Corporate Affairs Specialist - Navi Mumbai - Edgesetter Consulting Service LLP

Job Location: Taloja · CTC: 15 to 20 lacs · Position: AGM – Corporate Affairs (below 50 years) · This role requires frequent visits to multiple local and regional offices; hence candidates below 50 years are preferred due to the high mobility and energy levels required. · Preferr ...

Job Location: Taloja · CTC: 15 to 20 lacs · Position: AGM – Corporate Affairs (below 50 years) · This role requires frequent visits to multiple local and regional offices; hence candidates below 50 years are preferred due to the high mobility and energy levels required. · Preferr ...

We are looking for a highly skilled and experienced Regulatory Affairs Specialist to join our team at a reputed Pharma Company. · ...

Regulatory Affairs Specialist with 12+ years experience in EU market regulations. Expertise in EU compliance, dossier submissions, CE marking/EMA guidelines, and end-to-end regulatory processes. Strong documentation and coordination skills required. · Perks and benefits · Health ...

Job Overview · We are seeking a Medical Affairs Specialist to join our team full-time in Mumbai. The ideal candidate should bring 1 to 3 years of experience, contributing to our team in supporting pharmaceutical product launches, regulatory compliance, and medical communication. ...

Job summary · The Global Regulatory Affairs Service Center Team (GRASC – Team) supports regulatory compliance for Diversey chemical products across all business portfolios. · This is a Regulatory Specialist role in the GRASC Team. · ...

· Key Responsibilities: · Regulatory Expertise: Manage the regulatory process for Pharmaceutical Finished Formulations across CIS, LATAM, and Africa. · Dossier Management: Compile and review ACTD and CTD dossiers to ensure accuracy and compliance. · MOH Query Response: Address a ...

Working Experiance in API Industry. Need good experience from DMF preparation to submission · ...

We are seeking an experienced Regulatory Affairs professional to manage global regulatory submissions and lifecycle activities across Africa, LATAM, Asia, · and other assigned markets.Review batch manufacturing records. · Serve as Product Lead for assigned products. · ...

Managing regulatory submissions and reviewing labeling for herbal nutraceuticals and dietary supplements. · ...

You execute the regulatory affairs strategy for your respective category or categories and geographical area using your technical and regulatory knowledge. · ...

Fuse specialist for medical affairs position at TCS involves administering iEnvision tool administration enhancements configuring workflows templates dashboards publication planning processes creating submissions FUSE metadata entry categorization managing user access roles permi ...

Drive evidence-based medical affairs strategies to support the safe and effective use of Medtronic s cardiovascular technologies. · ...

Drive evidence-based medical affairs strategies to support the safe and effective use of Medtronic's cardiovascular technologies. · Lead scientific engagement, HCP education, and competitive intelligence to inform product positioning and clinical adoption. Collaborate cross-funct ...

Job Summary: · The Regulatory Affairs Specialist will provide end-to-end regulatory support for India-specific and APAC product-related activities. The role ensures timely and accurate execution of regulatory submissions, maintenance of product licenses, and coordination with Hea ...

+The candidate will be responsible for monitoring and interpreting changes in India's Medical Device Rules (MDR) and global regulatory standards including EU MDR/IVDR and US FDA. · + · +Candidate should have a B.Pharm / M.Pharm or equivalent qualification in Pharmacy or a relevan ...

This role requires a Lead Specialist to work within the focused flag state team in Regulatory Affairs. The specialist will develop and maintain relationships with governments to support LR's RO-obligations and business development. · ...

Lead Specialist for Governmental Affairs · Lloyd's Register · Location: Mumbai ,India · About The Role · Working within the focused flag state team in Regulatory Affairs, take a hands-on approach to ensuring that LR develops, maintains and capitalises on relationships with gove ...

Drive evidence-based medical affairs strategies to support the safe and effective use of Medtronic's cardiovascular technologies. · ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. · A Day in the Life · Drive evidence- ...