1019 Cgmp Jobs - Page 15

Job Title: Head Engineering & Maintenance Location: Vapi Number of positions : 1 Reporting To: Sr. VP Operations Department: Engineering & Maintenance Purpose of the Role To provide strategic leadership and operational excellence in managing plant engineering, utilities, and maintenance to support uninterrupted, compliant, and efficient API manufacturing operations. The role combines strategic engineering initiatives (capex, regulatory readiness, energy optimization) with maintenance operations (equipment reliability, preventive maintenance, troubleshooting), ensuring cGMP compliance and readiness for regulated markets. Accountability Tracks 1. Strategic Engineering Develop and execute engin...

Role Objective A key objective of this position is to serve as a strategic leader by providing scientific, technical, and managerial expertise in Quality Control (QC) and Analytical Development across diverse product portfolios. The position is responsible for establishing, validating, and implementing robust analytical testing methodologies in alignment with global regulatory requirements. In addition, the role emphasizes driving operational excellence, ensuring regulatory compliance, and fostering a culture of continuous improvement within the organization. Desired Candidate Profile Graduate/Postgraduate in Life Sciences, Pharmacy, Biotechnology, or a related field. Minimum 1822 years of r...

2–4 years of experience in tablet compression. Knowledge of tablet compression principles and machine operations. Attention to detail, reliability, and teamwork skills. Ability to work in shifts if required. Operate parle elizabeth machine

Role Overview: You will be responsible for developing and/or revising global procedural documents to support the business unit processes in the Quality Management System (QMS) process framework. Your activities will include working with subject-matter experts to ensure accurate document content and compliance with health authority regulations and expectations. Key Responsibilities: - Facilitate global procedural documents across areas of the QMS Framework and in association with electronic systems that support maintaining the QMS. - Conduct document authoring, coordinate review and comments resolution, approve, issue, implement, periodically review, and retire procedural documents. - Perform...

As a Lab Manager, your role involves overseeing and managing Mechanical, Electrical, and Chemical labs. Your key responsibilities include: - Direct oversight of incoming, in-process, and release testing in the labs. - Ensuring proper functioning of the labs by maintaining inventory levels of supplies, equipment maintenance and calibration, scheduling lab staff, and managing equipment AMCs. - Tracking assets and maintaining records as per Quality and Regulatory requirements. - Providing supervision and direction to employees, ensuring proper training on testing and methodologies. - Contributing to the development, updating, and review of Test Procedures, SOPs, and Protocols. - Performing trou...

Role Overview: As an Executive in the manufacturing department, your primary responsibility will be to supervise the manufacturing, processing, packaging, and holding of drug products according to approved procedures. You will also be in charge of maintaining the area and equipment in compliance with cGMP requirements. Additionally, you will be responsible for training subordinates on operational and cleaning procedures and coordinating IQ/OQ/PQ for new equipment/systems. Your role will involve following departmental SOPs for daily operations, handling material movement, and ensuring safety protocols are adhered to. Key Responsibilities: - Supervise manufacturing, processing, packaging, and ...

Work Your Magic with us! Ready to explore, break barriers, and discover more We know you've got big plans so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. The Manufacturing Site Quality Head plays a pivotal role in shaping the strategic direction of the organization by ensuring that all products meet the highest standards of quality and compliance....

Job Description JOB DESCRIPTION (Executive) Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. To perform online documentation with respect to departmental procedures as per good documentation. To impart training of operation and cleaning related SOP to all subordinates and operators. Co-ordination for IQ / OQ for any new equipments / system. To perform PQ for any new equipments / system. To follow all concern departmental SOPs for day to day operation a...

Position: Pharma Quality Control Officer - FDA Schedule M Documentation Qualification: Min. B. Pharma degree (mandatory) Location: Gurgaon, Haryana Experience: Min. 3 years Salary: Open/Negotiable - based on qualification, experience, and candidates expectation. Candidates are requested to mention their expected salary in the application / resume. Key Responsibilities: Ensure compliance with Schedule M requirements as per FDA and company SOPs. Prepare, review, and update QC/QA and other records, logbooks, and test reports. Maintain and review proper documentation in accordance with FDA Schedule M regulatory standards . Conduct sampling, testing, and analysis of raw materials, in-process mate...

You will be responsible for Vial washing, Depyrogenation tunnel, and filling with isolator activity for startup and routine operation. Ensure to adhere to cGMP and ALCOA in your daily tasks and follow organization policies and procedures. Your duties will include preparation and implementation of procedures related to qualification and maintenance activities for the Injectable facility. Review, implement, and maintain cGMP standards in all work areas. You will also be involved in preparing, reviewing, approving, and implementing Standard Operating Procedures and following guidelines. Your goal will be to meet the monthly productivity targets and ensure dispatches are made as per the schedule...

As a qualified candidate for the position, your role overview will involve being responsible for various tasks in the sterile manufacturing department. Some of your key responsibilities will include: - Updating on self-hygiene - Preparing, reviewing, revising, controlling, and implementing standard operating procedures - Reviewing master documents of production - Preparing and reviewing protocols and reports as required - Managing documentations such as BMRs, BPRs, and master SOPs - Handling change control, deviations, CAPA, investigations, etc. - Overseeing manufacturing, filling & sealing, labeling, and packing operations - Creating production planning on a monthly and daily basis - Genera...

We are looking for ambitious and detail-oriented Production professionals for our Oral Solid Dosage (OSD) and Injectable formulation plants located at Kathua & Jammu to execute day-to-day production activities as per cGMP and regulatory requirements. Required Candidate profile Experience in Pharma Production (OSD / Injectable). Strong knowledge of cGMP and regulatory guidelines. Good communication and documentation skills. Ability to handle shop-floor operations.

-Concept Engineering drawings (Process Flow Diagrams, Facility & Equipment Layouts/Sections/Elevations, Plot Plan) -Engineering drawings (Utility Generation & Distribution P&ID, Input info for detail eng.) -Revit modelling of Civil/Structure Drawings Required Candidate profile - Experience in development of Concept & Engineering for formulation facilities like Oral Solid/Liquid Dosages - Exp of 5-10 years (Pharma. consultancy / Design-Build-Contractor only) - cGMP norms

We required candidate for the position of AGM-Formulation Exp in OSD-Immediate Release (IR),Extended Release (ER),Powder for Suspension(PFOS) &Oral Liquid dosage forms for US,EU&Canada. T-Exp-15 + CTC-Upto 30.00Lacs Loc-Mumbai(Kandivali)

As a Senior Officer in Manufacturing at our company, you will play a crucial role in our Manufacturing team, focusing on executing complex production activities, providing technical guidance, ensuring compliance, and supporting the team lead in achieving production goals. Your strong foundation in pharmaceutical unit operations and problem-solving skills will be key in maintaining quality systems. **Key Responsibilities:** - Lead and execute manufacturing processes efficiently including Granulation, Compression, Coating, Filling, Lyophilization, Packaging. - Provide on-floor guidance, supervision, and training to officers & operators. - Review and verify GMP documentation such as BMR, Logboo...

Date: 28 Aug 2025 Location: Bangalore, KA, IN, 562158 Custom Field 1: Essential Functions Job Description Job Title: Assistant Manager Drug Substance QMS QA Job Location: Syngene Unit 3 Bangalore About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectati...

About Us We are a specialty chemicals manufacturing company with a full stack solution from R&D to manufacturing and doorstep delivery of innovative chemicals. Headquartered in Bengaluru, India we cater to pharmaceutical, agrochemical, personal care, and home care industries. Our B2B fulfillment platform supports businesses globally in developing and manufacturing chemicals from lab to commercial scale. With a team of in-house R&D experts and scientists, we offer custom synthesis and route scouting services to support manufacturers in product development. We are VC backed - here is a read. We are 400+ people strong and have offices in India, UAE and Indonesia. We are currently exporting to o...

To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to align with organization goal and other responsibilities assigned by reporting authority. Responsible to perform the calibration of instrument and to maintain instrument/equipment as per SOPs. Responsible to follow safety precaution as per laboratory procedure. Responsible for method development studies of Drug Substance, Drug Product & In process Materials related to Peptides. Responsible for method Validation studies of Drug Substance, Drug Product & In process Materials related to Peptides. Responsible for analysis of routine samples and stability studies of Drug Product & In process Material Dr...

Job Description: Technician Compression Job Purpose To operate and maintain tablet compression equipment in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality tablets. Key Responsibilities Set up and operate tablet compression machines and ancillary equipment (e.g., metal detectors, dedusters, friability testers, scales). Perform in-process checks such as tablet weight, thickness, hardness, and visual inspection as per Master Batch Records (MBR). Clean and sanitize equipment and manufacturing areas according to SOPs. Accurately complete equipment logs and batch documentation. Ensure proper execution of MBRs, SOPs, and validation protocols. Coordi...

Job Title Sr.Manager Warehouse Business Unit Sun Global Operations Job Grade G9B Location : Guwahati 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. Key Responsibilities Ensure compliance to regulatory requirements like cGMP,...

To maintain facility and equipment. To procure engineering consumables, proprietary spares and to maintain inventory of the same. To perform and to approve Qualification studies for equipment (Plant and Utility) and Facility. To schedule and to execute preventive maintenance program for plant equipment and utility equipment. To review and to participate in process validation program. To maintain and to update drawing like plant layout, equipment layout, P & ID for equipment (Plant and Utility), HVAC system etc. To schedule and to execute Annual Maintenance Program for Utility and material handling equipment. To arrange instruments for plant equipment and accessories. To review, authorize and...

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...

Job Summary Experienced Quality Assurance professional with a strong background in the Active Pharmaceutical Ingredient (API) industry. Responsible for implementing and maintaining GMP-compliant Quality Management Systems to ensure product quality, regulatory compliance, and operational excellence. Key responsibilities include managing documentation, handling audits (regulatory and customer), overseeing batch release, deviation investigations, and ensuring adherence to global regulatory standards (cGMP, ICH, FDA, etc.). The role demands expertise in validation, change control, and continuous quality improvement within a highly regulated API manufacturing environment. Quality Planning and Sch...

Company Name: Global calcium Pvt Ltd Location: Hosur Knowledge of ISO 9001, 14001, FSSC 22000, HACCP, Halal and cGMP standards requirement relevant to the function assigned and food & feed safety activities and ensure to comply the statutory and regulatory requirements Responsible for preparation & implementation of related SOPs and OCP (Operational Control Procedures) of the department. Reviewing PRPs (Pre-Request Program) & CCPs (Critical Control Points) as per relevant procedures under certification audits. Determination for right manpower strength for the assigned responsibilities and involving in the recruitment process for both new and replacement positions. Training the subordinates o...

Job Purpose To ensure the accuracy, completeness, and compliance of all Quality Control documentation and test results as per current Good Laboratory Practices (cGLP), regulatory guidelines, and internal SOPs before final release or submission. Key Responsibilities Review analytical raw data, calculations, and reports for accuracy, completeness, and compliance with approved specifications and methods. Ensure all laboratory documentation meets regulatory and internal quality standards (e.g., USFDA, EU-GMP, ICH, WHO, etc.). Review chromatographic data (HPLC, GC), wet chemistry reports, and other analytical test results. Verify results for routine analysis, stability studies, and validation rep...