About the Company Our client is a leading international healthcare company specialising in consumer health products across multiple sectors, including pharmaceuticals, cosmetics, medical devices, food supplements, and biocides. With a strong presence in global markets, the company is dedicated to ensuring high-quality, innovative, and regulatory-compliant products that enhance consumer well-bei...
Read moreCommercial Quality Director Location: Paris-based, with monthly travel to subsidiaries. Start Date: ASAP A global healthcare company is seeking an experienced Commercial Quality Director to ensure compliance with Good Distribution Practices (GDP) and regulatory requirements across its international sales subsidiaries. This role is key to maintaining quality standards and overseeing distribution...
Read moreSenior Manager, QMS & GMP Global Quality Assurance Our client are seeking a (Senior) Manager, GMP QA to join its dynamic Quality Assurance team. This role is essential for maintaining and improving the company’s Quality Management System (QMS) and ensuring compliance with Good Manufacturing Practice (GMP) standards. Key Responsibilities Enhance and implement the company’s QMS to […]
Read moreScienta are proud to be partnered with a leading Pharmaceutical company Head Quartered in the NRW area, on the search for a new QA Manager to join their teams. Overview: Ensure that assigned contract manufacturers, comply with EU-GMPs, international guidelines and internal quality standards. Support in analytical method transfer projects to new laboratories. Qualifications and […]
Read moreRole – QA Specialist Location – Pennsylvania Working type – Permanent Hours – 9-5 (Monday to Friday) Company: Scienta are proud to be partnering with Philadelphia’s leading CDMO in their Quality expansion. They focus on developing and manufacturing Cell and Gene Therapy products which are marketed across the globe and want an ambitious Quality Specialist […]
Read moreRole – Qualified Person Scienta are proud to be partnered with one of Germany’s leading innovators in ADC’s, who have recently put over a billion in funding to their German site – prompting the need for a new QP to join their teams! Qualified Person (m/f/d) for clinical investigational medicinal products All activities that fall […]
Read moreSummary Responsible Person for the maintenance of applicable Operational Licenses. Responsible for the implementation and maintenance of Quality Management System required as per local regulations and standards. The Responsible Person is the main contact for Quality Assurance (QA) topics to distributors and external bodies (e.g. Swissmedic, Cantonal Pharmacist). Responsibilities To ensure Quali...
Read moreMy client is looking for an energic consultant with a technical scientific background and initial (at least 2 years) experience in GMP/ GDP area (Packaging Labelling, Quality Operations and or Quality System) for a contracted role till end of the year. Daily Responsibilities Reviewing the Batch Record of the CMO with the intent to ensure […]
Read moreResponsibilities Perform Chemistry analysis of In process / Final product as per schedule and in accordance with regulatory requirements. Also perform analysis on Stability samples from a wide range of products Documenting all testing activities, results and raw data on time, accurately and legibly Use of laboratory IT systems including LIMS and Empower Reviews and […]
Read more(Sr) Director of Quality Scienta – Scienta are proud to be teaming up with a leading CDMO in the search for their new (Sr) Director of Quality Your role Creation, review and maintenance of training plans for the Quality Systems and Compliance Team Responsible for the main QMS processes at the site such as document […]
Read moreRole – Director of Quality Location – Paris – 80% remote working Scienta are teaming up with a leading gene therapy company seeking to apply pathbreaking science to help patients with severe inherited diseases of the eye and central nervous system. Under the responsibility of the VP Regulatory Affairs & Quality Assurance, the Director of […]
Read moreThe ideal candidate will be responsible for planning, coordinating, and implementing projects within the decided-upon budget, timeline, and scope. They will also effectively monitor and present project updates to relevant stakeholders, clients, or project team members. Responsibilities: Generation, Execution / Approval of Qualification Life Cycle documents from SLIA through to PQ and Fin...
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