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Development Quality Assurance
xecutive – Development QA (DQA) About VerGo Pharma Research VerGo Pharma Research is a leading Contract Development and Manufacturing Organization (CDMO) and CRO based in Goa, providing end-to-end pharmaceutical development services including formulation development, analytical development, ICH stability studies, cGMP manufacturing, technology transfer, and bioequivalence studies for regulated markets. The organization has exposure to global regulatory standards including USFDA, MHRA, Health Canada, and other international agencies. Position Details Designation: Executive Department: Development Quality Assurance (DQA) Role Category: R&D Experience: 2–4 Years Qualification: M.Pharm / M.Sc Location: Goa Preferred Candidate Profile Experience in Development QA (DQA) CRO / Formulation Development background preferred Exposure to OSD (Oral Solid Dosage) products Experience working with regulated markets Strong knowledge of QMS, GMP, and documentation systems Job Responsibilities Review and evaluate Stability Study Reports, DEC Reports, and Calibration Data Sheets. Track, manage, and close QMS activities including: Incidents Deviations Discrepancies CAPA Change Controls Handle Change Control activities through Kriya as per established procedures. Prepare and review Nitrosamine Risk Assessment and Elemental Impurity Risk Assessment reports. Conduct and coordinate phase-gate review meetings and ensure timely closure of action items. Manage item codification for Raw Materials, Packing Materials, and Innovator Samples in ERP. Oversee RLD and Pilot Bio-sample Management. Perform Audit Trail Reviews as per defined schedules. Coordinate vendor intimation activities with QA as per SOP requirements. Review, revise, and update SOPs as required. Mandatory Skills Development QA (DQA) QMS Management Change Control CAPA Deviation Handling Documentation Review Stability Documentation SOP Review & Management GMP Compliance Audit Trail Review Regulatory Compliance
Formulation Scientist
Job Title: Formulation Scientist (Oral Solids) Company: Vergo Pharma Research Laboratories Location: Goa Experience: 6–9 Years Open Positions: 2 Role Overview We are hiring experienced Formulation Scientists with strong expertise in Oral Solid Dosage (Tablets & Capsules) to join our growing formulation team. The role involves development and optimization of pharmaceutical formulations for regulated markets. Open Positions Formulation Scientist: 3–9 Years (2 Vacancies) Key Responsibilities Develop and optimize formulations for oral solid dosage forms (tablets & capsules) Conduct pre-formulation studies and compatibility analysis Handle technology transfer, scale-up, and exhibit batch activities Prepare and review development reports and documentation Work on regulatory filings for US & EU markets Ensure compliance with quality and regulatory guidelines Mandatory Requirements Qualification: M. Pharm (Only) Strong experience in Oral Solid Dosage (OSD) – Tablets & Capsules (mandatory) Hands-on exposure to regulated markets (US & EU) Good understanding of formulation development processes Interview Process 2 Rounds (Virtual) Why Join Us Opportunity to work with a growing pharmaceutical R&D organization Exposure to international regulatory markets Career growth in formulation development