5x Associate Specialist/Specialist, Site Analytical Sciences (SAS) - based in Carlow

Planet Pharma; Dublin; On-site; EUR 45,000 - 65,000; Full time

Job summary

Planet Pharma's Carlow site is seeking an Associate Specialist and Specialist to support analytical science teams, contributing to method validation, transfer, and verification to ensure compliant data.

The role requires GMP laboratory experience, proficiency in HPLC/UHPLC, CE-SDS, icIEF and ELISA, plus strong problem-solving, meticulous attention to detail, and effective collaboration in a fast-paced environment.

Qualifications

• 2–3 years experience for Associate Specialist; 3–5 years for Specialist in pharma/biotech.
• GMP-regulated lab experience.
• Proficient in HPLC/UHPLC, CE-SDS, icIEF, and ELISA.
• Strong analytical and troubleshooting skills, with meticulous attention to detail.

Skills

GMP-regulated labs

HPLC/UHPLC

CE-SDS

icIEF

ELISA

Analytical troubleshooting

Communication skills

Prioritization

Education

Bachelor's degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related discipline

Tools

Empower Software

Solo VPE

Cell-Based Assays

Job description

Join Our Team as an Associate Specialist/Specialist in Site Analytical Sciences

Ready to advance your career in the pharmaceutical and biotech industry? We are seeking dedicated and detail-oriented Associate Specialists and Specialists to support our analytical science teams at our Carlow location. This pivotal role offers an exciting opportunity to contribute to the development and lifecycle management of critical analytical procedures, ensuring the quality and compliance of our pipeline and commercial products. If you’re passionate about laboratory science, data integrity, and continuous improvement, this is your chance to make an impact in a dynamic environment.

What You’ll Bring

• Bachelor's Degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related discipline
• 2-3 years of experience for Associate Specialist level; 3-5 years for Specialist level within the pharmaceutical, biotech, or vaccine sectors
• Hands-on experience working in GMP-regulated laboratories
• Proficiency in analytical techniques such as HPLC/UHPLC, CE-SDS, icIEF, and ELISA
• Familiarity with analytical method validation, transfer, and verification processes
• Strong analytical and troubleshooting skills, with meticulous attention to detail
• Effective communication skills and a collaborative mindset
• Ability to manage multiple priorities in a fast-paced setting

Nice To Have Skills

• Experience with Empower Software, Solo VPE, and Cell-Based Assays
• Background in digital method development
• Knowledge of laboratory investigations, root cause analysis, and GMP documentation practices
• Experience with chromatography, electrophoresis, and compendial testing

Preferred Education & Experience

• Bachelor’s degree in a relevant scientific field
• Minimum of 2-3 years' experience for Associate Specialists; 3-5 years for Specialists in a similar setting
• Proven track record in analytical testing and technical documentation within regulated environments

Take this opportunity to elevate your career with a forward-thinking organization committed to scientific excellence and quality.