Quality Compliance Officer
Runcorn, United Kingdom, WA7 3FA
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. We are Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.
At Teva Runcorn, we develop, manufacture and market innovative and affordable medicines, specialising in sterile liquid products mainly used for treating respiratory conditions using Blow-Fill-Seal technology as well as injectable Combination Products.
Our values live within the work we do, these are: Leading The Way, Focus & Accountability, Getting It Done Together, Innovating Where We Can Create Value, Caring and Making Our Families Proud.
The opportunity
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.
You will join the team on a Full Time, Permanent basis, working Monday to Friday 9am - 5pm.
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:
- Vendor Assurance
- Complaint Management
- Product Quality Reports
- Document Control
- Internal & External Audit
- QMS performance i.e. KPI’s, SQC, Annual Reports etc.
- You will issue and control CGMP documentation to support business activity.
- You will support continuous improvement of quality documentation and processes to ensure compliance with CGMP.
- You will 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.
- You will maintain and update information on latest Regulatory standards for use by company personnel.
Your experience and qualifications
Do You Have?
- Relevant experience working in a Quality role within the Pharmaceutical Industry or other regulated 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
- 24 days holiday per year + bank holidays
- Company pension – flexible employee 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
Make a difference with Teva Pharmaceuticals
Apply online today!
Reports To
Associate Director - Quality Compliance
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