234 Gdp Jobs - Page 2

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 Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / IPQA (OSD) / Documentation (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. / B.Sc. MICROBIOLOGY (Officer / ...

Role & responsibilities Perform daily monitoring of laboratory activities as per defined SOPs. Experience in handling GMP documentation and regulatory audits preferred. Carry out calibration of instruments such as the pH meter and weighing balance. Conduct Environmental Monitoring (EM) through microbial methods. Perform water sampling and microbiological analysis of purified and process water. Conduct sterility and bacterial endotoxin tests (BET) as per standard methods. Perform Liquid Particle Count (LPC) testing and maintain trend data. Maintain all laboratory documentation and records in compliance with GMP and regulatory requirements.

Roles & Responsibilities: Good Communication skills (Hindi, Gujarati and English) candidate who has experience or are from pharma/biotechnology/medical devices industry. Experience with SAP S4 HANA is must. Good understanding of dispatch activities, understanding of inventory management, domestic and export dispatches etc. Familiarity with GMP, GDP, and 5S practices. Ensure proper documentation and control of records related to incidents, deviations, change controls, and other QMS-related activities. Maintain and update records as per established SOPs and regulatory requirements. Oversee day-to-day warehouse activities, including material receipt, storage, issuance, and handling. Manage mate...

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 ...

The Pre-Sales Consultant will be responsible for designing, presenting, and proposing comprehensive cybersecurity solutions to clients. The role bridges the gap between sales and technical delivery teams, ensuring all proposals Writing requirement

Role & responsibilities 1. To ensure that all documents are updated according to audits & regulatory. 2. To calibrate the instruments as per the calibration schedule and maintain the records. 3. To develop SOPs and updating documents based on audits. 4. To ensure the QMS activities of instrument department. 5. To impart training to the shop- floor staff on handling & operation of the instruments. 6. Overall responsibility for calibration 7. Responsible for maintain concerned area as per Audit requirement. 8. Identify and perform calibration activities of all instruments as per schedule. 9. To highlight the non-safe working practices and conditions to the department in-charge so that these is...

You will be responsible for conducting WET, GC, and HPLC analysis as an Expert in the field. Your role will involve ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and ALCOA+ guidelines. Key Responsibilities: - Conduct WET, GC, and HPLC analysis - Ensure compliance with GMP, GLP, GDP, and ALCOA+ guidelines Qualification Required: - M.Sc. in Chemistry - 3 to 5 years of experience - Good knowledge of GMP, GLP, GDP, ALCOA+ - Expertise in WET, GC, HPLC Analysis,

Role Overview: As a Quality Control Inspector at our company, your role involves performing inspections, tests, and evaluations to identify defects or deviations from specifications. You will be responsible for collecting and analyzing data to identify trends and areas for improvement. Additionally, you will ensure that all required documentation complies with industry standards such as GMP, ISO, and GDP. Your contribution in helping implement and maintain quality control processes and procedures will be crucial. Collaborating with production and manufacturing teams to identify and resolve quality issues will also be part of your responsibilities. Furthermore, you will play a key role in ass...

Experience - 17 20 Years Qualification - B.E. / B. Tech Electronics / Instrumentation/Mechanical Responsibilities Manage and lead the engineering department at the site, ensuring smooth operations. Oversee operation and maintenance of HVAC systems and utilities. Develop, implement, and monitor monthly planners and maintenance schedules. Ensure readiness of the department for customer and regulatory audits; represent the department during audits. Implement corrective and preventive actions (CAPA) and monitor their effectiveness. Monitor and ensure compliance with process equipment and facility maintenance activities in line with cGMP requirements. Maintain and control all engineering document...

You will be responsible for providing operational support to business functions in managing contractors and external services, as well as representing an interface between the internal community and external partners. Acting as a single point of contact for all activities in accordance with legislation, internal regulations, good practices, and business objectives via NOCC Engineering project team. - Provide operational and administrative support to the organization in coordinating and managing external contractors, and activities between internal stakeholders and external partners. - Create purchase orders and order equipment in SAP/ESHOP. - Care for and maintain electronic databases (Share...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Medtronic is seeking a dynamic Associate Engineering Director to lead embedded and platform software development and sustaining engineering programs for its Surgical Robotics platform. This role requires building and managing a high-performing team of engineers, driving both new product development and existing system enhancements. You will oversee cross-functional engineering effortsespecially in software development, verification, an...

Job Title: ESO QA Specialist Location: Ankleshwar, Gujarat, India Seeking experienced QA professionals with 5+ years in GMP environments. Responsible for quality lifecycle management, audits, CAPAs, change control, and regulatory compliance.

Job Summary: Responsible for executing molecular biology and mammalian cell culture techniques to support cell line development activities including vector construction, transfection, clone selection, and assay development. Ensures compliance with GLP/GDP and timely documentation of all work. Key Responsibilities: Perform molecular biology tasks: gene cloning, cDNA synthesis, plasmid prep, buffer prep, and bacterial culture handling. Execute cell culture work: transfection, minipool generation, cell cloning, media optimization, and early product characterization. Support development and optimization of clone evaluation assays and molecular/protein biology techniques. Maintain lab records (LN...

Dear All, We are seeking a highly motivated and talented GLP Specialist to join our innovative team. The ideal candidate will have a strong foundation in formulation development as well in Analytical Development. Location: Hyderabad(Dulapally) Required Experience: 4-7 Years Key Responsibilities: Ensure error-free and real-time documentation as per departmental and regulatory requirements. Prepare and revise departmental SOPs, GTPs, AMCCs, and APMCs for Analytical Development (AD) and Formulation Development (FD) departments. Receive and maintain logbooks, SOPs, and other issued documents from QA in a controlled manner. Ensure laboratory compliance with GLP (Good Laboratory Practices) and GDP...

As an Officer / Executive in the Engineering Department at the Indore Plant, your responsibilities will include handling various functions such as Electrical, Instrumentation, Mechanical, HVAC, Utilities, Engineering Stores, Control Systems, Documentation, and Equipment Qualification/Validation in a regulated Pharmaceutical / API / Chemical industry. Key Responsibilities: - Maintenance and troubleshooting of electrical panels, drives, and control systems (PLC/SCADA). - Calibration and validation of instruments and sensors to ensure accuracy. - Ensuring power supply reliability and effective energy management. - Compliance with electrical safety standards and audit requirements. For Mechanica...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary This role will develop experimental approaches and will be responsible for ana...

Job Type : Long-Term Contract About The Role We are looking for an experienced CSV Lead with deep expertise in Computer System Validation, SAP S/4HANA upgrades, and strong Japanese language proficiency (JLTP N1). This is a remote, long-term contractual role ideal for a proactive professional who can manage validation activities and compliance processes independently while collaborating in a global, cross-functional environment. Key Responsibilities Lead and manage CSV (Computer System Validation) activities across the project lifecycle, including concept, implementation, operations, and retirement phases. Work closely with teams involved in SAP S/4HANA upgrade initiatives. Review and approve...

Responsibilities Talent Acquisition and Management. Onboarding and Offboarding. Employee Relations and Engagement. Performance Management. Training and Development. Compensation and Benefits Strategy and Administration. HR Policies and Compliance. HR Analytics and Reporting. Change Management and Organizational Effectiveness. Stakeholder Management and Leadership. HR SOP training should be provided to the new joiners. HR SOP refreshment training to be provided to all employees across the board. HR Documentation in alignment with the Quality Management System standards (GDP, CAPA, Change Management, Risk Assessment, Deviation, Maintaining Training Records of planned and unplanned sessions, et...

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 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...

As a candidate for this role, you will be responsible for various tasks related to self-hygiene and the sterile manufacturing department. Your key responsibilities will include: - Updating on self-hygiene - Preparation, review, revision, control, and implementation of standard operating procedures - Preparation and review of protocols and reports - Document management including BMRs, BPRs, Master SOPs, etc. - Handling of Change Control, Deviations, CAPA, Investigation - Generating general purchase indents for departmental items - Preparation of production planning on a monthly and daily basis - Preparation of daily production reports - Ensuring validation and calibration status of equipment ...

As a Production Operator at ACG Group Company in Dahanu, India, your primary responsibilities will include: - Checking the allocated post production (ATS/Printing/camera) line(s) in each shift as per the CTQ (critical to Quality) /CTP (Critical to Productivity) checklist. - Following the plan as per color change note by ensuring minimal change over time at each sub section. - Following instructions from the shift lead for timely change over by ensuring availability of roller(s)/ink etc. - Executing IPQC after every roller cleaning and checking of rejections of camera(s) after every hour to achieve zero defects. - Operating cameras as per SOP to achieve productivity and quality. - Coordinatin...

Regulatory Affairs Associate Responsible for preparation, review & submission of regulatory documents (US FDA, EMA, ICH), ensuring compliance with guidelines, supporting product approvals, maintaining records & coordinating with authorities. Required Candidate profile BSC/MSC/B.Pharm or Life Sciences graduate with knowledge of regulatory guidelines, dossier prep, submission processes, documentation, compliance, MS Office, attention to detail & communication skills.

Be a part of the winning culture! At Zentiva, we are a team of 4,800 unique talents bonded together by our common mission. We believe our diversity is a source of great energy and strength, and we create a work culture and ethics where everyone feels appreciated, can be their true selves, and contribute to the best of their ability. Seeking a balanced team across the company we welcome applications from all qualified candidates with various educational and industry experiences, cultural or ethical backgrounds, and different life experiences or abilities, regardless of their religious or philosophical beliefs or whomever they choose to love. What Would Be Your Main Responsibilities Operationa...

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...