236 Bpr Jobs - Page 4

Responsibilities: * Conduct BMR reviews * Prepare SOPs and BPRs * Collaborate with R&D team on new product development * Ensure compliance with industry standards * Manage production processes Food allowance Office cab/shuttle

Role & responsibilities (1) To perform the daily IPQA related activity and line clearance related activity.. (2) To monitor the plant critical areas like clean room (Manufacturing / Filling), Packing, labelling, OBD verification, water system, utility supply area etc. for the GMP compliance. (3) To ensure the End to End Control in Manufacturing, packing and material storage activity (4) To prepare and review GMP documents such as SOPs, protocol and other relevant documents. (5) To review the executed batch manufacturing / packing records and review of COA & analytical data. (6) Handling of Control sample management and review of stability sample management procedure and its compliance. (7) T...

The Production Chemist will be responsible for executing and monitoring API manufacturing processes, ensuring compliance with cGMP, SOPs, and regulatory guidelines . The role involves operating chemical process equipment, documentation, troubleshooting, and process optimization to achieve efficiency, safety, and quality standards. Key Responsibilities & Duties: Process Execution: Perform batch manufacturing activities in line with Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and cGMP requirements. Equipment Operation: Operate and monitor reactors, centrifuges, multi-mill, shifter, tray dryer, filtration systems, GLR, and SSR equipment . Quality Assurance & Complianc...

Oversee QA For Contract Manufacturing: Draft Agreements, Review Batch Docs, CoAs, Deviations, And Artwork. Ensure GMP Compliance, Traceability, And Regulatory Alignment. Support IPQA Checks, Sampling, Audits, And Real-Time Issue Resolution. Required Candidate profile Skilled in corporate QA documentation, third-party coordination, and artwork review Manage change control, audit readiness, and traceability Ensure regulatory compliance and product release approval

Division Department Sub Department 1 Job Purpose Operate & maintain packing machines to achieve quality product & shift wise targeted output with maximum utilisation. Key Accountabilities (1/6) Prepare the machine for packing operation as per production plan by using proper resources to ensure smooth operations Perform calibration, clean and set different equipment and machines as per SOP and schedules for on-time completion of batch processing Check the suitable change part as per product requirement Arrange change parts & stereo for batch packing activity Key Accountabilities (2/6) Operate the packing machines by using minimum resources to get quality product Evaluate the product dimension...

Asst. Manager – External Preparation and Oral Liquid Finished Formulations Location - Paria Pardi Gujarat 10 to 15 Years B. Pharma / M. Pharma with FDA Approval Interested? Share your CV nidhi@iihcrecruiters.com OR Call/WhatsApp +91 73548 88500 Required Candidate profile Equipment qualification (DQ, IQ, OQ, PQ) Validation (HVAC, Water, Equipment, Systems) Regulatory compliance (WHO GMP, PIC/S, EU, MHRA, FDA) Audit handling (Internal, Vendor, Regulatory)

Job Description 1. Preparation and review of operational packing materials list, Packaging materials specifications, Packaging materials specifications base documents, BOM, BPR (PAS X and SAP), In House Labels for Exhibit Batches, Pack Split Up and Pallet Matrix. 2. To provided technical support to Production, QA, QC and RA. 3. Review of Artwork, Shade cards and print proof etc. Initiate Change controls, Deviation and CAPA and close all action item of change control, CAPA and deviation within time frame preparation of investigation report of deviation. Coordinate with R&D and QA for Primary Packaging Materials Specifications, Primary Pack Specification and Standard Test Procedures. 4. Prepar...

Responsible for IPQA, line clearance, preventive maintenance checks, BMR/BPR review, vendor qualification, audit support, QAMS documentation, APQR preparation, and compliance verification across departments. Required Candidate profile M.Sc or M.Pharm or BSc or BPharm 2-3 Years 2.5 to 3.5 LPA

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 departments to maint...

Officer Production, Vapi, Gujarat Responsibilities: Equipment cleaning as per ECR/SOPs Ensure cGMP compliance Execute batch charging (BMR/BPR) Maintain records Complete BMR/BPR/ECR documentation Apply at talent@hireindians.com or call 8882212459. Required Candidate profile Qualifications & Skills: * B.Sc. / M.Sc. in Chemistry (Analytical/Organic/Industrial) or B. Pharma. * 1–4 years of experience in pharmaceutical formulation/API manufacturing.

Walk-in interview For Sun Pharmaceutical Industries Limited, Dadra Date: 14th Sept 25 (Sunday) We are recruiting for our OSD manufacturing facility located at Dadra Time: 10 AM to 4 PM Interview Venue: Sun Pharmaceutical Industries Ltd, Survey No. 694, Dadra - 396193, (U.T. of D & N. H.), India, Following are the requirements for our manufacturing facility at Dadra Location. 1) Designation: Operator / Sr. Officer / Executive / Sr. Executive Engineering Education: ITI / Diploma / B. E (Elect. / E.C /Inst./ Mech) Department: Engineering Experience : 6 8 years of Experience of handling Engineering QMS, OSD Process Maintenance, Engineering Projects, Utility and Water System in OSD manufacturing ...

Role & responsibilities Perform daily IPQA activities and line clearance in the manufacturing facility. Conduct training for IPQA and production personnel regarding IPQA activities. Review and update artwork/shade cards as per proposed Change Control Note (CCN) details. Oversee language translation processes for documents such as quotations, PR, PO, and final artwork. Monitor plant critical areas for GMP compliance. Prepare and review GMP documents, including SOPs, protocols, and other relevant records. Review executed batch manufacturing/packing records, COA, and analytical data. Manage control sample handling and review stability sample management procedures for compliance. Participate in ...

As a Trainee Executive in the Packing Section with a requirement of 2 years of experience, your main responsibility will be to manage and schedule the packing plan for various products across different sections. This includes efficiently allotting manpower for packing tasks and ensuring that the packing is carried out effectively. You will be expected to report all activities to the senior management and prepare documents such as Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). It is essential to achieve the targets set for the Packaging Section and have a comprehensive understanding of Current Good Manufacturing Practice (CGMP). Furthermore, you should be familiar with fac...

Senior Executive QA 1 Post based in Kathua, Jammu & Kashmir The ideal candidate brings 8-10 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) S...

Quality Assurance Pharmacovigilance (PV) Specialist based in Hyderabad. The ideal candidate brings 3-5 and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Ka...

Senior Officer QA 3 Posts based in Kathua, Jammu & Kashmir. The ideal candidate brings 4-6 yrs exp and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen...

Senior Officer QA (QMS) 1 Post based in Kathua, Jammu & Kashmir. The ideal candidate brings 4 - 6 yrs exp and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean...

The ideal candidate brings 2 yrs exp and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Strengthen QMS: author/review SOPs, BMR/BPR, oversee IPQA/AQA,...

Designation - Sr. Executive / Asst. Manager - Quality Assurance Company - Leading Pharma Raw Material Mfg. Company Job Location - Ahmedabad Qualification - B.Sc. / M.Sc. / B.E.- Chemical / B.Pharm Experience - Min. 6+yrs. and above Required Candidate profile Company coming up with Greenfield Project Responsible for handling QA / GMP Related documentation QMS, Audit Preparation, Vendor Questionnaire, Market Compliant & Customer Compliance

As a Digital Solutions Consultant at Worley, you will have the opportunity to work collaboratively with a diverse and inclusive team to deliver complex projects for our clients. Worley, a global professional services company specializing in energy, chemicals, and resources, is at the forefront of bridging the gap towards more sustainable energy sources while meeting the current societal needs for energy, chemicals, and resources. In this role, you will be responsible for supporting strategic initiatives, contributing to continuous improvement efforts, adhering to governance structures, and assisting in reporting tasks. We are looking for a candidate who is eager to learn, open to feedback, a...

Title: Executive API Custom Field 2: 2806 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Preparation and Review of Standard Operation Procedures, Review of executed BMR, BPR, ECR, etc, Responsible for Change control management, Preparation and Review of Annual product review, Responsible QA Release, Responsible for Process Performance Qualification and Cleaning Validation, Handling of Deviation, Responsible for OOS, OOT investigation related to manufacturing, Responsible for reviewing of Line Clearance activities, Responsible for Finished product sampling Job Segment: QA, Quality Assur...

Roles and Responsibilites 1.In process Quality Assurance activity in Production and warehouse area 2.Provide line clearance as per SOP 3.Monitoring and QA rounds in production and Warehouse 4.Sample verification against TRF / BPCR 5.Carry out Semi-finished / finished product sampling for release, stability study and control samples 6.To send samples along with TRF to Quality control laboratory 7.Participate in media fill, process validation, cleaning validation activities as per requirement 8.Timely communication and co-ordination with all the stake holders 9.Participation in Change control, Deviation & Investigations as per requirement 10.Preparation / review of documents like; SOPs, risk a...

Officer Production, Vapi, Gujarat Responsibilities: Equipment cleaning as per ECR/SOPs Ensure cGMP compliance Execute batch charging (BMR/BPR) Maintain records Complete BMR/BPR/ECR documentation Apply at talent@hireindians.com or call 8882212459. Required Candidate profile Qualifications & Skills: * B.Sc. / M.Sc. in Chemistry (Analytical/Organic/Industrial) or B. Pharma. * 1–4 years of experience in pharmaceutical formulation/API manufacturing.

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety & quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture, and technology to become the best version of you. And we're counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. Position Transformation Manager, GDS PAS Tax, India Rank Manager Education: Any Masters or Bachelor's Degree. PMP/Agile/Prosci or other relevant certification preferred. Experience: Minimum 12-15+ years strong work experience in a consulting environment and proven track record as a program &/change manager leading large scale global and/or c...