Site Name: Italy - Parma
Posted Date: Oct 23 2024
We create a place where people can grow, be their best, be safe, and feel welcome, valued, and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.
The R&D Clinical Supply Chain Sterile Operations Parma department is looking for a PLM (Product Lyfe Cycle Management) project manager to support clinical manufacturing business growth at Global Supply Chain Parma.
The new team member will work on projects in cooperation with GSC Parma and the R&D Project teams.
In this role, you will… Define activities plan and manage Change Control process for the introduction of new drug products and new equipment/component for manufacturing at Pilot Plant.Coordinate and look after change controls actions.Assess cleaning requirements of new equipment, define cleaning activities plan, issue cleaning verification protocols/report and coordinate activities.Support internal and external audits, as process and cleaning validation SME.Elaborate plans and monitor/track activities to ensure overall project deliverables meet required timelines.Communicate with R&D stakeholders so that they are kept fully informed of progress and any issue or change impacting on execution.The role ensures knowledge acquisition on multiple R&D functions (Product Development, QA, Supply Chain) and interactions with several GSC Parma departments (Manufacturing Operations, QA, Regulatory, Validation, Micro and Chemical Labs).
Why YOU?Basic Qualifications & Skills: Master's degree in Chemical or Management Engineering.Good written and spoken knowledge of Italian and English.Project management experience.Good attitudes to team working and interactions with vendors/international stakeholders.Experience in change control management process.Basic knowledge of aseptically filled drug products manufacturing process and related GMPs.Preferred Qualifications & Skills: Experience in technical functions (e.g. engineering, technical area, validation).Knowledge of terminally sterilized drug products manufacturing process.Problem-solving tools knowledge.Knowledge in 3 stage approach validation and regulatory submission.Exposure to international and multi-functional environments.Excel advanced user.What We Offer: Permanent contract in a very Inclusive environment.Smart Working.Flexible Benefits.Company Healthcare Plan.Integrative pension fund.Employee Assistance Programme.Sustainable mobility programme.Company canteen.Performance Reward.Closing Date for Applications – November 2nd, 2024 Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above.
Why GSK? GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive.
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