Oq Manufacturing Specialist - Parma - Gsk

    Gsk
    Gsk Parma

    23 ore fa

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    Descrizione

    **Job Title:** Operational Quality Oversight Sterile Specialist

    We are seeking a highly skilled and detail-oriented individual to support our Quality Management team in the day-to-day operations of a manufacturing environment.

    About the Role:

    This is an exciting opportunity for you to join our team as an Operational Quality Oversight Sterile Specialist. In this role, you will be responsible for supporting the implementation and maintenance of an effective and robust quality management system.

    You will perform day-to-day quality operations to ensure lean and efficient ways of working to meet compliance standards. Your responsibilities will include:

    • Performing quality oversight directly on the shop floor in the Manufacturing Sterile department and Inspection department to guarantee that all GMP standards are met during operations.
    • Executing and delivering quality objectives, quality improvement plan, and trends against the quality key performance indicators to drive continuous improvement.
    • Monitoring quality performance and key performance indicators to ensure quality and compliance issues are identified; providing immediate production support in case of issues to ensure their correct initial management in accordance with GMP requirements.
    • Performing activities to support the risk management process to ensure effective management, timely reporting, review, and escalation of quality risks.
    • Supporting the Sterile Production and Quality System to ensure inspection readiness.
    • Ensuring appropriate documentation of batch records.

    Why You?!

    We are looking for a talented individual who possesses the following skills and qualifications:

    • Bachelor's degree in a science-related field.
    • Experience within the Pharmaceutical/Consumer Healthcare industries.
    • Experience in quality assurance systems, particularly in areas of batch manufacturing and release, product incidents, and performing self-inspection.
    • Experience with regulatory requirements pertaining to good manufacturing practices and good documentation practices.
    • Experience working with effective quality documentation systems.
    • Good level of written and spoken English.
    • Availability to work shifts: 6-14/14-22.

    What We Offer:

    We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, shares and savings programme, flexible benefits, company healthcare plan, integrative pension fund, employee assistance programme, sustainable mobility programme, company canteen, and performance reward.

    GSK is a global biopharma company with a special purpose - to unite science, technology, and talent to get ahead of disease together. We prevent and treat disease with vaccines, specialty and general medicines. Our success absolutely depends on our people, and we want GSK to be a place where people feel inspired, encouraged, and challenged to be the best they can be. A place where they can be themselves, feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing.

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