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Technical Specialist - BioAnalytical Science

Job Seekers Ireland Science Pharmaceutical

Job Summary

  • Dublin
  • Permanent
  • BBBH765593
  • Aug 31, 2020
  • Competitive
Job Description

Fantastic opportunity for an experienced analytical specialist to join a growing team in a global biopharma in South Dublin.

This role is on par with a managerial level role in terms of seniority without direct people management.

The role will be responsible for providing technical expertise with a focus on method transfers, continuous improvement and implementing a lean culture and Right First Time (RFT). The role also represents the QC unit by liaising with internal and external customers.

Key Responsibilities

  • Expert in a wide variety of analytical techniques including but not limited to Bioassays, Immunoassays, Cell Culture and Aseptic Technique. Experience with liquid-handling robots is also preferable.
  • Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays.
  • Responsible for providing technical guidance and applying expertise and critical thinking to independently resolve technical issues.
  • Lead training of staff on technical aspects of job as required.
  • Develop, revise and implement procedures that comply with appropriate regulatory requirements.
  • Experience of managing project groups and leading high performing teams and delivering results
  • Qualification of analytical equipment and related testing functions.
  • Co-ordinates & plans activities related to the successful method transfers and optimisation of BioAnalytical Methods into the site.
  • Compliance with Standard Operating Procedures and Registered specifications.
  • Ensure the laboratory is operated in a safe manner
  • Develop and maintain quality systems within the QC laboratories to ensure ongoing compliance to cGLP and cGMP.
  • Ensure timely completion of Laboratory Investigation Reports and deviations through the Non-Conformance procedures.
  • Keeps abreast of current Corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing.
  • Approval of SOP's, trend data, investigations, non-conformances, validation protocols, reports, method validation/verifications and equipment qualifications.
  • Participate in regulatory agency inspections as required.
  • Plan and implement procedures and systems to maximise operating efficiency.
  • Manage and contribute to the achievements of department productivity and quality goals.

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.

Consultant Details

Consultant Details

Aoife Duggan
Aoife Duggan
  • Senior Consultant
  • +353 21 2300300
  • aduggan@morganmckinley.com