What are the responsibilities and job description for the External Manufacturing Project Manager, Pharma position at Eliassen Group?
Description
Our F500 Pharma client is seeking a strong External Manufacturing Project Manager to provide disciplined, end-to-end project management to ensure the safe, reliable, and compliant delivery of externally manufactured APIs, intermediates, and starting materials for our client’s new manufacturing facility. Programs are expanding as pipeline assets progress from development into clinical and commercial supply, and this Project Manager will play a critical role in leading cross-functional and cross-company project execution across technology transfer, process qualification, batch release, and supply chain activities, enabling on-time commercialization and sustained supply.
Responsibilities
BUSINESS PROBLEM, CONTEXT & INITIATIVE DESCRIPTION
Our F500 Pharma client is seeking a strong External Manufacturing Project Manager to provide disciplined, end-to-end project management to ensure the safe, reliable, and compliant delivery of externally manufactured APIs, intermediates, and starting materials for our client’s new manufacturing facility. Programs are expanding as pipeline assets progress from development into clinical and commercial supply, and this Project Manager will play a critical role in leading cross-functional and cross-company project execution across technology transfer, process qualification, batch release, and supply chain activities, enabling on-time commercialization and sustained supply.
DUTIES / EXPECTATIONS OF THIS ROLE
MUST HAVES – QUALIFICATION SUMMARY
Onsite at client’s facility in Lebanon, IN full-time.
Work Schedule: Monday-Friday, Daylight
February 2026 start. Immediate contract through Dec 31 2027 with potential to extend.
CONSULTING RATE
Competitive
Our F500 Pharma client is seeking a strong External Manufacturing Project Manager to provide disciplined, end-to-end project management to ensure the safe, reliable, and compliant delivery of externally manufactured APIs, intermediates, and starting materials for our client’s new manufacturing facility. Programs are expanding as pipeline assets progress from development into clinical and commercial supply, and this Project Manager will play a critical role in leading cross-functional and cross-company project execution across technology transfer, process qualification, batch release, and supply chain activities, enabling on-time commercialization and sustained supply.
Responsibilities
BUSINESS PROBLEM, CONTEXT & INITIATIVE DESCRIPTION
Our F500 Pharma client is seeking a strong External Manufacturing Project Manager to provide disciplined, end-to-end project management to ensure the safe, reliable, and compliant delivery of externally manufactured APIs, intermediates, and starting materials for our client’s new manufacturing facility. Programs are expanding as pipeline assets progress from development into clinical and commercial supply, and this Project Manager will play a critical role in leading cross-functional and cross-company project execution across technology transfer, process qualification, batch release, and supply chain activities, enabling on-time commercialization and sustained supply.
DUTIES / EXPECTATIONS OF THIS ROLE
- Develop, execute, and oversee integrated end-to-end project plans for facility’s External Manufacturing activities, including timelines, milestones, deliverables, and dependencies.
- Proactively manage scope, risks, issues, and decisions using formal change control and governance processes.
- Drive on-time, compliant technology transfer and commercialization of externally manufactured products.
- Establish clear accountability across cross-functional stakeholders and external partners.
- Support and coordinate Internal Process Teams (IPTs) and Joint Process Teams (JPTs).
- Integrate facility’s External Manufacturing project plans with internal client functions and contract manufacturer operational plans.
- Strengthen collaboration across technical, quality, supply chain, and manufacturing teams to support batch release, shipment, and supply continuity.
- Utilize project management tools such as MS Project, Jira, dashboards, scorecards, risk registers, and decision logs to improve visibility and predictability.
- Provide clear, timely project status updates and metrics to technical teams and leadership.
- Maintain collaboration platforms (e.g., Microsoft Teams, SharePoint, Yammer).
- Identify opportunities for process improvement and standardization across the facility's External Manufacturing projects.
- Support Lean initiatives and continuous improvement efforts to enhance efficiency and execution discipline.
- Integrated cross-functional project schedules and status reports.
- Risk registers, dashboards, metrics, and scorecards.
- Decision logs, meeting minutes, and action trackers.
- Leadership-ready project insights and recommendations.
- Continuous improvement and Lean initiative outputs
MUST HAVES – QUALIFICATION SUMMARY
- Minimum Education: Bachelor of Science in Chemical Engineering, Science, Engineering, or a Project Management–related discipline with pharmaceutical manufacturing experience. Advanced Degree Preferred.
- Strong Project Management expertise within pharmaceutical external manufacturing environments
- 3–4 years minimum of experience in manufacturing operations, technology transfer
- Demonstrated experience working in team-based, cross-functional environments. Proven experience managing cross-functional and cross-company stakeholders.
- Strong problem-solving skills with a root cause analysis and corrective action mindset
- Excellent written and verbal communication skills across technical and leadership audiences
- High adaptability and effectiveness in fast-paced, multi-priority environments.
- PE or PMP
- Experience with unit operations for large molecule expression and purification, peptides, and/or small molecule manufacturing
- Experience managing capital delivery projects or commercialization/technical agenda projects
- Direct or indirect experience with commercialization activities, including Validation, Tech Transfer, CMC, GMP, Quality, and/or HSE
Onsite at client’s facility in Lebanon, IN full-time.
Work Schedule: Monday-Friday, Daylight
- Virtual calls may routinely occur outside of regular hours due to the time zones of contract manufacturers.
- International travel may be required to support process start-ups, troubleshooting, and commercial manufacturing. All travel expenses to be covered by our client.
February 2026 start. Immediate contract through Dec 31 2027 with potential to extend.
CONSULTING RATE
Competitive