4097 Gmp Jobs - Page 41

An apprentice will support daily departmental activities and gain hands-on experience in a hotel. This role is designed to provide foundational knowledge of hospitality operations through structured training, job rotation, and on-the-job learning under supervision. Essential Job Tasks - Assist in the execution of day-to-day departmental tasks under guidance, such as guest check-in/check-out, room cleaning, food service, administrative support, or kitchen prep, depending on the assigned department. - Follow all Standard Operating Procedures (SOPs) related to service delivery, cleanliness, safety, and quality. - Maintain cleanliness and hygiene standards at the workstation and ensure proper ha...

An apprentice will support daily departmental activities and gain hands-on experience in a hotel. This role is designed to provide foundational knowledge of hospitality operations through structured training, job rotation, and on-the-job learning under supervision. Essential Job Tasks - Assist in the execution of day-to-day departmental tasks under guidance, such as guest check-in/check-out, room cleaning, food service, administrative support, or kitchen prep, depending on the assigned department. - Follow all Standard Operating Procedures (SOPs) related to service delivery, cleanliness, safety, and quality. - Maintain cleanliness and hygiene standards at the workstation and ensure proper ha...

Roles and Responsibilities Develop new APIs through organic synthesis, method development, and optimization. Conduct literature reviews to stay updated on latest research trends and technologies. Ensure compliance with GMP guidelines during API manufacturing processes. Collaborate with cross-functional teams for product development, scale-up, and commercialization. Perform impurity analysis using techniques like NMR, DSC, etc. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Ph.D/Doctorate in Chemical Sciences from a recognized university. Strong expertise in areas such as API synthesis, organic chemistry, method development/validation/transfer/methodology. 9-14 years of exp...

General Manager Works – Unit Head is overall responsible for Intermediate - API Plant - Technical Production And Upcoming Project if any Statutory Compliance at Chemical Plant And All departments working under him Exposure In Pharma Plant Is Must Required Candidate profile GM - Works - Unit Head will report to Managing Director Project And Commissioning experience Also desirable Liaison with All Government Authority like GPCB, GIDC, Local, State And Central Government

The Assembly Supervisor will oversee assembly operations in a pharmaceutical machine manufacturing environment, ensuring compliance with GMP (Good Manufacturing Practices) and optimizing workflow using the SAP system. The role requires leadership, operational oversight, and adherence to safety and regulatory standards to maintain quality and efficiency. Responsibilities / Tasks Key Roles and Responsibilities: Pharma Machine Manufacturing: Demonstrate strong knowledge of pharma machine assembly , ensuring compliance with industry standards and customer specifications. GMP Compliance: Ensure all assembly processes adhere to GMP guidelines , maintaining documentation and process accuracy for re...

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 with account management teams to resolve client challenges Perform a budgeted number of audits weekly that ensures high customer satisfaction Access and leverage industry leading food safety practi...

Roles and Responsibilities Lead and manage CAPA process from initiation to closure. Coordinate root cause investigations and ensure robust corrective actions. Track and report CAPA metrics and trends to management. Drive quality improvement projects and cross-functional collaboration. Ensure timely documentation and regulatory compliance. Facilitate audits and provide CAPA-related evidence. Support risk management and preventive action initiatives. Qualifications Bachelor’s degree in Engineering, Mechanical or related field. 7+ years’ experience in Quality/Regulatory in the medical device industry. Strong knowledge of ISO 13485, 21 CFR 820, EU MDR, and risk management (ISO 14971). Project ma...

Role & responsibilities Monitoring and continuously up keeping food safety and hygiene standards of the kitchen Giving training to the kitchen team on various SOPs, quality and food safety standards Prepping kitchen to comply to FSSAI standards and other internal audits Proactively checking the quality of raw ingredients/products through sensory and its documentation Handling customer complaints by doing RCA and sharing CAPA Analyzing data to understand regional performance on various metrics Ready to travel to different locations of the city Key Competencies Good communication skills Good understanding of the domain of food safety, RCA & CAPA , quality standards Well versed with FSSAI regul...

JOB DESCRIPTION 1, PURPOSE OF THE JOB: Job Context: To support the running of the factory by resolving breakdowns and by delivering maintenance. Also required to drive improvement across the site in terms of new machinery, hygiene, quality, and performance. Responsible for supervising and improving production at plants and factories. Support engineering teams, draw up safety protocols, report issues to the manager, and develop strategies to improve efficiency and profit. 2, DETAILS OF THE JOB: Job Role/ Title: Shift Engineer Level: M01-M02 Business Unit: Gorakhpur Function: Production Country: India Work Location: Gorakhpur Reporting Manager: Manager’s Manager: Matrix Manager: - Team Size: -...

B.Pharm / M.Pharm with 2 to 6 years of experience in Regulatory Affairs. To Review dossier prepared by executives & trainees & submit to client along with artworks for countries like ASIA, LATAM & ROW Market. Follow up with FRD & Microbiology Dept. Required Candidate profile Ensure that a company's products comply as per current ICH & Country Guidelines. To work on Renewals of Registration Certificate for countries. Courier of Legalized Documents such as COPP, FSC, POA. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Position Summary: Ensure that clients receive high-quality data by reviewing laboratory data for accuracy, clarity, and compliance with GMP and/or GLP regulations. Essential Duties and Responsibilities: Apply GMP/GLP standards in all areas of responsibility, as appropriate. Review laboratory documentation, generated data, calculated results, and final reports to ensure they meet departmental, corporate, and client SOPs. Gain a technical understanding of the analytical techniques relevant to the data being reviewed. Read and interpret analytical procedures accurately. Utilize MS Windows applications including Excel, Word, Access, and Outlook for documentation and communication. Demonstrate an...

As the Manager Plant Quality at Perfect Poultry Products, your role will involve overseeing and ensuring the implementation of food safety and quality management systems in the raw chicken processing plant. Your proactive leadership will be crucial in monitoring hygiene, product integrity, and process control from live bird intake to final dispatch. Key Responsibilities: - Develop, implement, and monitor quality systems and SOPs in line with FSSAI, HACCP, and ISO 22000 standards. - Supervise incoming raw material inspection (live birds), processing stages, chilling, packing, and storage. - Conduct regular hygiene audits and ensure sanitation standards in production areas. - Monitor Critical ...

As a Quality Intern at iD Fresh Food, you will play a crucial role in ensuring the quality and safety of our range of fresh and authentic ready-to-cook products. Your responsibilities will include: - Monitoring product conformance of Raw Materials (RM), Packaging Materials (PM), and Finished Goods (FG). - Monitoring cleaning of processing areas and other plant areas to maintain cleanliness. - Maintaining Good Manufacturing Practices (GMP) and 5S standards across the plant. - Implementing quality and food safety systems to uphold our high standards. - Monitoring and verifying Critical Control Points (CCP), Operational Prerequisite Programs (OPRP), and Prerequisite Programs (PRP). - Handling c...

Role Overview: Zapcom is a global Product Engineering and Technology Services company that specializes in providing bespoke, customer-centric solutions across various industries. As part of our team, you will have the opportunity to work on impactful projects that transform ideas into tangible outcomes using technologies like AI, ML, Cloud solutions, and full-stack development. We foster a culture of accountability, ownership, and equality, empowering you to excel and grow professionally. Join us now to be part of something extraordinary and shape the future with global opportunities and expansion plans. Key Responsibilities: - Achieve and exceed sales targets by developing a robust sales pi...

As a Lead with 10-14 years of experience in Bangalore, you will be required to have extensive knowledge of serialization at all levels (L1 thorough L4 and supply chain) and vision inspections on packaging lines. It would be preferred if you have Line provisioning knowledge. Additionally, having extensive knowledge of serialization standards, regulations, and GMP would be a plus. Your key responsibilities will include: - Hiring and Training: Recruit, onboard, and provide comprehensive training for support staff. - Performance Management: Set performance goals, monitor individual and team performance, and provide coaching and feedback. - Employee Development: Motivate and mentor team members t...

In pursuit of future expansion, we need Formulation & Development Officer/ Sr. Officer - 2-4 years in advanced probiotic/ nutraceutical / food supplement /phyto-pharmaceutical formulation development in solid orals (Tablet/Capsule/Granules/Powder) /Liquid Orals (Syrup/Suspension/Liquids) / semi-solid (Cream/ointment/ gel/paste). The candidate should preferably possess one or more of below requisites: 1.Knowledge of steps involves in Formulation and development. 2.Experience in development of Nutraceutical/ advanced probiotic/herbal formulations 3.Knowledge of GMP, GLP, D&C Act, ICH guidelines, FSSAI & AYUSH. 4.Ability to take lab trail and other lab related activity. 5.Ability to prepare the...

Role Purpose: To manage, implement, and continuously improve the Quality Systems of the plant in compliance with Coca-Cola Operating Requirements (KORE), regulatory guidelines, and international standards, ensuring that products consistently meet quality and food safety expectations while building a strong quality culture across the organization. Quality Systems Management Develop, implement, and maintain the plant's Quality Management System (QMS) in alignment with KORE, FSSC 22000, ISO, and FSSAI requirements. Ensure QFS pillar compliance, traceability systems, and effective execution of mock recall exercises. Ensure effective documentation control, record-keeping, and traceability systems...

Role & responsibilities: •Raise material requisition and receive the materials from stores. •Prepare BMR for new products to be processed on the lines. •Online BMR, BPR entries to be updated and all formats of relevant SOPs to be completed. •Preparation of SOPs for the vials and cartridge processing area and ensure training of it for the line operators. •To improve the yield of the lines and to reduce the rejections. •To prepare the samples as per the customer requirements and complete the entries in BMR and logbooks. •To complete the SAP entries for the line activities online. •To ensure that the completed batch pallets are transferred to ready to ETO area/ nonsterile FG area and line is re...

You will be responsible for performing and reporting the analysis of In-Process samples, finished products, Stability samples, and Cleaning Validation. Your key responsibilities will include: - Ensuring timely completion of analysis and data completion for the same. - Being responsible for all activities in the Quality Control Laboratory, including cGLP, documentation, and implementation of departmental quality systems. - Performing the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples, and Cleaning validation. - Preparing Stability Trend Reports for Laboratory samples. - Collecting and maintaining various laboratory samples. - Gen...

Role Overview: Joining as a part of the region's leading Life Science consultants and a company with a strong brand and extensive experience in the industry, you will contribute to improving human life and quality of life by developing production, quality, and project operations together with clients. Your development will be a key focus, with continuous dialogue with your immediate manager about your growth opportunities to shape a plan that suits your ambitions. Additionally, you will be part of a team of knowledgeable colleagues who enjoy working together and supporting each other in assignments and projects. The office's location in Uppsala Business Park provides proximity to engaging di...

Job Summary: The Quality Control Manager is responsible for ensuring that all products meet internal and external quality standards before reaching consumers. This includes developing, implementing, and managing quality control systems designed to ensure continuous production of FMCG products (consistent with established standards, customer specifications, and production goals). Key Responsibilities: Develop and implement quality control procedures and product specifications. Monitor performance of the QC team and manage day-to-day lab activities. Ensure compliance with regulatory and company standards (e.g., FSSAI, ISO, HACCP, GMP, BRC). Conduct root cause analysis and implement corrective ...

M.Sc, Phd/ Doctorate Keyskills Scientific & Technical Leadership. Regulatory and Quality compliance. Ensure cost effective process development. Ensure that laboratory work is carried out in a safe manner. Ensure that the R&D unit complies with relevant statutes. Key roles Lead development of synthetic routes and scale-up processes for APIs and intermediates. Guide polymorphism studies, impurity profiling, and characterization using advanced analytical techniques. Ensure cost effective robust process chemistry and technology transfer to manufacturing units. Manage multiple projects Mentor and develop team members, fostering a culture of scientific rigor and continuous improvement. Ensure adhe...

We are looking for a skilled HSE Officer to join our team in the international sector. The ideal candidate will have 3-7 years of experience in the field. Roles and Responsibility Develop and implement effective health, safety, and environmental management systems. Conduct regular audits and inspections to ensure compliance with regulatory requirements. Provide training and guidance on health, safety, and environmental procedures. Investigate incidents and accidents to identify root causes and implement preventive measures. Collaborate with other departments to develop and implement emergency response plans. Maintain accurate records of health, safety, and environmental performance metrics. ...

- 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

Coordinate to ensure minimum stoppage during shift Ensure manpower allocation as per planning. Regularly checking the Production Rate as per the quality standards Maintain all the register for process parameters Checking stage wise process samples Perks and benefits Medical, Canteen