582 Bmr Jobs - Page 20

This role involves following cGMP, safety, and environmental standards. The ideal candidate will have experience in API manufacturing, knowledge of regulatory guidelines, and a focus on quality and safety. Description: Strictly following cGMP, Safety and Environmental Practices. Filling of Batch Manufacturing record and equipment cleaning record. Following Good Manufacturing practices during operation. Ensuring Good Housekeeping in the respective plant area and its equipment. Usage of Proper personnel protective equipment as per requirement. Planning and ensuring RM availability for daily production as per production plan. Maintaining the documents like Issue and dispensing register. Carryin...

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

Roles and Responsibilities: Production Scheduling, Coordination with Departments, Capacity Planning, Risk Assessment, Inventory Control, Lead Time Management, Adherence to Standards, Documentation, Collaboration with Sales team, Cost Control.

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...

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...

JD: 1) To be prepared document related to audit as per audit agenda. 2) Filled vendor questionnaires & prepared related documents. 3) Keeping record of key Customer. 4) To be prepared process validation protocol and report as per seniors guidance. 5) To be prepare cleaning validation protocol and report as per seniors guidance. 7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement. 8) To help the senior for preparation of CAPA according to audit report. 9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook. 10) To be prepared BPC...

Walk In Interview Interview Day & Date : 14-06-2025 (Saturday) Time : 08:00 to 11:00 Am Department : Production Sciences or Pharmacy Graduates (M.Sc. / B. Pharm. / M. Pharm.) with 0 to 6 years Experiences in parenteral manufacturing (vial / ampoules / bottles of glass or Plastic through BFS technology). Candidate worked in production compliances / remediation / and having experiences of managing quality system document (CCN / CAPA / investigation etc.) ACULIFE HEALTHCARE PRIVATE LIMITED. Formally known as nirlife Near Railway Crossing (Sanand - Viramgam Highway) Village: Sachana, Taluka : Viramgam District: Ahmedabad 382 150

Retrival& Issuance of documentation GDP CGMP Control Documents Dispatch verification Batch Manufacturing

Customer Segmentation / Value Proposition / Messaging 1. Create different target customer segments and create different service/product offerings for them. 2. Establish the key value proposition of the product / service portfolio of the company. 3. Create strong and simple messaging to address pain points of the customer. Campaign Management / Marketing assets 1. Create an integrated marketing operating plan in line with businesss annual business plan. 2. Ensure that the messaging reaches the customer through the right channel and is appreciated. 3. Identify the marketing assets required for different customer facing situations. 4. Identify various channels of creating thought leadership con...

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 th...

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

Roles and Responsibilities Should Have Formulation Experience. 1. Responsible for product registration in ROW (AFRICA, ANZ, ASIA, LATAM, CIS &, MENA). 2. Responsible and involving in the regulatory audits and coordinating with the auditors/customers. 3. Preparation, compilation and review of dossiers for RoW region in CTD /country specific format. 4. Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities. 5. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. 6...

• Manufacturing activities as per production plan for API / Intermediates • Production as per GMP & SOP • Review BMR Required Candidate profile • Ensure safety and other precautions during plant and RM handling • Ensure quality of products as per specification • Handling of manpower in shifts

Position Overview: We are looking for a Sr. Manager will be responsible for leading and managing end-to-end multiple API production blocks. The role requires ensuring optimal productivity, quality, cost control and regulatory compliance in alignment with cGMP standards. This position plays a critical role in driving continuous improvement, cross-functional coordination, and operational excellence within the production unit.. Key Responsibilities: Oversee daily production activities to ensure efficiency, quality, and cost-effective management of resources. Develop and implement production schedules based on inventory / market requirements / capacity constraints and provide feedback accordingl...

Role & responsibilities : Prepare and review documentation such as SOPs, BMRs, and logs with attention to detail and good command of English. SHARE RESUME TO hrd@stedmanpharma.com / 9786920463 Preferred candidate profile : Education: B.Pharm / M.Pharm / M.Sc. (Chemistry, Biotechnology, Microbiology) / B.Tech or B.E. in Chemical Engineering or related fields. Freshers or recent graduates looking to start their career in pharmaceutical production Basic understanding of GMP , manufacturing processes, and safety protocols Good written and verbal communication skills in English (especially for documentation purposes) Attention to detail, willingness to learn, and ability to work in a team Open to...

*Experience in production operations in Intermediate 1 API industry, Equipment & Utility Operations, Filing BMR I BPR, Distillation Process, having exposure of handling CF, Multi-Milling, AGNFD, FBD equipment. Required Candidate profile * Experience of working in API industry I Bulk Drug, having exposure of handling and preparation of Production cGMP documentation, Change Control, Deviation, 005 Investigation and CAPA etc.

Outlines quality assurance procedures and policies Oversees implementation of quality assurance procedures Ensures the efficiency of inspections through hands-on guidance Ensures data integrity and accuracy Prepares reports on the results of quality inspections Evaluates outcomes of quality inspections and proposes corrective measures. Preferred skills : IPQA, Line clearance, BMR/BPR preparation and & Exposure in review Qualification of equipment and HVAC (DQ, IQ, OQ, PQ) Process validation, Protocol preparation and review Documentation, Change Control, deviation, Market Complaint, CAPA, etc.

QA Senior Executive / Quality Assurance Manager CTC UPTO 6 LPA, Contact: 09990842892 Email: info@wellgen.in We are a 30-year-old Medicine Manufacturer Company is located in Baddi Experience : Minimum 7 years of Pharmaceutical Experience Qualification : B.Pharm You will also be responsible for identifying and resolving quality-related issues and ensuring that the company's products and services meet the requirements of customers Conduct regular quality audits to identify and resolve quality-related issues Develop and maintain quality metrics to track performance and identify areas for improvement Manage the documentation process for quality assurance procedures, including the creation and mai...

Job Responsibility Will be responsible for Production Planning, Allocation of manpower, Daily work distribution, Dispensing of RM & PM, Maintaining Daily cleaning, Calibration etc. records, Documentation etc. ERP& BMR Preparation and Review Maintain the SOPs, Log books & other documents. Oversee and manage the entire manufacturing process. Handle Granulation, Coating and all other production related activities. Active calculation, dispensing of raw materials and batch reconciliation at various stages. In process checking at various intermediate stages of granulation, compression and coating. Should handle process of validation batches. Ensure online documentation of production activity on ti...

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

*Experience in production operations in Intermediate 1 API industry, Equipment & Utility Operations, Filing BMR I BPR, Distillation Process, having exposure of handling CF, Multi-Milling, AGNFD, FBD equipment. Required Candidate profile * Experience of working in API industry I Bulk Drug, having exposure of handling and preparation of Production cGMP documentation, Change Control, Deviation, 005 Investigation and CAPA etc.