Associate Scientist

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 have a great contract opportunity for an Associate Scientist to join a Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.

If you have 5 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!

ABOUT THE PROJECT - KEY RESPONSIBILITIES:

• Own and/or support analytical change controls for changes to global test methods or regulatory filings. Author, review, and manage change control process for (e.g., method changes, specification updates, equipment/instrument changes, site transfers) within the electronic Quality Management System (eQMS). Track change control timelines, ensure on-time closure, and elevate delays or roadblocks to management.
• Own and/or support analytical method transfers and validations in GMP Quality Control labs, both internally and externally - including generation of protocols, reports and acceptance criteria, co-ordination of execution, project management, and provision of program updates to leadership.
• Partner with Quality, Manufacturing, Supply Chain, 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.

ABOUT YOU - ARE YOUR SKILLS A MATCH?

• Advanced degree (MS/PhD) in a science or pharmaceutical-related field - Chemistry, Pharmacy, Biology or Chemical Engineering.
• 1-4 years of experience in a pharmaceutical/biotech environment, 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, etc.) and method validation/transfer principles is desirable.

Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!