Asst Manager- Drug Regulatory Affairs- Pharma OSD/Soft Gelatin

**Vivanza Biosciences Limited** is seeking a highly motivated and detail-oriented professional to join our team as a **Regulatory Affairs Executive** in Ahmedabad, Gujarat. This role is ideal for an individual with foundational experience in the pharmaceutical industry who is keen to grow their career in regulatory compliance and submissions for global...

Sunrise Remedies Job Opening for Regulatory Affairs (RA) officer.Experience: 1 YearIndustries: Pharmaceutical CompanyEducation: B.Sc. | M.Sc | B.Pharm | M.PharmJob Location: Santej Ahmedabad.Facilities Provided:– Transportation Facility Available (As Per Circumference Of Sunrise Remedies)*– Mediclaim and Food Facility provide By Company.*Key...

Job Opening: Regulatory Affairs Executive | Vital GroupLocation: SG Highway, AhmedabadExperience: 1–3 years (Pharma Industry)Key Responsibilities:Preparation and submission of dossiers, CTD/ACTD, and regulatory documents.Handling regulatory queries and compliance requirements.Coordination with internal teams to ensure timely submissions.Support in product...

Role & responsibilitiesTo lead Regulatory affairs team engaged in dossier preparation in CTD and ACTD formats / and country specific format, DMF verification, technical data verification for all LATAM, MENA, CIS and ROW Countries and other country as per company requirements.Responsible for final review of dossier before submission.To coordinate with...

:Lead/support emerging markets (and Japan, Canada, ANZ) filing for Biosimilars, NCEs &ANDAs,Query responses, audit support, and lifecycle management.Regulatory support for the filing of IND/CTA to various regulatory agencies.Maintenance of IND/CTA through submission of protocol amendments, addition of investigators, EC approvals, SAE report submission,...

Job Title:Sr. International Regulatory Affairs Executive/OfficerCompanies: PharmaLocation: Ahmedabad BodakdevExp: 4-6 Yrsemail: Whatsapp: Openings: 02 Required Candidate profilePreparing & review Dossiers for registration of products in various ROW marketsLegalization of FDCA documents for respective country registrationPreparing, managing FSC & COPP...

Job Summary:We are seeking a skilled and motivated Research Scientist to join our Formulation & Development (F&D) Oral Solid Dosage (OSD) team. The ideal candidate will be responsible for the design, development, and optimization of oral solid dosage forms (tablets, capsules, etc.) from concept to commercial scale. The role involves conducting...

Company DescriptionCLAPS Industries Pvt Ltd. is a global pharmaceutical company founded by a team of visionary and successful individuals in the pharmaceuticals field. With a focus on delivering top-quality healthcare products and services worldwide, CLAPS is rapidly growing through product diversification, strategic manufacturing expansions, and strong...

Role & responsibilitiesJob PurposeTo ensure compliance of OSD packing operations with regulatory and company quality standards, by managing QMS activities such as deviations, change controls, CAPA, documentation, and audits.Key ResponsibilitiesEnsure packaging operations are carried out as per cGMP, SOPs, and regulatory guidelines.Handle QMS activities...

Prepare, submit regulatory dossiers for new product registrationsCoordinate and manage the submission of regulatory documents Facilitate communication with health authorities, responding to queries Required Candidate profileM. Pharm (Female Candidate Preferred)1 year of experience in Regulatory Affairs in Pharmaceutical Formulations unit desired.Excellent...