2778 Gmp Jobs - Page 26

MetLife is looking for Software Dev Engineer Test II to join our dynamic team and embark on a rewarding career journey Analyzing customer needs to determine appropriate solutions for complex technical issues Creating technical diagrams, flowcharts, formulas, and other written documentation to support projects Providing guidance to junior engineers on projects within their areas of expertise Conducting research on new technologies and products in order to recommend improvements to current processes Developing designs for new products or systems based on customer specifications Researching existing technologies to determine how they could be applied in new ways to solve problems Reviewing exis...

Armein Pharmaceutical is looking for QC Executive 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 e...

Oversee and lead all activities of assigned teams /projects; meet customer needs. Work according to appropriate standards for quality, ethics, health, safety, environment, protection and information security; lead initiatives to ensure continuous improvement; all activities have to be aligned with organizational workflows and procedures. Evaluate and interpret results, draw relevant conclusions; supervise project related activities; perform complex tasks without having established procedures. Oversees and may also write protocols, scientific reports, lab procedures or process. related SOPs; write scientific documents intended for external partners or for generation of registration documents;...

Independently handle microbial cultures (bacteria, yeast, actinomycetes, fungi) from shake flask to fermenter scale. Perform inoculum preparation, fermentation runs (batch, fed-batch, continuous), and monitor critical process parameters. Operate and troubleshoot bench-top fermenters ranging from 1 L to 100 L. Execute scale-up studies and support technology transfer activities. Ensure compliance with CIP (Clean-in-Place) and SIP (Sterilization-in-Place) protocols for fermenters. Participate in downstream processing, including recovery and purification of target molecules. Conduct biochemical and analytical assays such as sugar profiling, amino acid profiling, fatty acids/fatty alcohols estima...

Experience in Scale up from R&D to Commercial plant, Technology Transfer Strong understanding of key chemical engineering concepts of Fluid Flow, Heat transfer, mass transfer and Reaction engineering Exposure on Process optimization, debottlenecking, process intensification and Process Safety management Basic understanding for GLP, GMP, and other pharma regulatory standards. vacancyKeyroles":" Must have Expertise on Technology transfer & scaleup from Lab scale to commercial scale. Preparation BEP documents for Technology Transfer like Design Basis , BFD, PFD, Mass balance , energy balance, line sizing calculation , Instrument data sheet preparation & Suitable MOC Selection. Involves Process ...

Manage ETO projects in an international environment from definition to final approval Coordinate all activities for the project and create the final design and pricing Define specifications in cooperation with other departments like product development, quality, procurement, MSAT,sales and marketing for more complex projects Making technical and feasibility analyzes of projects Design new custom products using in-house design tool according to customer needs and internal design rules (Use of computer software design tool) Ensure product is manufacturable and define any qualification/testing that might be needed Calculate product cost and define price of the product in collaboration with mark...

Ensure timely reporting of deviations, appropriate investigations to identify root cause or most probable root cause and proposal & implementation of appropriate CAPA to prevent reoccurrence. Perform the manufacturing investigations for OOS results and Customer Complaints to identify root cause or most probable root cause and facilitate proposal & implementation of appropriate CAPA to prevent reoccurrence. Participate in the audits and inspections as SME for deviation management and manufacturing investigations. Ensure timely proposal and implementation of appropriate CAPA for any audit findings. Perform timely tracking of Operational and Compliance Metrics for Manufacturing Operations and m...

Maintain specimen signature logbook and ensure the signature of employees being recorded before starting the work. Prepare training curricula for an employee/ Job Description based on the need in consultation with the Department head and respective reporting manager. Ensure review of training file and LMS report for the completion of trainings, applicable OJT s and certify the trainees post completion of the same. Responsible for updating classroom/ OJT/ awareness training attendances and related data in the LMS. Responsible for archiving of training records of respective departmental employees. Ensures training records of resigned employees are stamped and archived as per the procedure. Cre...

Active involvement in all upstream manufacturing activities. Perform error free operation by eliminating operational gaps in advance. Active trouble shooting to minimize the various risks prior to execution and during execution. Initiate and process upstream deviations /investigations and closure. Pre -execution activity: Area and equipment readiness. Issuance of raw material /consumables and issuance batch records. Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data. Follow and practice on-line documentation all the time. Follow cGMP practices during the manufacturing ac...

Division Department Sub Department 1 Job Purpose Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines Key Accountabilities (1/6) Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner Collect data from all SPOCs with respect to received work plan for review Escalate any delays in receiving response from unit with respect to work plan Review of collected data for work plan fulfilment Send data to HO for compilation of deficiency response Take follow up with HO to receive updated dossier...

Job Description: Inventory Management: Manage inventory cover of all raw and packing materials basis the set norms and the factory plan. Highlight issues in terms of stock-outs, freshness and BBD crossed stocks. Review the stock levels daily and identify constraints. Ensure delivery on service levels and keep the commercial, factory, quality teams informed on going challenges WRT RM and PM. Ensure blind count as per defined schedule and timely highlight the differences with reasons to relevant teams Warehouse management: Manage the existing RM/PM warehouse operations. Definition and monitoring of the KPI s and the SOPs for the raws warehouse Training & induction of new staff and manpower man...

Position Title: Shift Executive- Quality Position Type: Regular - Full-Time Position Location: Mehsana Requisition ID: 32234 Job Details: Function/Department : QA Global Job Grade Job Title: Shift Executive Quality Region*: AMENA Global Grading System Job Code: Global Job Grade : Evaluation Date : Global Pay Band : 3 Global Benchmark Job : Yes This is a generic job title to be used for Job Administration. Job titles used by individuals may vary by country but the position should be aligned to the generic job title for Job Administration purposes. *e.g. Global/APMEA/NA/CE/etc. Instructions for Position Summary : Brief description of the primary purpose of the position, with emphasis on the ou...

This is where your work makes a difference. At Baxter, we believe every person regardless of who they are or where they are from deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. ...

This is where your work makes a difference. At Baxter, we believe every person regardless of who they are or where they are from deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. ...

Position Title: Assistant Manager - Production Position Type: Regular - Full-Time Requisition ID: 37306 We are passionate about food. But we re even more passionate about our People! About the role : To supervise and co-ordinate the processing and packing operation of production line, ensuring the product is packed within the product specifications. To manage production costs by optimizing productivity / yield, while utilizing the staff / equipment in a safe, effective and hygienic manner. Roles and Responsibilities & Key Deliverables: Manager the Team: Make sure performance of subordinates is achieved against their agreed KPI s. Performance appraisals are carried out every three months and ...

Job Summary: We are looking for a dedicated and detail-oriented Assistant Manager Documentation with strong exposure to various Quality Management System (QMS) elements. The ideal candidate should have hands-on experience in managing QMS documentation including Quality Risk Assessment (QRA), Cleaning Validation, Market Complaints, Self-Inspection, Quarterly Review Reports, Site Master File (SMF), Quality Manual, and Validation Master Plan (VMP). Key Responsibilities: Manage and control QMS documentation in compliance with regulatory and company standards. Prepare, review, and update documents including: Quality Risk Assessments (QRA) Cleaning Validation protocols and reports Market Complaint...

About The Role Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Analyst Qualifications: Master of Pharmacy Years of Experience: 3 to 5 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Regulatory, helping the world s leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, co...

Eligibility: Experience : 0-2 Years Position: Shift Chemist Departments: API Production Qualification: M.Sc, Diploma, B.Sc, B.Pharm Documents to Carry (Photocopies): Resume All Educational Certificates Previous Organizations Relieving Letters Current Offer / Increment Letter Last 3 Months Payslips Aadhar & PAN Card Must be willing to work in shift operations

The Opportunity: . Officer - Quality Control is responsible to perform Quality Control activities at AQAL. What we are looking for :- Responsible for Timely analysis of under test samples giving timely results Coordination with tollar for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis. B. Sc. / M. Sc. (Chemistry) 2-5 years of experience in Quality including cGMP, ISO and regulatory Audits Knowledge of Quality Control in Fine Chemicals and pha...

- Develop new or improve current Sweet products - Daily and as and when required documentation and record keeping as per compliances and company SOP - Make test samples of Sweets products and conduct trials - Source and select ingredients for Sweets products - Manage or supervise development and production of Sweets - Improve efficiency of manufacturing processes - Develop new or improve current packaging - Ensure food products meet specifications and standards (quality assurance) - Investigate the nutritional properties of foods - Should be open to accept any unforeseen tasks related to FT. - Following keeping controls, maintaining as per FSSI norms - Traceability, Batch card - Following IS...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experienc...

Job Description: We are seeking a dedicated and skilled Production Officer to join our team. The ideal candidate should have a minimum of 1 year of experience in a regulatory-approved manufacturing plant, with hands-on experience in handling critical production equipment and knowledge of cGMP standards. Key Responsibilities • Operate and manage production equipment such as reactors, centrifuges, dryers, multi-mills, and other machinery used in manufacturing processes. • Oversee and ensure thorough cleaning of production areas, maintaining compliance with cleanliness and hygiene standards. • Monitor and maintain environmental conditions on the shop floor, ensuring adherence to regulatory and ...

- Analysis of finished goods & RM & maintain its documents - Analysis of all products as per inspection plan - Conduct the in- house calibration of instrument and equipment - Laboratory reagent preparation, its standardisation for daily use Perks and benefits Medical, Canteen

Job Description: As a Quality Compliance Associate in a manufacturing environment, you will be responsible for ensuring quality compliance, documentation, and adherence to industry standards. Your key responsibilities will include conducting quality checks and inspections of raw materials and finished products, ensuring compliance with GMP, ISO, and regulatory standards, maintaining quality documentation, and assisting in audits. You will also be involved in supporting process validation and implementing quality control measures while collaborating with production and R&D teams for quality improvements. To excel in this role, you should possess a B.Sc/M.Sc in Chemistry, and freshers are enco...

We are looking for a dedicated and detail-oriented Manufacturing Chemist to join our production team. The ideal candidate will have a strong background in chemistry and practical experience in a manufacturing setup, preferably in the cosmetics, pharmaceutical, or chemical industry. Your key responsibilities will include assisting in the manufacturing and formulation of chemical products according to company standards, handling and operating lab and production equipment safely and efficiently, monitoring and ensuring the quality of raw materials and finished products, maintaining proper documentation of batch records, test results, and manufacturing data, ensuring compliance with GMP (Good Ma...