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    IT Manufacturing Project Manager - Co. West Midlands, United Kingdom - Planet Pharma

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    Description

    Position: IT Project Manager

    Type: Contract

    Duration: 6 Month

    We've currently partnered with a global Pharmaceutical company, who are look for a manufacturing PM. This position will manage the execution of IT/OT Projects for 3 manufacturing sites in the UK.

    This is a full-time position, with travel to Milton Keynes. You'd be apart of the Manufacturing IT Team, reporting into the IT Automation Lead. This contract role will initially be until December 2024.

    Requirements:

    • Data Integrity Knowledge
    • Pharmaceutical Industry Experience (GxP)
    • BMS, EMS and SCADA Systems Experience and Knowledge
    • Knowledge of IT and OT areas
    • Ability to understand complex application and OT asset landscape

    If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on or email me on: -

    If this role isn't suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated Planet Pharma offers a competitive referral scheme so you will be rewarded for your help

    About Planet Pharma

    Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

    Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

    We are an equal opportunities Recruitment Business and Agency.

    We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.


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