Validation Engineer - PE Global (UK)
  • Cork, Munster, Ireland
  • via BeBee.com
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Job Description

PE Global is currently recruiting for a Product Lead for a leading multi-national Biotech client based in Dublin South. This is an initial 12 month contract.

Overview

The Product lead – Process Development will report to the Sr. Manager Process Development in the Portfolio Management and Delivery group and will be responsible for leading a cross-functional product team in a matrix organisation to deliver new technologies and products to our client. The successful candidate will have at least five years experience within the pharmaceutical or biotech industry and will have demonstrated program leadership skills.

Responsibilities

- Act as the Product Health Steward and own product health for the products in their brief through product governance and effective product team leadership

- Manage and develop product lifecycle management programs (multiple products)

- Assist in developing long term site product vision and strategy

- Serve as main point of contact for global operations leads (GOLs) & product delivery teams (PDTs)

- Ensure that site's needs are presented and prioritized appropriately at site and global level

- Build and manage the relationship with the product & process knowledge SMEs at network and site level

- Develop site product risks and implements plans to remediate risks

- Make critical decisions and provide Process Transfer Technical Leadership on the cross-functional Tech Transfer/NPI project team and at Technology Development and Transfer Governance Forums

- Engage at site product governance meetings i.e., Product Weekly Review meeting, Site Ops meeting

- Ensure changes to global product roadmap and contract books are fed back to site through Product governance and prioritized appropriately

- Influence key stakeholders on site and above site and protect site strategy while meeting Network demands

- Support new product/market launch

Requirements

- Technical Degree and/or Masters' or equivalent

- 5-7 years in biopharma/pharma industry

- A working technical knowledge in a range of products and their associated manufacturing sciences, technologies and analytical processes from within parenteral fill-finish, or oral dosage forms and/or packaging

- Ability to identify gaps/risks and put appropriate remediation plans in place

- Technical or program leadership experience

- A proven track record in the ability to transfer goals and objectives into measurable plans

- Strong process and manufacturing background

Interested candidates should submit an updated CV.

Please click the link below to apply, or alternatively send an up to date CV to rebecca@peglobal.net

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***

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