GMP Operations Manager

  • Location

    London

  • Sector:

    Life Sciences

  • Salary:

    Negotiable

  • Contact:

    Connor Harknett

  • Contact email:

    Connor.Harknett@volt.eu.com

  • Job ref:

    75084-PHARM-CKT_1568370185

  • Published:

    over 4 years ago

  • Expiry date:

    2019-10-13

  • Start date:

    ASAP

  • Consultant:

    ConsultantDrop

Hi All, I'm currently recruiting for this GMP Operations Manager. Please
view the Job Description below and apply to it!


Would you like the chance to join an award-winning global biotechnology Company who focus on development and commercialisation of innovative gene therapies to change lives? My client has a broad pipeline with one clinical trial ongoing and two more coming in 2019/20 which allows more opportunities to change lives of patients by focusing on gene therapy with the aim to provide treatments for diseases with significant unmet patient needs.

This opportunity will allow you to be involved in establishment and the operations of a GMP manufacturing facility to ensure on time delivery of products for clinical supply. Furthermore, our client will provide you the freedom to coordinate and lead the production project where you can map out the campaign via daily and weekly meetings securing project execution.

Role and responsibilities

  • To be able to work closely with the GMP team to ensure project success. Ensuring the deadline is met for clinical supply.

  • Lead the production project planning with cross functional teams to ensure completion. Giving you freedom to manage the maintenance schedule and production schedule.

  • In this role you will be made the primary point of contact within the GMP manufacturing facility, providing guidance on activities in the facility including waste /material transfer, qualification activities, equipment maintenance, equipment transfer etc.

  • Moreover, must be able to lead GMP Operations meetings daily or weekly. Setting tasks, capturing actions, agenda and tracking completion.

  • Play a vital role with senior members of the company where you will be working closely with cross functional teams such QC, QA, Supply chain and Technical guaranteeing all are working towards the same goals such as successful regulatory inspections.

  • Furthermore, you will need to maintain detailed and accurate training for all GMP team members to follow such as auditing for compliance.

  • In addition, you are responsible for tracking open GMP deviations, change controls preventive quality and safety measures. Presenting weekly updates to GMP department ensuring actions are closed on time.

  • If you are a self-motivated individual with a proven track record in project management looking to join a company who are achieving a high standard of work, please do reach out below!


or 01737 761 697

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