Quality Compliance and Systems Officer

Who we are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. A Day In The Life Of A Quality Compliance And Systems Officer Are you interested in Quality Systems and want and develop your quality knowledge and skillset to become a Subject Matter Expert in a range of Quality System Processes? Our Quality Compliance Officers are responsible for providing guidance and support to the business ensuring designated Quality System processes are operated in compliance with Regulatory and Company standards. How you'll spend your day: • You will manage and maintain Quality System processes and associated documentation to ensure compliance with Regulatory Standards and Corporate expectations. This includes but is not limited to the following quality systems: • Complaint Management • Product Quality Reports • Document Control • Internal & External Audit • QMS performance i.e. KPI's, SQC, Annual Reports etc. • Issue and control CGMP documentation to support business activity. • Support continuous improvement of quality documentation and processes to ensure compliance with CGMP. • Deliver CGMP and Quality Systems training in line with Site requirements. • You will carry out internal and external audits in line with plan. To act as lead auditor, to identify, action and close out all non-compliance issues with adherence to schedule. • Maintain and update information on latest Regulatory standards for use by company personnel. Working Hours You will join the team on a Full Time, Permanent basis, working Monday to Friday 9am - 5pm. Your experience and qualifications Do You Have? • Relevant experience working in a Quality role within the Pharmaceutical Industry • Full understanding of cGMP, ideally Pharmaceutical GMP regulations (EU & USA) • A good knowledge of Quality System Processes (such as Change Control, Deviation, Document Control and CAPA etc.) Are you? • Degree level educated (although not essential) • A confident communicator and able to prioritise effectively and work to tight deadlines • IT Literate with good report writing and audit skills Enjoy a more rewarding choice • 25 paid holidays per year with the option to buy and sell up to 5 days annual leave each year • Private healthcare scheme through Bupa • A formal training and development programme specific to your role and department • Company pension - flexible employee and employer contributions • Competitive salary • Employee assistance programme • A number of health benefits including: Life Assurance, Critical Illness Insurance, Income protection • Plus many other flexible benefits via salary sacrifice: Cycle to work scheme, online and in store discounts and much more Reports To Quality Compliance and Systems Team Leader Deadline for internal applications will close on Tuesday, 26th November 2024. #TJ 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 is why we are 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. TPBN1_UKTJ