1027 Cgmp Jobs - Page 17

As a member of the Analytical Development team at Apotex Inc., you will be responsible for planning and executing various analytical method development and validation activities for new products, ensuring compliance with regulatory and safety requirements. You will review laboratory data, instrument logbooks, and reports, and initiate departmental Corrective and Preventive Actions (CCR) to track progress through the Quality Management System (QMS). Your key responsibilities will include: - Preparing working plans and timelines for assigned projects - Developing stability indicative analytical methods for drug substances and finished products - Ensuring compliance with cGLP, documentation, an...

We have been retained by a fast upcoming and highly reputed Pharma company to hire a "General Manager - Operations" to be based at Baddi (Himachal Pradesh). Details of the position are mentioned below: Company: Our client operates a WHO - GMP approved liquid oral manufacturing facility at Baadi (Himachal Pradesh). The company is a third party manufactures for Most of Top 50 Pharma companies in India. Designation: General Manager Operations Reporting to: Director Experience: 10 - 20 years of similar experience with a reputed Pharma company. Main Task: General Manager (GM) shall have responsibilities as enumerated below: To manage the manufacturing element of the organization ensuring high qua...

Department: Production Location: Plant ( Bavla) Shift: Rotational Shifts (Day/Night/General) To ensure smooth execution of capsule filling operations within the Oral Solid Dosage (OSD) manufacturing section, ensuring compliance with cGMP standards, safety protocols, and production targets. Key Responsibilities: Operate, monitor, and manage capsule filling machines (e.g., Bosch, ACG Pam, Fette, etc.) within the OSD manufacturing unit. Supervise and guide operators and contract workforce during production shifts. Ensure accuracy and completeness of Batch Manufacturing Records (BMRs) and adherence to Standard Operating Procedures (SOPs) . Perform line clearance , conduct in-process quality chec...

As a Document Controller at Ferring India Laboratories, your role involves handling the issuance, control, and retrieval of documents. You will be responsible for scanning and uploading approved paper-based documents in Veeva Vault. Additionally, maintaining master copies for SOPs, including issuance, control, and retrieval of SOPs will be a key part of your responsibilities. Your key responsibilities will include: - Managing and conducting training sessions - Organizing training programs - Maintaining vendor audit and technical agreement planners - Preparing and reviewing SOPs, Protocols, and other cGMP documents - Tracking Change control, CAPA, Deviation, OOS/OOT, and coordinating with sta...

As the Head of Quality Assurance and Compliance at our Biopharmaceutical company, your role will be crucial in maintaining the highest standards of quality, compliance, and regulatory adherence. Reporting directly to the executive leadership team, you will play a critical role in upholding and enhancing our reputation for excellence in the industry. **Role Overview:** You will be responsible for establishing and maintaining robust Quality Systems to support cGMP activities, ensuring compliance with regulatory requirements and industry standards. Your role will involve managing the Quality Control and Quality Assurance departments, overseeing document control and training systems, and leading...

As the Head of Engineering & Maintenance at Piramal Pharma Solutions, you will play a crucial role in leading all engineering and maintenance operations for a large-scale API pharmaceutical plant located in Digwal. Your responsibilities will include ensuring optimal performance, reliability, and compliance of plant equipment, systems, and facilities. Your extensive experience in API manufacturing, expertise in CGMP, FDA regulations, and managing regulatory audits will be essential in this role. **Key Responsibilities:** - Lead, manage, and develop the Engineering & Maintenance team to drive plant operational excellence. - Develop and execute a comprehensive maintenance strategy, ensuring a p...

Role Overview: You will be responsible for handling upstream operations in the biotechnology field, specifically focusing on mammalian cell culture process and microbial fermentation. Your tasks will include handling equipment such as Bioreactors and CEDEX Bioanalyzer, as well as activities like handling mammalian cell lines, cell bank preparation, media scouting, and process optimization at different scales to improve yields and product quality. Additionally, you should possess good documentation skills including SOP and STP. Key Responsibilities: - Hands-on experience in upstream process development and process characterization of mammalian and microbial culture - Sound scientific knowledg...

Beckman Coulter Life Sciences mission is to empower those seeking answers to life's most important scientific and healthcare questions. With a legacy spanning 80+ years, we have long been a trusted partner to our customers, who are working to transform science and healthcare with the next groundbreaking discovery. As part of our team of more than 2,900 associates across 130 countries, you'll help drive our vision of accelerating answersand our commitment to excellence. Beckman Coulter Life Sciences is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Do you want to work in Manufa...

Job Role : Documentation Liquid 1.To maintain safe and clean work environment by following current good manufacturing practices (cGMP), and standard operating procedures, complying with legal regulations, monitoring environment. 2.To train the workmen for their specific job. 3.To prepare and revise functional SOPs, where ever required. 4.To perform Calibration of applicable instruments. 5.Resonsible for CCF, Deviation and CAPA (If Applicable). 6.To Prepare Qualification Document of Manufacturing equipment. 7.To maintain plant assets in good condition and making optimum use of 8.Any other activities assigned by Department Head Job Role : Liquid Manufacturing Supervision 1.To maintain safe and...

Dear Candidate, WE ARE HIRING Department: - Production- DS Designation: - Dy Manager / Manager Qualification: - Preferably Post Graduation in Science Experience: - 15+ Years Age: - Between 35- 40Years Mandatory: - Should come in all shifts, including Night shifts Role: Shift-in-charge for entire DS floor Job Description: > Strong Functional knowledge of DS Biologics (Chromatography and related purification experience protein/ Insulin handling experience preferable). Capable of handling large teams as we have around 45 members in each shift, around 50% of contractual staff. Strong administration / team management capabilities to streamline GMP across the floor. Monitoring the efficiency of em...

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! 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 ...

Position: Executive TSD (Technology Support / Technology Transfer) Department: TSD Location: Ahmedabad Reports to: TSD Manager / Head of Department Experience: 510 Years Education: B.E / M.E Chemical / Chemical Engineering Key Responsibilities: Execute technology transfer from R&D to pilot and commercial production. Support process scale-up and optimization for cost, yield, and safety. Prepare and review tech transfer protocols, BMR/BPR, SOPs, and risk assessments . Troubleshoot and resolve issues during pilot and commercial batch production . Ensure compliance with cGMP, GLP, QbD, and regulatory guidelines . Liaise with R&D, QA, AR&D, Production, and Regulatory Affairs teams. Support audits...

Job Role : Documentation Liquid 1.To maintain safe and clean work environment by following current good manufacturing practices (cGMP), and standard operating procedures, complying with legal regulations, monitoring environment. 2.To train the workmen for their specific job. 3.To prepare and revise functional SOPs, where ever required. 4.To perform Calibration of applicable instruments. 5.Resonsible for CCF, Deviation and CAPA (If Applicable). 6.To Prepare Qualification Document of Manufacturing equipment. 7.To maintain plant assets in good condition and making optimum use of 8.Any other activities assigned by Department Head Job Role : Liquid Packing Supervision 1.To maintain safe and clean...

Role Overview: As a Head Quality Assurance (QA) at Instrumentation & Control Solutions in Indore, you will be responsible for leading and managing Quality Assurance activities in the pharmaceutical unit. Your main focus will be ensuring compliance with cGMP, regulatory standards (such as WHO-GMP, USFDA, EU, etc.), and internal QMS protocols. Key Responsibilities: - Lead QA operations which include documentation, audits, and compliance. - Handle deviations, CAPA, OOS investigations, and regulatory audits effectively. - Oversee the development and implementation of SOPs, validations, and training programs. - Ensure the robust implementation of Quality Management Systems within the unit. Qualif...

As a Packing Operator Executive at our pharmaceutical manufacturing team, you will be responsible for operating Blister and Alu Alu Machines. Your key responsibilities will include: - Operating relevant machines with a minimum of 1 to 2 years of experience - Demonstrating a strong understanding of cGMP and quality control principles - Working efficiently in a fast-paced environment to meet production targets - Possessing excellent communication and teamwork skills To qualify for this role, you must have: - Education from ITI Mechanical Join our team and contribute to the success of our pharmaceutical manufacturing operations.,

JOB DESCRIPTION: Followings will be the Core Job Responsibilities of the position holder: 1. Responsible for Operation, cleaning, and primary maintenance of compression machine, metal detector, Lifting and positioning device, IPQC instrument. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & Responsible for complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP's and good documentation practices. 3. To Ensure equipment cleaning before line clearance as per standard operating procedure 4. To perform all in-process checks and monitoring all intermediate processes in compression stages. 5. ...

JOB DESCRIPTION: Followings will be the Core Job Responsibilities of the position holder: 1. Responsible for Operation, cleaning and primary maintenance of negative isolator, Vibro sifter, Bin blenders and all other GEA granulation line equipment. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP's and good documentation practices. 3. To perform all in-process checks and monitoring of all intermediate processes in granulation. 4. To select recipes and set process parameters in Blender HMI & ensure its correctness before blender revol...

JOB DESCRIPTION: Followings will be the Core Job Responsibilities of the position holder: 1. Responsible for Operation, cleaning and primary maintenance of negative isolator, Vibro sifter, Bin blenders and all other GEA granulation line equipment. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP's and good documentation practices. 3. To perform all in-process checks and monitoring of all intermediate processes in granulation. 4. To select recipes and set process parameters in Blender HMI & ensure its correctness before blender revol...

As a Quality Control professional at Medivisual Healthworld in the Pharmaceutical & Cosmetic Manufacturing industry, you will be responsible for: - Performing testing of raw materials, in-process, and finished products such as tablets, syrups, skin care products, etc. - Ensuring quality checks are conducted following laid Standard Operating Procedures (SOPs) and regulatory standards - Making independent quality decisions (accept/reject) based on control parameters - Maintaining and updating all test records, reports, and logbooks in compliance with regulatory norms - Ensuring compliance with legal, safety, and quality standards Key Skills Required: - Hands-on experience in HPLC / GLC - Profi...

Salary Between 15-20 Lacs QA-Validation Sterile Injectables (Candidate with B1/B2 USA Visa Preferred) Experience Required: 10-15 years Location: Remote Department: Quality Assurance No. of vacancy: 01 Key Responsibility: Validation Activities: Prepare, review, and approve validation protocols and reports for media fill studies, ensuring aseptic process integrity. Analyze remote media fill results, identify deficiencies, and recommend corrective or preventive actions. Prepare and review area qualification protocols and reports for classified manufacturing areas (Grade AD) based on environmental monitoring and qualification data from the site. Prepare and review periodic requalification protoc...

Responsible for management of QC/QA function of Chemical Manufacturing Plant including: Day to day operations of quality function from Raw Material testing till Finished Goods Dispatch Compliance of Quality Systems including IMS, GLP, CGMP, 5S, Kaizen Documentation and Audits (Internal & External) Customer Complaints and CAPA Team Management and its competency development Lead the continuous improvement projects for quality improvement Preferred candidate profile Ideal Candidate must be a Full Time M.Sc. in Chemistry/B.Tech -Chemical (Through out First Class) with 18 - 23 years of experience out of which minimum 5 years of leading QC/QA function in a large scale chemical manufacturing unit. ...

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a w...

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...

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Share your Resume to hrd@stedmanpharma.com