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Sandoz

Leader in generic and biosimilar medicines

Quality Assurance Manager and QP

Regulatory & Quality (Life Sciences)Updated on Nov 12
Full-timeBracknell, UKIn-person

About the Job

Requirements

  • A life science degree or equivalent experience.
  • Eligibility as a Qualified Person, ideally with experience across multiple dosage forms.
  • More than five years of pharmaceutical industry experience and knowledge of GxP.
  • Detailed knowledge of GMDP requirements relating to manufacturing, packaging, licensing, release, and post-market responsibilities.
  • Knowledge of process-improvement techniques.
  • Working knowledge of problem-solving and evaluation techniques.
  • Experience developing quality systems and/or processes.
  • Coaching, training, and facilitation skills.
  • Good skills using computer-based systems and applications.
  • Interpersonal and collaboration skills, with communication skills sufficient to ensure information is effectively received, used, and shared at all levels.
  • Operational excellence, including problem-solving and continuous improvement.
  • Resilience, motivation, ability to manage multiple priorities, organization of own and team workload, self-direction, flexibility during workload peaks, and project-management skills.

Responsibilities

  • Lead local execution of quality systems, including compliance with GxP requirements, global standards and standard operating procedures, and local work practices; monitor locally owned quality activities and systems, including metrics, quality review, and self-inspection; liaise with global quality system owners and participate in expert networks or work with Centres of Excellence where appropriate.
  • Perform routine risk and impact evaluations associated with product-based decisions or the quality system, and participate in escalation situations.
  • Ensure local compliance with global standards and standard operating procedures, maintain relevant local procedures, communicate requirements and changes, and act as a content expert for audits and inspections using knowledge of associated systems.
  • Investigate, manage, and resolve quality investigations, including deviations, complaints, and corrective and preventive actions, at the country organisation, working with nominated third parties where necessary to minimise impacts on product availability and sales.
  • Develop expert knowledge of information technology platforms and applications supporting quality systems and perform multiple roles within those systems as applicable.
  • Ensure effective information flow and communication of quality matters within the country organisation and between the country and Global Quality Assurance organisation, including issue escalation.
  • Recommend productivity and quality improvements, and lead implementation of quality initiatives and continuous improvements, including project planning, milestone delivery, and cross-functional communication.
  • Perform quality compliance and governance tasks as appropriate to experience, which may include product launch evaluations, product divestments, quality oversight, marketing authorisation holder responsibilities, regulatory updates, developing documents such as a site master file or business continuity plan, metrics review, quarterly leadership presentations, or serving as a point of contact for e-compliance, data integrity, or document management.
  • Work with country organisation business brands to provide direction and support on quality and Good Manufacturing Practice matters, and provide GxP education and training to colleagues across the team and country organisation.
  • Support and develop personnel in the Sandoz Quality team using Capability Assessment and MyGrowth tools.
  • Plan resources with the team and ensure personnel are trained to undertake GxP activities.
  • Conduct batch assessment and release activities in a timely manner and in accordance with relevant regulatory standards.
  • Lead activities supporting batch release, oversee the Quality System, and perform tasks such as Qualified Person declarations and review of Annual Product Quality Reviews.
  • Perform agreed communications with the Medicines and Healthcare products Regulatory Agency.
  • Maintain knowledge in accordance with the Qualified Person’s Code of Practice.
  • Set and review objectives.

About the Company

Sandoz

Leader in generic and biosimilar medicines

What does the company do? Sandoz is a global leader in generic and biosimilar medicines, with a broad portfolio of about 1,300 products that address diseases from the common cold to cancer. How does its product work? The medicines are off-patent (generics) or biosimilars that match the reference brands in safety, quality, and efficacy, offering affordable treatment options to patients and helping healthcare systems save money while expanding access. How is it different from competitors? Sandoz emphasizes scale, a long heritage dating back to 1886, and a sizeable global workforce dedicated to broadening patient access, aiming for large social impact and substantial healthcare savings. Its leadership in biosimilars and the breadth of its portfolio set it apart in the market. What is the company's goal? To pioneer access for patients by making high-quality medicines more affordable and widely available worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1886

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