309 Gmp Compliance Jobs - Page 4

Position Summary: The Deputy Manager Warehouse will be responsible for planning, organizing, and overseeing all warehouse operations, ensuring efficient receipt, storage, dispensing, and dispatch of materials. The role requires strict adherence to cGMP and GDP standards, effective audit management, and strong leadership to guide the warehouse team. Key Responsibilities: Manage end-to-end warehouse activities, including material receipt, storage, dispensing, and dispatch . Ensure compliance with cGMP, GDP, and regulatory guidelines in all warehouse operations. Prepare for and actively participate in regulatory and customer audits ; implement corrective and preventive actions. Develop and moni...

As a General Manager Factory Operations at Madhu Jayanti International Pvt. Ltd., your role is crucial in leading and optimizing the manufacturing facility. The company, established in 1942, is a pioneering tea house with a strong presence in the international market. Your primary responsibility will be to ensure operational efficiency, waste reduction, and productivity improvement through hands-on leadership in factory automation, machine line operations, GMP compliance, and lean manufacturing principles. **Key Responsibilities:** - Oversee daily factory operations encompassing production, quality, maintenance, and logistics. - Lead factory automation initiatives to enhance process efficien...

As an experienced Regulatory Affairs Consultant with specialized knowledge in lipid-based pharmaceutical products, particularly Fish Oil Triglycerides such as EPA/DHA omega-3 fatty acids, your role will involve providing regulatory support and strategic guidance for drug, dietary supplement, or nutraceutical products containing fish oil derivatives to ensure compliance with global regulatory standards including FDA (CDER & CFSAN). You will be a crucial resource within the organization, offering technical expertise and regulatory guidance for the development, manufacturing, and commercialization of lipid-based pharmaceutical products. Your role will require strong cross-functional collaborati...

Role Overview: As a Quality Assurance Specialist at Apotex Inc., you will report to the General Manager, QA 3rd Party Ops, India, and play a crucial role in ensuring the quality systems required for Apotex Suppliers meet regulatory and GMP compliance obligations. Your responsibilities will involve negotiating Quality Agreements with external suppliers, monitoring the status of Quality Agreements, reviewing GMP Quality Documents, Stability protocols, and Change Controls of third-party manufacturers, and providing support for customer requests for products manufactured by Apotex for Third Parties. Your attention to detail, strong communication skills, and knowledge of pharmaceutical manufactur...

Required Experience: 2 to 6 years of hands-on experience in Downstream Processing Educational Qualifications: B.Sc / M.Sc in Life Sciences ITI / Diploma B. Pharmacy / M. Pharmacy B.Tech / Any relevant technical degree Key Skills & Responsibilities: Experience in handling equipment such as: Chromatography columns and systems Column Packing (BPG and Chromoflow) TFF (Tangential Flow Filtration) Systems Centrifuge Systems Filtration, Filter Integrity Testing, Buffer Preparation, CIP/SIP Systems Strong documentation skills QMS/GMP Compliance and process awareness Candidate Preferences: Immediate joiners are highly preferred Only male candidates are encouraged to apply Candidates with prior biolog...

Dear Candidate, WE ARE HIRING Department: - Production- DS Designation: - Dy Manager / Manager Qualification: - Preferably Post Graduation in Science Experience: - 15+ Years Age: - Between 35- 40Years Mandatory: - Should come in all shifts, including Night shifts Role: Shift-in-charge for entire DS floor Job Description: > Strong Functional knowledge of DS Biologics (Chromatography and related purification experience protein/ Insulin handling experience preferable). Capable of handling large teams as we have around 45 members in each shift, around 50% of contractual staff. Strong administration / team management capabilities to streamline GMP across the floor. Monitoring the efficiency of em...

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Role - Engineer & Sr. Engineer - Mechanical Location - Thane, Mumbai - Experience in Pharma consulting or consulting industry/ company providing design engineering and EPC services in the Pharma industry is mandatory. Key Responsibilities: 1. Activity & Resource Planning: Plan and manage activities and resources. 2. Site Inspections: Conduct inspections, prepare GAP analysis reports, and conduct FAT. 3. Travel: Visit sites as per project requirements. 4. Client Queries: Clarify technical queries in line with regulatory guidelines. Technical Skills: 1. Regulatory Compliance: Knowledge of local statutory requirements. 2. Team Leadership: Experience in leading teams. 3. Process/Utility Equipmen...

Job Description 1. Monitor raw material dispensing activity. 2. Perform daily IPQA activities as per SOP-defined frequency and ensure timely closure of IPQA observations. 3. Conduct validation sampling as per approved validation protocols. 4. Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and compliance. 5. Perform ERP-related transactions of IPQA. 6. Check BSR (Batch Summary Record) and Shipper inspection as per SOP. 7. Manage issuance, review, and reconciliation of formats across all departments. 8. Conduct IPQA rounds and share observations with concerned HODs for corrective action and compliance. 9. Ensure cleaning, sanitation, and hygiene in all depa...

Role - Senior Instrumentation Engineer Location - Thane, Mumbai - Experience in Pharma consulting or consulting industry/ company providing design engineering and EPC services in the Pharma industry is mandatory. Key Responsibilities: 1. Activity & Resource Planning: Plan and manage activities and resources. 2. Site Inspections: Conduct inspections, prepare GAP analysis reports, and conduct FAT. 3. Travel: Visit sites as per project requirements. 4. Client Queries: Clarify technical queries in line with regulatory guidelines. Technical Skills: 1. Regulatory Compliance: Knowledge of local statutory requirements. 2. Team Leadership: Experience in leading teams. 3. Process Equipment: Basic unde...

Role - Principle Engineer - Mechanical Location - Hyderabad - Experience in Pharma consulting or consulting industry/ company providing design engineering and EPC services in the Pharma industry is mandatory. Key Responsibilities: 1. Activity & Resource Planning: Lead and represent project meetings with clients. 2. Client Correspondence: Handle routine correspondence with clients and stakeholders effectively. 3. Marketing Support: Provide technical details as required. 4. Site Inspections: Conduct inspections, prepare GAP analysis reports, and conduct FAT. 5. Client Queries: Clarify technical queries in line with regulatory guidelines. Technical Skills: 1. Regulatory Compliance: Knowledge of...

We are looking for skilled committed Production Operators.candidate will be responsible for operating production machinery,maintaining production line efficiency,ensuring quality compliance cGMP environment. share resume to hrd@stedmanpharma.com

About Precision NanoSystems Inc. (PNI) Precision NanoSystems Inc. (PNI) is a manufacturer of instruments, kits and reagents in the global nanomedicine market providing tools for drug development and cell-specific delivery to study, diagnose and treat disease. PNI's NanoAssemblr family of instruments allow scientists to rapidly develop novel nanomedicine drug candidates for pre-clinical testing. PNI's NanoAssemblr Scale-up platform enables the translation of these drug candidates to clinical testing and eventually to commercial use. PNI's NanoAssemblr Transfection Reagents use nanomedicine technology to deliver genetic materials in primary cells vitro and in vivo, enabling disease researchers...

Key Skills :QMS, GMP, GDP, Audit & Compliance, SOP Management ,equipment qualification IQ/OQ/PQ,ICH, WHO, USFDA Qualifications: B.Pharm / M.Pharm / M.Sc. in Chemistry, Microbiology Experience : 7–10 pharmaceutical manufacturing setup. CTC : 6-9 LPA

We Are Hiring Officer: Purchase & Logistics Company: GreenSignal Bio Pharma Pvt. Ltd. Role: Officer Purchase Location: Kodambakkam , Chennai Industry: Pharmaceuticals / Biopharmaceuticals / Vaccine Manufacturing About the Company: GreenSignal Bio Pharma Pvt. Ltd. is a leading manufacturer of vaccines and sterile pharmaceutical products. We are committed to delivering high-quality, life-saving solutions globally. Join our team and contribute to ensuring Wellness for All through innovation and operational excellence. Job Description: We are seeking a proactive and detail-oriented Officer – Purchase & Logistics with experience in pharmaceutical or sterile manufacturing environments. The ideal c...

To ensure GMP compliance to approved procedures / practices as per SOP. Responsible for review of analytical records, handling of QMS related activities for Quality control.Ensure compliance for Quality Control.

Assist in the planning, designing, and drafting of HVAC layouts, duct routing & Cleanroom systems utility designs for pharma & industrial projects apply cleanroom classifications (ISO 14644, GMP) Drawings using AutoCAD or relevant design software

Role & responsibilities 1. To attend/supervise all jobs related to Engineering (Mechanical maintenance) and projects at site. 2. Preparation and Review of all documents related to Engineering Maintenance. 3. Execution of maintenance jobs of all utility equipment as per SOP and Good engineering practice. 4. To maintain critical spares related to mechanical for all equipment in site. 5. To attend emergency breakdown on all plant wide machines round the clock as and when the need arises. 6. Timely execution of all preventive maintenance jobs in co-ordination with vendor and users. 7. To maintain the preventive maintenance logs, area/ equipment log and preventive maintenance schedules for all th...

Role Overview: As an Engineer specializing in Static & 2D, you will be accountable and responsible for preparing and revising 2D engineering drawings for pressure vessels, tanks, reactors, and Heat Exchanger using AutoCAD or equivalent software. Your role will involve developing General Arrangement (GA) drawings, nozzle orientation, fabrication drawings, and bill of materials (BOM). Collaboration with cross-functional teams such as 3D and production will be essential to ensure seamless integration of 2D elements. It will be your responsibility to ensure that all designs meet technical standards, regulatory requirements, and project objectives. Additionally, you will assist in preparing docum...

Warehouse Manager for API Manufacturing Plant. Responsible for GMP compliance, material handling, inventory control audit & documentation. Must have experience in API, API Intermediate & Chemical industries with strong regulatory knowledge.7666036008 Annual bonus Provident fund Health insurance

Lead API chemical process ops, ensure cGMP & safety, optimize processes, supervise plant, train teams, handle audits, ensure compliance & quality. For executive- 2-8 years experience AM- 8-10 Years experience Manager- 12-14 years experience

Responsible for overall QA function.Handling of Customers complaint up to customer satisfaction level and to organize customer complaint meetings.Face customer audits and fulfil audit observations compliance. To do online survey of customers.

Walk-in Drive | TIL Healthcare | Multiple Openings in Production, QA, Engineering & QC TIL Healthcare is a part of "Jhaver Group of Companies" having a turnover of USD 450mn whose core activities include Manufacturing, Marketing, Engineering, Construction and Trading like diversified businesses. Our plants are accredited approvals like EUGMP, TGAAustralia, UK MHRAetc. TIL manufactures Tablets, Liquids, Powders in Sachets, and Capsules and with well-known partners for several European companies. We are considered as Pioneers in Amino Acids in India and few known brands include ApetaminT/AstyminT/Astyfer/Neutrosec/Urelog/Peglec/HappenzT. Walk-in Interview Details: Date: Sunday, 28th September ...

Role & responsibilities To ensure GMP practices are followed during various stages of production activities of finished drug product. To perform in process checks in Tablets/Capsule/Ointment/ Liquid/Dry powder To ensure various operations are complying as per SOP. Daily & Monthly calibration of IPQC instruments. Sampling of Control and Stability samples. To ensure that the facility is maintained in a clean and sanitary conditions. In-process checks during dispensing & secondary packing activities. To ensure timely sampling of finished products, control samples, validation samples & stability samples. To monitor Dispensing of raw material and packing material required for the manufacturing of...