Ra/Labelling Officer

This position is open for candidates with a first experience as Regulatory Affairs or QA Officer/Assistant (internship or working experience) or with experience in an administrative position within the pharma industry. For this role, a very good knowledge of French and Dutch and English is required. Job Description As RA/Labelling officer, you comply with...

This position is open for candidates with a first experience as Regulatory Affairs or QA Officer/Assistant (internship or working experience) or with experience in an administrative position within the pharma industry. For this role, a very good knowledge of French and Dutch and English is required. Job Description As RA/Labelling officer, you comply with...

**Site Name**: Belgium-Wavre, Italy - Siena, Switzerland - Zug, UK - London - New Oxford Street, USA - Maryland - Rockville, Warsaw Rzymowskiego 53 **Posted Date**: Oct 31 2024 **Global Regulatory Affairs Manager, Vaccines Therapeutic Group**: Job purpose: As a **Global Regulatory Affairs (GRA) Manager**, you will join the GRA Vaccines Therapeutic Group in...

As part of consulting you will collect, establish and control (on a quality and regulatory level) the labelling/specifications /packaging of raw materials, finished products or recipes and translate when required. Legal verification of labels / products in line with customer/market requirements. Various one-off projects (short-term quality assistance on...

**PRINCIPAL ACCOUNTABILITIES/RESPONSIBILITES** As part of the consulting elements you will collect, establish and control (on a quality and regulatory level) the labelling/specifications /packaging of raw materials, finished products or recipes and translate when required. Legal verification of labels / products in line with customer/market...

Location: **Wavre** **#22146** **Clinical R&D Leader** Brabant Wallon - Contracting Our partner is looking for a **Clinical R&D Leader **to join its team. This international company is well-known for its pharmaceuticals and vaccines. **Your responsibilities?** - Contribute to activities or components of a Clinical and Epidemiology Plan (CEP) as...

Belgium *** RESPONSIBILITIES **PRINCIPAL ACCOUNTABILITIES/RESPONSIBILITES** As part of the consulting elements you will collect, establish and control (on a quality and regulatory level) the labelling/specifications /packaging of raw materials, finished products or recipes and translate when required. Legal verification of labels / products in line with...

RESPONSIBILITIES **PRINCIPAL ACCOUNTABILITIES/RESPONSIBILITES** As part of the consulting elements you will collect, establish and control (on a quality and regulatory level) the labelling/specifications /packaging of raw materials, finished products or recipes and translate when required. Legal verification of labels / products in line with...

**Site Name**: Belgium-Wavre **Posted Date**: Sep 24 2024 Job Purpose To conduct Phase I-IV Clinical Development activities within a program or group of related programs within the context of the GSK process in order to ensure the high quality and on-time delivery of all clinical data that will allow world-wide registration in compliance with the clinical...

**Site Name**: Belgium-Wavre **Posted Date**: Sep 25 2024 **Job Purpose** To conduct Phase I-IV Clinical Development activities within a program or group of related programs within the context of the GSK process in order to ensure the high quality and on-time delivery of all clinical data that will allow world-wide registration in compliance with the...

**Site Name**: GSK HQ, Belgium-Wavre, Canada - Ontario - Mississauga **Posted Date**: Sep 3 2024 As SERM Associate Medical Director you will provide medical expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting. You will ensure scientifically sound review and interpretation of...

**Site Name**: GSK HQ, Belgium-Wavre, Canada - Ontario - Mississauga **Posted Date**: Sep 3 2024 As SERM Associate Scientific Director you will provide scientific expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting. You will ensure scientifically sound review and interpretation...

**Site Name**: GSK HQ, Belgium-Wavre, Canada - Ontario - Mississauga **Posted Date**: Oct 11 2024 As SERM Associate Scientific Director you will provide scientific expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting. You will ensure scientifically sound review and interpretation...