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Senior Manager/Associate Director, CMC Project Management

JR United Kingdom

Sheffield

Remote

GBP 70,000 - 100,000

Full time

2 days ago
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Job summary

A leading company in the pharmaceutical sector is seeking a Senior Manager/Associate Director for CMC Project Management in Sheffield. This remote role will oversee significant projects from initiation to completion, requiring extensive experience in the pharmaceutical industry and project management. Candidates should possess strong leadership and interpersonal skills to drive project success across diverse teams. An educational background in life sciences is essential, along with significant industry experience.

Qualifications

  • Master's or PhD in life sciences; chemistry preferred.
  • Minimum 10 years in pharmaceutical or CRO/CMO industry.
  • Proven problem-solving skills for complex challenges.

Responsibilities

  • Lead project initiation, planning, and execution.
  • Monitor project progression to ensure timely completion and budget adherence.
  • Support business development by attending client meetings and conferences.

Skills

Project Management
Problem Solving
Interpersonal Skills

Education

Master's or PhD in Life Sciences

Tools

MS Project

Job description

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Senior Manager/Associate Director, CMC Project Management, Sheffield, South Yorkshire

Location: Sheffield, South Yorkshire, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

7

Posted:

16.06.2025

Expiry Date:

31.07.2025

Job Description:

Overview

The Senior Manager/Associate Director Project Manager will be responsible for managing projects within STA, WuXi’s API and Drug Product development and manufacturing division. Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team, and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting STA’s services in conferences/trade shows.

Please note this is a remote (work from home) position within the UK.

Responsibilities

  • Lead all project initiation and planning efforts. Participate in the implementation and execution of a given project.
  • Establish project objectives, timelines, and deliverables. Define project tasks and resource requirements.
  • Closely monitor/control project progression to ensure project is completed on schedule and within budget. Report project progress to all key stakeholders.
  • Support the technical team to investigate any project challenges by necessary risk assessment tools & techniques, then implement corrective measures.
  • Serve as liaison with client contacts, manage day-to-day communications, and organize project team meetings.
  • Represent the company in project meetings, prepare meeting agenda and minutes, and follow up on action items.
  • Evaluate and assess project results and provide recommendations for future improvements.
  • Support the business development team by joining customer visits, conferences, or tradeshows.
  • Prepare Quotations/Proposals/Change Orders with inputs from key stakeholders for existing relationships.

Qualifications

Education and Experience:

  • Master's (MS) or PhD in life sciences; chemistry preferred
  • A minimum of 10 years pharmaceutical or CRO/CMO industry experience, preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing.
  • Prior experience in project management or managing external research collaborations, with PMP certification desired.
  • Strong and effective project management, problem-solving, and interpersonal skills with a proven track record working cross-functionally across technical, business, and operational areas.
  • Good understanding of the pharmaceutical industry and small molecule drug development.
  • Minimum of 5 years relevant experience in CMC process development and/or GMP manufacturing.
  • Knowledge of current regulations and industry trends for small molecule manufacturing and testing. Oligonucleotide and Solid State Peptide experience is a plus.
  • Experience in CRO or CMO is preferred but not required.
  • Proficiency in MS Office, especially MS Project.

Independence/Accountability:

  • Self-starter, self-motivated, and highly flexible; approximately 25% travel.
  • Organized and detail-oriented.
  • Proven problem-solving skills with successful plans and processes for complex problems.

Leadership Activities:

  • Coordinate efforts across all CMC-related business units and with STA management to ensure effective communication and effort alignment.

Communication Skills:

  • Proficiency in English required; Mandarin is a plus.
  • Excellent verbal, written, and presentation skills.
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