C

Cencora

Distributes medicines and supports patient care

QA Officer - Good Distribution Practice

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeUnited KingdomNo salary listedIn-person

About the Job

Requirements

  • Previous Quality Assurance experience within a Good Distribution Practice and/or Good Manufacturing Practice-regulated environment.
  • Good working knowledge of Good Distribution Practice regulations and the UK pharmaceutical regulatory framework.
  • Experience managing or supporting deviations, corrective and preventive actions, quality incidents, and change controls.
  • Experience supporting or conducting internal, supplier, client, and/or regulatory audits.
  • Ability to maintain accurate, compliant quality documentation and records.
  • Strong knowledge of Good Distribution Practice requirements and quality systems within a regulated pharmaceutical environment.
  • Strong written and verbal communication skills, including communication with clients and cross-functional teams.
  • Effective planning, organisation, and prioritisation skills.
  • Ability to investigate quality issues and apply sound judgement and problem-solving skills.
  • Strong attention to detail and commitment to quality and continuous improvement.
  • Ability to influence and collaborate effectively with internal stakeholders, clients, vendors, and suppliers.
  • Flexible, proactive, and able to use initiative when making decisions.

Responsibilities

  • Provide Quality Assurance oversight of operational activities to ensure compliance with Good Distribution Practice, applicable Good Manufacturing Practice, ISO 9001, company procedures, and client requirements.
  • Raise, investigate, review, and manage deviations and corrective actions, supporting other departments where required.
  • Perform internal and supplier audits in line with the agreed audit schedule.
  • Support and host client and regulatory audits.
  • Generate, monitor, and report quality metrics internally and to clients.
  • Attend client review meetings and provide updates on quality matters, deviations, and continuous improvement activities.
  • Support the Change Control process, ensuring quality-critical changes are appropriately documented, reviewed, and assessed.
  • Ensure quality incidents, customer and client complaints, and deviations are appropriately recorded, investigated, and followed through to completion.
  • Ensure corrective actions are completed within agreed timelines and effectiveness checks are performed where required.
  • Ensure quality documentation is appropriately approved, controlled, maintained, and reviewed.
  • Maintain up-to-date knowledge of applicable regulations, procedures, and client requirements, including Technical Agreements.
  • Review daily temperature records and ensure appropriate action is taken when required.
  • Ensure all Quality Assurance activities and records are completed in accordance with relevant procedures and regulatory requirements.
  • Comply with applicable Standard Operating Procedures and Health and Safety requirements.

About the Company

Cencora

Distributes medicines and supports patient care

Cencora buys and distributes medicines for pharmacies, hospitals and physician practices, while helping drug manufacturers bring treatments to patients. Its businesses combine wholesale supply networks with specialty distribution for complex therapies and services that support prescribing and patient access. Customers order medicines through its distribution systems, and its teams manage sourcing, storage and delivery alongside pharmacy operations and manufacturer support. It earns revenue from pharmaceutical sales and fees for logistics and healthcare services. The parent company was formed in 2001 through the merger that created AmerisourceBergen, adopted the Cencora name in 2023, and is headquartered in Conshohocken, Pennsylvania.

Company size
10,001+
Company stage
IPO
Headquarters
Conshohocken, PA
Founded
2001

Recently Posted Jobs

Explore more opportunities at Cencora

See more jobs