Hobson Prior are seeking for a Senior Quality Manager - Operations to join a brilliant pharmaceutical organisation on a permanent basis located in London. Our client is focused on manufacturing solutions that have the possibility of curing those who suffer from severe illnesses.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this role, you will be accountable for the quality operations and batch release teams.
• Guarantee that the KPIs are clearly outlined and handled.
• Serve as the main QA point of contact for operations.
• Uphold both capability and capacity of QA operations team to assure assistance to all operational areas, which involves deviation and CAPA management, GMP practices, etc.
• You will hose and serve as an SME for both regulatory and partner inspections.
• The ideal candidate will guarantee efficient communication with senior organisation and quality management for business-critical concerns.
• Accountable for guaranteeing that any GMP documentation such as Issues, CAPAs, Change Controls, BMRs & Audit/inspections actions, within own area of responsibility is closed in a RFT state and timely manner.
• As the Senior Quality Manager, you will be deputised for the quality director when necessary.
• Any other assigned duties.

Requirements:

• Expertise and comprehension of pharmaceutical quality assurance.
• Familiarity with GMP in an operations setting.
• Able to make sound decisions.
• Know-how of preparing for, hosting and following up on regulatory inspections.
• Knowledge and exhibited ability to execute quality management systems in compliance with suitable cGxP guidelines and regulations.
• Practical knowledge and acquaintance with enabling quality culture and forming a "quality mindset" for team members with limited work experience or have not worked within a GxP setting.
• At least 10 years of quality assurance experience.
• Know-how of GMP operations and quality systems for a sterile manufacturing facility implementing and with comprehension of the principles of sterile manufacturing.
• Expertise on the principles and regulations for GMP as set out in the Orange Guide, Eudralex Volume 4, U.S 21CFR part 210/211 and any other pertinent guidelines.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.