235 Bpr Jobs - Page 8

Supervise day-to-day operations of Dry Powder Filling, Mixing, and Packing activities. Ensure batch manufacturing records (BMR) and other documentation are filled accurately and in a timely manner. Ensure cleanroom discipline and maintain the required environmental conditions in the production area. Coordinate with QA, QC, Maintenance, and Warehouse departments for uninterrupted production. Follow and enforce adherence to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP). Perform and supervise line clearance, cleaning, and sterilization procedures for equipment and areas. Maintain production logs, equipment usage logs, and cleaning records . Participate in investiga...

Operate and monitor compression machines (e.g., Cadmach - ACC). Ensure smooth execution of batch production as per BMR/BPR and SOPs. Carry out in-process checks (IPC) like weight variation, hardness, thickness, friability, etc. Perform machine changeovers, cleaning, and line clearance. Maintain and update Batch Manufacturing Records (BMRs), logbooks, equipment usage logs. Adhere strictly to cGMP, GDP, and safety norms. Participate in audits (internal/external) and handle compliance requirements. Collaborate with QA, maintenance, and validation teams. Report deviations, breakdowns, and implement corrective/preventive actions (CAPA). Suggest and implement process improvements for yield and pro...

Execute daily coating production activities as per batch production records (BPRs). Supervise the mixing, blending, and application processes for various coating formulations. Ensure proper setup and maintenance of coating equipment (e.g., mixers, spray booths, curing ovens). Monitor in-process parameters and adjust formulations or processes to maintain product quality. Ensure compliance with ISO, GMP, and EHS guidelines. Coordinate with QC and R&D teams for sampling, trials, and product validation Maintain accurate production records, logs, and shift reports. Assist in preparing Standard Operating Procedures (SOPs) and work instructions. Report deviations, rejections, and ensure corrective ...

Preparation of MFR, BMR and BPR. Preparation of batch manufacturing records, Batch packing record of all dosage forms.

Role & responsibilities Routine activities of Production department Batch processing CGMP GDP SOP Preferred candidate profile Relevant experience from Pharmaceutical and Chemical industry. Must have cGMP experience.

Role & responsibilities - Review of Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and other related documentation. Implementation and monitoring of cGMP compliance across departments. Handling of deviations, CAPA, and change controls. In-process checks and line clearance during production activities. Conduct internal audits and support external regulatory audits (USFDA, EDQM, WHO, etc.). Review and preparation of SOPs and other quality documents. Training of personnel on GMP, GDP, and SOPs. Ensuring data integrity and documentation control. Preferred candidate profile 2 to 5 years of QA experience in An API manufacturing Unit Good communication and documentation Skill

Role & responsibilities Must have knowledge of dispensing of RM/PM. In-process quality checks Review BMR/BPR, regulatory books, online entries, sampling techniques. Calibration of IPQA instruments. Control sample and stability sample handling procedure. Preferred candidate profile Must have experience in OSD plant. Perks and benefits

Responsible for handling all activities pertaining to Tablets & Capsules & Pellets Mfg. Responsible to handle the team to achieve the set targets & maintain qualitative & quantitative as well as cGMP aspects. Perks and benefits Accommodation & Transportation And Mediclaim

Job Description: Operate, monitor, and optimize chemical production processes. Prepare chemical batches according to Standard Operating Procedures (SOPs). Ensure quality control through in-process testing. Coordinate with Quality Assurance (QA) and R&D teams for process improvement and new product trials. Maintain production documentation, including batch records, logbooks, and reports. Adhere to safety protocols, chemical handling procedures, and environmental regulations. Troubleshoot equipment malfunctions and process deviations. Support in scaling up lab-scale processes to full-scale production. Monitor inventory levels of raw materials and reagents. Train and guide plant operators and j...

Position : Assistant Manager- Production Location : Dahej Experience : 4-8 Years CTC Range : 5-9 LPA 1. Production Operations: Check and verify labels of raw materials, packing materials, and solvents before usage. Maintain appropriate storage conditions of raw materials and intermediates in the plant. Ensure adherence to process conditions during batch processing as per BMR (Batch Manufacturing Records). Take instructions from Shift In-charge / Managers for batch charging and monitoring. Report any deviations or discrepancies in plant/process to the Shift In-charge immediately. Complete assigned production tasks within the stipulated time. Maintain environmental conditions in the Production...

Roles and Responsibilities Prepare and review batch manufacturing records (BMR) and batch processing documents to ensure compliance with regulatory requirements. Monitor production processes to identify areas for improvement and implement changes to optimize efficiency and productivity. Collaborate with cross-functional teams to resolve issues related to product quality, process optimization, and equipment maintenance. Ensure adherence to cGMP guidelines throughout the production cycle.

Job Description 1. Preparation of SOPs of QA, review of other departments' SOPs, 2. To perform batch release of API material and review of related documents. 3. To prepare and review Quality Risk Assessment, Site Master File, Hold Time Study Protocol/Reports, and other study protocols/reports, Specifications, Stability Protocol, and Stability Report Data. 4. Review of Validation Master Plan. 5. To review the analytical method transfer protocol/report and method validation documents of the API. 6. To ensure and handle the investigation of out-of-specification Results, OOT, Deviations, Product failures, and Market Complaints. 7. To review Quality system documents such as Deviation, Change cont...

Role & responsibilities Job description Dosage forms experience: Solid Oral & Injectable experience in TTD/PDL/MS&T. Perform formulation development activities on differentiated formulations and innovative technologies as part of product development in R&D and in Pilot/Manufacturing Site. Follow good laboratory practices, good documentation practices (LNB writing) and maintain the logbooks and forms for equipment/instruments. Dedicate Experience in technology transfer of product(s) under development activities from scale up, exhibit batches. To lead and support the site transfer products from scale up to product launch. To prepare, review and hand-over the Technology Transfer Dossier to plan...

Handle BMR and batch repacking records, Verify daily balance checks and calibration activities, Maintain production records, Perform and verify line clearance at manufacturing and packing stages, Issue and retrieve production documents Required Candidate profile Graduate candidates with 2-5 Year experience and knowledge about cGMP Practice, QMS tools knowledge, Production and Manufacturing documentation process. We are looking for local candidates ONLY.

Key Responsibilities: Operating and monitoring processing equipment in a cleanroom facility. Ensuring compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Accurate completion and maintenance of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Troubleshooting and resolving minor operational issues. Collaborating with other departments to optimize production processes. Adhering to all safety protocols and company policies. Qualifications & Experience: Male candidates only. Educational Background: Bachelor of Engineering (B.E.) in Mechanical / Bachelor of Science (B.Sc.) / Bachelor of Pharmacy (B.Pharm). Work Experience: 2 to 5 years of ex...

#Gracure Pharmaceuticals Ltd Hiring For Production (Primary Packing) Designation - Operator (Primary Packing) Qualification - ITI /Diploma Experience: 4 to 8 Years Location : Bhiwadi Note: Experience Required from Pharmaceutical Industry Only. Interested candidates can share their resume at Shivani.singh@gracure.com

Role & responsibilities 1) To perform line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labeling and packing 2) To perform Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. 3) To issue and control of SOPs, BMRs, BPRs, BCRs and also finished product label/product container seals /sealing of the containers as the part of IPQA activities. Preferred candidate profile

Key Responsibilities: Operating and monitoring processing equipment in a cleanroom facility. Ensuring compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Accurate completion and maintenance of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Troubleshooting and resolving minor operational issues. Collaborating with other departments to optimize production processes. Adhering to all safety protocols and company policies. Qualifications & Experience: Male candidates only. Educational Background: Bachelor of Engineering (B.E.) in Mechanical / Bachelor of Science (B.Sc.) / Bachelor of Pharmacy (B.Pharm). Work Experience: 2 to 5 years of ex...

Material Compliance Engineer Qualification: B.E. Mechanical Experience Range: 3 to 5 Years Roles & Responsibilities: At least 3 years of significant experience focused on the field of material management for the automotive industry. Proficiency in IMDS software is essential, along with advanced skills in Microsoft Office (Excel, Word, PowerPoint). The candidate would need to interact and align with the global group companies and external partners for development areas. Thorough knowledge of GADSL substance list. REACH, IMDS, ELV & BPR are all acronyms commonly used in the industry. Review IMDS reports in accordance with customer requirements, national and international standards, laws, regul...

Hii, Greetings from Avaniconsulting ! We are hiring for Production associate for a leading Pharma API Manufacturing company Position- 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 departmental pro...

Hii, Greetings from Avaniconsulting ! We are hiring for Production associate for a leading Pharma API Manufacturing company Position- Associate Work Experience Min 3-10 yrs in API Notice Period - 1 month ( maximum) Location - Mysore ( Nanjangud) 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 Manu...

Roles and Responsibilities Ensure compliance with regulatory requirements, company policies, and procedures related to production quality management systems (QMS). Develop and maintain documentation for change controls, deviation management, and non-conformance reporting. Collaborate with cross-functional teams to resolve issues related to product quality, process validation, and equipment calibration. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma). Minimum 1-4 years of experience in the pharmaceutical industry with expertise in OSD formulation manufacturing. Strong understanding of BMR/BPR regulations and ability to apply them ef...

Walk-in interview @ Ahmedabad For Sun Pharmaceutical Industries Limited, Dadra Date: 15th Jun 25 (Sunday) We are recruiting for our OSD manufacturing facility located at Dadra Time: 10 AM to 4 PM Interview Venue: The Fern Residency, Ahmedabad Near Subhash Bridge Corner, RTO Circle Ahmedabad Gujarat 380027. India Following are the requirements for our manufacturing facility at Dadra Location. 1) Designation: Officer / Sr. Officer Manufacturing & Packing Education: B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 2- 6 years of experience in OSD manufacturing handling Granulation, Compression, Tablet Coating, Tablet Inspection, and Bottle Packing activities in an OSD manu...

Role & responsibilities Knowledge of buffer systems (pH, molarity, ionic strength) Familiarity with enzymatic reactions and storage conditions Ability to handle chemical solution preparation with precision Understanding of cleanroom, GMP, and GLP guidelines Good documentation practices (BMR, BPR, SOP compliance) Basic computer knowledge (MS Excel, SAP/ERP preferred) Preferred Experience: 13 years in production of diagnostic reagents, pharma, or biotech products Regards, Muskan vats muskan.v@head2hire.com

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