1753 Change Control Jobs - Page 19

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 The Principal Software Engineer, Embedded Software will be a member of the Medtronic R&D software team working on product development and support of capital platform products. Principal Software Engineer is considered an expert in embedded software development including the understanding of how software interacts with hardware and FPGAs. The position is a hands-on development role with a dynamic set of responsibilities in a complex sof...

Job Title Sr Executive/Manager 2 Business Unit Sun Global Operations Job Grade G11B/G11A 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 Responsible for Receipt of Raw, Packing & Misce...

Job Title DGM Operations (Sterile) Business Unit Sun Global Operations Job Grade G8 - DGM Location : Halol Key Responsibilities 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 Approving sign authority for...

Description Position at Wind River Lead Software Quality Assurance Engineer BANGALORE |INDIA WIND RIVER In a world increasingly driven by software innovation, Wind River is pioneering the technologies to accelerate the digital transformation of our customers with a new generation of Mission Critical AI Systems in an AI-first world with the most exacting standards for safety, security, performance, and reliability. Wind River is a global leader in delivering software for mission-critical intelligent systems. For more than four decades, the company has been an innovator and pioneer, powering billions of systems that require the highest levels of security, safety, and reliability. Wind River he...

Role & responsibilities Manufacturing area:- Line clearance before start of batch processing and after cleaning. In-process checks during manufacturing stages Verification of machines settings, process parameters and yield reconciliatoin Sampling of in-process materials for testing. Monitoring of environmental conditions and compliance during production Verification of online entries in BMR Packing area: Line clearance before start of packing and after product/pack change over. Monitoring batch coding, overprinting, labeling, and packaging operations Performaning in-process checks - correct packing components, label reconciliation, and proper sealing. Monitoring controlled area discipline, g...

Here is how, through this exciting role, YOU will contribute to BMC's and your own success: You like to develop, design, and deliver solutions that deliver sustained business value from our and associated solutions You enjoy working cross-functionally across Sales, Marketing, Operations, and IT organizations for supporting the customer success organization Youre a team player and believe in building synergies across BMC to create/continually evolve one integrated customer journey You like to innovate, and have an appetite for solving business problems, to continuously improve our quality of service You have a passion for development, and challenge yourself to learn new things You know how to...

Job Description Maintenance of GLP in the Laboratory Upkeep of Housekeeping in the Laboratory. Ensuring activity logs are maintained for all critical instruments /equipment’s. Timely preparation of Laboratory Documents. Timely review of analytical data generated in laboratory. Ensuring Analytical Technology transfer from transferring lab as per approved protocol. Review and approval of incident , out of specification ,out of trend report and approval of QC related activities. Involved in QAMS activities such as change control, CAPA , incidents, deviation etc. Approval of stability summery report. Timely review of Quality control procedures and initiation for up gradation of same. Compliance ...

Job Description As a Manager at Lupin Limited, positioned within the Mechanical (Unit I) division at our Pithampur facility, you will take the helm of our engineering operations, spanning the Mechanical, Electrical, and Instrumentation domains. Your role will be pivotal in ensuring the seamless functioning and reliability of pharmaceutical process equipment used in both formulation and active pharmaceutical ingredient (API) production processes. You will be responsible for the strategic oversight and execution of both preventive and breakdown maintenance activities, ensuring minimal downtime and optimal equipment performance. This will involve coordinating comprehensive maintenance schedules...

Project management skills as an Water system & HVAC Engineer. Installation, Execution & maintaining, repairing heating ventilation, air conditioning, water air quality in buildings. HVAC, Water system – QMS Deviation and Change control work. Required Candidate profile SAP – PR and Service entry work in Project Management system.

Roles and Responsibilities 1. Responsible for implementation & monitoring of cGMP/GDP practices at site. 2. Responsible for periodic review of all quality Documents for appropriateness. 3. Preparation of SOPs and handling of QMS tools like deviation change control, CAPA. 4. Responsible for approval/rejection of deviations /change controls pertaining to corporate activities. 5. Oversee the team of technical personnel handling order processing artworks finalization BOM updating of products and follow ups. 6. Responsible for co-ordination and submission of Quality documents for regulatory submissions. 7. Responsible for maintenance, periodical update and review of technical agreements with dome...

Role Overview: You will be responsible for ensuring the establishment, implementation, and maintenance of processes needed for the Quality Management System at the company. Reporting on the quality system's performance to the Head-QA for review and improvement will be a key part of your role. Additionally, you will plan and execute clinical activities, conduct audits, review equipment maintenance, data analysis, and support regulatory inspections. Key Responsibilities: - Ensure establishment, implementation, and maintenance of processes for the Quality Management System. - Report on the performance of the quality system to the Head-QA and suggest improvements. - Plan and execute clinical act...

As an Associate Database Administrator at NTT DATA, you will be an entry-level subject matter expert responsible for assisting in daily database administration tasks. Your role will involve tasks such as database monitoring, backup and recovery, user management, and data maintenance. You will work closely with Change Control, Release Management, Asset and Configuration Management, and other teams to establish user needs and ensure database security. - Assist with the installation, configuration, and maintenance of database management systems (DBMS) like SQL Server, Oracle, MySQL, etc. - Collaborate with software developers/architects to design and optimize database schemas and data models. -...

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 ...

Quality assurance, Change management, Change control, APQR's, Media fill, Microbiology Compliance and Documents handling in software

Job Description Maintain self-hygiene and ensure compliance with cGMP, GDP and departmental discipline. Prepare and review the master documents, protocols and reports of production as per requirements. Manage the Exhibit batch documents such as BMRs, BPRs, etc. Handle change control, deviations, CAPA, investigation, etc. Train all the subordinates, technicians and operators of the department. Perform other activities as per HOD's requirement and guidance. Attend and ensure training as per training schedule and TNI. Review BMR, BPR and other Exhibit batch related documents. Skills Change control, deviations, CAPA, investigation, BMR, BPR, SOP. Qualifications Qualification - B. Pharm

Jubilant Foodworks Limited is looking for Quality Professional to join our dynamic team and embark on a rewarding career journey Develop and implement quality management systems. Monitor and analyze quality performance metrics. Collaborate with production and operations teams to ensure compliance. Provide training and support to quality staff. Maintain documentation and records of quality activities. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

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...

We have urgent Requirement for : Department : Quality Assurance Designation : Executive Skills Required : Process Validation, Equipment Qualification, QMS, APQR, Capa, Cleaning Validation. Experience Required : 03 to 08 years Salary : Depend upon Interview Location : Nalagarh interested candidate can contact @ 7717304694 or can send their Resume at hr2@theonpharma.com

Role Overview: As a Specialist IS Business Systems Analyst at Amgen, you will play a vital role in managing and driving the qualification, validation, and compliance activities for the company's SAP ERP systems and platforms. Your responsibilities will include ensuring enterprise-wide ERP solutions meet regulatory requirements, industry standards, and Amgen's IT-QMS policies. You will lead a team of validation and compliance professionals, define and improve validation strategies, and collaborate with cross-functional teams to embed validation and compliance into project lifecycles and daily operations. Additionally, you will champion adoption of digital validation, automation, and AI-driven...

You will be responsible for the following tasks as Officer - API at Dishman Carbogen Amcis Limited in Bavla, Gujarat, IN: - Handling Manufacturing Compliance activities such as IPQA Activity - Managing QMS Documents including CAPA, OOS, and Change control - Handling APQR processes - Managing Batch release activities - Demonstrating strong communication skills - Having exposure to Regulatory audits If you possess the necessary qualifications and experience for this role, you are encouraged to apply.,

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....

Role & responsibilities Responsible for quality management system of injectable as well as OSD facility. Should have knowledge about Quality Risk Management. Should have Knowledge about Audit and Compliance in Pharmaceutical Industry. Should have Basic Knowledge about Qc & injectable facility.

As a Quality eCompliance professional at Piramal Pharma Solutions, your role will involve ensuring regulatory compliance of Laboratory Information Management System (LIMS) at Global Piramal Pharma sites. Your key responsibilities will include: - Having a good understanding and knowledge of LIMS application functionalities and its integration with other systems. - Providing SME support for the implementation of LIMS across sites and supporting key decisions for system workflow changes from Quality and e-compliance perspective. - Supporting the validation of LIMS application and other enterprise systems to comply with regulatory guidelines. - Defining validation strategy and providing inputs t...

As a PLM Support - Teamcenter at our company, you will be responsible for providing support for ongoing and future Teamcenter functionalities. Your key responsibilities will include: - Hands-on experience in Teamcenter support - Good Knowledge of Teamcenter modules such as Structure manager, Bom Management, Workflow, Access management, Classification.etc. - Good functional experience in Teamcenter Install/Upgrade and Business configuration - Experience in CAD (NX, Catia and Creo) integration and support - Optimize system architectural elements like FMSFSC, Pool Manager server, Webserver, Client distribution - Monitor System regularly, ensure that Teamcenter service and automate the service -...