Regulatory Affairs

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Salvavidas Pharmaceutical Pvt. Ltd. is a India based entity which is acknowledged as one of the prominent companies in the global market, engaged in the field of pharmaceutical drugs manufacturing and pharmaceutical drugs exporting, Finish Formulation, API Bluk Drug.

Regulatory Affairs

1 to 3 yeras

Surat

Job Description

  • Vacancies: 1 Opening
  • Department: Regulatory Affairs
  • Gender: Male / Female
  • Function Area: Pharma
  • Industry: Pharma Export
  • Job Type: Full-time
  • Experience: 1 to 3 years

What we expect from you

• Studying scientific and legal documents • Gathering, evaluating, organising, managing and collating information in a variety of formats • Ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA) • Maintaining familiarity with company product ranges • Planning, undertaking and overseeing product trials and regulatory inspections • Keeping up to date with changes in regulatory legislation and guidelines • Analysing complicated information, including trial data • Outlining requirements for labelling, storage and packaging • Using a variety of specialist computer applications • Liaising and negotiating with regulatory authorities

Key skill

clinical data management

drug safety

clinical trials

pharmacovigilance

regulatory affairs

medical affairs

good clinical practice

Teamwork

Qualification

M.Pharm /M.Sc

Experience

1 to 3 yeras

Interested person can send their resume to us hr@salvavidashpharma.com

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