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Regulatory Affairs Manager
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Cpl Life Sciences Kent, United KingdomJob Description · Job Title: Regulatory Affairs Manager (Parallel Import) · Job Type: Full-time, permanent position · Location: East London/ Kent – (Hybrid, 3 days on-site, 2 days from home) · Remuneration: Competitive salary and benefits package · Overview: · Regulatory Affair ...
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Regulatory Affairs Manager
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Regulatory Affairs Manager
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Cpl Life Sciences Kent, United KingdomJob Title: Regulatory Affairs Manager (Parallel Import) · Hit Apply below to send your application for consideration Ensure that your CV is up to date, and that you have read the job specs first. · Job Type: Full-time, permanent position · Location: East London/ Kent – (Hybrid, 3 ...
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Regulatory Affairs Manager
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Cpl Life Sciences Kent, United KingdomJob Title: Regulatory Affairs Manager (Parallel Import)Job Type: Full-time, permanent positionLocation: East London/ Kent – (Hybrid, 3 days on-site, 2 days from home) Remuneration: Competitive salary and benefits package Overview:Regulatory Affairs Manager opportunity working for ...
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Regulatory Affairs Manager
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Cpl Life Sciences Kent, United KingdomJob Title: Regulatory Affairs Manager (Parallel Import) · Job Type: Full-time, permanent position · Location: East London/ Kent – (Hybrid, 3 days on-site, 2 days from home) · Remuneration: Competitive salary and benefits package · Are you the right candidate for this opportunity ...
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Compliance Manager
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Cpl Life Sciences Kent, United KingdomJob Description Job Title: Regulatory Affairs Manager (Parallel Import) · Job Type: Full-time, permanent position · Location: East London/ Kent – (Hybrid, 3 days on-site, 2 days from home) · Remuneration: Competitive salary and benefits package · Regulatory Affairs Manager opp ...
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Director of Quality and Regulatory Affairs - Kent, United Kingdom - Cpl Life Sciences
Description
Job Title:
Regulatory Affairs Manager (Parallel Import)
Job Type:
Full-time, permanent positionLocation: East London/ Kent - (Hybrid, 3 days on-site, 2 days from home)
Remuneration:
Competitive salary and benefits package Overview:Regulatory Affairs Manager opportunity working for a family-run pharmaceutical company that specialise in generic, OTC, medical devices, and prescription medicines.
The business is increasingly growing and is looking for a personable and detail-oriented professional to join the team and support all areas of Regulatory Affairs.
Seeking a detail-oriented Regulatory Affairs Manager with experience in Parallel Imports of medicines to join the business. The ideal candidate will ensure compliance with regulations and laws governing the industry.Responsibilities:
Prepare and submit regulatory filings and documentation to appropriate regulatory parallel import agencies (MHRA).Monitor and interpret regulatory requirements and communicate changes (variations) to stakeholders.
Develop strategies for regulatory submissions in coordination with stakeholdersCollaborate with cross-functional teams (QA) to ensure compliance with regulationsMaintain current knowledge of regulations, guidelines, and standardsManagement of packaging components stock levels.
Skills:
A degree in a related fieldleast 4+ years of experience working in the Regulatory Affairs sectorPrevious experience in Parallel Imports Understanding of quality assurance principles in parallel importsStrong written and verbal communication skillsAble to work independently and in a team environmentPlease note to apply for this position you will need to be based in the UK and hold the full right to work in the UK.
