Recipharm

project manager in pharmaceutical manufacturing

In short

This role leads and standardizes project management across a pharmaceutical CDMO, overseeing a portfolio of Technology Transfer, NPI, and Engineering projects across multiple sites. The company is Recipharm, a Contract Development and Manufacturing Organisation with a biologics division, ReciBioPharm, working on advanced therapy medicinal products. It demands significant PM experience in CDMO/pharma/biotech manufacturing, a formal PM qualification (PMP/PRINCE2 or equivalent), and the ability to align stakeholders across Quality, Regulatory, Engineering, Manufacturing, and Supply Chain without direct authority. The role is fully remote but restricted to candidates with EU/UK citizenship or valid work/residence permits and permanent residence in the UK, Sweden, Germany, Italy, France, Spain, or Portugal.

About Recipharm
Recipharm is a Contract Development and Manufacturing Organisation that provides pharmaceutical manufacturing, clinical trial material development and manufacturing, and pharmaceutical product development services. Its biologics segment, ReciBioPharm, develops and manufactures advanced therapy medicinal products, including products based on live viruses and viral vectors, live-microbial biopharmaceutical products, mRNA, and plasmid DNA.
Responsibilities
•Define, implement, and maintain project management systems, tools, and reporting frameworks across the business
•Manage and prioritize a portfolio of projects, including Technology Transfer/NPI and Engineering
•Align project management practices across the organization through training, governance, standards, and templates
•Lead and execute complex, multi-site projects from initiation through completion
•Coordinate contributing disciplines and ensure clear communication and project execution
•Identify and manage portfolio risks, dependencies, and resourcing conflicts
•Provide structured project and portfolio status reports to senior stakeholders
Requirements
•Significant project management experience in a CDMO, pharmaceutical, or biotech manufacturing environment
•Direct experience with technology transfer and/or NPI projects
•Formal project management qualification such as PMP or PRINCE2, or equivalent demonstrated experience
•Proven experience managing a portfolio of concurrent projects
•Experience designing or improving project management tools, templates, standards, or governance frameworks
•Ability to lead multi-site or cross-country projects and align stakeholders without direct line authority
•Ability to collaborate across Quality, Regulatory, Engineering, Manufacturing, and Supply Chain teams
•Strong communication and stakeholder management skills, with the ability to influence at all levels
•Applicants must have EU/UK citizenship, or a valid work/residence permit and permanent residence in the UK, Sweden, Germany, Italy, France, Spain, or Portugal
Nice to have
•Engineering project experience
Conditions
•Global remote-based role

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