Kiniksa Pharmaceuticals
Healthcare & Life SciencesDirect Greenhouse career site

CMC Project Manager

Pay
$145,000 – $150,000 per year
Location
Lexington, MA · On-site
Job type
Full-time
Level
Senior
Experience
2+ years
Education
Bachelor's degree
Listed
31 days ago

Skills & highlights for this role

  • GMP manufacturing
  • CDMO management
  • technology transfer
  • project management tools

Also useful

  • large molecule process development
  • small molecule process development

Responsibilities (including, but not limited to)

  • Support development and management integrated project plans for one or more products
  • Partner with technical project leaders to coordinate project meetings, communicate progress, and prioritize activities
  • Manage relationships with CDMOs to enable successful outcomes and on-time/on-budget development and manufacturing activities
  • Prepare clear communication documents such as meeting minutes and registers capturing decisions, actions, risks, and assumptions
  • Assist with routine project health assessments including maintenance of risk registry, risk identification, mitigation development, and communication/escalation to key stakeholders as appropriate
  • Support project team preparation for governance meetings
  • Oversee day to day contract activities with external vendors from scope development through progress tracking, accruals, and invoicing
  • Participate in scenario development and strategic planning
  • Support budget development and long-range forecasting

Standout Skills for Impact

  • Prior experience working with CDMOs and managing external tech transfers

Qualifications and Experience

  • Requires a Bachelor's Degree in Science, Engineering or a related field with at least 2-5 years relevant biopharmaceutical industry experience
  • A minimum of 1 year of project management experience as either a designated project manager or PM responsibilities as part of a technical role
  • Strong written/oral communication skills
  • Working knowledge of large (preferred) and/or small molecule process development and GMP manufacturing
  • Working knowledge of project management tools and techniques
  • Informed on current biopharmaceutical industry requirements, news and trends
  • Independent, motivated, team member with experience in a matrix environment
  • Strong business acumen
  • Ability to foster effective relationships and collaboration, motivate others, influence without authority
  • Ability to accommodate flexible working hours to support business relationships in different time zones
  • Some domestic and international travel may be required

Additional information

Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.

Pay Range $145,000—$150,000 USD

Kiniksa does not accept unsolicited resumes from staffing agencies or search firms. Any resumes submitted without a signed agreement will be considered property of Kiniksa, and no fees will be paid.

About Kiniksa Pharmaceuticals

Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications.

With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST®, the first and only FDA-approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders.

At Kiniksa, talented individuals are trusted and empowered to make a real impact-shaping the future of medicine while improving the lives of patients who need it most.

Reporting to the Sr. Director Tech Ops Business Operations, this individual will serve as an integral member of technical process development, analytical, manufacturing and supply chain teams at Kiniksa Pharmaceuticals. This person will partner with team and technical leads to manage complex CMC activities for one or more products, analyze product development scenarios, and play a key role in budget forecasting and management.

This cross-functional position requires a solid understanding of the functional operations involved in Chemistry, Manufacturing, and Controls for biologics including (but not limited to) drug substance, drug product, analytical development and quality control. Direct experience managing technical transfers is a must.

The ideal candidate will also be proficient in the planning and integration of combination product, supply chain, and regulatory activities.

The CMC project manager will support technical teams and manage associated projects both in-house and at external development, testing, and manufacturing organizations. Ability to work some flexible hours is a must to manage activities and interactions with global partners.

This role is based in our Lexington, MA office and requires employees to be onsite five days per week.

Read the original posting

From Kiniksa Pharmaceuticals's careers page, first listed on Rolev.ai on October 10, 2026. Rolev.ai is not the employer.

How Rolev.ai helps with this application

Rolev.ai is a job search and application tool for US job seekers. For this CMC Project Manager role at Kiniksa Pharmaceuticals, it shows how your resume fits, tailors your resume to the posting, and prepares the application for you to review.

  • See how you fit

    Openings from employer career sites are ranked against your whole resume—and searchable inside Claude, ChatGPT, and Cursor via Rolev.ai MCP.

  • Tailor without inventing

    Every change to your resume is checked against your original. New experience goes in only with your yes—zero fabricated claims.

  • Draft the full kit

    Tailored and Full Match resumes, role-specific cover letters, and answers to employer screening questions are prepared in seconds.

  • 1-Click Extension Autofill

    The Chrome extension fills the employer's Greenhouse, Workday, Lever, or Ashby form in 1 click. You review it and press Submit.

Common questions

What is the salary for the CMC Project Manager role at Kiniksa Pharmaceuticals?

The CMC Project Manager posting at Kiniksa Pharmaceuticals states compensation of $145,000 – $150,000 per year. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on Kiniksa Pharmaceuticals's official career site.

Where is the CMC Project Manager job at Kiniksa Pharmaceuticals located?

This CMC Project Manager position at Kiniksa Pharmaceuticals is located in Lexington, MA (On-site). Always check Kiniksa Pharmaceuticals's application page for specific state eligibility or relocation policies.

What qualifications are required for CMC Project Manager at Kiniksa Pharmaceuticals?

For the CMC Project Manager role, Kiniksa Pharmaceuticals highlights 2+ years of relevant experience; a bachelor's degree; experience with GMP manufacturing, CDMO management, technology transfer, project management tools. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.

How do I apply for the CMC Project Manager position at Kiniksa Pharmaceuticals?

This listing links directly to Kiniksa Pharmaceuticals's Greenhouse application page. You can apply directly on Kiniksa Pharmaceuticals's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Greenhouse application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.