1120 Change Control Jobs - Page 44

Manage QA documents and records Handle deviations, changes, CAPA, complaints Conduct audits and supplier evaluations Monitor quality metrics and improvements Train staff and ensure ISO compliance

Candidates should have good hands on Experience on HPLC, GC, Stability, Wet Lab, RM Sampling & Analysis, Documentation, Standardization of Karl fisher Titrator. Responsible for Calibration of Instruments. Can handle QMS & AMV activities Required Candidate profile Preferred immediate Joiners. USFDA preferable. Interested candidate can share CV on sachin.kapte@enaltec.com Mob.8976826875

6-10 years of Duck creek Billing Business Analyst. Excellent P&C Commercial Insurance Lines of business knowledge and work experience, Min 6 years of Duck Creek Billing platform work experience and should have worked on end-to-end on both Direct and Agency billing implementation projects for US insurance company. Sound knowledge in billing system workflow and in different integrations (internal and 3rd party) Good experience needed in requirements gathering, conducting client workshops and collaborating with multiple stakeholders, Ability to understand client requirements, perform business analysis Develop, analyze and document requirements, including business, functional and non-functional ...

Role & responsibilities 1. To maintain the technical details of all manufacturing sites. 2. Review of received URS from site for new procurment/Equipment. 3. Global review of URS requirement,technology and software for harmonization 4. Review of proposal as & when required. 5. Co-ordination with plant & HO. 6. Knowledge of quality assurance & documentation.

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top manag...

Greetings from Zydus, We are looking for a Production QMS Head for our SEZ 1, Matoda plant . Key Responsibilities would be: Responsible for monitoring of all manufacturing related activity performed in GEN & ONCO OSD facilities subjected to QMS . To ensure effective implementation of organization vision, mission and goals at site to achieve the expectation. To provide leadership and direction to the QMS team. To participate in monthly Technical Review Meeting, ensure implementation of actions derived against this review and provide recommendations for continuous improvement. To support planning, scheduling and achieving production targets with optimum utilization of resources. Responsible fo...

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

Job summary The SOACC team member to monitor and respond to Access Control & CCTV system failure alarms in real-time. The team member to proactively track failures collaborate with Physical Security leads and tech ops across multiple regions and ensures timely resolution. Additionally the team member to manage badge administration which involves overseeing access badge requests in ServiceNow enabling/disabling physical access in Enterprise application generating monthly reports supporting audits and Responsibilities Access Control & CCTV System Monitoring: Continuously monitor ACS and CCTV system applications for device failures across globe in real-time provide timely response and proper tr...

Job Purpose: To ensure that all outbound finished goods includingcosmetics and pharmaceutical products meet regulatory, safety, and qualitystandards before dispatch. The QA Officer is responsible for final productverification, documentation review, and compliance. Key Responsibilities: Inspectand verify packaging integrity, label accuracy, and batch traceability offinished goods ready for dispatch. Ensureall packed units comply with quality specifications, including packagingappearance, batch numbers, MRP, expiry dates, etc. Perform line clearance and final product release checksprior to warehouse transfer or dispatch. Review and maintain QA checklists, dispatch logs, and batchrelease docume...

Job Receiving user indents, verifying with approved budget, and floating RFQ to the vendor (minimum 2 to 3 vendors). Preparing a worksheet to validate supplier quotes based on cost, quality, OEM, and delivery lead time Knowledge of SAP for PO release. Create PSR and follow the PSR approvals stage-wise. PO release. Monitoring material delivery against committed vendor dates. Coordinating with the maintenance team for installation and commissioning. Coordinating with the logistics team. Coordinating material in warding and acceptance, and vendor payment. Asset management and handling the Audits Generating and circulating reports to management. Relevant Experience: Mechanical and Electrical, Co...

Role & responsibilities Review of the executed manufacturing documentation at contractual partners and ensure its compliance with internal Quality Management System and applicable Regulatory Guidelines in cooperation with Quality Management at Krka. Reviewing the manufacturing documentation of pharmaceutical products and identifying potential errors or irregularities. Participates in investigation of deviations, complaints, unfavorable trends, and OOS results with contractual manufacturers. Participate in harmonization of applicable change controls. Takes part in organizing audits of our contractual partners in line with the audit plan and monitors its realization. Monitors the manufacturing...

Roles and Responsibilities: Work experience of Accounts Payable/Procure to Pay Knowledge on GST, IGST, CGST, TDS, VAT Invoice Processing/Invoice audit/vendor payments experience must SAP end user experience in FI Module for Financial accounting is must. Advanced Excel, PPT, MIS report and other analytical reporting knowledge & experience is an added advantage. Knowledge about different kind of payment methods and payment term. PO and non PO invoices handling

Looking for a proactive and detail-oriented Mechanical Design Engineer to support the development, modification, and lifecycle management of mechanical components and systems. The role involves working on design activities , managing concessions , handling Change Control Documents (CCD) , and using ZAMI for configuration and documentation control. Key Responsibilities: Create and modify mechanical designs in compliance with engineering standards and project requirements. Analyze and process concessions for non-conformities or deviations from standard designs. Prepare and manage CCD (Change Control Documents) to ensure traceability and compliance with engineering change processes. Use ZAMI fo...

This role is responsible for leading a project team in delivering a solution to the client using the appropriate business measurements and terms and conditions for the project according to the project charter, project agreement or contract. They have overall performance responsibility for managing scope, cost, schedule, and contractual deliverables, which includes applying techniques for planning, tracking, change control, and risk management. They are responsible for managing all project resources, including subcontractors, and for establishing an effective communication plan with the project team and the client. They provide day to day direction to the project team and regular project stat...

This role is responsible for leading a project team in delivering a solution to the client using the appropriate business measurements and terms and conditions for the project according to the project charter, project agreement or contract. They have overall performance responsibility for managing scope, cost, schedule, and contractual deliverables, which includes applying techniques for planning, tracking, change control, and risk management. They are responsible for managing all project resources, including subcontractors, and for establishing an effective communication plan with the project team and the client. They provide day to day direction to the project team and regular project stat...

As a Solution Tester, you will be responsible for: 1. Designing and automating test suites to ensure reliability of the system z(s390x) platform technology 2. Having a client-first mindset to test at scale and imitate customer-like environments 3. Creating strategies and scripts to test new features and functionalities 4. Contributing and reviewing code for internal and external repositories 5. Documenting processes (Test plans) and procedures for clarity and reproducibility 6. Interacting with counterparts in US/Germany teams and Red Hat Required education Bachelor's Degree Required technical and professional expertise Required Technical and Professional Expertise with relevant experience o...

Work in an agile, collaborative environment to understand requirements, design, code and test innovative applications, and support those applications for our valued customers Automate testing in both on premise and cloud environments Build and manage testing environments, assisting in debugging application issues Contribute to our continuous improvement and continuous delivery while increasing maturity of our agile adoption practices Perform exploratory testing, discover defects/bugs and works with coders to determine root cause and how to prevent similar issues from happening in the future Required education Bachelor's Degree Preferred education Master's Degree Required technical and profes...

This role is responsible for leading a project team in delivering a solution to the client using the appropriate business measurements and terms and conditions for the project according to the project charter, project agreement or contract. They have overall performance responsibility for managing scope, cost, schedule, and contractual deliverables, which includes applying techniques for planning, tracking, change control, and risk management. They are responsible for managing all project resources, including subcontractors, and for establishing an effective communication plan with the project team and the client. They provide day to day direction to the project team and regular project stat...

This role is responsible for leading a project team in delivering a solution to the client using the appropriate business measurements and terms and conditions for the project according to the project charter, project agreement or contract. They have overall performance responsibility for managing scope, cost, schedule, and contractual deliverables, which includes applying techniques for planning, tracking, change control, and risk management. They are responsible for managing all project resources, including subcontractors, and for establishing an effective communication plan with the project team and the client. They provide day to day direction to the project team and regular project stat...

Novo Nordisk Global Business Services (GBS) India Department GCM DP RoW Job Location Hyderabad Are you an expert in aseptic manufacturing with a strong quality mindset and a desire to make a tangible impact on global healthNovo Nordisk is seeking a dedicated Manufacturing Specialist to join our Global Contract Manufacturing Drug Product (GCM DP) team in Hyderabad, India. In this role, you''ll be crucial in ensuring the high-quality production of life-saving insulin and GLP-1 products through our Contract Manufacturing Organizations (CMOs). ! The Position As a Manufacturing Specialist (SME), you''ll be the go-to expert driving Technology Transfer projects for commercial products, ensuring top...

The Apex Group was established in Bermuda in 2003 and is now one of the worlds largest fund administration and middle office solutions providers. Our business is unique in its ability to reach globally, service locally and provide cross-jurisdictional services. With our clients at the heart of everything we do, our hard-working team has successfully delivered on an unprecedented growth and transformation journey, and we are now represented by over circa 13,000 employees across 112 offices worldwide.Your career with us should reflect your energy and passion. Thats why, at Apex Group, we will do more than simply empower you. We will work to supercharge your unique skills and experience. Take t...

Working on unit operations related to upstream processing during DS Manufacturing. GMP Documentation related to DS manufacturing. Preparation of documents like SOPs, MMDs and QMS related documents like change control, deviation, CAPA, Risk assessment. Preparation and maintenance of virus stocks. Coordination with cross-functional team. Involvement during regulatory audit preparation.

Major purpose of the job : • To ensure compliance of procedure and practices in line with GMP guidelines and regulatory expectations for concerned manufacturing facilities and products of Biotech division, Cadila Pharmaceuticals Ltd. • To coordinate and ensure execution of validation/qualification activities Principal Tasks and Responsibilities: Ensure timely release of Drug Substance (Bulks) manufactured in Biotech Division Managing, mentoring and tracking activities of team, Troubleshooting of key issues and reporting to HOD and management Managing External as well as Internal Audit and Audit compliance related activities Ensure Training index/training needs and completion of Team Ensure t...

Looking for a proactive and detail-oriented Mechanical Design Engineer to support the development, modification, and lifecycle management of mechanical components and systems. The role involves working on design activities , managing concessions , handling Change Control Documents (CCD) , and using ZAMI for configuration and documentation control. Key Responsibilities: Create and modify mechanical designs in compliance with engineering standards and project requirements. Analyze and process concessions for non-conformities or deviations from standard designs. Prepare and manage CCD (Change Control Documents) to ensure traceability and compliance with engineering change processes. Use ZAMI fo...

Looking for diligent person with good attention to detail for the role of quality manager. Responsible for monitoring &evaluating production processes, examining products to determine quality, engaging with customers & gathering product feedback