Pharma Project Lead: CDMO & Manufacturing Tech

Polpharma

Starogard Gdański

Hybrid

PLN 180,000 - 240,000

Full time

12 days ago

Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Benefits offered by this job

Company car / car allowance

Hybrid work model

Private medical care

Multisport card

Pension program

Relocation package

Job summary

Polpharma is seeking a seasoned Project Manager to oversee API manufacturing projects and drive strategic goals. You will coordinate cross-functional teams, including R&D and external CDMOs, to ensure timely delivery and compliance with GMP standards.

The role emphasizes strong budgeting, risk management, and excellent communication, with a hybrid work model and competitive compensation.

Qualifications

Minimum 5 years of experience in project management.
Knowledge of GMP manufacturing processes.
CDMO experience is an advantage.
Budgeting, risk analysis, and negotiation skills.
Very good English (spoken and written).

Responsibilities

Projects’ management within API Business Unit, especially development of manufacturing technologies for active substances to implement strategic goals.
Plan and implement projects based on best practices, including external customer (CDMO) projects.
Collaborate with API BU R&D and other departments to achieve project goals.
Help build a cross-functional CDMO organization; streamline processes and set up new ones.
Lead project teams at all stages; ensure seamless execution using effective communication tools.
Develop cooperation skills within the team and organization; manage conflicts.
Apply change and risk management to projects.