Quality Officer

Alliance Healthcare UK; Woking; On-site; GBP 30,000 - 45,000; Full time

Job summary

Alliance Healthcare UK is seeking a Quality Officer in Woking to support the Quality Management System across their pharmaceutical operations. You will collaborate with the European Quality Manager to enhance and maintain compliance frameworks for Almus and Alvita product lines.

The ideal candidate should possess a degree in Chemistry or a relevant Life Science and previous experience in a Quality Assurance role. This position offers a hybrid working model following a probationary period.

Qualifications

• Experience in a Quality Assurance role within the pharmaceutical industry.
• Ability to interpret European regulatory guidance.
• Proven capability to communicate both orally and in writing.

Responsibilities

• Support the operation and continuous improvement of the Quality Management System.
• Coordinate quality documentation and periodic activities.
• Support audit, inspection, and compliance activities.
• Administer quality event management processes.
• Maintain records and performance indicators.

Skills

Experience within the Pharmaceutical industry

Good working knowledge of European regulations

Ability to work independently

Communication skills

Education

Degree in Chemistry or relevant Life Science

Job description

## Quality OfficerApplylocations: Woking, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R269843Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!# **Job Details**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..### 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.