Batch Preparation Operator
Department: Production
Key Responsibilities:
Perform gowning, hygiene, and line clearance procedures in the batch preparation area. Operate and monitor process vessels, autoclaves, and CIP/SIP systems per SOPs. Execute batch manufacturing activities and complete Batch Manufacturing Records online. Carry out calibration of weighing balances, pH meters, DO meters, and oxygen analyzers. Perform pre- and post-integrity testing of product filters. Conduct periodic aseptic media fill validations and equipment qualification. Ensure timely submission of logbooks and GMP documentation to QA.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience in pharmaceutical batch preparation, compounding, or production environments. ✔ Strong understanding of GMP, CIP/SIP, and aseptic processing. ✔ Familiarity with equipment qualification, calibration, and filter integrity testing. ✔ Hands-on experience with autoclave operations and Batch Manufacturing Record documentation. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
Filling Operator
Department: Production
Key Responsibilities:
Operate Blow Fill Seal, Ampoule Filling, and Vial Filling machines within isolators. Follow gowning and aseptic behavior per SOP; perform line clearance before filling. Verify environmental conditions and settle plate/NVPC data before start-up. Perform in-process checks per BPCR and attend filling interventions per SOP. Perform pre- and post-integrity testing of product filters. Support installation, validation, calibration, and qualification of filling machines. Record production data, output, and equipment performance.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience in pharmaceutical aseptic filling operations. ✔ Hands-on experience with isolators, Blow Fill Seal, ampoule, or vial filling machines. ✔ Strong attention to detail in aseptic technique, environmental monitoring, and BPCR documentation. ✔ Familiarity with filling machine validation, calibration, and qualification activities. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
Component Preparation / Autoclave Operator
Department: Production
Key Responsibilities:
Follow gowning and hygiene procedures in the component/compounding preparation area. Prepare autoclave loads per validated patterns; operate and monitor steam sterilizers. Inspect and manage production consumables (tubing, filters, gloves, garments, gaskets). Perform integrity testing and replacement of vent filters. Support installation, commissioning, and qualification of steam sterilizers and accessories. Conduct periodic aseptic media fill validations and equipment qualification. Maintain GMP documentation, load patterns, logbooks, and BMRs.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience in pharmaceutical component preparation and autoclave/steam sterilizer operations. ✔ Working knowledge of steam sterilization, pressure hold testing, and validated load patterns. ✔ Familiarity with production consumables handling and vent filter integrity testing. ✔ Strong documentation and GMP compliance skills. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
GMP Washing Operator
Department: Production
Key Responsibilities:
Operate equipment washers, CIP/SIP systems, and drying cabinets per SOPs. Carry out washing, rinsing, and drying of parts per validated wash cycles. Verify cycle parameters — temperature, time, conductivity, flow rate. Maintain segregation between clean and dirty areas to prevent cross-contamination. Complete GMP documentation: logbooks, usage logs, and cleaning records. Perform filter integrity testing where applicable. Report equipment faults and support new equipment qualification.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience in pharmaceutical GMP washing, cleaning, or equipment preparation operations. ✔ Familiarity with CIP/SIP systems, drying cabinets, and validated wash cycles. ✔ Strong hygiene, cross-contamination control, and cleaning chemical handling awareness. ✔ Comfortable maintaining detailed GMP documentation and equipment usage logs. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
Lyophilizer Operator
Department: Production
Key Responsibilities:
Prepare and operate lyophilizers per validated batch records and SOPs. Set up, start, and shut down lyophilization cycles. Monitor critical process parameters — shelf temperature, vacuum, chamber pressure. Perform routine cleaning, sanitization, and preventive maintenance. Perform integrity testing and replacement of vent filters. Record process data accurately in batch records or electronic systems. Report equipment malfunctions or deviations immediately to supervisor.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience operating lyophilization/freeze-drying equipment in a pharmaceutical setting. ✔ Understanding of critical process parameters — shelf temperature, vacuum, and chamber pressure. ✔ Comfortable with preventive maintenance routines and vent filter integrity testing. ✔ Strong documentation and batch record accuracy. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
Terminal Sterilization Operator
Department: Production
Key Responsibilities:
Perform loading/unloading of BFS bottles, ampoules, and vials per validated load patterns. Operate and monitor terminal sterilizers per SOPs. Perform line clearance and ensure utilities are available before operation. Transfer sterilized products to the visual inspection area. Perform integrity testing and replacement of vent filters. Maintain load parameters, logbooks, and BMR documentation. Record production data and QC results.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience in pharmaceutical terminal sterilization operations. ✔ Knowledge of steam sterilizer operation, validated load patterns, and BFS/ampoule/vial handling. ✔ Familiarity with vent filter integrity testing and production data recording. ✔ Strong attention to detail and GMP documentation practices. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
Officer – QC Microbiology
Department: Quality Control
Key Responsibilities:
Analyze starting materials, packaging, intermediates, and finished products using aseptic techniques. Run environmental monitoring programs across lab and manufacturing clean rooms. Conduct method validation, verification, and stability testing. Manage culture conservation and growth promotion testing. Prepare specifications, test methods, and Microbiology QC procedures. Prepare OOS/OOT investigation reports and Microbiology trend reports. Ensure lab compliance with GLP, GMP, and Good Documentation Practices.
Ideal Candidate Profile:
✔ Post Graduate in Microbiology, Biotechnology, or Life Sciences. ✔ Experience in pharmaceutical QC microbiology and aseptic testing techniques. ✔ Strong background in environmental monitoring across lab and manufacturing clean rooms. ✔ Experience with method validation, stability testing, and OOS/OOT investigations. ✔ Knowledge of culture conservation and growth promotion testing is an advantage. ✔ Full compliance with EHS, cGMP, and highest Data Integrity standards.
Container Closure Integrity Testing (CCIT) Operator
Department: Production
Key Responsibilities:
Perform CCIT testing using validated methods (vacuum decay / high voltage leak detection). Select representative samples across batches, container sizes, and closure types. Verify and calibrate CCIT equipment (vacuum decay tester, high voltage leak detector). Record testing parameters and evaluate results against acceptance criteria. Document and investigate deviations, including re-testing as needed. Support equipment, facility, and process qualification activities. Maintain logbooks, BMR, and BPR documentation.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience in pharmaceutical container closure integrity testing (CCIT). ✔ Strong knowledge of vacuum decay and high voltage leak detection methods. ✔ Comfortable with equipment calibration, sample selection, and deviation investigations. ✔ Detail-oriented with strong documentation skills. ✔ Full compliance with EHS, cGMP, and highest Data Integrity standards.
Packing Machine Operator
Department: Production Reports to: Manager / Supervisor
Key Responsibilities:
Set up, operate, and monitor packaging machines (cartoners, blister packers, shrink-wrappers, flow-wrap). Verify machine parameters and printing details (batch no., expiry, MRP, barcode). Perform in-process checks — sealing quality, print clarity, carton integrity, count. Execute changeovers for different SKU sizes/pack configurations. Operate inline printers, scanners, vision systems, and serialization equipment. Reconcile packaging materials and handle rejected units per procedure. Maintain logbooks, BMR/BPR, and IPC documentation.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience operating pharmaceutical packaging machinery (cartoners, blister packers, shrink-wrappers). ✔ Familiarity with serialization, inline printers, vision systems, and changeover procedures. ✔ Strong attention to detail in sealing, print clarity, and carton integrity checks. ✔ Comfortable reconciling packaging materials and handling rejected units per procedure. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
Visual Inspection Testing Operator
Department: Production
Key Responsibilities:
Conduct visual inspections of products, materials, and components against quality standards. Identify, document, and report defects or non-conformities. Use measuring/testing equipment (calipers, gauges, micrometers) for dimensional checks. Maintain accurate inspection records and support equipment/process qualification. Collaborate with production and quality teams to resolve quality issues. Ensure logbooks and BMR/BPR are completed and closed on time. Manage consumables inventory and support production targets.
Ideal Candidate Profile:
✔ D. Pharmacy or Diploma in Engineering (Mechanical/Electrical/Instrumentation). ✔ Experience in pharmaceutical visual inspection or quality control checks. ✔ Strong attention to detail and defect/non-conformity identification skills. ✔ Familiarity with measuring/testing instruments (calipers, gauges, micrometers). ✔ Comfortable maintaining inspection records and supporting process qualification. ✔ Full compliance with EHS, cGMP, and highest Data Integrity standards.
Officer – QC / Analyst
Department: Quality Control
Key Responsibilities:
Perform analytical testing using HPLC/GC/FTIR/UV and CDS software (Labsolutions/Chromeleon/Empower). Analyze starting materials (APIs, excipients), intermediates, bulk, and finished products. Conduct stability testing and prepare protocols/reports. Prepare and review Certificates of Analysis (COAs) and specifications. Execute qualification/validation of laboratory equipment and Method Verification/Validation. Prepare OOS/OOT investigation reports and Annual Product Reviews. Maintain lab compliance with cGMP and Good Documentation Practices.
Ideal Candidate Profile:
✔ Graduate or Post Graduate in Chemistry or Pharmacy. ✔ Experience in pharmaceutical QC and analytical testing. ✔ Hands-on experience with HPLC, GC, FTIR, UV, and CDS software (Labsolutions/Chromeleon/Empower). ✔ Strong background in method validation, stability testing, and OOS/OOT investigations. ✔ Comfortable preparing Certificates of Analysis and Annual Product Reviews. ✔ Full compliance with EHS, cGMP, and highest Data Integrity standards.
Manufacturing Operator
Department: Production
Key Responsibilities:
Carry out activities per SOPs and specified parameters. Fill Batch Manufacturing Records, in-process checklists, and logbooks online. Perform in-process checks during tablet compression/capsule filling. Check area and machinery before requesting IPQA line clearance. Report process deviations or machinery breakdowns. Carry out cleaning (CIP) of equipment, machinery, and instruments per SOP. Rotate across sections as assigned by the Section Head.
Ideal Candidate Profile:
✔ D. Pharmacy / B.Sc / ITI or Diploma in Engineering. ✔ Experience in pharmaceutical manufacturing, tablet compression, or capsule filling environments. ✔ Good understanding of GMP and SOP-driven production practices. ✔ Comfortable completing Batch Manufacturing Records and in-process checklists online. ✔ Strong teamwork and hygiene discipline. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
Validation Officer
Department: Quality Assurance
Key Responsibilities:
Execute SAT, IQ, OQ, and PQ activities for pharmaceutical equipment, instruments, and systems. Support qualification activities related to thermal validation, including steam sterilizers, vessels/tanks, lyophilizers, and tunnels. Perform equipment qualification for filling and sealing machines, vial washing machines, HVAC systems, isolators, VHP processes, LAFs, and dynamic pass boxes. Conduct temperature mapping activities for areas and equipment. Prepare, compile, and review validation/qualification protocols, reports, SOPs, Validation Master Plan, and Site Master File. Support media fill activities, including preparation/review of protocols, intervention trend review, execution support, and report compilation. Review relevant documentation including logbooks, calibration records, preventive maintenance records, and CSV documents. Ensure timely completion of validation schedules and qualification planners. Support QMS documentation, investigations, and compliance with GMP, ISO, cGMP, EHS, and Data Integrity requirements.
Ideal Candidate Profile:
✔ Experience in pharmaceutical validation and qualification activities. ✔ Strong understanding of GMP, validation lifecycle, and regulatory compliance. ✔ Experience in equipment qualification, thermal validation, temperature mapping, and documentation. ✔ Knowledge of Computer System Validation is an advantage. ✔ Strong coordination, documentation, and problem-solving skills. ✔ Quality Assurance background is preferred.
QMS Officer
Department: Quality Assurance
The selected candidate will join the Quality Assurance Department and will be responsible for leading investigations, managing CAPA processes, and strengthening quality systems in line with GMP, ALCOA+, and Data Integrity requirements.
Key Responsibilities:
Lead and coordinate investigations for deviations, non-conformances, OOS/OOT results, and market complaints. Apply root cause analysis tools (5-Why, Fishbone, Fault Tree Analysis) to identify true root causes. Develop, review, and track CAPA plans arising from investigations, audits, and quality reviews. Verify effectiveness of implemented CAPAs through follow-up and trend monitoring. Prepare investigation reports, CAPA reports, and root cause analysis documentation per Good Documentation Practices. Prepare periodic trend reports on deviations, CAPA closure rates, and repeat occurrences for management review. Support internal and external audits/inspections by providing investigation and CAPA documentation.
Ideal Candidate Profile:
✔ B. Pharmacy / M. Pharmacy or Graduate/Post Graduate in Life Sciences or Chemistry. ✔ Experience in pharmaceutical Quality Assurance, with a focus on investigations and CAPA management. ✔ Strong understanding of root cause analysis techniques and risk assessment tools (FMEA). ✔ Familiarity with regulatory guidelines (GMP, ICH Q9/Q10) and QMS documentation practices. ✔ Comfortable maintaining CAPA trackers and driving continuous improvement initiatives. ✔ Full compliance with EHS, cGMP, ALCOA+, and Data Integrity standards.
