Director, Quality

JR United Kingdom; Sheffield; Remote; GBP 60,000 - 90,000; Full time

Job summary

A prominent company in the clinical research sector is seeking a Director of Quality based in Sheffield, with an opportunity for remote work. This leadership role entails managing compliance, directing quality initiatives, and ensuring regulatory adherence across clinical projects. Ideal candidates will have substantial experience in Quality Assurance and a proven record in clinical research environments.

Qualifications

• 10 years of experience in clinical research with emphasis in Quality Assurance/Compliance.
• Working knowledge of GCP/ICH guidelines and FDA regulations.
• Availability to travel up to 30% domestically and internationally.

Responsibilities

• Manage audits and ensure compliance with regulations.
• Support Quality & Compliance team members.
• Lead initiatives to enhance quality throughout clinical development.

Skills

Leadership

Problem Solving

Communication

Project Management

Attention to Detail

Education

Bachelor’s degree in a science, healthcare or related field

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

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Director, Quality, sheffield, south yorkshire

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Client:

Location:

sheffield, south yorkshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

4

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

Precision for Medicine is hiring Director, Quality based in Europe. The position can be covered fully remotely from one of our European locations: UK, Spain, Poland, Slovakia, Hungary, Serbia or Romania.

Position Summary:

The Director, Quality manages the audit program and supports clinical projects to ensure compliance with regulations and Precision procedures.

Essential functions of the job include but are not limited to:

• Manage Quality and Compliance functional activities, including implementation of the QMS, inclusive of SOPs, Training and CAPAs
• Work closely with the Quality and Compliance staff and Operations to provide strategic compliance development advice and guidance for optimal conduct of clinical trials and performs ICH/GCP quality reviews/audits to ensure overall compliance with applicable regulations.
• Initiate the process of follow-up when suspicion of suspected scientific misconduct/serious non- compliance
• Support and mentor Quality & Compliance team members
• Audit regulatory documents for submission to the Food and Drug Administration (FDA) and global regulatory authorities (e.g. MHRA)
• Provide ICH/GCP guidance, auditing advice and training to internal and external clients
• As part of the Management Team help counsel on and direct quality initiatives to Provide ICH/GCP compliance guidance throughout the clinical development life cycle enhance/ensure quality is assessed and maintained cross-functionally
• Support and enhance Precision’s Corporate Compliance functions and facilitate business development and proposals for these areas as the need arises, including bid defense meetings and project kick-off meetings
• Lead system, site, documentation & Trial Master File audits to ensure compliance with internal
• SOPs/project plans and industry standards
• Review/audit documents intended for submission to the FDA to assure compliance with regulatory standards
• Build upon the current QMS in establishing additional company standards and metrics to ensure the highest quality of services provided to clients
• Participate in leading, maintaining and executing the corporate quality initiatives within Precision for Medicine
• Maintains current knowledge of regulations and guidance documents, providing expert analysis to project teams.
• Other duties as assigned

Qualifications:

• Bachelor’s degree in a science, healthcare or related field of study or equivalent
• Requires 10 years of experience in clinical research with emphasis in Quality Assurance/Compliance or equivalent relevant experience and/or demonstrated competencies
• CRO, Pharmaceutical and/or medical device experience
• Working knowledge of GCP/ICH guidelines and FDA regulations and standards
• Availability to travel up to 30% domestically and/or internationally

Skills:

• Strong leadership skills, excellent interpersonal and problem-solving skills, strong verbal and written communication, excellent computer skills
• Demonstrates mastery knowledge of GCP/ICH guidelines, FDA regulations and Precision SOPs - Motivates other members of the project team to meet timelines and project goals
• Ability to review and evaluate clinical data, with advanced proficiency in Microsoft Word, Excel, and PowerPoint, and some knowledge of Access or similar database
• Understands financial management to review proposals and budgets
• Exhibits high self-motivation and is able to work and plan independently as well as in a team environment
• Must possess a customer service demeanor; demonstrate collaboration and flexibility, teamwork, and keen attention to detail
• Ability to work with cross functional groups and management under challenging
• situations
• Ability to prioritize work and handle multiple and/or competing assignments
• Fluent in English language, with excellent verbal and written communications skills

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [emailprotected] .

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