About this role

  • Posted on

  • Location

    Allschwil, Arlesheim

  • Salary

    £54.14 - £60.80 per hour

  • Type

    Contract

  • Division

    Quality Assurance Jobs

  • Reference

    BBBH17874_1616588386

  • Start date

    1/5/21

  • Managing this role

Executive Consultant

Jon Martin

+44 203 8540 262

jon.martin@xplorelifescience.com

154-158 Shoreditch High Street, E1 6HU

Description

My client, a fast growing, reputable pharmaceutical business is seeking a Quality Assurance Manager (GMP / GDP) to join the business on a 12 month contract. This is an exciting opportunity to work in a collaborative, multicultural & solution-orientated environment where you can make a difference.
Key Responsibilities include

  • Provide GMP/GDP quality assurance expertise during development and commercialization of Idorsia’s products
  • Ensure all required quality activities are initiated and completed according to the development stage with advice from management
  • Ensure that medicinal products are designed, developed, manufactured and controlled according to adequate quality standards with advice from management
  • For assigned projects, provide guidance on the resolution of complaints, testing issues, deviations, discrepancies and Out of Specifications (OOS), investigations and propose Corrective and Preventive Actions (CAPA) as needed, with advice from management
  • Establish a quality risk management approach in projects based on six sigma concepts and training to ensure that quality is understood and managed by all stakeholders throughout the product life cycle, with advice from management
  • Manage all required activities to support release of active ingredients, commercial products and/or investigational medicinal products including approval of master process documentation, batch record review and assessment of change controls
  • Notify CMC team and management of potential quality, regulatory and lead time issues
  • Participate, represent and defend quality activities in CMC team meetings
  • Assist GMP/GDP onsite audits at Contract Manufacturing Organizations (CMOs) on demand
  • Preparation of GMP/GDP Agreements in collaboration with CMOs and the CMC team, with advice from management
  • Write, review, and/or approve internal SOP’s and other GMP/GDP related documentation
  • Support review and optimization of the company’s pharmaceutical quality system by preparing review of relevant CMO’s Key Performance Indicators
  • Pro-actively participate to the optimization of the quality system by proposing new procedures, tools or modification of existing ones

Candidate’s Requirements

  • University degree in Pharmacy, Chemistry or alternative technical/science university degree: master level minimum
  • 3-6 years of experience in different positions like pharmaceutical product development/ quality control/ analytical development/ chemical production or similar operational positions in the pharmaceutical industry
  • 3-6 years of experience in quality assurance of drug substance and/or drug product
  • Knowledge and understanding of drug substance and/or Drug Product development, manufacturing process, quality control, packaging and distribution
  • Good knowledge of (c)GMP/GDP’s
  • Ability to interpret and implement Quality standards with advice from management
  • Ability to manage complex projects and prioritize workload according to the project importance
  • Ability to pro-actively initiate and lead quality activities with coaching from management
  • Ability to manage multiple tasks with competing priorities
  • Good interpersonal and influencing skills
  • Self-confident, assertiveness and autonomy to deal with complex stakeholders/situations with some advice from management
  • Ability to communicate clearly and professionally both verbally and in writing
  • Fluent in English and at least basic knowledge of an additional European language, German or French advantageous
  • Provide coaching and advice to Junior QA Managers and QA Managers when required

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