Facilitator QC

at  Teva Pharmaceuticals

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Facilitator QC
Date: Apr 23, 2024
Location:Waterford, Ireland, X91
Company: Teva Pharmaceuticals
Job Id: 55514

WHO WE ARE

We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us. We’re Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world and we currently have a fantastic opportunity for a Facilitator QC to join our team on a Full Time, Permanent basis in Waterford.

INTERNAL ELIGIBILITY FOR JOB POSTINGS

Teva designs eligibility to empower and enable employees to manage their careers internally and provides an easy and smooth process to view and apply. To be considered for an open internally posted position, an employee must:

• Be a current employee of Teva
• Meet the basic requirements for the job
• Have received a rating not lower than “Successful” on their most recent performance review and must not currently be on a performance improvement plan
• Apply to the posted requisition within the allotted time frame
• Have been in their current position for a minimum tenure of twelve (12) months

Unless explicitly stated in the job description, no company sponsored work authorisation no relocation assistance should be assumed.

TEVA’S EQUAL EMPLOYMENT OPPORTUNITY COMMITMENT

At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.
Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That’s why we’re constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice
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• To Facilitate and lead the QC team to achieve agreed customer service levels
• Deliver Customer Service level of >95% by testing components/raw materials/finished product/stability samples in an efficient and timely manner
• Provide coaching, feedback and ongoing support to team members to ensure they have the necessary skills to perform their duties to the required standards
• Review work schedule in advance to ensure all relevant components and equipment are available
• Prioritise daily work schedule to ensure effective analysis of product and adherence to Operational schedule and Stability program timelines as required
• Plan and organise calibration, maintenance and validation of instruments as required
• Select and assign people to specific projects and tasks
• Ensure that all QC documentation is completed correctly and right first time
• Investigate and authorise Out of Specification investigations with QC Analysts
• Issue and control of worksheets
• Perform a detailed review of all analytical data generated in QC on raw materials, and finished products as required to meet the production schedule