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Quality Oversight & Compliance Manager

CK Group

Stone Cross

Hybrid

GBP 60,000 - 80,000

Full time

2 days ago
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Job summary

An established industry player seeks a Quality Oversight and Compliance Manager to enhance regulatory processes in the pharmaceutical sector. This role involves driving improvements, managing compliance initiatives, and collaborating with global teams to ensure quality and compliance in drug development. The ideal candidate will possess strong knowledge of regulatory affairs, project management skills, and the ability to influence stakeholders effectively. Join a leading biopharmaceutical firm where your expertise will contribute to the development of life-changing medicines and healthcare solutions, making a significant impact on patients' lives worldwide.

Qualifications

  • Experience in leading investigations and managing CAPA plans.
  • Strong knowledge of the drug development process and Regulatory Affairs.

Responsibilities

  • Drive improvements to existing processes and support regulatory initiatives.
  • Identify compliance gaps and implement remediation plans.

Skills

Investigation Leadership
CAPA Management
Regulatory Affairs Knowledge
Project Management Skills
Data Analysis
Stakeholder Management

Education

Degree in Life Sciences or related field

Tools

Regulatory Compliance Systems
Electronic Technologies for Regulatory Processes

Job description

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


Salary:

PAYE £23.39 - £28.59 per hour or UMB £26.21 - £32 per hour (inside IR35).


Quality Oversight & Compliance Manager role:

  1. Responsible for driving improvements to existing processes.
  2. Supports implementation and monitoring of initiatives related to pan-regulatory (e.g. Manufacturing, Regulatory Strategy, CMC, Submissions, Translation) information and processes globally through data reporting/metrics analysis.
  3. Works with global delivery teams to improve the quality and compliance associated with regulatory processes and product/license information.
  4. Identifies procedural/compliance gaps and establishes and monitors remediation plans to close identified gaps.
  5. Supports and drives implementation of initiatives targeting improvements in inspection readiness, audit preparedness and training compliance.

Your Background:

  1. Experience in leading investigations and managing CAPA plans.
  2. Strong knowledge of the drug development process, Regulatory Affairs, Regulatory Strategy and Submissions Management.
  3. Proven fluency with use of soft skills and ability to adapt core project management skills successfully within a dynamic line environment.
  4. Understanding of systems and electronic technologies used to support regulatory and submission process and planning activities and experience in process development and new technology implementation.
  5. Translates data into information to support the business in taking action and decision making.
  6. Management of change in partnership with key stakeholders.
  7. Ability to lead and operate seamlessly to influence colleagues across the organization and ensure delivery to time and quality driving highly complex projects to meet evolving business needs.
  8. Proven aptitude in project management.

Company:

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.


Location:

This role can be based at our clients sites in Sandwich, Kent or Tadworth, Surrey or worked remotely.


Apply:

For more information, or to apply for this Quality Oversight & Compliance Manager role please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@ckagroup.co.uk. Please quote reference 131 553.


It is essential that applicants hold entitlement to work in the UK.


Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

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