Quality Oversight & Compliance Manager

TN United Kingdom; Stone Cross; Hybrid; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Quality Oversight and Compliance Manager to join their team on a contract basis. This role offers the opportunity to drive process improvements and enhance compliance in a dynamic environment. You will collaborate with global teams to ensure quality delivery of regulatory processes while leading initiatives for inspection readiness and audit preparedness. If you are passionate about improving lives through quality management in the biopharmaceutical sector, this is the role for you. Enjoy the flexibility of remote work while making a significant impact in the industry.

Qualifications

• Strong knowledge of drug development and regulatory submissions.
• Experience in quality oversight and compliance management.

Responsibilities

• Drive improvements to existing processes and enhance compliance.
• Lead investigations and manage CAPA plans effectively.

Skills

Process Improvement

Data Reporting

Regulatory Affairs

Project Management

CAPA Management

Soft Skills

Education

Bachelor's Degree in Life Sciences

Relevant Certifications in Quality Management

Tools

Electronic Submission Systems

Job description

Quality Oversight & Compliance Manager

CK Group is recruiting for a Quality Oversight and Compliance Manager to join a pharmaceutical company on a contract basis for 6 months initially.

Role Responsibilities:

• Drive improvements to existing processes
• Support implementation and monitoring of initiatives related to pan-regulatory information and processes globally through data reporting and metrics analysis
• Collaborate with global delivery teams to enhance quality and compliance of regulatory processes and product/license information
• Identify procedural and compliance gaps; establish and monitor remediation plans
• Support initiatives to improve inspection readiness, audit preparedness, and training compliance
• Lead investigations and manage CAPA plans
• Maintain strong knowledge of drug development, Regulatory Affairs, and submissions management
• Utilize soft skills and adapt project management skills within a dynamic environment
• Understand systems and electronic technologies supporting regulatory and submission processes
• Translate data into actionable information for decision making
• Manage change in partnership with stakeholders
• Lead and influence across the organization to ensure timely and quality delivery of complex projects
• Demonstrate project management aptitude

Company Information:

Our client is a leading biopharmaceutical company providing medicines, vaccines, and healthcare products globally, improving lives worldwide.

Location:

This role can be based at client sites in Sandwich, Kent, or Tadworth, Surrey, or can be performed remotely.