236 Bpr Jobs - Page 5

Lead and optimize sterile injectable production, ensuring cGMP compliance, timely delivery, and continuous improvement GMP compliance, planning, output/yield/OEE monitoring, team management, audits, BMR/BPR approval, coordination with QA/QC,

Role & responsibilities 1. Documentation Issuance & Control - Issue Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and logbooks to production as per SOP. - Maintain master documents for BMR, BPR, SOPs, and other controlled documents with proper version control. - Implement and maintain document control systems as per GDP and cGMP requirements. 2. Batch Record Review & Compliance - Review executed BMR and BPR for completeness, accuracy, and compliance with approved specifications. - Coordinate with production to resolve discrepancies, deviations, and documentation errors. 3. SOP & Change Control - Assist in preparation, review, and revision of SOPs related to QA and documenta...

Job Title: Quality Assurance Officers (4 Positions) Company: Nourish Pharmaceutical Pvt Ltd Location: Kheda, Gujarat Job Type: Full-time Nourish Pharmaceutical Pvt Ltd is a leading pharmaceutical company committed to delivering high-quality products. We're expanding our Quality Assurance team and looking for talented professionals to join us. Positions: 1. Quality Assurance Officer - Production 2. Quality Assurance Officer - QMS 3. Quality Assurance Officer - Validation & Qualification 4. Quality Assurance Document Control Officer Job Descriptions: 1. Quality Assurance Officer - Production - Key Responsibilities: - Ensure cGMP compliance in production areas - Manage and review Batch Manufact...

Execute and monitor production activities as per SOPs and cGMP guidelines. Ensure compliance with safety, health, and environmental regulations during production operations. Handle day-to-day production activities for API and intermediate products. Required Candidate profile B.Sc. / M.Sc. (Chemistry) / B.E / B.Tech. (Chemical Engineering) with 2 to 7 years in API or Intermediates Manufacturing Strong knowledge of API / Intermediates manufacturing processes.

Hiring for Production Chemist Job Location - Jammu (Sambha) Interview Location - Chandigarh Salary bar - 5LPA - 5.5LPA Max Industry pref. - Pharma (API) Interested one share resume on meenakshikandpal@tdsjobs.com 9041666549

Key Responsibilities Execute daily production operations as per approved SOPs, BMR/BPR, and production plan. Handle manufacturing processes, equipment operations, cleaning, and changeover activities. Prepare, review, and maintain production documentation (BMR, BPR, logbooks, and SOPs). Ensure adherence to cGMP, GDP, and EHS standards across production processes. Actively participate in QMS activities deviations, CAPA, change controls, incident handling. Coordinate with QA, QC, Engineering, and Warehouse for smooth batch execution. Assist in audit preparation (internal, regulatory, and customer audits) with proper documentation. Monitor yield, productivity, and process improvements to minimiz...

Hiring for Production Chemist Job Location - Jammu (Sambha) Interview Location - Chandigarh Salary bar - 5LPA - 5.5LPA Max Industry pref. - Pharma (API) Interested one share resume on meenakshikandpal@tdsjobs.com 9815675900

We are looking for an experienced Production Executive with strong expertise in Liquid Injection and Parenteral Manufacturing . The ideal candidate will independently manage sterile production operations, ensure compliance with quality standards, and drive efficient utilization of resources. Key Responsibilities Supervise and manage the manufacturing of Liquid Injections and Parenterals . Oversee and maintain the sterile filling area of liquid parenterals. Handle the Liquid Injection section independently . Supervise the washing section, autoclave, and tunnel operations . Manage batch preparation, filling, washing, visual inspection, and packing sections . Prepare Sterile Water for Injection...

Designation - Manager - Quality Assurance Company - Leading Pharma Raw Material Mfg. Company Job Location - Dahej, Bharuch Qualification - B.Sc. / M.Sc. / B.E.- Chemical / B.Pharm Experience - Min. 8yrs. and above share with your friends Required Candidate profile company will provide transportation facility from Bharuch. Responsible for handling QA / GMP Related documentation QMS, Audit Preparation, Vendor Questionnaire, Market Compliant & Customer Compliance

Develop SOPs for production, filling, packaging & QA/QC; ensure FDA, EU, BIS & Drug Act compliance; conduct audits; review BMR, BPR & MFR; implement QMS; train staff on GMP/GLP; manage labelling, claims & documentation for regulatory compliance.

Company Name Gangwal healthcare Job Title Manager - production Job Location: Maharashtra Description Department: Production Location: Boisar/Tarapur Reports To: Sr. Production Manager / Plant Head Industry: Nutraceuticals & Food Manufacturing Employment Type: Full-time Job Summary The Manager Production is responsible for planning, organizing, supervising, and executing daily manufacturing operations in compliance with GMP, FSSAI, HACCP, and other regulatory requirements. The role includes managing resources, ensuring production targets, quality control, equipment efficiency, and safety standards. Key Responsibilities Production Planning & Execution: Assist in preparing and executing daily/m...

You will be working as a Production Chemist with a focus on knowledge of BRM, BPR, and exposure to GDP, GMP. Your role will involve experience in Sterile and Sterilization processes. As a Production Chemist, your responsibilities will include Batch Planning and Batch Manufacturing. The qualifications required for this position include relevant education details. The required skills for this role are a strong knowledge of BRM, BPR, exposure to GDP, GMP, and experience in Sterile and Sterilization processes. Preferred skills include proficiency in Batch Planning and Batch Manufacturing. Our company is committed to diversity and inclusivity, promoting an equal opportunity environment for all em...

As a key member of the Company OE projects team, you will actively participate in Business Transformation Projects encompassing roles in Business Analysis, Consulting, Offshoring, Project Management, and Process design/ Re-engineering (BPR). This diverse role offers real-world consulting experience with a global perspective and provides opportunities to engage in various Business-related endeavors. Your primary responsibilities will include: Consulting responsibilities: - Leading customer meetings to assess business problems and identify opportunities within OE business groups. - Analyzing and interpreting data to uncover weaknesses and problems, understanding their root causes. - Formulatin...

As an IPQA Specialist in an API manufacturing environment, your primary responsibility will be to monitor production activities and ensure cGMP compliance on the shop floor. You will be required to review and approve Batch Manufacturing Records (BMR), Batch Cleaning Records (BCR), and related analytical records before releasing API. Preparation and revision of SOPs, BMRs, BCRs, and other QA-related documents will also be part of your duties, aligning them with regulatory and internal requirements. Sampling of APIs, maintaining related records, overseeing proper cleaning and maintenance of sampling tools, and managing storage of control samples of API will be crucial tasks to uphold quality s...

As the Quality Control Officer, you will be responsible for ensuring the overall quality of products and compliance with GMP at the site. This includes conducting line clearance prior to dispensing, manufacturing, packing, and validation activities. You will also be involved in sampling during the manufacturing of validation, exhibit, and commercial batches, as well as in-process control, routine inspection, and online process verification and documentation. Your duties will involve the preparation, review, and approval of various documents such as SOPs, BMRs, BPRs, SMFs, VMPs, APQRs, MFR validation protocols/reports, and qualification protocols/reports. Additionally, you will be responsible...

The Supply Chain Executive is responsible for maintaining and monitoring Finished Goods (FG) made to stock (MTS), analyzing stock readiness, ensuring timely customer service, coordinating material movement, and supporting procurement planning through effective data management and reporting. The role requires strong coordination with cross-functional teams, especially Customer Care and Production Planning Control (PPC), to ensure smooth supply chain operations. 1. Finished Goods (FG) MTS Management Maintain FG MTS inventory to ensure readiness of materials for timely customer fulfillment. Analyze stock gaps against predefined inventory norms and highlight variances. Prepare and update the FG ...

Set up and manage the Project Implementation Unit for a 5-year duration. Improve access for businesses and beneficiaries to e-government services. Undertake Business Process Re-Engineering (BPR) and Government Process Re-Engineering (GPR) for identified service areas. Study existing business processes and organizational structures of government departments. Prepare as-is process maps and workflow charts to identify duplications and inefficiencies. Analyze gaps and propose to-be processes, including layers of decision-making, time analysis at each level, and required documentation. Ensure improved and efficient delivery of G2G (Government to Government), G2B (Government to Business), and G2C ...

Division Department Sub Department 1 Job Purpose Monitor and execute the packing activities in a shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target Utilise shift resources optimally to get desired production output Regulate usage of consumables in the production process at optimum level to save cost Key Accountabilities (2/6) Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement Review and monitor critical in-process parameters like NFD, camera ...

Responsible for leading production operations, coordinating production staff and equipment, ensuring product quality and profitability, and overseeing and managing the production operations involved in injectable products.

Role & responsibilities Production chemist and QC chemist Preferred candidate profile HPLC,GC wet lab,BPR,BATCH PLAN,REACTORS,ANALYSIS,WET LAB,INSTRUMENTATION, Perks and benefits As per company norms

The candidate will be responsible for the proper receipt, storage, and GMP-compliant dispensing of raw materials used in pharmaceutical production Perform raw material dispensing activity in designated dispensing booths under controlled conditions.. Required Candidate profile Receive, inspect & label incoming raw materials as per SOP Coordinate with the QA, Production & QC department during material movement Ensure adherence to GMP, GDP & safety guideline during dispensing

To perform IPQA activities at shop floor in every stage of OSD manufacturing and packing. Review of BMR & BPR. Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release. Review of documents of respective areas and logbooks for adequacy and completeness. QA overview for receipt of material from warehouse to production. IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities. Review and Control of SOP’s, Specification, BPR issuance, Master Formulae and Records. Preparation & Review of process validation protocols and reports. Any job activity assigned by HOD

Handle BMR and batch repacking records, Verify daily balance checks and calibration activities, Maintain production records, Perform and verify line clearance at manufacturing and packing stages, Issue and retrieve production documents Required Candidate profile Graduate candidates with 2-4 Year experience and knowledge about cGMP Practice, QMS tools knowledge, Production and Manufacturing documentation process. We are looking for local candidates ONLY.

As an intern at ThinQ Pharma, your day-to-day responsibilities will involve assisting in formulation and pre-formulation studies, supporting the development of stability and bio batches, helping in maintaining lab records including BMR/BPR and SOPs, coordinating with cross-functional teams such as QA/QC/Production, and performing basic lab tests while ensuring accurate data recording. ThinQ Pharma is an integrated pharmaceutical company with a strong global presence and a reputation for offering world-class products and services. Headquartered in Singapore and operating a fully equipped research center in Mumbai, India, ThinQ Pharma has been a key player in the global market for more than 25...

To perform IPQA activities at shop floor in every stage of OSD manufacturing and packing. Review of BMR & BPR. Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release. Review of documents of respective areas and logbooks for adequacy and completeness. QA overview for receipt of material from warehouse to production. IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities. Review and Control of SOP’s, Specification, BPR issuance, Master Formulae and Records. Preparation & Review of process validation protocols and reports. Any job activity assigned by HOD