Senior Project Manager, CMC Biologics, Commercial Manufacturing and Supply Chain - (Pharma OR B[...]

LS Solutions; Massachusetts; On-site; USD 100,000 - 130,000; Full time

Job summary

A leading company in the pharmaceutical industry seeks a Senior Project Manager to oversee CMC strategies within the POVE program. The role requires extensive experience in biopharmaceutical project management and excellent communication skills. This position involves working with cross-functional teams to ensure project delivery and compliance with GMP standards.

Qualifications

• At least 8 years in biopharmaceutical industry.
• 5+ years in project management of biopharmaceuticals.

Responsibilities

• Track milestones and decision points, driving project delivery.
• Communicate project status, risks, and mitigation strategies effectively.

Skills

Communication

Analytical

Problem-Solving

Education

Bachelor’s degree in engineering

PMP

Tools

Microsoft Office

Project Management Software

Job description

Senior Project Manager, CMC Biologics, Commercial Manufacturing and Supply Chain - (Pharma OR Biotech exp mandatory)

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Senior Recruitment Consultant at LS Solutions ##Hiring Top Talent!! (Validation/CSV/CQV/MES Developer/Automation Engineer/Project Manager All over…

Job Title: Senior Project Manager, CMC Biologics

Location: Massachusetts (On-Site)

12+ Months of Contract

JOB DESCRIPTION:

Senior Project Manager, Commercial Manufacturing and Supply Chain (CMSC) POVE

POSITION SUMMARY

This role involves supporting cross-functional project teams executing CMC manufacturing strategies within the POVE program, working with CMSC Program Management, CMC functional leads, and interfacing with CDMOs and internal teams. Responsibilities include tracking and reporting project scope, timelines, milestones, manufacturing, process validation, release and stability testing, capacity planning, and external partner strategy. The role requires a detail-oriented individual with experience managing CMC strategies in biotech, GMP knowledge, external manufacturer interaction, drug development understanding, and risk management skills. Excellent communication, high attention to detail, and ability to work in cross-functional teams are essential.

RESPONSIBILITIES:

• Partner with program management, manufacturing leads, and CDMOs to develop and monitor project plans, identifying dependencies and critical paths.
• Track milestones and decision points, driving project delivery.
• Communicate project status, risks, and mitigation strategies effectively to stakeholders.
• Maintain team communications, meeting documentation, decision logs, and risk analyses.
• Update project tools like action logs, risk registers, budgets, and dashboards.
• Assist in creating templates for team activities.
• Operate within SOPs and GxP requirements.

QUALIFICATIONS:

• Bachelor’s degree in engineering, life sciences, or related field; advanced degrees and PMP preferred.
• At least 8 years in biopharmaceutical industry, with experience managing external CDMOs and biologics manufacturing.
• 5+ years in project management of biopharmaceuticals.
• Experience with CMOs, GMPs, drug development, and regulatory processes.
• Proficiency in Microsoft Office and project management tools; experience with other PM software is a plus.
• Strong communication, analytical, problem-solving skills, and ability to manage multiple priorities in a matrix environment.

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Analysis, Manufacturing, and Project Management

Industries

• Pharmaceutical Manufacturing, Biotechnology Research, and Manufacturing