Overview

Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.Role Objectives

The WEP Clinical Quality Assurance Manager will be responsible for the leadership and operational execution of the site quality assurance function regarding the distribution and manufacturing (secondary packaging and labelling) activities. They will oversee and drive day-to-day site operations, driving compliance with regulatory Good Manufacturing and Distribution Practice standards and operational improvements. The Quality Manager will also act as a primary expert and interface between supply chain and logistics, project management, and other departments to drive delivery of client solutions with respect to Post Approval Named Patient/Expanded Access Program and Clinical Trial supply service lines for the site.The Ideal Candidate

Detail-OrientedProcess-DrivenAdaptableCollaborativeWhat You''ll Do

Accountable for day-to-day site quality operations at the site, ensuring critical quality records and activities are completed in a timely manner and that patient safety and product quality are protected.Lead and maintain the site Quality Management System, ensuring ongoing compliance with GDP/GMP, procedural standards, and regulatory requirements (e.g. FDA, MHRA, HPRA, EMA).Monitor and report operational key performance indicators, identify trends, and drive data-driven quality improvements and decisions.Provide hands-on quality oversight of the warehouse distribution and manufacturing activities.Complete or oversee risk assessments that drive key decisions to avoid/mitigate business and quality risks.Ensure a presence on the warehouse floor where necessary, supporting the supply chain and logistics team in making compliant, risk-based decisions.Point of escalation for site-specific issues and proactively mitigating product quality or patient safety issues.Attendance on site in the case of emergencies (e.g. business continuity, GxP critical issues).Oversee and ensure timely completion of quality records (e.g., deviations, complaints, CAPAs, Change Controls, Customer Verification), ensuring effective investigation and root cause analysis where applicable.Oversee and mentor team members in ensuring that effective quality decisions are made (e.g. robust CAPAs addressing the root cause, managing changes effectively)Complete critical warehouse reviews as the Responsible Person, Deputy Responsible Person or Equivalent Delegate, verifying warehouse maintenance programs have been completed (e.g. pest control, cleaning reports, calibration reviews).Support in developing secondary packaging strategies for the business, coordinating activities with key stakeholdersLead, coach, and develop the QA site operations team to drive a cohesive and highly effective team.Line manage QA site operational personnel, coaching them and developing them to meet their own personal in line with business goals.What You''ll Need

Bachelor''s Degree or higher (preference for pharmaceutical, life sciences, or engineering concentration)5+ years of related industry experienceProven leadership and management capabilities.Experience with UK, FDA, and EU regulations, pertinent to manufacturing and distribution operations, is required and may vary based on geographical considerations.Extensive knowledge of Good Manufacturing and Distribution Practice.Strong understanding of fundamental principles for core Quality Management System processes (e.g. risk assessments, deviations, change control, supplier/customer management).The use of initiative is essential to making day-to-day decisions and guiding the site.It is essential to be solution-focused to avoid causing business disruption and to understand various business models and apply risk-based approaches to the site.Ability to take a proactive and reactive risk-based approach with their day-to-day activities.Ability to balance business needs and Quality requirements, identifying ways to meet both aspects.What We Offer

Private healthcare insuranceLong-term illness CoverDeath in service coverSalary sacrifice pensionAnnual leavePaid maternity and paternity leaveVolunteer dayWhat Sets Us Apart

WEP Clinical partners with sponsors to help patients and physicians gain early access to medicines when no other treatment options are available. WEP Clinical has over 15 years of experience distributing products to over 120 countries worldwide to treat unmet patient needs.We\''re Committed to Our Team

WEP has many initiatives to encourage wellness, growth, development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all we do to support our employees.We\''re Committed to DEI

At WEP Clinical, acceptance, recognition, and engagement are the core of our DEI values. We are committed to giving employees opportunities for personal and professional success and growth, and embracing everyone\''s unique identities.Our services include

Access ProgramsClinical Trial ServicesPatient Site SolutionsClinical Trial SupplyMarket Access and CommercialisationWEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual\''s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.Job Details

Seniority level: Mid-Senior levelEmployment type: Full-timeJob function: Quality AssuranceIndustries: Research Services

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