This role is in support of Cencora's wholesale distribution services in Europe operating through our Alliance Healthcare business.

We have an exciting opportunity to support the continued development of the Almus and Alvita businesses. This role will provide support to the central Quality function. The role involves carrying out and being responsible for specific technical and quality related activities, under the supervision of the European Quality Manager, necessary to introduce new and maintain existing Almus and Alvita branded products on the market in a legally compliant manner throughout their entire product lifecycle.

Key Responsibilities will include:

• Support the European Quality Manager in the effective operation, maintenance and continuous improvement of the Quality Management System, ensuring key quality processes are managed in accordance with applicable regulatory, business and procedural requirements.
• Take ownership of allocated QMS processes, ensuring associated schedules, records, documentation, actions and reporting requirements are maintained accurately and completed within agreed timelines.
• Co-ordinate the preparation, review and follow-up of quality documentation and periodic quality activities, liaising with internal stakeholders, suppliers and contract service providers to obtain required information and evidence.
• Support audit, inspection and compliance activities, including preparation, follow-up, tracking of findings and monitoring of corrective and preventative actions through to closure.
• Administer and support quality event management processes, including complaints, incidents, deviations, alerts and other reported quality issues, ensuring appropriate investigation, documentation, escalation and closure.
• Support risk management and regulatory compliance activities by maintaining schedules, coordinating data collection, assessing the impact of new or updated information, and ensuring appropriate records are retained.
• Support the operation of change control and continuous improvement processes, including creation of records, coordination of actions, progress tracking and confirmation that agreed actions are implemented effectively.
• Maintain QMS tracking tools, performance indicators and management information to provide visibility of process status, compliance performance and outstanding actions.
• Contribute to the development, review and implementation of quality policies, procedures, working instructions and supporting templates to ensure the QMS remains effective, practical and aligned with business needs.
• Develop and maintain effective working relationships with colleagues, suppliers, contract service providers and other stakeholders to support the delivery of quality activities across the business.
• Attend and contribute to relevant project, operational and functional meetings, providing quality input, updates and follow-up on agreed actions as required.
• Prepare, maintain and deliver quality training materials as required to support effective implementation of QMS processes across relevant business units.
• Support the management of supplier and contract service provider Quality Agreements , including coordination of documentation, review cycles, stakeholder input and approval activities.

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We would value the following attributes:

• Degree in Chemistry or a relevant Life Science (or equivalent)
• Experience working within the Pharmaceutical industry within a Quality Assurance role.
• Good working knowledge of interpreting relevant European Regulation and guidelines within the pharmaceutical industry impacting on a Quality function.
• Self-motivated dynamic individual, with the ability and desire to work proactively.
• Ability to work independently and prioritise and organise workload and to the ability to work effectively under pressure.
• Ability to assimilate and interpret regulatory guidance into development of concrete action plans necessary for Almus to remain compliant.
• Proven ability to communicate clearly and logically, both orally and in written form.
• Good working knowledge of European regulatory guidelines and legislation.
• Experience of writing Quality documents.

This role will be based in our Woking (Surrey) Office and there will be a requirement to be in the office 5 days a week during the probationary period. The role will quality for hybrid Working, following the successful completion of the period.

What Cencora offers

​Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.

Full time

Affiliated Companies

Affiliated Companies: Alliance Healthcare Management Services Limited

Equal Employment Opportunity

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.

The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.

Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned