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Location
In office (Oslo)
Employment
Contractor

Confirmed on the employer's own hiring board on Nov 14, 2026. First seen by Alion on Nov 11, 2026. QCS Staffing scores A on the Alion truth index.

Overview
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QCS Staffing, formerly Quanta Consultancy Services, is a specialist recruitment agency headquartered in Berkhamsted, Hertfordshire, that places contractors, permanent staff and executives in life sciences, data centres, IT, renewable energy and heavy lift. Founded in 1992, it has worked for clients in more than 30 countries and runs offices in the UK, the United States, Ireland, Puerto Rico and the Netherlands, including one in Research Triangle Park, North Carolina. Its assignments include project, process, CQV and automation engineers, construction and electrical design managers, procurement advisers and network engineers on client capital projects.
CMC Program Manager - Norway - Initial 12-Month Contract - Life Sciences Our client is undergoing major growth, supported by substantial investment aimed at increasing its overall manufacturing capacity in the medical device sector. Recent upgrades include the development of new, advanced automation systems and additional infrastructure enhancements designed to meet growing global healthcare demands. With a long-established presence and a highly skilled workforce, the site requires the role of a CMC Program Manager to support their project based in Norway. What you’ll deliver:

Lead CMC programmes from development through regulatory submission, approval and implementation.Develop and maintain the integrated programme plan, critical path, milestones, budget and resource requirements.Coordinate formulation, analytical development, stability, process development, validation, manufacturing readiness and regulatory activities.Partner with Regulatory Affairs to drive submission readiness, health-authority responses and approval timelines and clear risk communication.

Experience required:

Bachelor's or advanced degree in Pharmacy, Chemistry, Pharmaceutical Sciences, Chemical Engineering or related discipline.Significant pharmaceutical industry experience, including leadership of complex CMC or product-development programmes.Strong understanding of pharmaceutical development, GMP, CMC requirements and global regulatory submissions.Demonstrated experience coordinating multidisciplinary teams through major development and regulatory milestones.Strong programme planning, risk management, stakeholder management and executive communication skills.

If this assignment is of interest, apply now! #LI-JS5

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