1740 Change Control Jobs - Page 19

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 -...

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...

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research and Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research...

Understand the project requirements and deliverables from manager as specified by the client Understand the reaction protocol and search literature as required Efficiently delegate work and monitor team members for effective planning, execution and delivery Understand and discuss the MSDS (Material Safety Data Sheet) with team members Identify and mitigate any potential safety risk with the help of supervisor Plan and execute reactions with proper reagents and equipment (glassware, stirrers, vacuum pumps etc.) maintaining specified conditions (temperature, pressure etc.), with optimum usage and minimum wastage Ensure parallel execution of multiple reactions Monitor the reaction by observing ...

Engineering and Architecture of open source and commercial products Provide architectural leadership and support for existing and new technologies, assess business requirements, and create product roadmap, product standards and automation pipelines Expected to be running spinning off the effort from the ground and running it all the way through final implementation and operationalize the tool or product Provide technical support for business and client partners for product integrations Develop and document technical and non-technical infrastructure related processes

Key Responsibilities Understanding the specific needs of internal customers to the product portfolio of our Piston, Screw and Centrifugal compressors and its accessories Optimize the (re)use of engineering standardization concepts and actively steer the adoption of these concepts within Product Management team Optimize ways of working of mechanical engineers within Product Management team To mentor and guide Mechanical Engineers towards the best design possible and handling questions/problems during engineering process Responsible for the (check of the) quality of the design Minimise Cost to quality Checking execution of risk analysis Reviewing easy maintenance of the machine (serviceability...

Your Role Design and implement seamless integration solutions between Teamcenter and enterprise platforms Develop custom BMIDE (Business Modeling Integrated Development Environment) extensions Configure Solid Edge and Teamcenter integration Create data mapping and synchronization strategies Develop interfaces between PLM, ERP, and CRM systems Ensure data integrity and consistency across multiple platforms Troubleshoot and resolve complex integration challenges Create comprehensive technical documentation Your Profile XML/JSON data mapping BMIDE customization Web services and API integration SQL and database integration Enterprise system architecture Integration middleware technologies Siemen...

Title: Senior Executive/ Manager - Corporate Quality Compliance Business Unit: Global Quality and Compliance Job Grade: G10 Location: Vadodara 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.” ...

Perform daily, weekly, and monthly reconciliations of bank statements with internal accounting records. Investigate and resolve discrepancies in a timely and efficient manner. Record and monitor all cash transactions including bank fees, interest, and transfers. Collaborate with Accounts Payable and Accounts Receivable teams to ensure alignment of transactions. Maintain documentation and audit trails for all reconciliation activities. Prepare monthly reconciliation reports and assist with month-end and year-end closing processes. Liaise with banks to resolve any issues or discrepancies. Support internal and external audits by providing necessary reconciliation documentation. Identify opportu...

Associate - Clinical Quality Assurance (CQA) Department: QA - MakroCare and DDi Job Roles and Responsibilities: Perform maintenance, review, and approval of company Standard Operating Procedures (SOPs) in compliance with ISO standards and applicable international and national regulations. Prepare and review Quality Management System (QMS) documents, CQA procedures, and assist in reviewing department SOPs as needed. Manage SOPs in mLMS, create users, review training records, and escalate non-compliance issues to the Head of CQA or relevant department heads. Maintain the CQA document repository and archive validation protocols and documents in line with regulatory requirements. Conduct interna...

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...

As a Systems Engineer at Arcadis, you will play a crucial role in producing System Engineering plans and implementing Systems Engineering processes such as requirements management, Interface management, systems integration, assurance, verification and validation, engineering safety, EMC, and RAMS. You will be responsible for delivering Systems Engineering elements of Projects within set timelines, budgets, and quality standards. Your role will involve advising teams on adherence to processes, training designers on requirements and technical assurance techniques, providing Technical Assurance expertise, and assisting in system and software model development. Your responsibilities will also in...

As a member of the Process Engineering (Instrumentation) team at Knovea Pharmaceutical Pvt. Ltd. in Indore, MP, you will play a crucial role in the pharmaceutical manufacturing industry. Your responsibilities will include: - Reviewing equipment design qualification documents such as PI&D, FS, DQ, SDS, HDS, IQ, OQ, and drawings for approval if necessary. - Verifying process equipment instruments according to PI&D and electrical drawings for commissioning if needed. - Conducting FAT for process equipment as required and providing support for installation and commissioning activities. - Supporting qualification activities for equipment including IQ, OQ, and PQ. - Identifying all field instrumen...

Dishman Carbogen Amcis is looking for Senior Executive - API QC to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel an...