1027 Cgmp Jobs - Page 20

As a Deputy Manager in Stores within the pharmaceutical sector located in Surendranagar, Gujarat, India, you have an exciting opportunity to leverage your over 10 years of experience in pharmaceutical warehouse operations to ensure efficient and compliant warehouse management. **Key Responsibilities:** - Oversee warehouse operations, including receipt, verification, storage, and dispatch of raw materials, packaging materials, and finished goods while adhering to cGMP and GDP standards. - Maintain accurate inventory records through physical stock counts and reconciliation with SAP/ERP systems to minimize waste and identify non-moving or expired materials. - Develop, review, and implement Stan...

As a QC Microbiologist I, you will be responsible for performing various microbiological testing activities under minimal supervision. This includes water testing, environmental monitoring, media preparation, growth promotion of media, raw material testing, finished product testing, stability testing, antibiotic assay testing, gram staining, microbial enumeration suitability testing, antimicrobial effectiveness testing, and other required microbial testing. Your role requires maintaining quality and efficiency in all tasks performed to ensure accurate results. Your responsibilities will include routine water testing, media preparation, growth promotion of media, and environmental monitoring....

Responsibilities: * Prepare SOPs, review BPRs, adhere to CGMP guidelines. * Collaborate with R&D on new product development. * Ensure compliance with GMP standards during production.

As a Validation Specialist at our company, your primary responsibility will be to plan, execute, and document analytical method validation activities for raw materials, in-process samples, finished products, and cleaning validation. This will involve assessing various parameters like accuracy, precision, specificity, linearity, robustness, LOD/LOQ, and others. You will also review and approve validation protocols and reports to ensure compliance with ICH Q2(R1), USP, and other regulatory standards, maintaining adherence to GMP, GLP, and cGMP guidelines. Your role will require collaboration with R&D, QA, and Production teams to facilitate seamless tech transfer and validation support. Trouble...

Qualification :- M. Pharm Experience :- 3 to 5 year Location :- Vatva (Ahmedabad) Experience in Formulation Plant , Product Development .

Position Overview: We are seeking a knowledgeable and results-driven CSV Engineer to join our team, specializing in providing expert validation services to our clients. In this role, you will work closely with a diverse range of companies, ensuring the compliance, reliability, and quality of their computerized systems while adhering to industry regulations and best practices. Key Responsibilities: Validation Strategy and Planning: - Collaborate with clients to develop tailored validation strategies and plans based on their specific needs and regulatory requirements. - Assess project scope, goals, and timelines to design efficient validation approaches. Validation Execution: - Design, develop...

Manage the technology transfer process for established products, ensuring robust and compliant manufacturing processes e.g. implementation of new API sources. Write, review, and maintain regulatory response documents, justification reports, and risk assessments related to technology transfer activities. Oversee the preparation and review of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for smooth transfer and manufacturing. Review process validation protocols and reports. Coordinate with R&D, production, quality assurance, and regulatory teams to ensure alignment on project deliverables and timelines. Troubleshoot and optimize manufacturing processes addressing deviatio...

We're Hiring!!!! Candidates with experience in API & Formulation are encouraged to attend our Walk in Interview. API MANUFACTURING Designation : Sterile Officer/Sr. Officer Experience: 5-10years Educational Qualification: B.Sc/M.Sc(Chemistry)/B.Pharma/M.Pharma Designation: Shift Incharge Experience: 10-12years Educational Qualification: B.Sc/M.Sc(Chemistry)/B.Pharma/M.Pharma Designation: Non-Sterile Operator/Officer Experience: 2-8years Educational Qualification: B.Sc/M.Sc(Chemistry)/BE/B.Tech Designation: Non- Sterile Shift Incharge Experience: 8 to 12 years Educational Qualification: B.Sc/M.Sc(Chemistry)/BE/B.Tech WAREHOUSE Designation: RM/PM - Head Experience: 12 to 15 years Educational Q...

Project Engineer (PEB) - High Voltage Products Breakers/disconnectors and switches Manufacturing Plant projects This role is responsible for coordination all on-site PEB construction works activities in alignment with project delivery schedule/activities to assure cost-effective execution of project deliverables in accordance with contract specifications, quality standards, schedule, and safety requirements. Job Description About the Role: Review and verify PEB designs including general arrangement drawings, structural calculations, connection details, and fabrication drawings. Coordinate with PEB vendors and consultants to align structural design with pharmaceutical layout, HVAC systems, an...

Hi, Greetings from Avani Consulting!! We have job opportunities with API Manufacturing Company for the Sr. Executive/Executive- Electrical position, Mysore Location. Position- Sr. Executive/Executive- Electrical & Instrumentation Work Experience +8 in API / Pharmaceutical / Chemical / FMCG / Continuous Process Industry Location Mysore Qualification- B.E. / B.Tech / Diploma in Electrical Engineering. Knowledge of SAP. Must Have Electrical Supervisor License Must have experience in 66KV Job Summary: To lead and manage all electrical maintenance activities and ensure optimal performance, reliability, and safety of electrical systems in an API manufacturing facility. The role also includes effic...

Role Overview: As a Packaging Planning Executive in the Sterile Manufacturing Department, your primary responsibility will be to prepare packaging planning on a monthly and daily basis based on material availability. You will also be responsible for updating self-hygiene practices, attending training sessions, and working in accordance with standard operating procedures. Key Responsibilities: - Prepare packaging planning on a monthly and daily basis according to material availability - Update self-hygiene practices - Attend training sessions as per schedule and ensure compliance with Training Needs Identification (TNI) - Adhere to standard operating procedures in the general area of the Ster...

Role Overview: You will be a Senior Chemist at Scimplify, located in Kurkumbh, Pune. Your primary responsibility will involve tasks related to sampling and analysis of raw materials, packing materials, and finished goods. This includes conducting analysis of finished products, in-process samples, stability samples, raw materials, and packing materials. Key Responsibilities: - Maintain and calibrate various lab instruments such as HPLC, Gas Chromatography, Karl-Fischer Titrator, Melting-Boiling Point Apparatus, Refractive Index, Moisture Analyzer, pH meter, and Weighing Balance. - Work in compliance with approved methods, SOPs, cGMP, and CGLP standards. - Proper documentation of laboratory da...

As an Officer/Sr. Officer, your role will involve operating the PCC, Diesel Generator, and utility Equipment efficiently. You will be responsible for maintaining the critical spares inventory for utility (Electrical Power) and plant equipment. Additionally, you will provide necessary utility to the production department or other users as required. Key Responsibilities: - Update and maintain all PCC and utility equipment records per SOP - Qualification, preparation, and qualification of utility and plant equipment - Carry out all work as per cGMP and GEP standards - Perform preventive maintenance of utility and plant equipment as per SOP - Handle any breakdown efficiently and in line with the...

Role Overview: As a leader in utility systems management within an API manufacturing facility and drug product filling and packing line equipment, you will be responsible for overseeing the operation and maintenance of various utility systems. Your primary focus will be to ensure the 24x7 availability of utilities to support uninterrupted manufacturing processes. Key Responsibilities: - Plan and implement preventive and breakdown maintenance schedules for utility systems including Brine chillers, Air compressors, HVAC, N2 plant, Air dryer, and Chilled water chillers. - Ensure compliance with cGMP, USFDA, and other regulatory standards. - Lead utility qualifications and support audits and ins...

JOB DESCRIPTION: MAIN PURPOSE OF ROLE Job Responsibilities: Third Party Manufacturing (TPM) Site Compliance: Perform regular and ad-hoc visits to TPM facilities across the West Zone to evaluate compliance with current Good Manufacturing Practices (cGMP) primarily Revised Schedule M, Abbott's internal quality standards, and applicable regulatory guidelines. Identify non-conformities, process inefficiencies, and documentation gaps during site inspections. Collaborate with TPM quality teams to develop robust corrective and preventive action (CAPA) plans. Monitor CAPA implementation timelines and effectiveness through follow-up visits and reviews. Audit CAPA Oversight: Review audit findings from...

A. Job Objective Planning, scheduling, coordinating and staffing of shift activities to meet the production targets and achieve the desired quality. Shift In charge in particular will be responsible for managing all the above shift activities for the entire Hall/all machines. Strategic Planning Activities: Core: Monitoring and verifying all shift activities (Machine checking, IPQC (Dimensional and Attribute), FT change, DB change, Greaser Change, Colour change, daily machine performance report, process parameters, ) Implement Quality corrections ( Dimension correction, moisture correction, process parameters) to minimize defects & achieve the target DAFOE Ensures that all process parameters ...

A QC Officer performs visual inspections, tests, and measurements on raw materials, in-process products, and finished goods. This is done to identify any defects or deviations from the quality standards and specifications. Required Candidate profile Previous experience in a quality control, quality assurance, or manufacturing environment is highly valued. A strong understanding of quality control principles, testing methods

This is where your work makes a difference. At Baxter, we believe every personregardless of who they are or where they are fromdeserves 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. He...

Biocon Biologics is a fully integrated pure play biosimilars organization globally committed towards transforming patient lives through innovative and inclusive healthcare solutions. It is engaged in developing high-quality, affordable biosimilars aimed at expanding patient access to cutting-edge class of therapies across the world. Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led-global biopharmaceuticals company and India&aposs ?rst publicly listed biotech enterprise. Biocon Biologics has one of the largest biosimilars portfolios, a wide global footprint, state-of-the-art manufacturing facilities, world-class R&D ecosystem, and high quality & compliance standards, enabling...

Role Overview: As a Raw Material Quality Control Analyst, your main responsibility will be to ensure that all raw materials (API & excipients) used in manufacturing are sampled, tested, and released according to pharmacopeial/in-house specifications and regulatory standards before they are utilized in production. You will play a crucial role in maintaining the quality and integrity of raw materials used in pharmaceutical manufacturing processes. Key Responsibilities: - Receive and verify raw material intimation from the warehouse. - Conduct GMP-compliant sampling using appropriate tools and in classified environments (if applicable). - Properly label samples and maintain sampling logbooks. -...

B.Sc/M.Sc Chemistry, 1–8 yrs exp in API/Pharma QC. Must handle HPLC/GC/UV/IR, cGMP, stability, and docs. Local preferred Dahej. Only male candidates are required. Only pharma experience required.

Role Overview: At Unijules Life Sciences Ltd., we believe in the immense potential for growth and innovation in the pharmaceutical industry. As new technologies continue to emerge, we understand the importance of expertise and skill to stay ahead in this rapidly evolving field. We provide a learning platform for individuals who are energetic, enthusiastic, and dedicated to learning and excelling in their careers. If you are committed to growth, development, sincerity, and quality, we welcome you to join the Unijules Pariwar family. Key Responsibilities: - Conduct audits in the pharmaceutical manufacturing plant, preferably specializing in Liquid/Solid dosage. - Implement cGMP system to ensur...

Job Alert Sr. GM / Associate Vice President – Quality Control Location: North India Industry: API / Chemicals Manufacturing Salary: Open (Attractive hike on current package) Experience: 16+ Years | Age: 50 Years We are seeking a dynamic Quality Control leader for a reputed API Manufacturing organization . The candidate must have strong exposure to regulatory-driven companies with proven expertise in leading global regulatory audits (USFDA, EMA, MHRA, etc.) and managing large QC operations. Key Responsibilities: Head the Quality Control department ensuring compliance with cGMP & international regulatory guidelines. Lead a QC team of 150–200 employees , driving efficiency, compliance, and tech...

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical a...

The ideal candidate should have at least 3 years of experience of working in Pharmaceutical Production floor where the person is responsible for shift operations. The incumbent would typically be responsible for: Ensuring the targets are met keeping in mind safety and quality guidelines. Management and upkeep of facility, materials and manpower. Troubleshooting in operations, validations and equipment qualification Coordination with other functions like QC, QA, Warehouse among others. Knowledge and Adherence to SOPs , regulatory requirement Preparing Batch Manufacturing Records, Protocols, Reports, Investigation Reports, and Qualification Reports. Work on Continuous improvement Plans (like C...