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Scientific & Laboratory

Job Description

MANUFACTURING PROCESS SPECIALIST, PURIFICATION required by CareerWise Recruitment to work within Downstream manufacturing for a new start up 15,000 litre scale fed-batch facility for our BioTech client in Cork, initial 12 month contract on offer. The MANUFACTURING PROCESS SPECIALIST, PURIFICATION will involve 10 weeks of being on the manufacturing floor full time to build relationships and competency in the area. After this the successful candidate will be moved to a Core team member role for an exciting introduction of a new product to the Suite.

Role of this position

  • Lead by example and strive to perform to high standards at all times
  • Responsible and accountable for assuring the safe accomplishment of job activities, following good environmental practices and procedures. Commit to and demonstrate safe behavior in every activity.
  • Carry out routine and non-routine tasks delegated by the Team Lead according to appropriate procedures, values and standards.
  • Carry out all activities in compliance with corporate and cGMP/EHS regulatory requirements.
  • Compliance with Manufacturing and general site procedures at all times.
  • Completion of all documentation in compliance with site procedures and GDP.
  • Execution of activities as necessary to meet operational and business needs.
  • Lead, support and participate in commissioning and qualification activities both current and future projects (and annual re-qualification activities). Also support to validation activities.
  • Prioritize and schedule activities to support business needs and to meet requirements of Master Production Schedule.
  • Lead and Support investigation and resolution of problems on plant.
  • Participate in and lead Cross-Functional teams as necessary.
  • Generate and assist with generation, review and revision of Manufacturing documentation as necessary.
  • Ensure that personal training requirements are completed in compliance with site procedures. Training and support for new recruits to the Manufacturing group
  • Support ongoing studies by Validation, OTS and other support functions.

JOB REQUIREMENTS

  • A relevant third level qualification in either Microbiology, Biochemistry, Pharmacy, Biotechnology, Science or Engineering
  • Postgraduate Qualification
  • Bio-pharmaceutical Manufacturing experience
  • Experience executing GMP change controls and investigating quality issues
  • Experience of Purification either in a manufacturing or a lab-based environment.
  • Experience of DCS (e.g. Delta V)
  • Experience on MES, PasX Werum or similar
  • 6-Sigma/Kepner-Tregoe or similar problem solving/decision making methodology training.

Please call Conor Twomey today for further information on 087-0907204 or email: ctwomey@careerwise.ie
CareerWise Recruitment (In Search of Excellence) Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin. By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your consent.

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Scientific & Laboratory

Cork Office

CareerWise Recruitment. EastGate Village, EastGate, Little Island, Cork.

Phone: +353 (0) 21 206 1900

Email: info@careerwise.ie