2778 Gmp Jobs - Page 27

You will be joining Vimson Derma, a renowned contract manufacturer of cosmetic and medicated products located in Ahmedabad with over 45 years of experience in the cosmetics and dermatology industry. As a trusted name in the field, Vimson Derma holds certifications such as GMP, GLP, and ISO 9001:2015, ensuring the highest quality standards. The company's product range includes dusting powders, talcum powders, shampoo, conditioner, cream, gel, lotions, oil, soaps, sunscreen, serums, and more. With a substantial client base of over 200 companies across India, Vimson Derma is committed to delivering excellence in the products they manufacture. As the R&D Senior Executive in Cosmetics, your prima...

You will be responsible for operating and maintaining a variety of equipment including injection molding machines (Arburg, Engel, Batten field, Nissei, Fanuc Roboshot, etc.), CNC milling machines (Mazak, Makino, DMG Mori, etc.), EDM machines (AGIE, Sodick, etc.), surface grinders (Okamoto, HMT, Proth, etc.), as well as utility equipment like transformers, electrical switchgear, diesel generators, air handling units, air compressors, sewage treatment plants, UPS, PLCs, etc. Your key accountabilities and essential functions will include carrying out routine scheduled maintenance work, responding to equipment faults, designing maintenance strategies, procedures, and methods. You will also be re...

You will be responsible for analyzing Vendor Approval samples and preparing Standardization of Solutions as needed. You will also need to implement GLP/GMP requirements and analyze Raw Materials, Finished Products, Stability samples, and Packing materials. Ensuring samples and related documentation meet cGMP requirements is crucial. Additionally, you will need to oversee the analysis of Raw Materials, Finished Products, and Stability Samples from outside commercial labs. Reviewing laboratory chemicals, calibrating instruments such as HPLC, UV, IR, Dissolution, KF Potentiometer, and performing Working standard qualification are part of your duties. Maintenance of Stability Incubators, loading...

As a sLIMS Implementation Specialist at Sun Pharmaceutical Industries Ltd., you will play a crucial role in the successful deployment, configuration, and ongoing support of our Laboratory Information Management System (SLIMS). Your responsibilities will include supporting the implementation and configuration of sLIMS to ensure alignment with laboratory workflows and regulatory requirements. You will work closely with cross-functional teams to execute tasks defined in project plans, adhering to timelines for a successful implementation of sLIMS. In this role, you will configure the sLIMS software to meet the specific needs of the laboratory, including configuring workflows and setting up user...

About Shalina Healthcare: Shalina Healthcare is among the largest privately owned pharmaceutical businesses in Africa with its Global Headquarters based in Dubai, UAE. The company has recently diversified into new lines of businesses such as Digital Healthcare, Diagnostics, and Consumer Healthcare. Shalina Healthcare has a remarkable track record and its brands are highly trusted across Africa. With a vision to become the health champion of Sub-Saharan Africa by 2030, the company is seeking individuals who can contribute to its growth and make a positive impact on the communities it serves. If you share our Core Values and are passionate about our Mission, we welcome you to join us on this j...

As the QA Manager in plastic injection moulding, you will be responsible for developing and implementing quality assurance policies, procedures, and systems. Leading the QA team, you will monitor and evaluate product quality across all stages to ensure compliance with internal standards, customer specifications, and relevant regulatory bodies such as ISO, GMP, HACCP, and IATF. Conducting root cause analysis (RCA) and implementing corrective and preventive actions (CAPA) for process and product non-conformances will be a key aspect of your role. Managing customer complaints, performing root cause analysis, and implementing quality improvement plans will also be part of your responsibilities. ...

As a QC & R&D Chemist (Biological) at Sikandrabad, Uttar Pradesh, your primary responsibilities will include conducting chemical, microbiological, and biological testing of raw materials, in-process samples, and finished products. You will be required to ensure adherence to quality standards, regulatory requirements, and specifications for biological formulations. Additionally, you will perform stability testing and prepare detailed reports on product shelf-life and efficacy. It will be essential for you to maintain documentation and lab records as per regulatory and internal compliance guidelines. You will also be responsible for calibrating and maintaining laboratory instruments and equipm...

As an Associate R&D (DQA) at our company located in Jhagadia, you will play a crucial role in the Research & Development department. You are required to have a qualification of M.Sc. in Chemistry or a related science field along with a minimum of 4 years of experience, preferably in the pharmaceutical industry. Your primary responsibilities will include reviewing Lab Validation Protocols/Reports (CRD) and Method Development/Validation documents (ADL), as well as reviewing specifications and STPs for raw materials, intermediates, and finished products. Additionally, you will be supporting DMF filings, stability studies, and regulatory documentation, preparing/reviewing SOPs, logbooks, and ens...

The VP of Supply Chain at Piramal Critical Care (PCC) plays a pivotal role in overseeing and developing the Global Supply Chain operations under the strategic direction of the Executive Committee (Excom) and the EVP of Global Operations. In this position, you will be responsible for managing External Supply Operations, end-to-end Global Planning, Logistics, Procurement, revenue forecasting, and Supply Chain Operations across the three regions where PCC operates. As the VP of Supply Chain, you will collaborate with key stakeholders both internally and externally. Internal stakeholders include Regional Supply Chain heads, Excom Vice Presidents, Sales General Managers, and Alliance Management H...

As the General Manager - R&D at Gujarat Fluorochemicals Limited, you will play a crucial role in leading a team to drive the research and development efforts of the organization. Your primary responsibilities will include conducting literature surveys, identifying innovative and cost-effective processes for fluoro-specialty molecules, developing new products, and ensuring the scalability of lab processes to commercial levels. You will be tasked with managing a team of scientists and chemists to facilitate new product and process development while enhancing existing products. A deep understanding of synthetic and analytical methods, along with proficiency in interpreting data from various ana...

As a Production Manager, your role is crucial in ensuring that food production processes run reliably and efficiently. You will be responsible for planning, coordinating, and controlling production processes to ensure the correct amount of food is produced at the right cost and quality level within the stipulated time. Your duties will include estimating budgets and timescales in coordination with the operations manager, monitoring product quality from raw materials to the final products, and ensuring that the production team strictly follows Standard Operating Procedures (SOPs). Additionally, you will oversee the packing and timely handover of prepared food to the distribution team. In this...

You are seeking an experienced and highly skilled Quality Control (QC) Manager to lead the QC team at Inducare Pharmaceutical & Research Foundation in Jejuri, Pune. As the Quality Control Manager, you will be responsible for overseeing all QC operations, ensuring compliance with regulatory standards, and driving continuous improvement in processes. The ideal candidate should have a minimum of 12 years of QC experience, with at least 5 years in a managerial role. Your key responsibilities will include leading and mentoring the QC team, managing team performance, and providing training and development opportunities. You will oversee all QC activities, including testing of raw materials, in-pro...

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. Key responsibilities: Timely validation of analytical methods of the drug products and API (intermediates and key starting material) for the drug products I drug substances to be filed globally. This role necessitates understanding of cGMP requirements and good technical knowledge to validate analytical methods and establish their suitability for the intended use Documentation of data as per laid down pro...

Ecosure, a division of Ecolab and a global leader in food safety and brand protection, is rapidly expanding. We are currently seeking a freelance Food Safety & Brand Standard Auditor in Bangladesh. This role involves conducting on-site evaluations and delivering tailored training to clients in the food service and hospitality industries. Our auditors help ensure compliance with food safety, cleanliness, and brand standards, supporting clients in delivering exceptional guest experiences. What you will do: Conduct food safety, brand standards and workplace health and safety audits at client locations Consult, coach and train clients on the latest food safety, health, and hygiene practices Work...

Division Department Sub Department 1 Job Purpose Perform sampling, execute and document the analysis of raw materials, packing materials, products assigned for testing and complete all the stability studies in order to ensure its compliance to the laid down quality parameters and predefined specifications / standards and meet SRB targets Key Accountabilities (1/6) Analyse the assigned samples and chromatographic tests for analysis by using the suitable valid procedure and calibrated instruments to ensure the compliance to the set specification / standards Perform analysis for release of RM, PM, FP & water analysis and process/cleaning validation as per commitment dates Perform analysis for s...

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...

Division Department Sub Department 1 Job Purpose Execute analysis of allocated samples and Produce reliable and reproducible results in order to ensure their compliance to the microbiological quality parameters and predefined specifications and standards. Key Accountabilities (1/6) Analyse and review samples based on work allocation to meet the service level agreement Analyse samples as per priority and work allocation Review the data as per respective specification, Microbiological Methods and results obtained Prepare, review and submit reports to Team leader within stipulated timelines in order to support individual sample release within stipulated timelines to achieve SLA Key Accountabili...

Division Department Sub Department 1 Job Purpose Monitor and execute the packing activities in a shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute shift packing activity by managing available resources and reduces micro stoppage of machine to achieve shift target Utilise shift resources optimally to get desired production output Regulate usage of consumables in the production process at optimum level to save cost Key Accountabilities (2/6) Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement Review and monitor critical in-process parameters like NFD, camera ...

Oversee and manage daily production activities Ensure adherence to cGMP and EHS guidelines Coordinate with cross-functional teams for smooth operations Optimize processes for efficiency and quality

USV, a top-15 pharmaceutical company in India, excels in the diabetes and cardio sectors. We have a presence in over 65 countries with our dynamic team of over 7,000 across generations. Our commitment to brand building is evident in our popular products like Glycomet GP, Ecosprin AV, Jalra, Tazloc, Glynase, MVI and more. Join USV and be part of our journey as we continue to innovate, transform lives, and shape the future of healthcare. Job Title: Manager / Sr. Manager (Quality Assurance) - API Only Designation - Manager / Sr. Manager - CQA - API Direct Reportees: No Location: HO @ Govandi, Mumbai Working Days: 5 days from Office + Alternate Saturdays - 1st, 3rd & 5th Working (sometimes 2-3 d...

Job Overview We are looking for a qualified and experienced Manufacturing Chemist having worked in cosmetics and OTC production background to oversee the manufacturing processes of cosmetics and OTC products in accordance with industry standards, regulatory requirements, and company protocols. The ideal candidate will ensure accurate batch preparation, maintain compliance with GMP standards, and support production efficiency. Key Responsibilities Take batches of cosmetic & OTC Supervise and manage the manufacturing of cosmetic and OTC topical formulations (creams, ointments, gels, etc.). Oversee end-to-end production management, including planning, scheduling, and resource optimization. Ensu...

Role & responsibilities Responsible for formulation and process development (QbD approach) of following categories of Pharmaceutical products: Oral Immediate-Release Dosage Forms. Oral Modified-Release Dosage Forms Including Pelletization technology and Wurster technology. Topical Semisolids (Creams, Ointment and Gels). Oral Liquid Dosage Forms Topical Liquid Dosage forms. Solid (Suppositories), Semisolid & Liquid dosage forms for Rectal and Vaginal applications. Design and execute formulation trials and evaluate stability data to finalize formulation composition. Execution of technology transfer batches for manufacturing processes from laboratory scale to production scale. Oral Immediate-Re...

Designs, implements and maintains quality assurance protocols and methods for processing materials into partially finished or finished products Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution Designs methods and procedures for inspecting, testing and evaluating the precision and accuracy of production processes, production equipment and finished products Performs analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary May assure compliance to i...

Anjan Drugs is looking for QC Chemist to join our dynamic team and embark on a rewarding career journey The QC Chemist is responsible for conducting chemical and physical testing on raw materials, intermediate products, and finished goods to ensure they meet quality and safety standards This role involves analyzing data, maintaining documentation, and contributing to quality control processes Key Responsibilities:Chemical Analysis: Conduct chemical and physical testing on raw materials, in-process samples, and finished products to assess their quality and compliance with specifications Instrument Operation: Operate and maintain laboratory equipment and instruments, such as HPLC, GC, UV-Vis s...

Quality Control Analysts needed with 4+ years of experience in HPLC/GC, troubleshooting, and software integration (mpower 3, LIMS). GMP, GLP, GDP, and DI knowledge required. Shift operations experience necessary. Pharma API experience Mandatory.