Associate Scientist: Method Transfer & Change Control

LSC, Life Science Consultants; Dublin; On-site; EUR 48,000 - 70,000; Full time

Job summary

LSC, Life Science Consultants partners with a Dublin-based biopharmaceutical company to recruit an Associate Scientist focused on analytical change controls, method transfers, and quality systems in a GMP setting. The role requires 1–4 years in pharma/biotech, an MS/PhD in a science field, and familiarity with eQMS like Veeva; hands-on with HPLC and method validation will be valued. This is a contract opportunity with Ireland visa eligibility noted.

Qualifications

• Advanced degree (MS/PhD) in a science or pharmaceutical-related field (Chemistry, Pharmacy, Biology, or Chemical Engineering).
• 1–4 years in pharma/biotech with exposure to Change Control, Technology Transfer, Quality Systems, or Analytical Sciences.
• Experience with eQMS platforms (e.g., Veeva) is a plus.
• Familiarity with analytical techniques (HPLC, Empower) and method validation/transfer principles is desirable.

Responsibilities

• Own and/or support analytical change controls for changes to global test methods or regulatory filings.
• Own and/or support analytical method transfers and validations in GMP QC labs, including generation of protocols, reports and acceptance criteria, coordination of execution, and leadership updates.
• Partner with Quality, Manufacturing, Regulatory Affairs, Technical Services, and external stakeholders to ensure successful execution of analytical and process-related changes.
• Ensure all activities comply with cGMP, regulatory guidelines (FDA, EMA, ICH), and internal SOPs.

Skills

Change Control

Technology Transfer

Quality Systems

Analytical Sciences

Education

MS/PhD in Chemistry or Life Sciences

Tools

Veeva eQMS

Job description

LSC, Life Science Consultants partners with a Dublin-based biopharmaceutical company to recruit an Associate Scientist focused on analytical change controls, method transfers, and quality systems in a GMP setting. The role requires 1–4 years in pharma/biotech, an MS/PhD in a science field, and familiarity with eQMS like Veeva; hands-on with HPLC and method validation will be valued. This is a contract opportunity with Ireland visa eligibility noted.