234 Gdp Jobs - Page 3

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...

Role & responsibilities: Ensure training management and compliance on the shop floor. Preparation of training materials including presentation for the effective training at shop floor. Coordination with the cross functional team for the execution of training as per the plan. Updating of employees, courses, modules and other amendments in the training system. Follow-up the reconciliation of training materials with cross functional teams on shop floor. To ensure 100% training execution of every employee working on the shopfloor. To ensure the training of new employees with respect to job description within the timelines to ensure smooth transition of employees in company roll shall ensure re-t...

As a Manager - Quality at Dishman Carbogen Amcis Limited, located in Bavla, Gujarat, your role will involve the following responsibilities: - Handling of Change control - Handling of Deviation and CAPA management system - Handling of Internal and external audits - Sound knowledge about Equipment and Utility qualification - Should have thorough understanding about regulatory guidelines, cGMP norms, GLP, GDP, Data integrity requirements etc. - Should have experience of regulatory audits The company, Dishman Carbogen Amcis Limited, operates in the General business unit and is committed to maintaining high quality standards in accordance with regulatory requirements.,

Role Overview: As a Production Supervisor in Pharmaceutical Manufacturing at Makshi, Madhya Pradesh, your role will involve supervising daily production operations to ensure compliance with Good Manufacturing Practices (GMP). You will be responsible for overseeing the production of tablets, capsules, liquids, or injectables, ensuring adherence to Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and Standard Operating Procedures (SOPs). Additionally, you will monitor equipment readiness, coordinate with Quality Assurance/Quality Control (QA/QC) for in-process checks, maintain shop floor hygiene and discipline, and train staff on GMP, Good Distribution Practices (GDP), and safet...

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...

Title: Manager - Quality Custom Field 2: 2490 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Handling of Change control, Handling of Deviation and CAPA management system, Handling of Internal and external audits, Sound knowledge about Equipment and Utilty qualifcation, Should have thorough understanding about regulatory guidelines, cGMP norms, GLP, GDP, Data integrity requirements etc. Should have experience of regulatory audits. Job Segment: Quality Manager, Law, CAPA, Manager, Quality, Legal, Management

Job Title: Manager Admin & Facility Location: Expeditor, Sholavaram / Polivakkam Department: Warehouse Operations Reporting To: Senior Manager – Logistics Type: Full Time – Onsite Job Purpose: To ensure seamless management of administrative, facility, infrastructure, statutory, compliance, and safety functions within the warehouse and office environment, supporting operational efficiency and regulatory readiness. Key Responsibilities: Documentation & Record Maintenance Maintain organization chart, yearly training calendar, training attendance & records. Update and preserve attendance sheets, manpower cost sheets, and petty cash details. Ensure proper handover of monthly provision details and...

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 ...

You will be responsible for supervising and managing day-to-day production activities during the shift. Your key responsibilities will include: - Ensuring adherence to cGMP, safety, and quality standards in all production processes. - Managing manpower and allocating tasks effectively to meet production targets. - Monitoring batch processing, documentation, and timely reporting. - Coordinating with Quality Assurance, Quality Control, and Maintenance teams for smooth operations. - Handling equipment operations, troubleshooting, and ensuring preventive maintenance schedules are followed. - Maintaining production records as per regulatory requirements and internal SOPs. - Ensuring compliance wi...

Key Skills :QMS, GMP, GDP, Audit & Compliance, SOP Management ,equipment qualification IQ/OQ/PQ,ICH, WHO, USFDA Qualifications: B.Pharm / M.Pharm / M.Sc. in Chemistry, Microbiology Experience : 7–10 pharmaceutical manufacturing setup. CTC : 6-9 LPA

Roles and Responsibilities To be handle all API pharma equipment w.r.t. manufacturing. Perform operation related activities. Ensure compliance with regulatory requirements. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records, reports, and documentation. Desired Candidate Profile having experience in API pharma industries. Strong understanding of Good Manufacturing Practices (GMP) regulations. Experience with Cleaning Validation & Equipment Qualification procedures.

SKILLS & RESPONSIBILITIES: Minimum 2- 4 years relevant experience and/or training related to systems engineering Knowledge of medical device technology, applicable quality and safety standards, and regulations (ISO 60601-x) Demonstrated ability to deal with a fast-paced environment, high levels of ambiguity, multiple concurrent projects, and conflicting assignments Demonstrated initiative, attention to detail, customer focus, and commitment to ongoing process improvement Experience with requirements specification and traceability Knowledge of product life-cycle management Experience with project management a plus Experience with documentation of design/development activities Understanding of...

You will be joining Biocon Biologics, a subsidiary of Biocon Ltd, a global biopharmaceuticals company focused on developing high quality and affordable biosimilars to provide cutting-edge therapies to patients worldwide. As a fully integrated pure play biosimilars organization, Biocon Biologics aims to improve patient lives through innovative and inclusive healthcare solutions. With a large portfolio of biosimilars in global clinical development and commercialized products in developed markets like EU, U.S., and Japan, Biocon Biologics is committed to transforming healthcare and impacting millions of lives. Your role at Biocon Biologics will involve the following key responsibilities: - Adhe...

Planning and execution of preventive maintenance of Process equipment- Vial filling, vial washing, Tunnel, isolators. Online entering check list for carrying a preventive maintenance as per SOPs. Attending breakdown maintenance in compliance with cGMP of process equipment's. Following the cGMP, GDP and safety while carrying out all activities. Maintaining good co-ordination with other department to sort out plant maintenance issues. Spares Management for all process equipment's. Operation and maintenance of HVAC system. Ensure maintaining of clean room parameters and trouble shooting. Operation of HVAC Requalification. To communicate relevant EHS issues to concerned person. Plan and preparat...

Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led global biopharmaceuticals company. Biocon Biologics is engaged in developing high quality, affordable biosimilars that can expand access to a cutting-edge class of therapies to patients globally. It is uniquely positioned as a fully integrated pure play biosimilars organization in the world and aspires to transform patient lives through innovative and inclusive healthcare solutions. The Company has a large portfolio of biosimilars under global clinical development with three of these commercialized in at least one of the developed markets of EU, U.S. and Japan. Biocon Biologics has a product pipeline of 28 molecules, including...

Immediate joiner who can join within a week time with having experience in CSV, QC area. Hands on Quality Control system- software as, Chromeleon, TIAMO, LAB Solution. Knowledge of 21 CFR Part 11, GAMP 5 GDP, GMP. Preparing documents GxPA, URS, VPP,

As a QMS Project Reviewer at Syngene International Limited in Bengaluru, you will play a vital role in drug substance development and manufacturing processes. Syngene is an innovation-led contract research, development, and manufacturing organization that offers integrated scientific services from early discovery to commercial supply. Safety is a top priority at Syngene, and you will be expected to adhere to safety guidelines, procedures, and SOPs to ensure a safe working environment for yourself, your team, and the lab/plant. **Key Responsibilities:** - Following GMP, GDP, and GLP procedures - Creating, revising, and reviewing procedures such as SOPs and protocols - Reviewing and approving ...

As a Manufacturing Supervisor, your role involves ensuring efficient line clearance activities, preventive maintenance of machines, cleaning and sanitizing visual inspection and packing areas, operating machines, and maintaining logs as per SOPs. You are also expected to uphold cGMP, GDP standards, and enforce discipline within the department to ensure uniform compliance among all employees. Key Responsibilities: - Perform line clearance activities before commencing operations - Follow the preventive maintenance schedule of machines - Clean and sanitize visual inspection and packing areas - Operate machines and maintain logs according to SOP - Ensure adherence to cGMP, GDP, and discipline st...

As a Manufacturing Specialist in our company, your responsibilities will include: - Performing line clearance activities before commencing operations to ensure a clean and sanitized visual inspection and Packing area - Following the preventive maintenance schedule of machines - Operating the machines efficiently and filling the log of general areas as per SOP and work execution - Adhering to cGMP, GDP, and maintaining discipline in the department - Ensuring that all employees comply with the same standards Your role will also involve: - Ensuring that all equipment and production lines are in validated and calibrated status - Preparing daily production reports based on achieved targets - Crea...

As a Commissioning and Qualification Engineer for Pharmaceutical equipment, your role will involve working with a range of equipment including RMG, CoMil, Tablet press, Coating Machine, blister packing machine, Vial Filling Line, PFS Line, Isolators, RABs, GL Reactors, Dryer, Nutsche Filters, Centrifuges, Lyophilizers, etc. You will be responsible for developing various protocols such as CQMP, VMP, FRA, cGMP review sheet, URS, SCA/SLIA, CLIA, DQR, SRA/QRA, SAT protocol, commissioning protocol, IQ protocol, OQ protocol, PQ protocol, process validation, and cleaning validation protocol. In addition, you will execute Commissioning, qualification, and validation activities for Pharma Process Equ...

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 ...

1. Product Planning 2. Inventory Control 3. Inventory Optimization 4. Raw Material & Packaging Material Management 5. Demand Forecasting & Planning 6. Regulatory Compliance

Exciting Career Opportunities at Natco Pharma Limited for the following requirements Work Location: Kothur (Formulation Division) Interview Date: Saturday, 20th September 2025 Time: 9:00 AM to 2:00 PM Venue: Natco House, Road No.-2, Banjara Hills, Hyderabad 500034 (Opp. A.P. Productivity Council) Open Positions: Analyst - Quality Control (OSD & Sterile) Experience: 3 to 5 Years Qualification: B. Pharmacy / M. Pharmacy / M.Sc (Organic/Analytical/General) Chemistry Key Responsibilities: Adherence to GLP, GDP, cGMP, and ALCOA+ standards. Analysis of RM / IP / FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus. Demonstration of QC testing...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Role & responsibilities Responsibility of Upstream activities in bulk manufacturing facility. To ensure that upstream batches are carried out as per manufacturing instructions following relevant Process Development description document, MFR, SOPs, BMRs, Protocols etc. and to ensure appropriate documentation in order to maintain cGMP compliance. ESSENTIAL JOB FUNCTIONS: (Details of key job functions) 1. Preparation of process documents (PCS, MFR, BMR), SOPs, protocols, related documents for upstream activity. 2. Hands on experience in operations of seed and production fermenters, continuous centrifuge, homogenizer and continuous involvement and support for commercial batches etc., 3. Involvin...