582 Bmr Jobs - Page 12

Greetings from Avani Consulting ! Hiring Production associates for API (Pharma Production ) Walkin drive face to face interview on 30th August'25 in Bangalore Company: a leading Pharma API Manufacturing company || Location - Mysore ( Nanjangud) Position- Associate || Work Experience Min 5-10 yrs in API if interested kindly share their updated resume with below details to priyanka@avaniconsulting.com or whatsapp to 9518220852 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change: Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments co...

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...

Key Responsibilities: Documentation and Compliance: Review batch manufacturing records (BMR) and batch packing records (BPR) for completeness and compliance with Good Manufacturing Practices (GMP). Prepare, review, and approve standard operating procedures (SOPs), work instructions, and specifications. Ensure compliance with pharmacopeial standards (USP, BP, IP, EP) and regulatory requirements (FDA, WHO, ICH, etc.). Batch Release: Evaluate and approve batch documentation for the release of raw materials, intermediates, and Active Pharmaceutical Ingredients (APIs). Ensure that all deviations, change controls, and out-of-specification (OOS) results are resolved prior to batch release. Audits a...

Dear Candidates, Urgent opening in MNC company at Pawne, Navi Mumbai for Jr .production officer in well know manufacturing company. The details are as follows:- Interviews on 14th August 2025 , Thursday and 18th August 2025,Monday Please send your profile on pranali.karanje@humancaliber.com Type -Permanent Education - BSC/MSC -Chemistry/Diploma in chemical Experience -2+ years in Batch process & Unit Operations Industry Preferred :- Chemical/Petrochemical / Fertilizer/Pharma/refinery CTC upto 4.5 +Bus+ Canteen Facility ( Two holidays in a week) Will get hike 20% only Immediate joiners are preferred Notice period max upto 1 month Mumbai candidates are preferred.

Company:Pharma API Unit Location Mysore Role: Production Associates Salary: up to 25% hike > Note: No Consulting Charges Roles & Responsibility for Production Associate 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure growing practices, entry / exit procedures, usage of PPEs are followed by the team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the pro...

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...

You will be responsible for strictly following cGMP, Safety and Environmental Practices, as well as ensuring Good Manufacturing practices during operation. This includes filling Batch Manufacturing records and equipment cleaning records, maintaining proper personnel protective equipment usage, and ensuring good housekeeping in the respective plant area and its equipment. You will need to plan and ensure raw material availability for daily production as per the production plan, maintain documents like Issue and dispensing register, and carry out processes as per Batch Manufacturing Records (BMR) without any deviation. It is essential to adhere to data integrity in online documentation and han...

Equipment Knowledge of Plant area i.e. Reactor, Centrifuge, Dryer, Sparkler & Sifter etc. Knowledge of documentation as required in GMP like BMR, ECR, Usage Log Book etc Handling of Workmen in Plant area Knowledge for using of Safety Equipments which are using in Plant area Experience of general Computer knowledge.

Role & Responsibilities: To carryout the processes of different products as per the respective approved BMR from Q.A. To make entry in BMR while the process is in progress. To follow written standard operating procedure while working in the plant. To follow instructions given by the Production Executive and other superiors related to Personnel safety, product safety, product quality and its yields. To follow instructions relating to cGMP, GDP, Personal hygiene and other documentations related to regulatory requirements. To ensure operational control, availability of BMR, raw materials, packing material as per requirement. To report any ill health, injury, unfitness regarding work to Producti...

He should know computer good computer knowledge He should know and having expertise in Good Manufacturing Practices (Developing, implementing. Required Candidate profile And maintaining quality systems and procedures ( Deviation/OOS investigation , batch card /SOP drafting ) that align with regulatory requirements.

Interview for Production Dept on 02-08 in Bharuch for API Pharma Company in Dahej Qualification: BE / Diploma Chemical / BSC / MSC Chemistry / ITI AOCP Experience: 3 to 13 Years CTC: Up to 8 LPA No Charges Free Jobs Share with Your Friends!!! Required Candidate profile Send CV on sdpbharuch@gmail.com with Subject: Production Dahej & Call on 760033423 Interview Venue: SDP HR SOLUTION, Sixth Floor, 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch

Role & responsibilities -To perform the manufacturing process of products and to fill all the quality records in shift as per GMP. (BMR/BPR/ECR/Log Books/etc.) Following the SOP. -To give the requisition for Raw material/Packing material to Raw material store and verification of the same after receipt. -To give requisition for any consumable items to engineering store and verification of the same after receipt. -To give requisition for forms / formats and other quality related documents to QA and submission of the same to QA. -To make sure that all production deviations, non-conformance & accidents are reported along with investigation report. - To schedule training of plant personnel on SOP...

Ensure current versions of all GMP documents are in use. Prepare, revise, and control SOPs . Implement and enforce (GDP). Conduct internal audits, maintain summaries and CAPA tracking Support in process validation, equipment qualification etc Required Candidate profile Ensure all QA activities comply with cGMP, regulatory requirements & internal quality standards for API & Specialty manufacturing. Contact Mr Deep at 9867038868, Email Id: ops@empowerrecruitments.com

B.Sc/M.Sc. with 1–4 years in QA (API preferred). Strong in GMP, documentation, audits, and QMS. Detail-oriented, compliant, and reliable. Ready to ensure quality excellence in a world-class pharma environment. Required Candidate profile B.Sc/M.Sc. with 1–4 years’ QA experience in API. Skilled in GMP, documentation, audits, and QMS. Detail-oriented, disciplined, and committed to quality compliance. Perks and benefits GMP GLP plant |Growth |Safety |Compliance |Perks

You will be responsible for managing the operations of chemical processes involving the addition of Diketene reactions for the production of Arylides. This will include handling batch processes, drying operations, and creating acidic strength as per the requirements. You will also be involved in pressure nutch filtration, BMR filling, and operating water ring vacuum pumps. Additionally, you will be required to handle DCS panel operations efficiently. This is a full-time position with a rotational shift schedule. The ideal candidate should have at least 1 year of relevant work experience. The work location for this position is on-site. The expected start date for this role is 04/10/2024.,

Role & responsibilities Operate and monitor critical equipment such as reactors, centrifuges, blenders, sifters, multi-mills, etc. Ensure strict compliance with cGMP guidelines during all stages of production. Maintain accurate and timely documentation in accordance with regulatory requirements, including handling of change controls, deviations, and batch records. Identify and escalate technical issues and implement corrective and preventive actions (CAPA). Coordinate with cross-functional teams (QA, QC, Maintenance) to ensure smooth plant operations. Adhere to standard operating procedures (SOPs) and safety protocols. Support process improvement initiatives to enhance productivity and effic...

Responsibilities: * Manage production processes from BMR to dispatch. * Oversee liquid oral, syrup, ointment, GMP compliance, cream & manpower handling. * Ensure quality control measures are implemented.

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

KPMG India is looking for Executive - Adobe QA to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing exis...

Responsibilities: * Collaborate with cross-functional teams on product development & launch * Conduct BMR reviews & SOP maintenance * Ensure compliance with GMP standards through audits & inspections Food allowance Annual bonus Provident fund

Role & responsibilities Granulation Supervisor Responsibilities: Supervise the granulation process, ensuring compliance with Batch Manufacturing Records (BMR) and adherence to Good Manufacturing Practices (GMP) . Ensure effective process adherence, timely production, and achievement of department goals. Focus on yield improvement , identifying and implementing strategies to optimize production efficiency and minimize waste. Monitor and maintain granulation equipment, ensuring smooth operation and troubleshooting as needed. Collaborate with cross-functional teams to address any production or quality-related issues. Provide training and mentorship to junior staff, ensuring operational efficien...

Role & responsibilities 1. Drive product robustness for all products in area of responsibility and lead the third party operation team. 2. Lead and manage all TPO Process activities and process validation for products developed and manufactured at outside contract facilities. 3. This includes, providing product stewardship by ensuring the performance of all products are monitored and maintained in a validated state, supporting root cause investigations by providing Technical intelligence to deviations, technical complaints, OOS & CAPAs. 4. Identifying and executing continuous improvement opportunities, leading New Product Launch third party teams and leading technical activities related to t...

Handled hazardous chemicals like Tri-phosgene or Phosgene