Sr. Bio-process Associate

Desired Skills: cGMP,Manufacturing,Biologics

PE Global is currently recruiting for a Senior Bioprocess Associate for a leading multi-national Biotech client based in Meath.

This is an initial 11-month contract position working on a 24/7 shift.

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:

• Bachelor’s degree in Biotechnology, Chemistry, Biology, Pharmacy, or Process engineering.
• 3 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 Seán on +353 86 3514962 or alternatively send an up-to-date CV to sean.molloy@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***