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- ...Pharmaceutical Quality Assurance (QA) role ensures drug products meet safety, efficacy, and regulatory standards by overseeing documentation, processes, audits, and batch release, focusing on building quality into manufacturing (cGMP) through activities like SOP review,...Suggested
- ...,000 per month Are you looking to start your career in the pharma industry and gain hands-on experience in Computer System Validation... ...Youll learn: Computer System Validation concepts Documentation & regulatory compliance Real-time exposure to pharma validation...SuggestedInternship
- ...About Company : Top 10 Pharma Company having an API, Formulation and Biologics business. Job Title: Assistant General Manager – EHS... ...inspections. Drive closure of audit observations. 8. Documentation & Reporting Maintain EHS records, MIS reports, and compliance...SuggestedFull timeFor contractorsLocal area
Rs 5 lakh p.a.
...Production Supervisor to manage day-to-day operations on the chemical/pharma manufacturing floor, ensuring safety, quality, and output... ...; assign tasks and track performance. Ensure proper documentation of batch records, logbooks, and production reports. Coordinate...SuggestedFull timeLocal areaShift workRotating shift- ...Education: B. Pharma Experience: Min 8 years in Pharma (MDI / DPI / Derma & Nasal) (USFDA exposure mandatory) CTC: 10–12 LPA Key Responsibilities: • Preparation and review of Validation Master Plan, Cleaning Validation Master Plan, Protocols & Reports • Execution...Suggested
- ...Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing... ...instruments failures, replacement, maintenance of PLC / HMI / SCADA and documentation Key Roles & Responsibilities To take care of Plant...SuggestedContract workWorldwideShift work
- ...responsibilities include managing batch release auditing processes handling deviations conducting risk assessments and maintaining documentation to guarantee patient safety. Lab Manager Lab Manager 4 Key Responsibilities Batch Record Review & Release: Review...SuggestedFull time
- ...targets with optimum utilization of manpower and equipment. Monitor and control process parameters, yields, and material usage. Documentation & Compliance Review and ensure completion of Batch Manufacturing Records (BMR) and related GMP documents. Ensure adherence...SuggestedShift work
- ...Immediate Hiring | Computer System Validation (CSV) Pharma Industry Were looking for passionate professionals to join our team in the... ...of manufacturing systems (SCADA, HMI, PLC). Conduct and document Computer System Validation (CSV) activities for pharmaceutical/life...SuggestedImmediate start
- ...during scale-up and identifying all critical process parameters for a seamless scale-up Knowledge on IUT, VQ, LFR/PDR reports documentation. Understand the scalability of the chosen process, in coordination with TSD and Production. Amicable relationship with PRD and...SuggestedFlexible hours
- ...Minimum work experience- 10-15 years of experience in sales & Marketing and at least 2 years of experience as Regional Sales Manager in pharma company in specific area of speciality Skills & attributes Technical Skills In depth understanding of Indian...SuggestedFull timeRelocation package
- ...reliability and efficiency of utilities. Compliance, QMS & Documentation Prepare and maintain all GMP and GDP documentation for utility... ...areas and documentation. Ensure 100% compliance with Pharma GMP and regulatory expectations. Prepare quarterly and monthly...SuggestedFor contractorsShift work
- ...Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing... ...related modifications, ensuring thorough safety reviews and proper documentation. Conduct incident investigations for process safety-related...SuggestedContract workWorldwide
- Company Description Founded in 2021, Naukri Pay is a forward-thinking human resources and talent solutions company headquartered in Kolkata, West Bengal, India. The company bridges the gap between job seekers and employers by providing customized solutions tailored...SuggestedFull time
Rs 1 - 7 lakhs p.a.
We are looking for a meticulous and dedicated Pharmacist / Senior Pharmacist to join our healthcare team. The ideal candidate will be instrumental in ensuring the safe, effective, and economical delivery of pharmaceutical care, working closely with various healthcare professionals...SuggestedLocal area- ...inspections, audits, and CAPA implementation Ensure proper documentation of maintenance records, logbooks, and change controls Participate... ...formulation manufacturing facility Strong knowledge of pharma manufacturing equipment and utilities In-depth understanding...Contract workFor contractorsShift work
- ...through robust appraisals as part of the credit approval process and by reviewing the loan sanctioning, disbursement process and documentation to ensure controlled operations . Review financial risk via analysis of regional operations MIS and Data Analytics reports ....
- ...Support risk and review process through the credit approval process and by reviewing the loan sanctioning disbursement process and documentation to ensure controlled operations Review financial risk via analysis of city/ branch operations MIS and Data Analytics reports...Full timeLocal area
- ...Company Description JD Pharma Consultants Pvt Ltd specializes in offering comprehensive turnkey solutions tailored for the pharmaceutical industry. The company manages end-to-end projects, including design, supply, installation, and commissioning, ensuring excellence...Full time
- ...Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a...Contract workWorldwide
- ...Ensure adherence to approved BPR/BMR, SOPs, and packing specifications. Achieve daily, weekly, and monthly production targets. Documentation & Compliance Complete and review Batch Packing Records (BPR) accurately and on time. Ensure compliance with cGMP, GDP, SOPs,...Shift work
Rs 3 - 6.5 lakhs p.a.
...Assist in processing reactivation requests. Welcome newly onboarded customers. Verify policy issuance details and update system records if required. Make introductory calls to new customers within a defined time frame. Confirm receipt of policy documents....- ...Purpose The Warehouse Executive is responsible for managing receipt, storage, issuance, and documentation of raw materials, packaging materials, finished goods, and other inventory in compliance with GMP (Good Manufacturing Practices) and company SOPs. The role ensures...Shift work
- ...shutdown, and any production requirement. Compliance, GMP & Documentation Maintain all documentation as per GMP, GDP, and engineering... ...deviations, abnormalities, or near misses. Ensure utilities meet pharma requirements for PW, Compressed Air, HVAC utility supply, etc....For contractorsImmediate startShift work
- ...inspections investigations interviews and key control audit. Monitor Closed Circuit Televisions and alarm systems. Authorize monitor and document access to secured areas. Assist guests/employees during emergency situations. Respond to accidents contact EMS or administer first...Full timeShift work
- ...process parameters (CPPs) and critical quality attributes (CQAs). Support equipment qualification and process capability studies. Documentation & Compliance Prepare and review manufacturing instructions, BMR/BPR, SOPs, and process flow diagrams. Ensure compliance with...
- ...within specified on monthly review the location portfolio and report early/potential stress that all collections activities are properly documented in the form of Collection that all collections processes and Risk governance mandates rolled out are completely adhered to at each...Full time
- ...Solid Oral / Cream and Ointment experience is must Job Responsibilities / Deliverables - Well versed in the analytical review of documents, which includes those from GLP section. Handling of OOS, OOT, Events, Change control and CAPA. Review and ensure compliance of...Shift work
- ...in the implementation of best practices, new technologies, and software solutions to optimize PPIC functions. ~ Compliance and Documentation: Ensure that all PPIC activities comply with Good Manufacturing Practices (GMP), pharmaceutical regulations, and company policies...
- ...maintenance, calibration, electrical EHS compliance, and active participation in regulatory and Quality Management System (QMS) documentation in accordance with cGMP requirements. Position / Job Title Executive Engineering Department Engineering Reporting...

