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UK Group Quality Director Pharmaceutical, Qualified Person/QP

Vacancy Title: UK Group Quality Director Pharmaceutical, Qualified Person/QP
Contract Type: Permanent
Location: Cheshire
Industry:
Salary: Competitive
Start Date: 2024-04-23
REF: J91978564
Contact Name: Tom Hammond
Contact Email: tom.hammond@russell-taylor.co.uk
Vacancy Published: 30 days ago

Vacancy Description

UK Group Quality Director Pharmaceutical, Qualified Person/QP

Type: Permanent
Location: Onsite, 5 days a week - Cheshire based
Our client, a multi sited pharmaceutical company is looking for an experienced QP /QM/QD to work onsite at their Cheshire site - reporting directly to the MD, the QD will manage the quality function/s / teams for multiple sites within the group. The QD will be responsible for 5 direct & 40+ indirect reports.

The role:

• Manage the Quality Function across business entities ensuring Compliance status is maintained in support of business strategy
• Provide assistance to all functions within the business on technical and regulatory matters to ensure changing regulatory landscapes are accommodated in support of business objectives
• To lead, motivate and develop the quality teams in support of business plans and profitability goals
• Performing duties as required by a Pharmaceutical Qualified Person under pertinent regulations
• Ensure delivery of quality oversight in in-house and external third-party manufacturing operations
• Provide guidance to Sales and Marketing teams engaged in UK and Export territories as appropriate
• Liaise with and undertake the role of principle point of contact for UK MHRA and UK Home Office Departments in support of business strategy
• To promote and adhere to Health, Safety and Environmental regulations to ensure the wellbeing of the company's employees, contractors and visitors in compliance with legislative requirements.
• To act as a pharmaceutical qualified person to certify products as suitable for release to market

The Person:
• QP qualification essential
• Significant experience working as in a senior quality role within solid dose and none - sterile liquid pharmaceutical settings working and implementing QMS strategies.
• Significant experience working with cGxP regulations
• Previous management/ supervisory experience in a quality setting



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