NPI QC Sr Associate

LSC, Life Science Consultants; Dublin; On-site; EUR 46,000 - 83,000; Full time

Job summary

LSC, Life Science Consultants is seeking an NPI QC Senior Associate for a South Dublin based biopharmaceutical company specializing in formulation, fill finish and packaging. 2-3 years ofQC/GMP experience in pharma/biotech is preferred.

You will support NPI activities as QC, handling analytical testing, method validation, and technology transfer. The role requires strong cGMP/LIMS knowledge, excellent communication and data analysis skills, and the ability to work independently in a fast-paced

Qualifications

• Bachelor's degree in Chemistry, Biology, or another relevant scientific discipline.
• 2-3 years of Quality Control or GMP lab experience within the pharmaceutical, biotechnology, or medical device industry.
• Strong analytical chemistry and laboratory testing experience, with knowledge of cGMP and LIMS.
• Experience with method validation, method transfers, technical writing, and GMP documentation.
• Excellent communication, problem-solving, and data analysis skills with the ability to work independently.

Responsibilities

• Support New Product Introduction (NPI) activities as the Quality Control representative across cross-functional teams.
• Perform analytical testing, sample management, method validation, and technology transfer activities.
• Prepare and approve protocols, SOPs, sample plans, and GMP documentation.
• Coordinate LIMS data management, analytical results, and QC documentation.
• Ensure compliance with cGMP, regulatory requirements, and laboratory quality standards.
• Support audits, investigations, equipment qualification, and continuous improvement initiatives.

Skills

Analytical chemistry

Laboratory testing

cGMP

LIMS

Technical writing

Data analysis

Independent work

Education

Bachelor's degree in Chemistry, Biology, or another relevant scientific discipline

Tools

LIMS

Job description

LSC have a great contract opportunity for an NPI QC Senior Associate to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.

If you have 2-3 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:

• Support New Product Introduction (NPI) activities as the Quality Control representative across cross-functional teams.
• Perform analytical testing, sample management, method validation, and technology transfer activities.
• Prepare and approve protocols, SOPs, sample plans, and GMP documentation.
• Coordinate LIMS data management, analytical results, and QC documentation.
• Ensure compliance with cGMP, regulatory requirements, and laboratory quality standards.
• Support audits, investigations, equipment qualification, and continuous improvement initiatives.

ABOUT YOU - ARE YOUR SKILLS A MATCH?

• Bachelor's degree in Chemistry, Biology, or another relevant scientific discipline.
• 2-3 years of Quality Control or GMP laboratory experience within the pharmaceutical, biotechnology, or medical device industry.
• Strong analytical chemistry and laboratory testing experience, with knowledge of cGMP and LIMS.
• Experience with method validation, method transfers, technical writing, and GMP documentation.
• Excellent communication, problem-solving, and data analysis skills with the ability to work independently.

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!