Cpl Life Sciences

Quality Manager (GCP)

Central London / West End
30 Apr 2021
30 May 2021
Ed Taylor
Quality, QA / QC
Full Time
Contract Type
Experience Level

Quality Manager (GCP)
Location: London
Salary: Competitive

The Manager, Clinical Quality, is responsible for the designing, establishing, maintaining and executing a robust GCP and GVP compliance program, including conduct and oversight of audits, to ensure consistent adherence to relevant regulations, guidelines, company policies, strategies, procedures as well as contracts/agreements.

This position will establish and maintain strong relationships with internal and external stakeholders to ensure that quality standards are adhered to at all time and collaborate with global GCP and GVP QA members to ensure the initiation/completion of global initiatives.

In addition, this position will serve as the GCP subject matter expert on various clinical
development projects by providing high standard of quality guidance, advice and support on GCP regulatory compliance matters, and participate in and support health agency inspections as required.

Responsible for designing, setting up, maintaining and executing robust GCP and GVP compliance programs for both Local and Global GCP and GVP Audit Programs including proper management of audit schedules and execution of audits, ensuring compliance with regulatory standards, company policies, and procedures.
Ensure the timeliness and completeness of reports and assessment of appropriate
Serve as a subject matter expert by providing high standard of quality guidance, advice and support on GCP compliance
Contribute to the development of local quality management systems, including contributing/writing policies/procedures.
Partner with Quality Systems group to develop and enhance the GxP Quality
Management System, looking for cross-GxP efficiencies and synergies.
Manage and identify potential systemic compliance risks including Investigations of
deviations and monitoring of corrective actions and preventative (CAPA)relating to
non- compliance issues and findings
Manage and perform/handle GCP investigations regarding Quality Issues, Misconduct
Investigations including Serious Breaches etc.
Establish and maintain GCP and GVP regulatory inspection readiness; Participate in
preparation and execution of health agency inspection activities.
Support the development and delivery of GCP training programs.
Lead development of process improvement strategies and tools related to GCP and
GVP compliance efforts.
Assist with Clinical activities (e.g. deviations, CAPAs) when requested.
Ensure key performance indicators for GCP and GVP are set-up, maintained, performed
and reported to detect and monitor any significant compliance deviations to the
company quality standards and/or regulatory requirements
Maintain expert knowledge of regulations, company procedures, auditing, and quality
Facilitate the sharing of best practices and help to drive continuous improvement and
Continuously build and innovate in all aspects of GCP and GVP Compliance
Perform other quality or compliance related duties as needed.

Bachelors degree in a scientific field required or relevant experience.
Good understanding of GCP, knowledge of PMDA/EMA/FDA, ICH and applicable regulations
Knowledgeable of basic statistics
Proficient in Microsoft Office Applications (Excel, PowerPoint and Word)
Ability to travel at least 10% of the time (International travel is required)

Extensive knowledge and practical hands-on experience in GCP and applicable legislation
Comprehensive understanding of pharmaceutical regulatory requirements and impact
on the various functions within the business
Familiarity with database and GLP audit practices
Ability to identify proactively and anticipate risk of non-compliance in a complex
Ability to develop and manage efficient and effective compliance systems
Excellent planning and organizational skills
Ability to project manage, set clear strategic goals, align priorities and lead multiple
tasks/activities within a virtual/remote team to successful business conclusion
Strong decision-making skills and ability to use independent judgment to quickly set
priorities, solve problems and resolve conflict
Excellent oral and written communication skills and ability to adjust communication to
different target groups
Good working knowledge and comprehension of written English and/or Japanese
Exceptional attention to detail
Inter-cultural awareness, proven ability to work in an international environment and
cross functional team
Ability to work independently with minimal supervision.
Ability to effectively multi-task, be proactive and self-motivate
Ability to work to tight deadlines, with incomplete information, handle unexpected
events and work under the pressure
Good analytical and judgment capabilities to understand/analyze/synthesis and
Proven ability to influence senior leaders within the organization on matters of importance
Customer-focused, good interpersonal skills, assertiveness, team spirit and coaching skills.
Able to delegate but committed to providing proactive support to the business and
teams to achieve successful outcomes.
A team player able to work with and through others; someone people proactively seek out for help, guidance and advice

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