CMC Project Manager

Kiniksa Pharmaceuticals; Lexington (MA); On-site; USD 145,000 - 150,000; Full time

Job summary

Kiniksa Pharmaceuticals seeks a CMC Project Manager to join our Lexington, MA team, onsite five days a week. You will partner with cross-functional teams to manage complex CMC activities for one or more products, and support budget forecasting and management.

The role emphasizes CDMO relations, external tech transfers, and planning across development, manufacturing, and regulatory activities, with a focus on timely, on-budget execution.

Qualifications

• Bachelor's Degree in Science, Engineering or related field with 2-5 years relevant biopharmaceutical industry experience
• At least 1 year of project management experience as either a designated project manager or PM responsibilities as part of a technical role
• Working knowledge of large (preferred) and/or small molecule process development and GMP manufacturing
• Prior experience working with CDMOs and managing external tech transfers
• 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

Responsibilities

• 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
• Support budget development and long-range forecasting

Skills

Project management

Cross-functional collaboration

Budget forecasting

Communication

Travel flexibility

Strategic thinking

Education

Bachelor's degree

Job description

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.

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
• Support budget development and long‑range forecasting

StandoutSkills forImpact:

• 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
• Working knowledge of large (preferred) and/or small molecule process development and GMP manufacturing
• Prior experience working with CDMOs and managing external tech transfers
• 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

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 is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities areprovidedreasonable accommodation toparticipatein the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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.