Proclinical - IT - Administration

Seeking a Sr Manager GMP QA in Boston to lead batch disposition and core QMS activities. This role requires hands-on GMP Quality experience in pharmaceutical manufacturing, with expertise in deviations, CAPAs, and change control. Strong preference for candidates familiar with small-molecule drug ...

Medical Affairs Manager sought to lead rare disease nephrology and cardiorenal strategy across the Netherlands and Belgium. This role blends scientific insight with external expert engagement, requiring a scientific degree, Dutch fluency, and pharma experience. Based in Breda or Mechelen, you wil...

We are seeking a Warehouse Operator in Visp, Switzerland, to manage material movement, storage, and distribution. This role involves inspecting shipments for quality, tracking inventory, and operating hand trucks. Ideal candidates possess strong attention to detail, organizational skills, and the...

Proclinical seeks a Workplace Solutions Facility Manager to lead soft services and operational excellence across multi-site pharmaceutical labs and offices in Lexington, US. This role requires proven experience in facilities management, vendor oversight, and EHS compliance within life sciences. Y...

Proclinical is seeking a QA Associate to join a highly regulated quality function in Angleton, US. This role requires a Bachelor’s in Life Sciences and experience in GxP sterile manufacturing operations. Key responsibilities include managing QMS documents, supporting audits, and ensuring GMP comp...

Proclinical seeks an Infrastructure & Utilities Engineer for an onsite role in Visp, Switzerland. You will ensure the reliability and lifecycle management of small equipment within a GMP-compliant facility. The role demands fluency in German and English, expertise in GMP standards, and skills in ...

Proclinical is hiring a QA Document Control Associate in Rockville, MD to ensure GMP compliance through precise document lifecycle management. You will maintain electronic and hardcopy records, utilize Veeva, and support audits within the QMS. Ideal candidates have experience in Quality Systems D...

Proclinical seeks a Project Manager in Melbourne to lead end-to-end clinical studies across all phases. You will manage budgets, risks, and cross-functional teams while ensuring ICH GCP and regulatory compliance. Ideal candidates have a relevant degree and CRA background. This role offers the cha...

Lead regulatory labelling strategy for medicinal products in Hertfordshire. Develop and maintain Core Data Sheets and EU/US product information, ensuring global compliance. Collaborate cross-functionally, providing strategic guidance throughout the product lifecycle. Requires strong regulatory af...

Lead regulatory lifecycle management projects in Paris, driving pharmaceutical innovation. Coordinate cross-functional CMC, regulatory, and supply teams to advance a portfolio of products. Ideal candidates have strong project management and CMC expertise within the pharma industry.

Join our team as an EHS Project Manager in Lexington, MA. You will develop and implement critical safety programs for facilities and construction projects within biotech/pharma. This role requires strong EHS regulatory knowledge and experience with risk assessment and management systems. We seek ...