QC, QA, Research & Development

Roles & Responsibilities
• Perform analytical testing, analysis, and documentation activities in API manufacturing (QC)
• Ensure compliance with GMP standards, audits, and quality documentation systems (QA)
• Support process development, synthesis, optimization, and scale-up activities (R&D)
• Maintain adherence to SOPs, ICH guidelines, and regulatory requirements
• Collaborate with cross-functional teams to ensure product quality, safety, and efficiency

Qualification
• B.Sc / M.Sc in Chemistry OR B.Pharm / M.Pharm or related discipline

Experience
• Quality Control (QC): 2–5 years in API/pharma testing and analysis
• Quality Assurance (QA): 2–4 years in GMP compliance and quality systems
• Research & Development (R&D): 2–5 years in process development or synthesis
• Note: Only male candidates are eligible

Skills
• Experience with API manufacturing and analytical instruments (HPLC, GC, etc.)
• Strong knowledge of GMP, ICH guidelines, and pharma documentation
• Good problem-solving skills and teamwork

Walk-in Details
• Date: Sunday, 08 February 2026
• Time: 9:00 AM – 2:00 PM
• Venue: Pharma Jobs Talent Acquisition Center, 2nd Floor, Bhagayarathi Talent Acquisition Center, Near IDPL Degree College, IDPL X Road, Chinthal Road, Hyderabad
• Documents Required: Updated resume, educational certificates, experience letters, passport-size photographs

About the Organization
Vital Syntheticlabs Pvt Ltd is a Hyderabad-based manufacturer of pyridine derivatives, speciality chemicals, APIs, and intermediates, known for its quality-driven processes and innovation in pharmaceutical manufacturing.