139 Bmr Jobs - Page 5

We are looking for Production Officer for our Company Hindustan Platinum Location: Turbhe, Navi Mumbai Exp: 3+ years JD: Experience in Centrifuge GLR ,SSR Reactors Blender Dryer Distillation, Filtration , ANFD BMR Batch process Interested candidate please share resume on rakshita.banjan@hp.co.in

Aragen is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey. Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant.

Roles and Responsibilities (Hiring for AQA Role, IPQA Role, QMS Role - API Background is Must) Ensure compliance with GMP, BMR, BPR, SOPs, and quality systems. To Perform Analytical QA Role IPQA Activities QMS Activities Validation Activities Collaborate with cross-functional teams to ensure timely completion tasks Person Should be from the API Background

S.K.AGARWAL&SON. is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant. Good Presentation, Communication and Reporting Skills. Working Knowledge of Computers and Accounting Software. Strong inter-personal skills to deal with Clients and Team Members

ASTER DM HEALTHCARE LIMITED is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey. Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant.

Walk-in interview For Sun Pharmaceutical Industries Limited, Dadra Date: 30th March 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: Officer / Sr. Officer / Executive Granulation & Packing Education: B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 2- 6 years of experience of handling Granulation and Bottle Packing activities in an OSD manufacturing plant, should have knowledge of cGMP. 2) Designation: Technician – Manufacturing & Packing Education: ITI / Diploma/ B. Sc Department: OSD Manufacturing & Packing Experience: 4 - 8 years of work experience in pharmaceutical company, handling Granulation, and Primary & Secondary Bottle Packing activities in a regulated OSD manufacturing plant. 3) Designation: Officer / Sr. Officer / Executive/ Sr. Executive - Microbiology Education: M. Sc / B. Pharm / M. Pharm Department: New Product Quality Control Experience: 2 - 10 years of experience of handling Environment monitoring, MLT Analysis, Culture Maintenance, Media Management & Micro GLP should have knowledge of cGMP. For all the positions, we are looking for candidates with experience in regulated plants like USFDA, MHRA, ANVISA, TGA etc. Interested candidates meeting with criteria should carry their updated resume along with photograph, Photocopy of Salary Supporting/Appointment/latest Increment letters giving salary breakups of Monthly & Annual Salary is must. Those who are unable to attend the personal interview may send their resume by e-mail to rupeshkumar.upadhyay@sunpharma.com

We are seeking a highly motivated and detail-oriented QA Executive to join our team. The ideal candidate will have a strong background in the pharmaceutical, API, or chemical industry with hands-on experience in quality assurance activities. This position requires a keen eye for detail, the ability to work efficiently under pressure, and a commitment to maintaining the highest standards of quality. Key Responsibilities: Document Management: Manage and control the issuance and reconciliation of essential quality documents including BMR, ECR, BPR, SOPs, Logbooks, and Labels. Quality Systems: Perform tasks related to VQ (Validation Qualification), change control, deviation management, market complaints, and DMF readiness. Audit Readiness: Ensure that all documentation and processes are in place for successful audit outcomes and maintain compliance with regulatory requirements. Process Validation: Work closely with the process validation team to ensure that all processes meet required specifications. GMP Compliance: Maintain and ensure daily GMP (Good Manufacturing Practices) formats are followed across operations. Team Collaboration: Collaborate with other departments to support continuous improvement initiatives and maintain the quality of products in production. Required Qualifications & Skills: Education: BSc/MSc/B Pharm/M Pharm (Chemistry/Microbiology/Any other related field). Experience: Minimum of 2-3 years of experience in the pharmaceutical API, intermediate, or chemical industry. Skills: In-depth knowledge of document issuance and control (BMR, ECR, BPR, SOPs). Hands-on experience in VQ, change control, deviation management, and market complaint handling. Experience with audit readiness and process validation. Strong understanding of GMP compliance and daily GMP formats. Excellent teamwork and collaboration skills.

FinAdvantage is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant.

Handling production reactors. GLR SLR, monitoring processes. Maintain BMR as per SOP. Ensuring compliance with GMP and safety protocols. Centrifuge. Handling raw materials and maintaining production logs.

You will be responsible for overseeing the production, ensuring product quality, maintaining production efficiency, and troubleshooting any manufacturing issues. Supervise & manage day-to-day production processes in the manufacturing plant. . Required Candidate profile - Diploma / ITI - Exp in a manufacturing plant - Stays near Taloja .

Role & responsibilities * Candidate should have minimum 3 years of experience in Production - OSD Formulation handling Granulation / Blending / Compression / Coating / Packing etc. * Should have machines operating experience & trouble shooting experience. * Should have BMR / BPR Preparation and online documentation experience. * Should be from USFDA approved plant only. Perks and benefits Best in the industry.

Company: Strides Pharma Department: IPQA Profile: - Executive Office Locations: Alathur Qualification – B. Pharmacy/ M. Pharmacy Experience – 2 to 6 years (Must have exposure to OSD) Job Description: • To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing. • QA overview for clean room behaviour and aseptic activity. • Review of batch processing records. • 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. • Executing the validation/revalidation activity in the absence of authorized person. • Any job activity assigned by HOD • Responsible for regulatory audits with exposure equivalent to WHO Geneva PQ/USFDA Competencies: • Execute IPQA Excellence by setting clear benchmarks. • Smart Thinker and displays smart/ tactical moves & mental agility. • Is open and flexible when faced with changing circumstances and finds ways and means of doing things and not get struck with the past. • Comes up with ideas which are different and can be used commercially, profitably and growth. • Support and guide subordinates by giving appropriate examples & feedback. Encourage team to come up with new ideas. • Proposes solution which has elements of sustainability.

Company: Strides Pharma Department: IPQA Profile: - Executive Office Locations: KRSG Plant, Bangalore Qualification – B. Pharmacy/ M. Pharmacy Experience – 2 to 6 years (Must have exposure to OSD) Job Description: • To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing. • QA overview for clean room behaviour and aseptic activity. • Review of batch processing records. • 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. • Executing the validation/revalidation activity in the absence of authorized person. • Any job activity assigned by HOD • Responsible for regulatory audits with exposure equivalent to WHO Geneva PQ/USFDA Competencies: • Execute IPQA Excellence by setting clear benchmarks. • Smart Thinker and displays smart/ tactical moves & mental agility. • Is open and flexible when faced with changing circumstances and finds ways and means of doing things and not get struck with the past. • Comes up with ideas which are different and can be used commercially, profitably and growth. • Support and guide subordinates by giving appropriate examples & feedback. Encourage team to come up with new ideas. • Proposes solution which has elements of sustainability.

Hii, Greetings from Avaniconsulting ! We are hiring for Production associate for a leading Pharma API Manufacturing company Position- Associate Work Experience Min 3-8 yrs in API Location - Mysore ( Nanjangud) Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical Salary- 20% to 25% hike on current ctc Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by 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 product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. if intrested kindly share their updated resume with below details to jyotsna@avaniconsulting.com or whatsapp to 7780363938 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change:

Job description: Providing Line Clearance to the equipment's and areas. Issuance of documents as per procedures. Review of all online documentation activities. To monitor the cGMP at the shop floor periodically. Monitoring process validation activities of various products. Review of GMP records and ensuring compliance for any observations. Responsible for coordinating self-inspection. Assist in deviation, incidence, OOS/ OOT investigations. Awareness in guidance on ICHQ7 Candidates with less than 1 month notice period or immediate joiners will be preferred.

Hiring for "Executive " for Leading Biotechnology company Knowledge of Protein Purification Knowledge of GMP standards, SOPs and quality management systems Awareness of QMS as per ISO13485: 2016 and ISO 9001:2015 standards.

1. Good Documentation Practices, Compliance for Standard Operating Procedures, Quality Management Systems shall be followed. 2. Review and understanding of product related technicalities for smooth transfer of products to Internal Manufacturing facility of Strides or External Facility. 3. Co-ordination and collection of technical documents from internal sites. 4. Review of Tech pack documents and sharing (MFR, MPR, Spec/STP, BMR, BPR, Tool drawings layouts etc.) to Internal or external manufacturing sites. 5. Review of Master documents before initiating validation batches at Internal or external manufacturing sites. 6. Handling of Investigation related to OOS/OOT/Deviation occurred/reported for New Products and Site Transfer Projects. 7. Conducting/Monitoring of Feasibility trials/ Scale up trials at R&D or Manufacturing site. 8. To be involved in cost improvement program for identified product, to change the formula and improvise the process as required. 9. Handling of Product Robustness Projects and related activities like conducting the trials at R&D, Execution and Monitoring of Optimization batches and Registration/Commercial batches for PR projects. 10. Handling of Trouble shooting to improve the product quality attributes. 11. Review of APQR, RCI, CAPAs, PDR and other related documents. 12. Handling of QMS events (CC/Deviations) in Trackwise. 13. Ensure Test license availability at R&D & Plant. 14. Ensuring Toolings and RMs availability for execution of lab trial batches, PO/PE/Scale up batches and monitoring the batches during execution. 15. Preparation and Review of Trial Reports, and Investigational Summary Reports. 16. Preparation and Review of Documents i.e. MFRs, BMRs, BPRs, Protocols/Reports, QRM for Trial/Feasibility, PO and New Products, various batch sizes and subsequent revisions of all kinds. 17. Review & Approval of PVP & PVR. 18. Preparation and review of stability protocol for experimental batches. 19. Initiation/approval of the test request for the analysis. 20. Process optimization activities for internal/external products as identified and assigned. 21. GMP, GDP, Quality Management systems and SOP shall be followed to ensure the continuous compliance.

Hii, Greetings from Avaniconsulting ! We are hiring for Production associate for a leading Pharma API Manufacturing company Position- Associate Work Experience Min 3-8 yrs in API Location - Mysore ( Nanjangud) Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical Salary- 20% to 25% hike on current ctc Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by 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 product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. if intrested kindly share their updated resume with below details to mona@avaniconsulting.com or whatsapp to 7327039030 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change:

• Responsible for QA activities & review of documents in the area of: • Quality Management Systems, Incidents & Investigations, IPQA, Internal Audits • Document control • Batch review and release, Dispatch • Validations, Qualifications • Product Quality review • Logging, Investigating and closing Quality events (Deviations, OOS&OOTs, Complaints), Participate in Investigations • Logging, Tracking, Closing Changes, CAPAs • IPQA and Internal Audits • Document Management – Issuance, Retrieval, Archival • Review of Quality System documents such as -Batch records, Validation reports, Qualification reports, calibration reports • Review Dispatches and documentation • Review Vendor Qualification, • Coordinate Training Management, Samples dispatch • Sampling of intermediate/ APIs

Aster Medcity is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey. Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant.

Batch Charging and Manufacturing, CGMP compliance, BPR compliance

RESPONSIBILITIES Preparation and review of master batch records / batch manufacturing records, qualification documents (URS, DQ, IQ, OQ, PQ, volumetric calibration, surface area calculation etc.) & QMS documents. Preparation and review of standard operating procedure. Preparation and review of organogram, job responsibility, training needs & list of list. Preparation and review of training matrix & training plan. To ensure online documentation related to all CGMP activities including data integrity. Initiate, review & complete required change control, deviations, investigations & CAPA impact. Reviewing & maintaining all logbooks in the manufacturing area and plant. Operation of primary and secondary water treatment plant as per standard operating procedure and look after operations in solvent recovery plant. Responsible for performing validation & qualification activities in the plant (equipment qualification, process validation, cleaning validation). Responsible for the execution of validation & scale up batches for all the products to be manufactured. Proper utilization of available manpower (no contract people) & manufacturing facilities to enhance productivity. Ensuring timely manufacturing schedule as per production planning & maintaining quality & safety parameters. DESIRED SKILLS Must have experience in API production in reputed pharma organizations. Should have hands on experience of Manpower Handling Strong knowledge of operating DCS (Distributed Control System) One Should Manage Shift Planning Handling of Water System Operation Handling of Process Equipments like Reactor, Centrifuge, RCVD, RVPD, FBD, Bin Blender, Co-mill, etc Good Knowledge of preparing BMR and BPR. Should have sound knowledge of drafting and reviewing of SOP’s. Good Communication and problem solving skills. Should be assertive, proactive, and self-driven. Ability to work in dynamic environment.

- Experience of Calcium Lactobionate Manufacturing - Responsible for preparing work instruction for Production and manufacturing activities - Maintain online documentation related to production activities like BMR, BPRs, logbooks and daily records. Required Candidate profile Relocation from Maharashtra only - Qualification of production equipment and participation in validation activities - Maintaining documentation such URS, DQ, IQ, OQ, PQ validation protocol with report

1. Responsible for reviewing, approving and distributing work instruction for manufacturing activities. 2. Carry out production activities as per production plan. 3. Review online documentation related to production activities BMR, BPRs, logbooks

Position- Junior/ Senior Production Executive Work Experience +3 in API Location Mysore MSc (Chemistry)/ BE (Chemical) Job Description 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by 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 product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. If interested, kindly send your updated resume on jyotsna@avaniconsulting.com or whatsapp@7780363938