Assoc. Spclst, Quality Control

539

Dunboyne, Ireland
Hybrid
Biochemistry and cell biology methods
Analytical methods
Elisa, sds-page, bio-assays, pcr
The Associate Specialist in Quality Control at a biotechnology facility in Dunboyne, Ireland, is responsible for quality control support testing, method establishment, and driving a high-performance culture within the Quality Control team. Candidates should possess a Master's degree in a relevant field or a PhD with significant industry experience, particularly in biochemistry and cell biology methodologies

Job Summary

  • This individual will be responsible for quality control support testing by providing technical expertise for the following activities: method execution troubleshooting, establishment of methods, input in investigations, building capability related to Biochemistry and Cell Biology methods and Analytical methods.
  • Develop lead and coach the Quality Control team in relation to the technical aspect of the lab activities and drive a high-performance organisational culture that accommodates rapid growth and highly dynamic expectations, ensuring attainment of site operational and development goals.
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA and cGMP regulations.

Matching Summary

Match Score: 85

The Associate Specialist in Quality Control at a biotechnology facility in Dunboyne, Ireland, is responsible for quality control support testing, method establishment, and driving a high-performance culture within the Quality Control team. Candidates should possess a Master's degree in a relevant field or a PhD with significant industry experience, particularly in biochemistry and cell biology methodologies.

Skills & Requirements

Must-have

  • Biochemistry and Cell Biology methods
  • Analytical methods
  • ELISA, SDS-Page, Bio-Assays, PCR
  • cGMP requirements
  • Data integrity and compliance

Nice-to-have

  • Lean Six Sigma experience
  • Continuous quality/process improvement tools

Key Requirements

  • Master’s degree with 5 years’ experience
  • PhD with 3 years’ experience
  • Leadership skills and experience managing daily activities
  • Excellent written and oral communication skills
  • Strong understanding of cGMP requirements
  • Excellent time management and organisational skills
  • Strong understanding of biochemical and cell biology methodology
  • Strong understanding of GMP, ICH, USP and global compendia regulations

Work Rights

Not specified

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