mfhkgkgjlhjhk;jk;jlkl'k';l; l;l;l' l '; Job Type: Full-time Pay: ₹242,400.40 - ₹796,586.02 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Experience: Civil engineering: 1 year (Required) Construction: 1 year (Required) Language: English (Required) Location: T Nagar, Chennai, Tamil Nadu (Required) Willingness to travel: 25% (Required) Work Location: In person
mfhkgkgjlhjhk;jk;jlkl'k';l; l;l;l' l '; Job Type: Full-time Pay: ₹242,400.40 - ₹796,586.02 per year Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Experience: Civil engineering: 1 year (Required) Construction: 1 year (Required) Language: English (Required) Location: T Nagar, Chennai, Tamil Nadu (Required) Willingness to travel: 25% (Required) Work Location: In person
Job Summary: We are seeking a dedicated and detail-oriented QC Microbiologist with 2 to 4 years of experience in pharmaceutical/biotech microbiology labs. The ideal candidate will be responsible for performing microbiological testing to ensure compliance with GMP standards and regulatory requirements. Key Responsibilities: Perform routine microbiological testing including: Sterility testing Water and air sampling Environmental monitoring (EM) Bioburden and endotoxin testing Identification of microorganisms Microbial limit tests Maintain microbiological data and logbooks. Participate in media fill validations and aseptic process simulations. Prepare and review SOPs, protocols, and reports related to microbiology activities. Ensure all testing and documentation complies with GMP, USP, EP, and regulatory guidelines. Support microbiological investigations (OOS, deviations, CAPAs). Operate and maintain laboratory instruments such as autoclaves, incubators, particle counters, etc. Coordinate with production, QA, and validation teams for sample planning and testing timelines. Assist in audits and regulatory inspections as needed. Qualifications: · B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life science discipline. · 2 to 4 years of hands-on experience in QC Microbiology within a regulated pharmaceutical or biotech environment. · Knowledge of cGMP, GLP, and regulatory guidelines (FDA, EMA, WHO). · Familiarity with microbiological techniques and cleanroom classifications. · Good documentation practices and understanding of data integrity principles. · Proficiency in MS Office and LIMS (Laboratory Information Management System) is a plus. Job Type: Full-time Pay: ₹300,000.00 - ₹800,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Experience: APIs: 5 years (Required) Work Location: In person
Job Title: QC Executive – Analytical (2 to 4 Years’ Experience) Industry: Biopharmaceutical Location: Puducherry Department: Quality Control – Analytical Reports To: QC Manager Job Summary: We are seeking a motivated and detail-oriented QC Analyst (Analytical) with 2 to 4 years of experience in a regulated pharmaceutical or biopharmaceutical QC laboratory. The role involves performing analytical testing of raw materials, in-process samples, and finished products in compliance with cGMP and regulatory requirements. Key Responsibilities: Perform routine and non-routine analytical testing of: Raw materials, intermediates, in-process, finished products, stability samples Water and cleaning validation samples (if applicable) Operate and calibrate analytical instruments such as: HPLC, GC, UV-Vis, FTIR, Karl Fischer, pH meter, Dissolution, etc. Prepare and review test records, logbooks, and related documentation as per GMP and data integrity standards. Conduct analysis as per pharmacopeial methods (USP, EP, IP, JP) Support in method validation/verification and equipment qualification activities. Review and interpret analytical results and escalate OOS/OOT results promptly. Maintain compliance with laboratory SOPs, GLP, and safety procedures. Participate in stability studies, trending data, and document control activities. Support investigations, deviations, and implementation of CAPAs related to QC analytical operations. Participate in internal and external audits and regulatory inspections. Qualifications: M.Sc. (Chemistry, Analytical Chemistry, Biotechnology) / B.Pharm / M.Pharm 2 to 4 years of hands-on experience in QC Analytical in a cGMP-compliant pharmaceutical or biopharma lab Key Skills: Handling of oncology molecules is plus Proficient in handling HPLC, GC, and other analytical instruments Familiarity with pharmacopeial testing (USP, EP, IP) Good understanding of cGMP, GLP , and data integrity practices Strong documentation and observation skills Working knowledge of LIMS or electronic data systems is an advantage Job Type: Full-time Pay: ₹11,407.45 - ₹27,703.75 per month Benefits: Provident Fund Experience: Laboratory: 3 years (Required) Clinical laboratory: 3 years (Required) Laboratory procedures: 3 years (Required) Laboratory techniques: 3 years (Required) Work Location: In person
Job Summary: We are seeking a proactive and detail-oriented IPQA professional with 2 to 4 years of hands-on experience in pharmaceutical or biopharma manufacturing. The IPQA Executive will be responsible for ensuring in-process compliance on the shop floor, monitoring production activities, and ensuring adherence to cGMP and quality standards. Key Responsibilities: Perform line clearance before the start of manufacturing, packaging, and batch changeovers. Monitor in-process checks during manufacturing and packaging activities (e.g., weight variation, hardness, uniformity, yield reconciliation). Review of batch manufacturing records (BMRs) and batch packaging records (BPRs). Ensure compliance to approved SOPs, Master Batch Records, and current GMP guidelines during operations. Verify and document critical process parameters during production activities. Handle and escalate on-the-spot deviations, discrepancies, and non-conformances. Ensure appropriate environmental conditions, gowning practices, and material handling in cleanrooms or controlled areas. Participate in routine area audits, inspections, and self-inspections. Support in investigations related to deviations, OOS, OOT, implementation of CAPAs. Ensure proper labelling, status control, and traceability of materials and equipment during operations. Coordinate with production, engineering, and warehouse teams to maintain compliance on the shop floor. Qualifications: B.Pharm/B.Tech/M.Sc/M.Tech in Life Sciences, Microbiology, Biotechnology. 2 to 4 years of IPQA experience in a regulated pharmaceutical or biopharma manufacturing facility (formulations, sterile/non-sterile, or biologics). Key Skills: Experience in Oncology plant is plus Sound knowledge of cGMP, GDP, and IPQA practices Familiarity with regulatory guidelines (USFDA, EU-GMP, WHO, etc.) Ability to detect quality issues in real-time and act decisively Good documentation and communication skills Ability to work in shifts and under pressure Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicheri, Puducherry: Reliably commute or planning to relocate before starting work (Required) Experience: Pharmaceutical: 2 years (Required) Oncology: 2 years (Required) Work Location: In person
[Exp: 2 to 5 years] We are looking for an experienced and detail-oriented professional to support downstream operations in a Bulk Manufacturing (BM) facility for small molecule API production. The role involves equipment handling, documentation, compliance, and coordination with cross-functional teams to ensure efficient and cGMP-compliant manufacturing processes. Key Responsibilities: · Facility readiness, monitoring, and routine maintenance; ensure operational efficiency of key equipment including mixing vessels, centrifuges, AGR, GLR, SSR. · Participate in shift operations to support continuous manufacturing activities for small molecule APIs. · Prepare, review, and maintain process-related documentation including MFRs, BPRs, SOPs, protocols, and other downstream process documents; ensure timely submission and closure. · Good understanding in chemical engineering concepts like Extraction, Distillation, TFF, Column chromatography, Centrifugation, Filtration, Drying · Manage Quality Management System (QMS) activities, including initiation and closure of change controls, deviations, and CAPAs related to bulk manufacturing. · Track and manage inventory of raw materials and consumables used in the manufacturing process. · Adhere to and promote safety protocols and proper use of PPE within the bulk manufacturing environment. · Support the scale-up and execution of development batches in coordination with R&D · Coordinate with the engineering team and external vendors to track and complete preventive maintenance and calibration activities for downstream equipment and instruments. · Ensure compliance with Good Documentation Practices (GDP) and cGMP standards in all facility and process operations. · Liaise with vendors for equipment and instrument qualification, troubleshooting, and resolution of technical issues related to downstream processes. · Collaborate with internal stakeholders and actively participate in technical and safety training to ensure seamless production operations. Preferred candidate profile · Expertise in handling aseptic operation and critical equipment’s in downstream process. · Ensure compliance with quality management systems. · Must have knowledge on GDP, GMP practices during batch operation in commercial campaign. · Must have work experience in manage the team Industry Type: Pharmaceutical & Life Sciences Department: Production, Manufacturing Employment Type: Full Time, Permanent Education: Diploma/B.Tech/MSc/ in Chemistry/Chemical Job Type: Full-time Pay: ₹10,000.00 - ₹25,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Experience: Pharmaceutical: 3 years (Required) Life science: 3 years (Required) Analytical chemistry: 3 years (Required) Chemical engineering: 3 years (Required) Work Location: In person
Job Summary: We are seeking a diligent and organized Stores Executive to manage the receipt, storage, and issuance of raw materials, packaging materials, and finished goods in a pharmaceutical setup. The role requires strict adherence to GMP guidelines, proper documentation, and coordination with cross-functional departments to ensure smooth inventory operations. Key Responsibilities: Receive, inspect, and verify incoming materials (Raw, Packaging, and Finished Goods) as per SOPs. Maintain accurate stock records in ERP/manual system (e.g., GRN, stock registers). Ensure proper storage of materials in designated areas with correct labeling, status tagging (quarantined, approved, rejected), and environmental conditions. Follow FEFO/FIFO systems for material issuance. Issue materials to production and other departments based on material requisition slips. Conduct periodic physical stock audits and report discrepancies. Maintain hygiene and orderliness of the stores area in line with GMP and GDP guidelines. Coordinate with QA/QC for material sampling, approval, and release. Ensure compliance with SOPs, regulatory requirements, and safety norms. Monitor inventory levels and initiate procurement requests when required. Handle documentation such as GRNs , MRNs , bin cards , and stock ledgers . Manage returned goods and rejected materials as per protocols. Support during audits (internal, external, regulatory) by providing required documents and clarifications. Requirements: Diploma/Bachelor’s degree in Pharmacy , Science , Logistics , or a related field. 2–5 years of experience in pharmaceutical stores or warehouse operations. Sound knowledge of GMP , GDP , and warehouse best practices in a regulated environment. Familiarity with ERP systems (e.g., SAP, Oracle, Tally) and MS Office. Basic understanding of material classification (API, excipients, packaging, consumables, etc.). Preferred Qualifications: Experience in handling stores for formulations , injectables , or API manufacturing . Exposure to controlled substances or temperature-sensitive products. Knowledge of cGMP documentation and audit preparation. Key Competencies: Attention to detail Organizational and record-keeping skills Understanding of pharmaceutical material handling Ability to work under pressure and meet deadlines Good communication and coordination skills Job Type: Full-time Pay: ₹300,000.00 - ₹500,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Pondichéry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Experience: pharmaceutical: 3 years (Required) Clinical pharmacy: 1 year (Required) Work Location: In person
Job Summary: We are seeking a detail-oriented and motivated Accounts Executive to support daily accounting operations, financial recordkeeping, and reporting. The ideal candidate will have a strong grasp of accounting principles, be proficient with accounting software, and contribute to accurate financial management. Key Responsibilities: Maintain day-to-day financial transactions, including accounts payable/receivable, journal entries, and bank reconciliations. Prepare invoices, receipts, and other financial documents. Process vendor payments, staff reimbursements, and other disbursements. Reconcile ledger accounts and assist in month-end and year-end closing activities. Maintain proper documentation of financial records in compliance with internal controls and regulatory requirements. Assist in preparing GST, TDS, and other statutory filings. Coordinate with auditors during internal and external audits. Monitor company expenses and support budget tracking. Provide administrative support to the finance department as required. Qualifications: Bachelor’s degree in Commerce, Accounting, or Finance (B.Com, M.Com, MBA Finance, or equivalent). 1–3 years of experience in a similar accounting or finance role. Working knowledge of accounting software such as Tally, QuickBooks, Zoho Books, or ERP systems. Strong understanding of accounting standards and financial regulations. Proficient in MS Excel and other MS Office tools. Good analytical, organizational, and communication skills. Preferred Skills: Experience with GST/TDS filings and statutory compliance (specific to country). Knowledge of payroll processing and basic HR accounting. Ability to handle multiple tasks and meet deadlines in a fast-paced environment. Working Conditions: Office-based role with standard working hours. May require occasional extended hours during month-end/year-end closings or audits. Let me know if you'd like this version adapted for: A senior executive or manager-level role. A specific industry (e.g., manufacturing, IT, retail). A particular country’s tax or accounting system (e.g., India, US, UAE). Job Type: Full-time Pay: ₹10,000.00 - ₹15,000.00 per month Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Work Location: In person
Job Summary: We are seeking a highly motivated and detail-oriented Quality Control Analyst to join our biotechnology team. The ideal candidate will be responsible for performing laboratory testing to ensure products meet established specifications and regulatory requirements. This position plays a critical role in maintaining the integrity and safety of our biotechnological products. Key Responsibilities: Perform routine and non-routine analytical testing (e.g., ELISA, PCR, HPLC, SDS-PAGE, spectrophotometry) on raw materials, in-process samples, and finished products. Ensure all laboratory activities are performed in compliance with cGMP, GLP, and company SOPs. Conduct environmental monitoring of cleanroom and production areas. Maintain accurate and detailed laboratory records, including test results and observations. Perform calibration and maintenance of laboratory instruments. Investigate and document deviations, OOS (Out of Specification), and OOT (Out of Trend) results. Support method validation, equipment qualification, and technology transfer processes. Participate in internal and external audits as required. Collaborate with cross-functional teams including QA, R&D, and Manufacturing. Qualifications: Bachelor’s or Master’s degree in Biotechnology, Microbiology, Biochemistry, or related field. 1–3 years of experience in a GMP-regulated quality control laboratory (biotech or pharma preferred). Proficient in analytical techniques such as ELISA, qPCR, HPLC, and microbiological assays. Knowledge of regulatory standards including FDA, EMA, and ICH guidelines. Strong organizational and communication skills. Ability to work independently and in a team-oriented environment. Preferred Skills: Experience with LIMS or other electronic data management systems. Familiarity with biologics or cell & gene therapy products. Experience in stability testing and trending of quality data. Working Conditions: Laboratory and cleanroom environments. May involve occasional weekend or shift work depending on project needs. Job Type: Full-time Pay: ₹200,000.00 - ₹300,000.00 per year Education: Bachelor's (Required) Location: Pondy, Puducherry (Required) Work Location: In person
Key Responsibilities: Assist in performing microbiological tests on samples (e.g., pharmaceutical products, environmental swabs, etc.). Prepare media, reagents, and microbial cultures as per standard protocols. Support aseptic techniques, culturing, streaking, incubation, and colony counting. Maintain and clean laboratory equipment and workspaces. Record and analyze test results under supervision. Participate in environmental monitoring and sampling procedures. Follow Good Laboratory Practices (GLP) and safety guidelines. Assist in maintaining proper documentation and logs. Support research projects or ongoing experiments as assigned. ________________________________________ Requirements: Pursuing a Bachelor’s or Master’s degree in Microbiology, Biotechnology, Biology, or a related field. Basic understanding of microbiological techniques and lab safety. Strong attention to detail and willingness to learn. Good communication and teamwork skills. Ability to work in a fast-paced, regulated environment. Familiarity with MS Office (Excel, Word, PowerPoint) for documentation. ________________________________________ Preferred Qualifications: Previous lab coursework or hands-on experience with microbiological methods. Knowledge of aseptic technique and microbial culturing. Familiarity with ISO, GMP, or GLP standards (if applicable). Job Type: Contractual / Temporary Contract length: 6 months Pay: ₹9,000.00 - ₹10,000.00 per month Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Work Location: In person
Job Purpose: To ensure seamless planning, procurement, inventory management, logistics, and distribution of pharmaceutical products in compliance with regulatory standards and company goals. Key Responsibilities:1. Procurement & Vendor Management Coordinate with approved vendors for timely procurement of raw materials, packaging materials, and APIs. Monitor vendor performance and maintain strong supplier relationships. Assist in vendor audits and ensure compliance with regulatory standards. 2. Inventory & Material Planning Plan and maintain optimal inventory levels to avoid stock-outs or overstocking. Use forecasting tools or ERP systems to support production planning. Track material movement and reconcile inventory variances. 3. Production Coordination Align material availability with production schedules. Collaborate with production and quality teams to ensure on-time product availability. 4. Logistics & Distribution Ensure timely dispatch of finished goods to domestic and international markets. Coordinate with logistics providers for transportation, customs clearance, and cold chain compliance (if applicable). Monitor lead times and delivery performance. 5. Documentation & Compliance Prepare and maintain all supply chain documentation including invoices, shipping documents, and import/export paperwork. Ensure adherence to GDP (Good Distribution Practices), GMP (Good Manufacturing Practices), and regulatory guidelines (e.g., FDA, CDSCO, EU GMP). 6. ERP & Data Management Use ERP systems (SAP / Oracle / Tally / customized tools) for purchase orders, inventory tracking, and reporting. Analyze supply chain KPIs and prepare reports for management. Key Skills & Competencies: Strong understanding of pharma supply chain regulations Knowledge of ERP tools Analytical and problem-solving skills Attention to detail Strong communication and negotiation skills Ability to work cross-functionally Qualifications & Experience: Bachelor's degree in Pharmacy, Supply Chain, or related field MBA/PGDM in Supply Chain or Operations (preferred) 2–5 years of experience in pharmaceutical supply chain operations Job Type: Full-time Pay: ₹400,000.00 - ₹600,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Kodambakkam, Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required) Experience: Pharmacy software: 3 years (Required) Laboratory information management systems: 2 years (Required) Research laboratory: 2 years (Required) Work Location: In person
Job Summary: We are seeking a dedicated and detail-oriented QC Microbiologist with 2 to 4 years of experience in pharmaceutical/biotech microbiology labs. The ideal candidate will be responsible for performing microbiological testing to ensure compliance with GMP standards and regulatory requirements. Key Responsibilities: Perform routine microbiological testing including: Sterility testing Water and air sampling Environmental monitoring (EM) Bioburden and endotoxin testing Identification of microorganisms Microbial limit tests Maintain microbiological data and logbooks. Participate in media fill validations and aseptic process simulations. Prepare and review SOPs, protocols, and reports related to microbiology activities. Ensure all testing and documentation complies with GMP, USP, EP, and regulatory guidelines. Support microbiological investigations (OOS, deviations, CAPAs). Operate and maintain laboratory instruments such as autoclaves, incubators, particle counters, etc. Coordinate with production, QA, and validation teams for sample planning and testing timelines. Assist in audits and regulatory inspections as needed. Qualifications: · B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life science discipline. · 2 to 7 years of hands-on experience in QC Microbiology within a regulated pharmaceutical or biotech environment. · Knowledge of cGMP, GLP, and regulatory guidelines (FDA, EMA, WHO). · Familiarity with microbiological techniques and cleanroom classifications. · Good documentation practices and understanding of data integrity principles. · Proficiency in MS Office and LIMS (Laboratory Information Management System) is a plus. Job Type: Full-time Pay: ₹10,000.00 - ₹30,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Work Location: In person
Job Summary: We are seeking a dedicated and detail-oriented QC Microbiologist with 10 years of experience in pharmaceutical/biotech microbiology labs. The ideal candidate will be responsible for performing microbiological testing to ensure compliance with GMP standards and regulatory requirements. Key Responsibilities: Perform routine microbiological testing including: Sterility testing Water and air sampling Environmental monitoring (EM) Bioburden and endotoxin testing Identification of microorganisms Microbial limit tests Maintain microbiological data and logbooks. Participate in media fill validations and aseptic process simulations. Prepare and review SOPs, protocols, and reports related to microbiology activities. Ensure all testing and documentation complies with GMP, USP, EP, and regulatory guidelines. Support microbiological investigations (OOS, deviations, CAPAs). Operate and maintain laboratory instruments such as autoclaves, incubators, particle counters, etc. Coordinate with production, QA, and validation teams for sample planning and testing timelines. Assist in audits and regulatory inspections as needed. Qualifications: · B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life science discipline. · 7 to 10 years of hands-on experience in QC Microbiology within a regulated pharmaceutical or biotech environment. · Knowledge of cGMP, GLP, and regulatory guidelines (FDA, EMA, WHO). · Familiarity with microbiological techniques and cleanroom classifications. · Good documentation practices and understanding of data integrity principles. · Proficiency in MS Office and LIMS (Laboratory Information Management System) is a plus. Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Work Location: In person
Job Title: QC Manager– Analytical (10Years’ Experience) Industry: Biopharmaceutical Location: Puducherry Department: Quality Control – Analytical Reports To: QC Manager Job Summary: We are seeking a motivated and detail-oriented QC Analyst (Analytical) with 2 to 4 years of experience in a regulated pharmaceutical or biopharmaceutical QC laboratory. The role involves performing analytical testing of raw materials, in-process samples, and finished products in compliance with cGMP and regulatory requirements. Key Responsibilities: Perform routine and non-routine analytical testing of: Raw materials, intermediates, in-process, finished products, stability samples Water and cleaning validation samples (if applicable) Operate and calibrate analytical instruments such as: HPLC, GC, UV-Vis, FTIR, Karl Fischer, pH meter, Dissolution, etc. Prepare and review test records, logbooks, and related documentation as per GMP and data integrity standards. Conduct analysis as per pharmacopeial methods (USP, EP, IP, JP) Support in method validation/verification and equipment qualification activities. Review and interpret analytical results and escalate OOS/OOT results promptly. Maintain compliance with laboratory SOPs, GLP, and safety procedures. Participate in stability studies, trending data, and document control activities. Support investigations, deviations, and implementation of CAPAs related to QC analytical operations. Participate in internal and external audits and regulatory inspections. Qualifications: M.Sc. (Chemistry, Analytical Chemistry, Biotechnology) / B.Pharm / M.Pharm 2 to 4 years of hands-on experience in QC Analytical in a cGMP-compliant pharmaceutical or biopharma lab Key Skills: Handling of oncology molecules is plus Proficient in handling HPLC, GC, and other analytical instruments Familiarity with pharmacopeial testing (USP, EP, IP) Good understanding of cGMP, GLP , and data integrity practices Strong documentation and observation skills Working knowledge of LIMS or electronic data systems is an advantage Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Provident Fund Experience: Laboratory: 10 years (Required) Clinical laboratory: 10 years (Required) Laboratory procedures: 10 years (Required) Laboratory techniques: 10 years (Required) Work Location: In person
Job Summary: We are seeking a qualified and proactive Safety Officer with a mechanical engineering background to ensure compliance with occupational health and safety (OHS) guidelines. The Safety Officer will be responsible for implementing safety policies, conducting risk assessments, and promoting a culture of safety in all mechanical operations and projects. Key Responsibilities: Enforce safety protocols and regulations across mechanical engineering activities. Conduct regular site inspections, hazard identification, and risk assessments. Investigate incidents/accidents, determine root causes, and recommend corrective actions. Assist in the development and implementation of safety management systems (SMS). Ensure proper usage and maintenance of Personal Protective Equipment (PPE). Organize and conduct safety training and toolbox talks for employees and contractors. Maintain records of safety inspections, incidents, and training. Ensure compliance with local, state, and national safety regulations. Collaborate with engineers and project managers to integrate safety into project planning and execution. Monitor mechanical operations (e.g., heavy machinery, fabrication processes) for safety compliance. Qualifications & Skills: Bachelor’s Degree or Diploma in Mechanical Engineering or related field. Certification in occupational health and safety (e.g., NEBOSH, OSHA, IOSH). 2–5 years of experience in a safety role, preferably in a mechanical or industrial environment. Strong knowledge of mechanical systems and associated risks. Familiarity with safety laws, regulations, and best practices. Excellent communication, observation, and problem-solving skills. Ability to work independently and as part of a team. Preferred: Experience in sectors like construction, oil & gas, manufacturing, or power plants. First Aid and Fire Safety certifications. Working knowledge of safety software or digital reporting tools. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicheri, Puducherry: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) License/Certification: OSHA (Required) NEBOSH (Required) IOSH (Required) Work Location: In person
Job Summary: We are seeking a dedicated and detail-oriented QC Microbiologist with 2 to 4 years of experience in pharmaceutical/biotech microbiology labs. The ideal candidate will be responsible for performing microbiological testing to ensure compliance with GMP standards and regulatory requirements. Key Responsibilities: Perform routine microbiological testing including: Sterility testing Water and air sampling Environmental monitoring (EM) Bioburden and endotoxin testing Identification of microorganisms Microbial limit tests Maintain microbiological data and logbooks. Participate in media fill validations and aseptic process simulations. Prepare and review SOPs, protocols, and reports related to microbiology activities. Ensure all testing and documentation complies with GMP, USP, EP, and regulatory guidelines. Support microbiological investigations (OOS, deviations, CAPAs). Operate and maintain laboratory instruments such as autoclaves, incubators, particle counters, etc. Coordinate with production, QA, and validation teams for sample planning and testing timelines. Assist in audits and regulatory inspections as needed. Qualifications: · B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life science discipline. · 6 to 10 years of hands-on experience in QC Microbiology within a regulated pharmaceutical or biotech environment. · Knowledge of cGMP, GLP, and regulatory guidelines (FDA, EMA, WHO). · Familiarity with microbiological techniques and cleanroom classifications. · Good documentation practices and understanding of data integrity principles. · Proficiency in MS Office and LIMS (Laboratory Information Management System) is a plus. Job Type: Full-time Pay: ₹30,000.00 - ₹60,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Work Location: In person
Job Summary: The Safety Officer is responsible for ensuring compliance with occupational health and safety (OHS) guidelines and regulations. This role includes monitoring operations to eliminate hazardous activities, conducting risk assessments, and enforcing preventative measures to ensure a safe working environment in the factory. Key Responsibilities: Develop, implement, and monitor health and safety plans, policies, and procedures specific to the factory. Conduct regular risk assessments and safety audits to identify hazards and recommend corrective actions. Ensure all safety equipment and machinery are functioning properly and compliant with regulations. Conduct toolbox talks and safety training sessions for workers and supervisors. Investigate accidents, incidents, and near-misses; prepare reports and recommend solutions to prevent recurrence. Ensure compliance with local, state, and national safety regulations and standards (e.g., OSHA, ISO 45001). Maintain records of inspections, incidents, and training activities. Coordinate with various departments to ensure adherence to safety protocols during maintenance, production, and logistics operations. Liaise with external health & safety inspectors during visits and audits. Promote a culture of safety awareness among all employees. Qualifications and Skills: Bachelor’s degree or diploma in Occupational Health & Safety, Engineering, or a related field. Certification in industrial safety (NEBOSH, IOSH, or equivalent) preferred. 2–5 years of experience as a Safety Officer in a factory or industrial environment. Strong knowledge of safety regulations, risk assessment, and incident investigation. Excellent communication and interpersonal skills. Ability to train and guide employees in safety protocols. Proficient in Microsoft Office and safety management systems. Working Conditions: Factory environment with exposure to machinery, noise, and potentially hazardous materials. Requires use of personal protective equipment (PPE). May involve shift work depending on factory operations. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicheri, Puducherry: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: Pharmaceutical: 5 years (Required) License/Certification: OSHA (Required) NEBOSH (Required) IOSH (Required) Work Location: In person
Job Summary: We are seeking a dedicated and detail-oriented QC Microbiologist with 10 years of experience in pharmaceutical/biotech microbiology labs. The ideal candidate will be responsible for performing microbiological testing to ensure compliance with GMP standards and regulatory requirements. Key Responsibilities: Perform routine microbiological testing including: Sterility testing Water and air sampling Environmental monitoring (EM) Bioburden and endotoxin testing Identification of microorganisms Microbial limit tests Maintain microbiological data and logbooks. Participate in media fill validations and aseptic process simulations. Prepare and review SOPs, protocols, and reports related to microbiology activities. Ensure all testing and documentation complies with GMP, USP, EP, and regulatory guidelines. Support microbiological investigations (OOS, deviations, CAPAs). Operate and maintain laboratory instruments such as autoclaves, incubators, particle counters, etc. Coordinate with production, QA, and validation teams for sample planning and testing timelines. Assist in audits and regulatory inspections as needed. expertise in environmental monitoring, sterility testing, microbial limit testing, and GMP compliance. Adept at leading teams, training staff, and coordinating with cross-functional departments to ensure regulatory compliance and product quality. Core Competencies Qualifications: · B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life science discipline. · 7 to 10 years of hands-on experience in QC Microbiology within a regulated pharmaceutical or biotech environment. · Knowledge of cGMP, GLP, and regulatory guidelines (FDA, EMA, WHO). · Familiarity with microbiological techniques and cleanroom classifications. · Good documentation practices and understanding of data integrity principles. · Proficiency in MS Office and LIMS (Laboratory Information Management System) is a plus. Microbial Limit Testing (MLT), Sterility Testing, Environmental Monitoring, Water Analysis (TOC, Conductivity, Bioburden), Media Preparation & Validation, Cleanroom Validation, Regulatory Compliance (GMP, GLP, FDA, MHRA), Quality Risk Management, Audit Preparedness & CAPA, Team Leadership & Training. Expertise in environmental monitoring, sterility testing, microbial limit testing, and GMP compliance. Adept at leading teams, training staff, and coordinating with cross-functional departments to ensure regulatory compliance and product quality. Job Type: Full-time Pay: ₹10,000.00 - ₹40,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Work Location: In person