587 Bmr Jobs - Page 23

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 applic...

JOB DESCRIPTION: Knowledge about Log Book. Have a deep overview regarding the SOP and Preparation of BMR with its theoretical terms. To Follow Safety Instruction & Norms During Manufacturing should be kept in mind. In Process Sampling for Reaction Monitoring/In Process Drying. Cleaning Manufacturing Area as Per Respective SOP to be assured. Movement, Labelling & Proper Segregation of Materials as Per SOP & BMR. Knowledge about the documentation process that need to be followed in different production segments. Report to Shift Manager If Any Kind of Deviation/Unsafe Working Condition is Observed. Document like BPR, Equipment Log Book, ECR, Calibration of weight balance. Working on a product p...

Please download the comprehensive job description, including the position summary, specific responsibilities, and qualifications . APPLICATION DEADLINE: Applications will be reviewed as they are received, so interested candidates should apply immediately.

Roles and Responsibilities Assist in production activities such as BMR, sterilization, dispensing, mixing, formulation, and parenteral operations. Monitor and control process parameters to ensure compliance with quality standards. Maintain accurate records of production data and batch logs. Collaborate with team members to resolve issues and improve productivity. Ensure adherence to cGMP guidelines and company policies. Desired Candidate Profile Strong understanding of BMR, sterilization techniques, dispensing procedures, mixing processes, formulation development, and parenteral manufacturing principles. Ability to work effectively in a fast-paced environment with attention to detail and abi...

Seeking a Quality Assurance professional to oversee daily QA activities, review compliance documents, enforce safety standards, and ensure timely production with focus on quality, cost, safety, and delivery.

Role & responsibilities Job Title : Executive / Sr. Executive Blending Department (Aroma Chemicals) Department : Production / Blending Location : Daund Reports To : Production Manager Job Summary : Responsible for managing the blending operations of aroma chemicals in accordance with batch production schedules, ensuring product quality, safety, and compliance with SOPs and regulatory standards. Key Responsibilities : Batch Preparation & Execution : Execute daily blending operations as per the batch manufacturing record (BMR). Accurately weigh and mix raw materials and aroma chemicals. Ensure proper sequencing to avoid cross-contamination. Quality & Compliance : Coordinate with QC/QA for in-p...

Ensure that the products are manufactured as per the cGMP. Maintain documentation as per regulatory authorities requirements like change control, and deviations. Highlight technical problems and take corrective actions.

Help in Day To Day Production Of Pharmaceutical Products Manpower Allocation For Smooth Working In Shift Supervision Of Production Activity BMR And BPR Report Preparation Data Preparation For Internal And External Audit -IE. US FDA - EU GMP Etc Required Candidate profile B. Pharm - M. Pharm - B.Sc - M. Sc Experience In Production Or Packaging Working Experience US FDA Approved Plant is Desirable FDA Approval in Tablet - Capsule Or Any will be an added advantage

Help in Day To Day Production Of Pharmaceutical Products Manpower Allocation For Smooth Working In Shift Supervision Of Production Activity BMR And BPR Report Preparation Data Preparation For Internal And External Audit -IE. US FDA - EU GMP Etc Required Candidate profile B. Pharm - M. Pharm - B.Sc - M. Sc Experience In Production Or Packaging Working Experience US FDA Approved Plant is Desirable FDA Approval in Tablet - Capsule Or Any will be an added advantage

Role & responsibilities We are seeking a diligent and experienced QA & QC & production. The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance ( QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range: 15,000 to 25,000 (negotiable based on experience & skills) Experience: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile Quality control analyst Responsible for testing and analyzing pharmaceutical prod...

QA & QC Executive Job Description Position Overview The QA & QC Executive is responsible for ensuring that products meet quality standards and regulatory requirements through systematic inspections, testing, and process monitoring. This role involves collaboration with production teams to implement corrective actions and continuous improvement initiatives. Key Responsibilities Quality Control & Inspection Conduct inspections on raw materials, in-process products, and finished goods to identify defects or deviations from quality standards. Utilize measurement tools and testing instruments to verify dimensions and other quality criteria. Monitor all operations that affect quality and report ma...

Role & responsibilities Conduct in-process checks during various stages of sterile injectable manufacturing, including dispensing, compounding, filtration, filling, and sealing. Perform line clearance and area clearance before the start of manufacturing and packaging operations. Monitor aseptic practices and personnel hygiene compliance inside cleanrooms and controlled areas. Verify critical process parameters and environmental conditions during batch processing. Ensure compliance with SOPs, batch manufacturing records (BMR), and batch packaging records (BPR). Participate in visual inspection activities and oversee container-closure integrity checks. Monitor the usage and replacement of ster...

Exciting opportunity for IPQA Executive at our EU approved OSD Manufacturing faculity (UNIT 1) @ Moraiya, Ahmedabad!! Company : Unison Pharmaceuticals Pvt Ltd Website : www.unisonpharmaceuticals.com Location : UNIT 1 , Moraiya, Ahmedabad Experience : 4 - 9 Years Dept. & Sub Dept. : QA - IPQA - OSD MFG Designation : Executive Job description (Not limited to): Collect in-process and Finished sample as per Specifications and Protocol. Check documents like equipment log books, temperature & humidity records. Line clearance of machine & manufacturing area . Checking of batch manufacturing record. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free tra...

Role & responsibilities We are looking for candidate on below criteria at our Nalagarh Plant Himachal Pradesh location. Candidate must have completed Pharma, M.Sc. or B.Sc. in Chemistry. Experience of regulatory industry would be preferred. Candidate should have 1-3 years of working experience Preferred candidate profile Responsible for Line clearance in Warehouse and Production area during dispensing, MFG, Filling and Packing & review of log books and status label of each equipments before start of activity. Responsible to carry out in-process checks as per respective Batch Production Record in Manufacturing, packing and warehouse. To ensure that the manufacturing and packing operations are...

Job Description Preparation & Review of SOP’s of QA system and review / approval of SOP’s of other departments. Review of master BMR/BPR of commercial and exhibit batches. Review of BMR / BPR, scale-up and placebo batches. Review of executed BMR/BPR of commercial and exhibit batches for batch release. Issuance, Retrieval & Destruction of SOP’s, STP, specification, BMR/BPR, annexures & other formats. Login and review of quality system documents such as Deviation and IPOOS. In-process Quality Assurance during Production / Packing activities. Sampling at different stages of manufacturing / packing as per the requirement (In-process, BU, CU, finished, control, QP, Hold Time & stability etc.) Rev...

Hii, Greetings from Avani consulting ! We are hiring for Production Officer/associate for a leading Pharma API Manufacturing company Position- officer/Associate Work Experience Min 3-10 yrs in API Location - Mysore Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical/BSC Chemistry 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...

Office Administration HO Asset Tracking, asset allocation and Records1) 0 Gap 2) No Policy Violation 3) No Customer GrievanceCheck all AIS Admin on-line portals as a checker and escalate deviations to Sr Executive Admin1) No Gap 2) Maximum 1 working day to escalate gapsBooking of Hotels, Guest House, Taxi for outstation employees, expats etc1) 0 Gap 2) No Policy Violation 3) No Customer GrievanceVehicle Fuel, R&M and Trackers1) 0 Grievance 2) No SOP violation 3) Within budgeted costMISAll Corp Admin MIS except MIS handled by Unit Head Admin for specific office1) Maximum 3 working days gap to updatation 2) No Policy Violation Location Issue Logs- Plan, execute, Record and share MoM1) No Gap 2...

Develop thorough test plans and document the results and progress Develop in-depth functionality and stability automatic tests that will map customer use cases Research the right set of workloads and benchmarks Develop automated test scenarios and environments for End2End automatic evaluation Collect test evidence measurements to ensure system functionality, stability and scalability Establish automatic measures to assess the accuracy Analyze results to find ways to improve functionality coverage Analyze root causes and identify areas for improvement Collaborate with development teams to drive resolution for issues and improvement Generate test automation summary reports for stakeholders rev...

Roles and Responsibilities Ensure compliance with BMR, SOPs, and quality standards through regular audits and inspections. Develop and maintain documentation for QA procedures, protocols, and reports. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of batch manufacturing processes, including BPR reviews.

1. Quality Management Systems: Implementing, monitoring, and maintaining Quality Management Systems to ensure compliance with CGMP/regulatory guidelines. 2. Documentation: Reviewing and approving technical and quality documents. Required Candidate profile Should be minimum Post Graduation in Science having the work experience of about 10 Yrs in Chemical .

Opening for Pharma company Location : Mahemdabad Role & responsibilities : Continuous process Monitoring Batch Release of Finished product Collection of Sample ie in-process, Finished Product , Control, Stability and Tendor Knowledge of Collection of Validation samples i.e process validation, cleaning and hold time validation. Knowledge of review of Master and executed MFR/BMR and MPR/BPR Adequate knowledge of Inprocess checks of Tablet ,Capsule ,Liquid and Ointment. Adequate knowledge of Shop floor related Non-compliance ,its root cause and compliance. Adequate knowledge of calibration of instruments ie weighing balance , friabilator, DT apparatus, hardness tester, Vernier calliper, Moistur...

Manage QA documents and records Handle deviations, changes, CAPA, complaints Conduct audits and supplier evaluations Monitor quality metrics and improvements Train staff and ensure ISO compliance

Roles and Responsibilities Conduct quality audits, inspections, and IPQA activities to ensure compliance with GMP regulations. Perform BMR reviews, CAPAs implementation, and participate in process validation activities. Ensure timely completion of documentation related to quality control processes. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of all quality-related documents and reports. Desired Candidate Profile 1-2 years of experience in Quality Assurance/Quality Control or Regulatory Affairs department. Bachelor's degree in Chemistry (B.Sc) or Dairy Technology (B.Tech). Strong understanding of Good Manufactur...

- Sterile Injectable Manufacturing (Core) - Liquid ampoules, vials, lyophilized products - BMR/BPR Documentation - cGMP - Production Line Operation - Pharmaceutical Equipment Handling - Cleaning/Sterilization - Internal Audit/Validation - Maintenance

- 8+ yrs in Sterile Injectable Manufacturing - 3+ yrs as Production Manager in Injectable Plant - Handling Liquid Ampoule, Vial, and Lyophilized Vial Lines, BMR/BPR Documentation - Leadership & People Management - cGMP; WHO-GMP; FDA Guidelines, SOP