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Lead bioprocess associate

Pe Global
Posted: 4 July
Offer description

PE Global is currently recruiting for a Lead Bioprocess Associate for a leading multi-national Biotech client based in Meath.
This is an initial 11-month contract position that requires flexibility to work on a shift basis.
ROLE: Lead/Guide team members to support on floor manufacturing of pipeline products on a shift rotation Provide guidance, coaching and mentoring to the rest of the production team Operate equipment according to electronic batch records,?sampling plans and standard operating procedures.
Work as part of a dedicated process team where flexibility and teamwork are a key requirement.
Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop.
Conduct all work activities with a strict adherence to the safety and compliance culture on site Support the Authoring of electronic batch records, sampling plans, work instructions and standard operating procedures.
Lead, facilitate and participate daily in cross-functional teams to collaborative effectively to ensure compliance REQUIREMENTS: Bachelors degree in Biotechnology, Chemistry, Biology, Pharmacy, or Process engineering.
5 years + Biotech Industry (bulk manufacturing of pharmaceutical or biological components) Competent in troubleshooting and show practical problem-solving capabilities.
Ability to work independently and within a cross-functional team.
Understanding of multi column chromatography concepts Familiarity with contamination control and batch release requirements Familiarity with Emerson DeltaV, Pas X,?and the use of Automation in a manufacturing Process.??
Proficiency in various SingleUse technologies in a manufacturing environment Problem, Deviation, and Change Management experience?
Commissioning and Qualification experience?
?
Experience of Upstream and Downstream Unit Operations for mAb manufacturing with in depth knowledge of key unit operations.
Understanding of both continuous and batch fed manufacturing processes ?
Experience leading, presenting, or supporting Regulatory Inspections and Site Internal Audits Interested candidates should submit an updated CV.
Please click the link below to apply, call Sen on or alternatively send an up-to-date CV to ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application.
You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you.
You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy.
Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert.
Skills: GMP Biotech Production

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