EMPREGO REGULATORY AFFAIRS CMC SPECIALIST

Job description the scientist is responsible for developing regional cmc strategy, preparation of cmc documentation and execution of regional post-approval cmc submissions...

We are currently seeking a senior regulatory affairs specialist (cta - clinical research field))... you will feel confident providing regulatory advice and carry...

The senior regulatory affairs specialist will provide regulatory support on a range of endoscopy devices and activities which include new product introduction...

regulatory affairs specialist - maternity cover (2 years)   as a regulatory affairs specialist you will act as the person responsible for regulatory compliance for...

• onboarding responsible for the quality assurance and regulatory affairs (qa&ra) part... • ensuring alignment of regulatory objectives with regional/ global regulatory...

* management of submission and follow-up of maa requests, variations, renewals and mah transfers until regulatory approval with national authority for products under...

Experience:       minimum 3 years of work experience in a regulatory affairs department within the healthcare sector or pharmaceutical sector...

Funções: verificação e garantia da conformidade regulamentar de dispositivos médicos; preparação de documentação técnica segundo mdr ; libertação de lotes, tratamento...

We are currently seeking a principal regulatory affairs specialist to join our global regulatory affairs department – regulatory science team...

We are currently seeking a senior regulatory affairs specialist to join our global regulatory affairs department –   regulatory science   team...  we are a global organisation but...

With adequate supervision, the regulatory affairs specialist ii is responsible for planning, managing, and implementing regulatory submissions to the us fda, eu...

With adequate supervision, the regulatory affairs specialist ii is responsible for ensuring continued compliance with regulatory agency approvals through change...

As an european regulatory affairs specialist, your role will serve as a crucial link between our business operations and the european regulatory environment...

Supports country-level intelligence on start-up (su) and clinical trial regulatory (ctr)... we translate unique clinical, medical affairs and commercial insights...

Advanced knowledge of quality, process optimization, gmp´s, ich/cfr guidelines, iso norms and industrial safety guidelines and regulatory affairs with the ability...