582 Bmr Jobs - Page 9

Nexdigm (SKP) is looking for Senior Executive - FDD 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 implementi...

Esskay Compu Services Pvt Ltd 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 ...

Role & responsibilities To take plant round and monitor production activities at shop floor. To prepare appropriate Quality related documents like SOP, BMR, BCR, BPR etc. To review BMRs, BCRs, and analysis records before release of API. To perform sampling of APIs and maintain its records. To maintain control samples of API and its records. To perform and ensure the cleaning of sampling tools. To provide line clearance at the time of product changes over. To review dispatch of finished product and maintain record for the same. To Investigate the deviations identified in co-ordination with QA-Head/Designee. Product quality review of API Process and cleaning validation monitoring in plant Pref...

IPQA, IPQA Officer, IPQA Chemist ,GPM,BMR SOP, Pharma Process, FDA Approval, COsmetic Healthcare Industry, Direct Call:9974756637 whatsapp Resume:9974756637

Job Description 1 Should have knowledge of Ophthalmic Dosage Forms manufacturing process – Solutions, Suspensions and Emulsions 2 Should be well versed with Process Development, Process Design and Process validation. 3 Should have awareness of regulatory guidance for USA/EU and other regulatory markets. 4 Execution of Development, Scale up, exhibit and validation batches. 5 Review of scale up / exhibit documents – Scale up protocols, Reports, BMRs etc. 6 Should have good communication and writing skills and aware of Good Documentation Practices. 7 Should have well versed with SAP handling and Quality system software. Work Experience 2-4 years Education Masters in Pharmacy or Pharmaceutical T...

Preferred Skills: 1. Knowledge of API manufacturing processes and regulations. 2. Familiarity with quality management systems (QMS) and audit processes. 3. Strong communication and interpersonal skills. Key Responsibilities: 1. Assist in conducting audits and inspections of production areas, warehouses, and laboratories. 2. Support the QA team in reviewing and updating SOPs, Batch Records, and other quality documents. 3. Collaborate with production and quality teams to identify and resolve quality issues.

Job Description Department: Production Designation: Jr. Officer - Production (E0) Working Section: Granulation / Compression / Coating Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/ managers. Manufacturing / processing of batches of assigned products under supervision as per ...

Job Description Key Responsibilities 1. Monitoring of IPQA activities in all functional departments. 2. Responsible for BMR correction/ quantity verification before batch execution along with QC. 3. Responsible for area and line clearance in production area. 4. Responsible for BMR verification for the completion and online inspection of batch execution at site. 5. Responsible for dispatch verification along with dispatch checklist, BMR, labels (at site and godown) 6. Site inspection for any abnormalities with respect to Raw materials, Packing materials, Products, labels, BMR, Dispatch. 7. Responsible for implementation of 5S at site. 8. Handling of Deviations, failure investigation, Change m...

Global Study Centre (GSC) is looking for Documentation Assistant to join our dynamic team and embark on a rewarding career journey Prepare, organize, and manage company documentation and records. Ensure documents are properly filed, easily accessible, and securely stored. Assist in the creation and revision of company policies, procedures, and manuals. Coordinate with various departments to gather and verify documentation. Maintain documentation databases and ensure data integrity. Prepare reports and summaries as needed for management review. Candidates of with proficiency in English and work experience are preferred. Freshers can be applied for the post of trainees.

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.

hi we are hiring Experience- 4-7 years Location- Baddi Salary Range- 40-50 k Position;- R& D Key Responsibilities: Interested candidate Apply;- Mail;-Tisha.singh@unitedgroupmail.com Contact No';- 9041666549

Looking for Production Chemist for Vasai Location, daily production of colour cosmetics quality control and batch consistency formulation and process improvements understanding of manufacturing processes

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 ...

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.

Role & responsibilities Solid Oral - Production & Packing Officer - Executive and Plant Operator - Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Tablet/ Capsule - Blister Line (BQS), CVC Bottle Line Warehouse (Supervisor / Machine Operator): Officer Senior Executive and Plant Operator - Technical Assistant: RM, PM, FG, Dispensing, Dispatch , Documentation Engineering Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumentation) of OSD Plant like preventive maintenance and breakdown related activities of equipment of OSD plant such as FBD, FBP, RMG, coating, compression, capsule, Packing machine ...

We are looking for a meticulous Chemist Production to manage production documentation preparation and batch record review at Synnat Pharma Private Limited. As a key member of our API Manufacturing Unit, you will play a crucial role in ensuring seamless production processes and adherence to the highest quality standards. Your responsibilities will include verifying daily logbooks, reviewing online Batch Manufacturing Records, and managing all production-related documents, including Process Deviation Control Orders (PDCOs). You will also be responsible for raw material indenting, updating activities in our ERP system, and participating in preventive maintenance programs. This role requires clo...

Role & responsibilities Solid Oral - Production & Packing Officer - Executive and Plant Operator - Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Tablet/ Capsule - Blister Line (BQS), CVC Bottle Line Warehouse (Supervisor / Machine Operator): Officer Senior Executive and Plant Operator - Technical Assistant: RM, PM, FG, Dispensing, Dispatch , Documentation Engineering Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumentation) of OSD Plant like preventive maintenance and breakdown related activities of equipment of OSD plant such as FBD, FBP, RMG, coating, compression, capsule, Packing machine ...

Deloitte 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 re...

Lodha Group is looking for Senior Executive - Community Lifestyle 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 ...

Performing Gap analysis of the existing facilities with the required regulatory requirements for API / Excipients / Packaging Material companies / Testing Laboratories. Preparing report and CAPA review in timely manner Preparation of technical documents as per regulatory expectations. Providing Validation / Qualification Services. Imparting training to the employees/site team members To take part in remediation projects allotted by company.

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...

Execute day-to-day production activities as per production plan. Operate and monitor production equipment (Granulation, Compression, Coating, Packing, etc. based on plant). Ensure adherence to cGMP, SOPs, and regulatory guidelines during all production activities. Maintain batch manufacturing records (BMRs), logbooks, and online documentation. Coordinate with QA, QC, Maintenance, and Warehouse for smooth operations. Implement safety, quality, and housekeeping standards within the production area. Support investigations (deviations, OOS, incidents) and assist in CAPA implementation. Train new operators / apprentices on processes and equipment. Participate in qualification/validation activitie...

Greetings from MSN Laboratories...! We are conducting a walk-in interview for Experienced & Freshers candidates in Our APICHEM Unit Vangapalli (Near to Yadagirigutta) on 5th Sept 2025 (Friday). Department- Production Req Exp- 3 to 8 Yrs Qualification- B. Sc Chemistry/ Any Graduate Designations- Executive/ Jr. Executive/ Sr. Executive Department- QC Req Exp- Freshers Qualification- M. Sc Chemistry Designations- Trainee Eligibility- 2022/23/24/2025 Passed Outs only Venue Details- APICHEM Laboratories Pvt. Ltd, Vangapalli (V), Yadagirigutta (M), Yadadri Bhuvangiri (D), Telangana. Date- 05th Sept 2025 (Friday)

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...