling toxicology and pharmacology, CMC and analytical development for biologics, regulatory documentation and IND submission processes.
  • Proven ability to lead highly matrixed, cross‑functional teams without direct authority.
  • Excellent communication, facilitation, organizational, and stakeholder management skills.
  • Strong problem‑solving abilities with demonstrated experience managing complex timelines, dependencies, and risks.
  • Experience preparing executive‑level presentations, status reports, and governance materials.
Preferred Qualifications
  • Advanced degree (MS, PhD, PharmD, or MBA) in a relevant scientific or business discipline.
  • Experience with monoclonal antibodies, bispecifics, ADCs, or other complex biologic modalities in oncology.
  • Mandarin‑English bilingual ability.
  • PMP or related project management certification is a plus and biotherapeutics life cycles.
  • Experience in a fast‑paced, innovation‑driven biotech environment.
Core Competencies
  • Strategic thinking with strong operational execution.
  • Cross‑functional leadership and influence.
  • Decision facilitation and issue resolution.
  • Planning discipline and attention to detail.
  • Agility in a dynamic R&D environment.
  • Strong sense of ownership and accountability.
Success in this role will be defined by the ability to:
  • Keep complex oncology biologics programs aligned and moving forward from discovery to IND.
  • Create clarity across scientific and development teams around priorities, timelines, and decisions.
  • Anticipate risks and dependencies before they become delays.
  • Enable efficient governance and high‑quality decision‑making.
  • Build trust across functions as a strategic and operational partner.
Position Type/Expected Hours of Work
  • May need to work outside of standard working hours at times.
  • This role is currently working onsite and is expected to work onsite during working hours, with flexibility to work start time. The work location for this role is in Redmond, WA.
Compensation and Benefits

The expected base salary range for this position is $100,000 - $160,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills. While most offers typically fall within the low to mid‑point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.

SystImmune offers a comprehensive benefits package, including: 100% paid employee premiums for medical/dental/vision, STD, LTD, a 401(k) plan with a 50% company match up to 3% and a vesting schedule of 5 years, 15 PTO days per year, sick leave, 11 paid holidays and additional benefits.

We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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