Senior Supervisor Production

24 hours ago


madhya pradesh, India TAPI Full time

Company Description At TAPI, we're not just a company—we're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide.Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description We're looking for a hands-on Senior Supervisor Production with strong expertise in batch manufacturing, process optimization, and team leadership. If you thrive in managing daily production planning, driving yield and cost improvements, overseeing documentation and compliance, and leading technology transfers and audits—all while fostering a culture of safety and GMP excellence—this opportunity in a fast-paced pharmaceutical environment is for you.Main Responsibilities: Assist in preparing daily and monthly production Planning and adherenceProcess optimization, team supervision, and continuous improvement initiatives to meet quality and efficiency goals.Ensuring proper solvent recovery, yield, waste management, and preventive maintenance.Ensure timely execution of batch manufacturing as per SOPsMonitor raw material availability and coordinate with stores and planningSupervise critical process parameters and troubleshoot deviationsResponsible for Process validation and equipment qualifications.Ensure & Approve production-related documentation including BMRs, logbooks, and deviation reports.Support scale-up and technology transfer activitiesDrive yield improvement and cost reduction initiatives.Ensure adherence to cGMP, EHS, and regulatory guidelinesReview and approve batch manufacturing records (BMRs) and logbooksCoordinate with QA/QC for in-process checks and batch release.Lead and train production operators and shift supervisorsConduct performance reviews and skill development sessionsFoster a culture of safety, discipline, and accountability.Implementing and monitoring GMP standards with 24*7 ATR.Participate & Lead in internal and external audits.Implement CAPAs and ensure timely closure of audit observationsStrong knowledge of chemical reactions, equipment handling, and process safetyFamiliarity with GMP documentation and regulatory expectationsLeadership, problem-solving, and communication skillsManaging technology transfer and scale-up of new products.Lead and manage production staff and Responsible for conducting training sessions on departmental Standard Operating Procedures (SOPs) and overseeing the qualification process of departmental personnel. Qualifications The ideal candidate will have: Education: M.Sc./ Diploma (Chemistry).Experience: 8 to 15 years of experience in Pharma API industry. Additional Information Make Your Mark with TAPIYour journey with TAPI is more than a job—it's an opportunity to make a lasting impact on global health. If you're ready to lead, innovate, and inspire, we're excited to welcome you to our team. Together, let's shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon



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