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        Specialist Quality Operations

        REQ-10015901
        9月 03, 2024
        India

        摘要

        Provide quality support in compliance with cGMP requirements and Novartis Quality Management System. Manage Quality aspects & projects within area of responsibility.

        About the Role

        Major accountabilities:

        Have expertise in Supplier Quality management and QMS activities. Drafting of QRA, QAA and AMR documents. Handling Supplier Qualifications and change notification.

        Interpret and compile APQR and/ or extracted data from Internal Novartis systems into a pre-defined template and draft conclusion of product quality review.

        Create and review GxP documents including SOPs, working procedures, trend reports, qualification

        reports and technical investigations, as and when needed.

        · Provide active support during internal and external audits by collecting and presenting the requested process/ data and reports

        · Adherence to the current GxP and compliance policies of Novartis Perform and deliver Quality

        Operations services in support of product quality compliance and regulatory workflows

        · Hold accounts in workflow applications (such as SAP, Dragon, SUBWAY, TEDI etc.) to ensure

        appropriate execution of service deliverables

        · Generate and analyze predefined and ad-hoc reports in various applications (such as AGILE PLM, AQWA etc.) and perform follow-up actions if required

        · Ensure compliance to the Novartis internal quality standards, relevant regulatory requirements, filed

        product quality standards and service level agreements

        · Support implementing service quality and process improvement projects, CAPA management within

        Quality Service Centers

        · Comply with all internal functional operating procedures like time tracking, KPI reporting, ticket

        management tools and other internal systems and processes

        Requirements for the role

        • Minimum 6 years of experience in Quality assurance activities in pharmaceutical company.
        • GxP knowledge, Basic IT knowledge
        • Good communication, presentation and interpersonal skills
        • Experience of working closely with the global stakeholders

        Skills:

        • Continuous Learning.
        • Dealing With Ambiguity.
        • Gmp Procedures.
        • Qa (Quality Assurance).
        • Quality Control (Qc) Testing.
        • Quality Standards.
        • Self Awareness.
        • Technological Expertise.
        • Technological Intelligence.

        Languages :

        • English.

        Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? http://www.novartis.com/about/strategy/people-and-culture

        Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: http://talentnetwork.novartis.com/network

        Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: http://www.novartis.com/careers/benefits-rewards

        A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
        REQ-10015901

        Specialist Quality Operations

        Apply to Job

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        2. http://talentnetwork.novartis.com/network
        3. http://www.novartis.com/careers/benefits-rewards
        4. http://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Hyderabad-Office/Specialist-Quality-Operations_REQ-10015901
        5. mailto:[email protected]
        6. http://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Hyderabad-Office/Specialist-Quality-Operations_REQ-10015901