4089 Gmp Jobs - Page 16

Job Title: Executive Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” JOB Description: - Method development & Validation by using sophisticated...

DEAR CANDIDATE , WE ARE HIRING! LET'S JOIN OUR TEAM NOW! Department: R&D Position: Research Trainee / Research Associate Preferred Qualification: M.Sc. Biotechnology / M.Sc. Biochemistry Preferred candidate: Male Preferred Experience: 2 to 3 years of experience Should have good documentation skills and knowledge of GDP, GMP, GLP. Should have basic knowledge about proteins and protein purification. Should be a good team player with good interpersonal skills. Job description: Perform R&D related documentation like SOP preparation, data management and data analysis. Perform routine laboratory procedures, including buffer preparation, gel electrophoresis, western blot. Operation and maintenance ...

Dear Candidate , we are hiring for QC Jr Executive ,Down stream process executives & Operators. Open Positions-50 Down Stream Process Executives & Operators Required • Qualification: Bsc/Msc/ITI/B Pharmacy Experience in handling the following Equipment 1 Chromatography column and system handling. 2 Column Packing (BPG And Chromoflow) 3 TFF System 4 Centrifuge system 5 Filtration, Filter Integrity,Buffer Preparation,CIP_SIP PRODUCTION-DS M Pharmacy/Diploma/B tech/Any Degree 6 Expertise in documentation QMS/GMP Compliance / Process Awareness Biologics Company's only Preferable. • Experience: 2 to 6 years in Total Downstream CTC :up to 5.0 LPA. IMMEDIATE JOINERS ARE PREFERABLE" Interested candi...

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Job Description: 1 . Hands on Experience in regulatory submissions preferably for Blood products and Biologics. 2. Review/Submission of applications for new products Manufacturing licenses and renewals. 3. Experience on procedures for application of new drugs (NOC's and Test licenses). 4. Monitoring and ensuring allp certificates (COPPs, GMP, GLP, WHO-GMP and FSC Production Capacity and Performance Certificate) renewals and approvals up to date. 5. Review of Tender certificate. 6. Co-ordinate with Drug control authority personnel for License approvals. 7. Review of Dossiers. 8. Submission of Samples and Documents to NIB, Noida for testing. 9. Updation of the National and international legisl...

KnJ Projects Private Limited is looking for Material cum Quality Expert to join our dynamic team and embark on a rewarding career journey. Develop and implement quality assurance policies and procedures. Conduct quality audits and inspections. Analyze data to identify areas for improvement. Provide training on quality standards and processes. Ensure compliance with regulatory requirements. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

KGVK (NGO & CSR Arm of Usha Martin Limited) is looking for Quality Control/Assurance Professional to join our dynamic team and embark on a rewarding career journey. Develop and implement quality control systems to ensure products meet regulatory and customer standards. Conduct inspections, audits, and testing to identify deviations or defects. Collaborate with production and R&D teams to address quality issues and implement corrective actions. Maintain documentation and compliance with ISO and GMP standards for continuous improvement. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourag...

KGVK (NGO & CSR Arm of Usha Martin Limited) is looking for Quality Control/Assurance Professional to join our dynamic team and embark on a rewarding career journey. Develop and implement quality control systems to ensure products meet regulatory and customer standards. Conduct inspections, audits, and testing to identify deviations or defects. Collaborate with production and R&D teams to address quality issues and implement corrective actions. Maintain documentation and compliance with ISO and GMP standards for continuous improvement. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourag...

Manage day-to-day office operations, including administrative tasks and employee coordination. Handle communications, both internal and external, ensuring timely responses and follow-ups. Organize meetings, prepare agendas, and take minutes for effective documentation. Maintain office supplies and ensure all equipment is in working order. Assist with budgeting, invoicing, and other financial tasks as needed.

Manage day-to-day office operations, including administrative tasks and employee coordination. Handle communications, both internal and external, ensuring timely responses and follow-ups. Organize meetings, prepare agendas, and take minutes for effective documentation. Maintain office supplies and ensure all equipment is in working order. Assist with budgeting, invoicing, and other financial tasks as needed.

Mail your resume on pooja.kalse@orcapod.work Support audit teams in the review and evaluation of UK DB pension schemes, focusing on compliance with IAS 19 and FRS 102. Test clerical accuracy of actuarial and financial reports. Review actuarys reports for reasonableness, consistency, and compliance with relevant standards. Test the appropriateness of actuarial assumptions used in pension scheme valuations. Participate in planning calls and contribute to the preparation of planning memos. Perform initial review of all audit materials related to pension schemes. Collaborate with the audit Owner and Firm Actuary (FA) to resolve technical issues. Prepare final deliverables , including memos and w...

Job Description JOB Responsibilities: - Location: Ahmedabad 1. Ensuring the GMP compliance at CMO and Release of batch manufactured for US market at CMU. 2. Monitoring of process starting from dispensing to packing including witness analysis of Lupin products manufactured at CMO for US market and Domestic market. 3. Handling of market complaint with root cause identification and ensuring the CAPA implementation. 4. New product review to be carried out at manufacturing site after availability of all the documents. 5. Review and authorize Master Batch Records, stability protocol, process validation protocol, temperature cycling protocol, specification of in-process, intermediate and finished p...

Job Description : We're seeking a highly skilled Quality Person with 3-5 years of experience in the biscuits, breads, wafers, and cakes industry. The ideal candidate will have a strong background in quality control and assurance, with a focus on ensuring compliance with industry standards. Requirements: - 3-5 years of experience in the biscuits, breads, wafers, and cakes industry - Strong knowledge of GMP, GHP, and HACCP - ISO 22000 certification is preferred - Excellent communication and problem-solving skills - Work proactively in 3 shifts to ensure consistent quality control Key Responsibilities: - Implement and maintain quality control processes to ensure product safety and quality - Con...

Location: Delhi | Experience: 58 years | Employment Type: Full-time Are you passionate about food quality and safety, and ready to lead quality initiatives in a fast-growing premium fresh food brand Join Pluckk as a Lead Quality , where you'll play a pivotal role in building and maintaining our high standards across production and supply chain operations. About the Role: As a Quality Lead , you'll oversee food safety and quality assurance systems end-to-end from raw materials to finished products. You'll lead audits, mentor QA teams, and drive continuous improvement initiatives to ensure compliance, consistency, and consumer trust. Key Responsibilities: Lead quality assurance processes acros...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary IPQA activities. Warehouse QA activities MMaR S / MPaR's Review. Job Responsibi...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary IPQA activities. Warehouse QA activities MMaR S / MPaR's Review. Job Responsib...

As a Lyophilization Specialist at our stem cells manufacturing company in Hyderabad, your role will involve overseeing the freeze-drying process and ensuring optimal performance. You will be responsible for preparing and executing lyophilization cycles, monitoring equipment, maintaining documentation, troubleshooting issues, and collaborating with cross-functional teams to meet production goals and quality standards. Key Responsibilities: - Oversee the freeze-drying process and ensure optimal performance - Prepare and execute lyophilization cycles - Monitor equipment and maintain documentation - Troubleshoot issues related to lyophilization - Collaborate with cross-functional teams to meet p...

As a Site Instrumentation & Automation Lead at Zydus Takeda Healthcare Pvt. Ltd., located in Navi Mumbai, India, you will play a crucial role in ensuring the smooth operation, reliability, and continuous improvement of automation and control systems in the healthcare manufacturing industry. Your responsibilities will include: - Leading troubleshooting and optimization of automated processes, such as PLC, DCS, SCADA, and HMI systems. - Managing the span of control for Budget, including Spares Management, Services, AMC, Asset Life cycle review, and Capex proposal. - Driving projects related to automation upgrades, expansions, MES integration, and integrations with IT/OT networks. - Ensuring co...

Location: Gujarat, GJ, IN, 382845 JRS India Corporation Private Limited is a wholly owned subsidiary of the J R Simplot Company The J R Simplot Company is a diverse, privately held organization, with roots firmly planted in agriculture and agriculture-related businesses The J R Simplot Company is a true farm-to-table company with operations that touch every aspect of agriculture, including seed production, farming and ranching, plant sciences, fertilizer manufacturing, food processing, commercial product development, and distribution, Summary Tends, maintains, and adjust machine that stock, fill, wrap, seal and label bags with finished product This individual ensures that product and bagging...

Job Title: Manager - Plant Engineering, Pharma Formulations Plant Maintenance Pharma Formulations Basic & Minimum Qualification: Degree in Mechanical Engineering from a reputed university . Experience: 12 to 15 years of working experience in a Pharmaceutical Formulations plant. Location: Ankleshwar Site . Job Description and KEY ACCOUNTABILITIES Engineering & Maintenance Operations Oversee preventive, predictive, and breakdown maintenance of plant equipment and infrastructure. Ensure optimal performance of manufacturing & packing, and warehouse equipment. Lead root cause analysis and corrective actions for equipment failures. Documentation and maintaining the History cards of all critical pl...

Ensures that the Product Quality Reviews / Annual Product Reviews for Teva products are completed in a timely and compliant manner as per Teva s CORP Quality Management systems. PQR/APR compilation and approval must be well associated with the Teva Manufacturing Sites, Global Quality Units and Commercial affiliates to meet the targets and ensure compliance. Ensures timely and accurate data migration in collaboration with sites and Global IT / IT Quality Ensures timely review of CMC documentation in collaboration with Global R&D sites Defines team operating standards and ensures essential CORP and local procedures are followed based on knowledge of own discipline. Manages and supervises a tea...

Candidate should be B.Pharm Candidate should have regulatory exposure/ in previous organisation Candidate should have well command on IPQA activities Candidate should have Command on packaging operations Candidate should be able to work in shift well aware with regulatory requirement

Jindal Advance Materials is looking for Quality - QMS Associate - Patherheri (- yrs) to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Storage, Issuance and Dispensing of Raw Material and Handling of ASRS for Store in Store out of materials, Troubleshooting and handling of TESTO software. Job Responsibilities Phisical stock verification (Cycle counting) and update the stock in SAP. To ensure cGMP compliance in respect of material segregation, ststus labels, calibration and performance checks of weighing balance. Maintain safety and good housekeeping practices at work place. Issuance of Raw Materials as per LVMP production plan as per standard operatin procedure. Responsible for Handling of materials and maintenance in rejected material storage area and cold storage area. Handling of raw material sampling. Handling of Reject...