Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Salary Range: ₹9.00 - ₹10.00 Salary/yearRole Definition:The Senior Research Associate(SRA) Regulatory Affairs (RA) is responsible for the strategic and operational aspects of regulatory, review, compilation, submissions, approvals,
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Position Type: Full TimeSalary Range: ₹5.00 - ₹8.00 Salary/yearJob Shift: Day Role Definition:The Research Associate(RA) Regulatory Affairs (RA) is responsible for the strategic and operational aspects of
Description: Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. Exposure of the Solid oral dosage form / Sterile dosage form / complex dosage form / topical-Inhalation dosage form and brief manufacturing process and key regulatory aspects. Ability to preliminary
Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. Exposure of the Solid oral dosage form / Sterile dosage form / complex dosage form / topical-Inhalation dosage form and brief manufacturing process and key regulatory aspects. Ability to preliminary review
Description: Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. API DMF and DMF Change Notification review with respect to USFDA regulatory requirement. Exposure of the Solid oral dosage form / Sterile dosage form / complex
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated
Job Description SummaryDesign, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within a multifunctional project team coordinated by a
Job Title: Lead Manager – Finance & Accounts Location: Goregaon Reporting To: Assistant Vice President – Finance Experience Required: 5–7 years Qualification: Chartered Accountant (CA)/ MBA Finance Working Days: 5 days a week About Inventia Healthcare:
UMEDICA is a vertically integrated company engaged in the manufacturing and export of a wide range of finished formulations i.e., Injectables, Tablets, Capsules, Suspensions, Dry Syrups, etc. UMEDICAs manufacturing facility, located in Vapi (Gujarat), is approved
Job Title: Assistant General Manager – Formulation R&D Location: Thane Reporting To: VP – FRD Team Structure: 5-6 Experience Required: 16-18 yrs Qualification: M.Pharm Working Days: 5 days a week About Inventia Healthcare: Inventia Healthcare is
About Inventia Healthcare: Inventia Healthcare is a pioneer in pharmaceutical development and manufacturing, with over 40 years of expertise in Oral Solid Dosage (OSD) forms. Our global presence spans 45 countries with over ten international facility approvals. Backed by Platinum
Job Title: Assistant Manager / Manager – Technical Services & Business Development Experience: 5 - 8 Years Qualification: M. Pharm Location: Mumbai Job Summary Responsible for providing technical formulation support and driving business development for a
Formulation Resarch & Development – Job Description (Pharmaceutical Company) Job Title Formulation Research & Development (FR&D) Executive Job Summary The Formulation R&D professional is responsible for developing pharmaceutical formulations, conducting trials, optimizing manufacturing processes, and supporting
Department Details Role Summary Urgent Requirement for Formulation Development - OSD role (Scientist / Senior Scientist) •Handling Formulation Development - OSD / Solidi Orals • Keeps abreast of current trends, practices, developments, and regulatory changes, which would
At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Senior Associate to join our team. The job responsibilities for this position includes post-marketing regulatory
Job Description Job Summary We are seeking a dynamic and experienced Lead in Polymorph SCreening - Process Engineering for invention/discovery of pharmaceutically acceptable novel forms that are commercially viable for Active Pharmaceutical Ingredient & formulation development within
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Department Details Role Summary Generic Formulations - Supervisor Packing Key Responsibilities •Responsible for Packing of solid oral dosage forms. • Candidate must have faced major regulatory audits (like USFDA, MHRA etc.) • Preparation and updatation standard procedures (SOP/EOP/IOP/SCP) for different
20 + years with extensive exposure to Technology Transfer in OSD & Opthal Proven leadership in technology transfer, scale-up, and process validation. About Our Client This is a leading pharma formulations company based in Mumbai with