582 Bmr Jobs - Page 10

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,...

A) Production Activiies 1)Handle Production Activities, line independently, maintain SAP & production records 2) Handle Shiftwise Planning to achieve production targets and with maximum efficiency 3). Ensure Optimum utilizing of resources (manpower, RM/PM) and machine operations with maximum productivity 4) Ensure budgeted manpower is available to run the shift without any production loss and no any additional hands kept on over time without management approval 5) Reduce product changeover, machine cleaning time and ensure machine is run at rated throughput/Speed 6) Handle Trouble shooting, Machine setting and optimizing output & increasing efficiency & utilization 7)Shift wise Job allocatio...

Ensure accurate and timely processing of invoices and monitor incoming payments. Manage and oversee the daily operations of the AR department including invoice processing, payment processing, and account reconciliation. Knowledge of TDS & GST. Secure revenue by verifying and posting receipts and resolving any discrepancies. Maintain accurate records and control reports for all AR transactions. Use accounting software and MS Excel to process business transactions and compile reports. Collaborate with other departments to ensure billing accuracy. Address and respond to customer inquiries regarding invoices and payments. Ensure compliance with accounting principles and company procedures. Parti...

Role & responsibilities Manufacturing of cell line/cell culture based AG for FG Cell culture operations, including inoculation and observatory monolayer work Compilation of all commercial batch data and BMR filling RM/PM issuance, sterilization, and monitoring of all supportive data Maintaining procell-related modules, areas, and utility fixed assets Receiving NPD from R&D and scaling up for commercialization Areas, equipment validation, and maintenance Cell bank passage history maintenance and reconciliation Preferred candidate profile Throughout knowledge of cell line/primary culture Propagation of cell line & maintenance Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

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

1. Oversee the production of tablets, capsules & Ointment 2. Ensure quality, efficiency & compliance with regulations like EU GMP 3. Monitor, Control, Plan production & Manpower handling 4.Responsible for carrying out production plan as per the BMR. Required Candidate profile 1. Must have minimum 2 Yrs of experience. 2. Willing to work in Chengalpattu. 3. Qualification : B.Pharma in Pharmaceuticals.

As an Assistant Manager in the Contracts_WMEL team, you will be responsible for managing and overseeing all aspects of contract administration within the organization. This includes but is not limited to drafting, reviewing, and negotiating contracts, ensuring compliance with labor laws and statutory requirements, and managing relationships with stakeholders. You will also be responsible for preparing and maintaining all necessary documentation and reports related to contracts.

Production Chemist / Senior Production Chemist /Production Executive Dear Candidate, We have an exciting opportunity for candidates who are interested to pursue their career as a Production Chemist / Sr Production Chemist / Production Executive's in Pharmaceutical / Nutraceutical Industry. Experience: 2-10yrs. Education: B.Sc. / M.Sc. Chemistry / BE/ B TECH / Diploma in Chemical Engineering. Shifts: Should have willingness to work in Rotational Shifts. Job Location: Hassan / Kunigal / Dobaspet. Gender: Only Males. Roles and Responsibilities : Manage and execute production processing activities. Work on Production Plan to achieve the dispatch commitment. Ensure the team to achieve "ZERO ACCID...

We are hiring Production Officer for pharma intermediate manufacturing Unit. Requirement:- Qualification :-B.Sc/M.Sc Experience :- 2 to 3 years in pharma industry. Benefits:- PF & Bonus Salary isn't a constrain for right candidates.

Role & responsibilities Handling of QMS for drug substance of bacterial products. Should have good process understanding of upstream and downstream unit operations. Experience to handle QMS documents such as deviation, Change control, Investigations through Track-wise software. Should have experience on audit compliance, Regulatory guidelines and knowledge on documentation such as SOP, BMR preparation. 5-8 years of experience on QMS and compliance, Documentation role along with good understanding about manufacturing process operations of bacterial and recombinant vaccine and biological therapeutics. Preferred candidate profile

As a candidate for this role, you will be responsible for handling various Quality Management System (QMS) activities such as managing Corrective and Preventive Actions (CCF), deviations, and Out of Specification (OOS) incidents. Your duties will include preparing and reviewing Standard Operating Procedures (SOPs), Equipment Operating Procedures (EOPs), Operating Control Plans (OCPs), Batch Manufacturing Records (BMR), and other production-related documents. Additionally, you will be required to review batch reports, participate in productivity improvement initiatives, and investigate batch failures. You will also be responsible for creating and maintaining the Asset Integrity Management (AI...

Skill Required Roles and Responsibilites 1. Media fill and qualification summary preparation knowledge. 2. To maintain track of qualification and validation activities. 3. To prepare and review the protocols and reports. Execution of various qualification / validation activities. 4. To review correctness of the technical documents received from the supplier (DQ/OQ/IQ/PQ,FAT). 5. Co-ordinate with production and other user department for qualification/validation activities 6. Timely compile and review of qualification validation reports. 7. To review the equipment documents like calibration reports and ensure correctness of documents. 8. To perform FAT. 9. To co-ordinate with outside agencies ...

Purpose of Job 1. Preparation and Review of PQR. 2. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. Skill Required 1. Having basic knowledge on Microsoft Word and Microsoft Excell 2. Have knowledge of Minitab software for statstical evaluation of data. Roles and Responsibilites 1. Preparation and review of PQR schedule. 2. Planining of PQR compilation as per PQR schedule. 3. Collection of data from all the CFT teams for compilation of PQR. 4. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. 5. Based of the PQR data recommendation to be recommended to concern depa...

Purpose of Job 1. Preparation of PQR. 2. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. Skill Required 1. Utilization of Microsoft Word and Microsoft Excell 2. Using of Minitab software for statstical evaluation. Roles and Responsibilites 1. Preparation of PQR schedule. 2. Planining of PQR compilation as per PQR schedule. 3. Collection of data from all the CFT teams for compilation of PQR. 4. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. 5. Based of the PQR data recommendation to be recommended to concern department and ensure implemenation of the same. Quali...

Job Description Required for IPQA acitities. Required for Batch manufacturing record review. Required for line clearnace and other shop floor related activity of QA. Work Experience 3 to 8 years. Education Graduation in Pharmacy Competencies

SKS Enterpprises is looking for Portfolio Review Analyst to join our dynamic team and embark on a rewarding career journey Analyst plays a crucial role in driving data-driven decision-making processes within the organization This position involves analyzing complex data sets, generating actionable insights, and providing strategic recommendations to support key business initiatives Key Responsibilities:Data Analysis:Conduct in-depth analysis of large and complex datasets to extract meaningful insights Utilize statistical and data visualization tools to present findings in a clear and concise manner Strategic Planning:Collaborate with cross-functional teams to understand business objectives 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

Execute production activities as per BMR, ensuring compliance to SOPs and timelines. BMR/BPR entry, line clearance, vial/ampoule loading-unloading, filtration operations, aseptic practices

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,

Hi Greetings form Avani consulting , We have job opportunity with API Manufacturing (pharma company) for production department. we are going to conduct Walk -in interview in Bangalore on 30-Aug-2025 Saturday . Job Description for Production-Associate Position- Associate Work Experience Min 3-9 yrs in API Location Mysore Gender Any Qualification- B.Tech Chemical Engineering/M Sc and Bsc Chemistry /Diploma in chemical Engg 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 de...

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...