277 Bmr Jobs

You will be responsible for strictly following cGMP, Safety and Environmental Practices, as well as ensuring Good Manufacturing practices during operation. This includes filling Batch Manufacturing records and equipment cleaning records, maintaining proper personnel protective equipment usage, and ensuring good housekeeping in the respective plant area and its equipment. You will need to plan and ensure raw material availability for daily production as per the production plan, maintain documents like Issue and dispensing register, and carry out processes as per Batch Manufacturing Records (BMR) without any deviation. It is essential to adhere to data integrity in online documentation and handle hazardous operations in a safe manner. Additionally, you will be expected to effectively utilize resources such as utility, men, and machines. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that offers end-to-end development and manufacturing solutions across the drug life cycle. PPS serves customers globally through a network of facilities in North America, Europe, and Asia. The services provided include drug discovery solutions, process and pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products and services, and potent solid oral drug products are also offered. PPS caters to the development and manufacturing of biologics such as vaccines, gene therapies, and monoclonal antibodies. With experience across varied technologies, PPS has established itself as a trusted service provider and a preferred partner for innovators and generic companies worldwide.,

Equipment Knowledge of Plant area i.e. Reactor, Centrifuge, Dryer, Sparkler & Sifter etc. Knowledge of documentation as required in GMP like BMR, ECR, Usage Log Book etc Handling of Workmen in Plant area Knowledge for using of Safety Equipments which are using in Plant area Experience of general Computer knowledge.

Role & Responsibilities: To carryout the processes of different products as per the respective approved BMR from Q.A. To make entry in BMR while the process is in progress. To follow written standard operating procedure while working in the plant. To follow instructions given by the Production Executive and other superiors related to Personnel safety, product safety, product quality and its yields. To follow instructions relating to cGMP, GDP, Personal hygiene and other documentations related to regulatory requirements. To ensure operational control, availability of BMR, raw materials, packing material as per requirement. To report any ill health, injury, unfitness regarding work to Production Executives. To ensure that proper dress code, work behavior, personnel hygiene is followed in plant as per SOP. To give training to sub-ordinates and take proper shift charge from reliever (production officer/executive.) To ensure batch processing is done strictly as per Batch Manufacturing record (BMR). To report any deviation occurred/odd observations in plant to the production Executive. To take all necessary safety precautions & to ensure all necessary personal protective Equipment is worn while working in the plant. To maintain equipments cleaning and good housekeeping in plant. Ensure that all work relevant to his area is carried out under his supervision in accordance with company procedures as regards Safety, Health and Environmental Protection. To co-ordinate with QC department for sampling/testing of in-process, equipments cleaning ,intermediate, finished products, purified water, Microbiological analysis Etc. To co-ordinate with Maintenance department regarding Utility, equipments cleaning, quarterly preventive maintenance, equipment/instrument calibration and major breakdowns. To fill and maintain daily documents in plant. To co-ordinate with QA department regarding issuance of documents like BMR, BCRs, SOPs Formats, Log-books, Intimations, Training sheet etc. Desired Candidate Profile: Qualification: B.sc /M.sc in Chemistry Experience: 01 to 05 Years of experience in API/Bulk Drug manufacturing. Job Location: Boisar( Tarapur)

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.

Interview for Production Dept on 02-08 in Bharuch for API Pharma Company in Dahej Qualification: BE / Diploma Chemical / BSC / MSC Chemistry / ITI AOCP Experience: 3 to 13 Years CTC: Up to 8 LPA No Charges Free Jobs Share with Your Friends!!! Required Candidate profile Send CV on sdpbharuch@gmail.com with Subject: Production Dahej & Call on 760033423 Interview Venue: SDP HR SOLUTION, Sixth Floor, 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch

Role & responsibilities -To perform the manufacturing process of products and to fill all the quality records in shift as per GMP. (BMR/BPR/ECR/Log Books/etc.) Following the SOP. -To give the requisition for Raw material/Packing material to Raw material store and verification of the same after receipt. -To give requisition for any consumable items to engineering store and verification of the same after receipt. -To give requisition for forms / formats and other quality related documents to QA and submission of the same to QA. -To make sure that all production deviations, non-conformance & accidents are reported along with investigation report. - To schedule training of plant personnel on SOPs, documentation and other cGMP compliances as per ICH Q7 and safety.

Ensure current versions of all GMP documents are in use. Prepare, revise, and control SOPs . Implement and enforce (GDP). Conduct internal audits, maintain summaries and CAPA tracking Support in process validation, equipment qualification etc Required Candidate profile Ensure all QA activities comply with cGMP, regulatory requirements & internal quality standards for API & Specialty manufacturing. Contact Mr Deep at 9867038868, Email Id: ops@empowerrecruitments.com

B.Sc/M.Sc. with 1–4 years in QA (API preferred). Strong in GMP, documentation, audits, and QMS. Detail-oriented, compliant, and reliable. Ready to ensure quality excellence in a world-class pharma environment. Required Candidate profile B.Sc/M.Sc. with 1–4 years’ QA experience in API. Skilled in GMP, documentation, audits, and QMS. Detail-oriented, disciplined, and committed to quality compliance. Perks and benefits GMP GLP plant |Growth |Safety |Compliance |Perks

You will be responsible for managing the operations of chemical processes involving the addition of Diketene reactions for the production of Arylides. This will include handling batch processes, drying operations, and creating acidic strength as per the requirements. You will also be involved in pressure nutch filtration, BMR filling, and operating water ring vacuum pumps. Additionally, you will be required to handle DCS panel operations efficiently. This is a full-time position with a rotational shift schedule. The ideal candidate should have at least 1 year of relevant work experience. The work location for this position is on-site. The expected start date for this role is 04/10/2024.,

Role & responsibilities Operate and monitor critical equipment such as reactors, centrifuges, blenders, sifters, multi-mills, etc. Ensure strict compliance with cGMP guidelines during all stages of production. Maintain accurate and timely documentation in accordance with regulatory requirements, including handling of change controls, deviations, and batch records. Identify and escalate technical issues and implement corrective and preventive actions (CAPA). Coordinate with cross-functional teams (QA, QC, Maintenance) to ensure smooth plant operations. Adhere to standard operating procedures (SOPs) and safety protocols. Support process improvement initiatives to enhance productivity and efficiency. Key Skills & Competencies: Good understanding of chemical processes and API manufacturing. Hands-on experience with chemical plant operations and equipment. Strong documentation and problem-solving skills. Awareness of regulatory and compliance requirements.

Responsibilities: * Manage production processes from BMR to dispatch. * Oversee liquid oral, syrup, ointment, GMP compliance, cream & manpower handling. * Ensure quality control measures are implemented.

Responsible for leading production operations, coordinating production staff and equipment, ensuring product quality and profitability, and overseeing and managing the production operations involved in injectable products.

Role & responsibilities Production chemist and QC chemist Preferred candidate profile HPLC,GC wet lab,BPR,BATCH PLAN,REACTORS,ANALYSIS,WET LAB,INSTRUMENTATION, Perks and benefits As per company norms

KPMG India is looking for Executive - Adobe QA to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

Responsibilities: * Collaborate with cross-functional teams on product development & launch * Conduct BMR reviews & SOP maintenance * Ensure compliance with GMP standards through audits & inspections Food allowance Annual bonus Provident fund

Role & responsibilities Granulation Supervisor Responsibilities: Supervise the granulation process, ensuring compliance with Batch Manufacturing Records (BMR) and adherence to Good Manufacturing Practices (GMP) . Ensure effective process adherence, timely production, and achievement of department goals. Focus on yield improvement , identifying and implementing strategies to optimize production efficiency and minimize waste. Monitor and maintain granulation equipment, ensuring smooth operation and troubleshooting as needed. Collaborate with cross-functional teams to address any production or quality-related issues. Provide training and mentorship to junior staff, ensuring operational efficiency and safety. Analyze production data and report on key performance indicators (KPIs) to senior management for continuous improvement. Granulation Pharmacist Responsibilities: Responsible for operating and overseeing more than two granulation machines during production, ensuring quality and quantity targets are met. Perform regular quality checks at various stages of production to maintain high-quality standards. Ensure proper machine performance, identify potential issues, and support troubleshooting and preventive maintenance activities. Ensure compliance with GMP and regulatory standards throughout the production process. Collaborate with Quality Control and Maintenance teams to resolve operational challenges and maintain machine performance. Maintain accurate production records, monitoring machine performance and production metrics. Pellets Supervisor Responsibilities: experience in pellets manufacturing in a regulated OSD pharmaceutical environment. Strong understanding of GMP, GDP, regulatory (USFDA/EU/WHO) guidelines. Good documentation, team management, and communication skills.

Role & responsibilities 1. Drive product robustness for all products in area of responsibility and lead the third party operation team. 2. Lead and manage all TPO Process activities and process validation for products developed and manufactured at outside contract facilities. 3. This includes, providing product stewardship by ensuring the performance of all products are monitored and maintained in a validated state, supporting root cause investigations by providing Technical intelligence to deviations, technical complaints, OOS & CAPAs. 4. Identifying and executing continuous improvement opportunities, leading New Product Launch third party teams and leading technical activities related to transfers of Drug Product Manufacture and Packaging. 5. Be familiar with statistical tools to analyze data. 6. Provide third party and techno-commercial leadership in the areas of production and packaging process and process optimization using pharmaceutical processes. 7. Knowledge of all pertinent technical information related to an assigned product. Detailed knowledge of the operation, maintenance, and utility of all manufacturing and/or packaging equipment for assigned projects. Thorough familiarity with cGMPs, SOP's, relevant government regulations, and current industry standards. 8. Responsible for Techno-commercial activities for all dosage form. 9. Responsible for Sourcing / coordinate with LL/TP manufacturers for product related documents. 10. Supplier Identification: • Identifying potential suppliers capable of meeting the quality, regulatory, and supply requirements for markets. 11. Supplier Qualification and Onboarding: • Developing and implementing a robust supplier qualification process to ensure that selected suppliers meet the necessary standards and regulations in coordination with quality team. Preferred candidate profile PHARMA THANKS YOU REGARDS MILAP RATHOD (7486829377) call or whtup HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

Handled hazardous chemicals like Tri-phosgene or Phosgene

Perform daily production as per SOPs & batch instructions. Operate reactors, filters, centrifuges. Maintain BMRs, ensure GMP/EHS compliance, proper labeling & raw material handling. Coordinate with shift in-charge for smooth operations.

Execute production as per plan & SOPs. Ensure quality, yield & safety. Maintain BMRs/logbooks. Coordinate with teams, support troubleshooting, report deviations, and uphold EHS, GMP & area cleanliness standards. Suggest process improvements.

Lead daily production to meet output, quality & safety goals. Manage schedules, manpower & equipment. Ensure GMP/SOP compliance. Review BMRs. Resolve issues, optimize processes, oversee key ops & ensure QMS, EHS & regulatory compliance.

The candidate will be responsible for the proper receipt, storage, and GMP-compliant dispensing of raw materials used in pharmaceutical production Perform raw material dispensing activity in designated dispensing booths under controlled conditions.. Required Candidate profile Receive, inspect & label incoming raw materials as per SOP Coordinate with the QA, Production & QC department during material movement Ensure adherence to GMP, GDP & safety guideline during dispensing

To perform IPQA activities at shop floor in every stage of OSD manufacturing and packing. Review of BMR & BPR. Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release. Review of documents of respective areas and logbooks for adequacy and completeness. QA overview for receipt of material from warehouse to production. IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities. Review and Control of SOP’s, Specification, BPR issuance, Master Formulae and Records. Preparation & Review of process validation protocols and reports. Any job activity assigned by HOD

Role & responsibilities To handle the production activities in rotational shift. Controlling manpower in the shifts. Ensuring safety and quality compliance in the shift. Following data integrity strictly at work place & Follow the Instructions as per BMR. Good exposure in Clean room and controlling of foreign particles. Knowledge on QMS document handling & Follow the SOPs during manufacturing process. Handling of different unit operations like Batch charging, Solvent receiving & Charging, Layer separation, Work up, Distillation & Sparkler filtration, Crystallization, Centrifugation, drying, milling, sieving and packing etc. Ensure the cleaning, sanitization as per procedure and recording the document. If any abnormality observed immediately inform to Shift incharge. Critical operations should be ensure Ex. Layer Separation, Work up, Solvent charging & Transfer the reaction mass. Update of Equipment usage log, Weighing balance log & Online documentation of BMR and ECR. Reaction monitoring as per the written procedure given in Batch manufacturing record. Preferred candidate profile Should have exposure to the regulatory requirements of documentation. Adherence to Quality, Safety, Health, and Environment measures and cGMP norms. Please share update cv on email :- hrd@apotheconpharma.com Perks and benefits 5 Lakhs Sum Assured Medical Insurance Canteen Transportation

Roles and Responsibilities Should Have Formulation Experience. Having vacancies in RoW (ASIA , MENA, LATAM, AFRICA) Regions Responsible for product registration RoW (ASIA , MENA, LATAM, AFRICA) Regions region Preparation, compilation and review of dossiers for region in eCTD/CTD/country specific format. 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. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. Responding to queries with in the time lines received from client/agency. Preparation of check list as per country specific requirements region. Review of documents like specifications/ MFC/ BMR/ PV/ Stability/ PDR/ DMF/ CoAs/Artworks and other quality related documents for their suitability for registration in MENA region. Co-ordinating for CoPP, GMP, License and other required documents/certificates legalization activity required for dossier compilation and registration. Archiving/Maintenance of the dossiers, renewal files and variation approvals along with supporting documents in regulatory data base. Identifying gaps in approved dossier, compiled and submit the post approval changes (Minor variations) to agent/agency. Filing of variations if any and registration renewals. Compilation and circulation of product approval package up on receipt of product approval/Minor variation approvals to concern departments. Maintaining the product status (Registered and Under registration) in excel sheet. Desired Candidate Profile Should Have Regulatory Affairs Relevant Formulation Experience Perks and Benefits