Analytical Sciences Associate Specialist

PSC Biotech® Corporation

Carlow

On-site

EUR 42,000 - 60,000

Full time

10 hours ago
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Job summary

PSC Biotech Corporation in Ireland seeks an analytical specialist to support end-to-end method lifecycle management, including method transfers, validations, and product testing. You will work across QC, Manufacturing, and Global teams to ensure compliant, high-quality analytical deliverables.

The role emphasizes analytical problem solving, data integrity, and continuous improvement within a GMP environment, offering exposure to top pharma clients.

Qualifications

  • Bachelor's degree in analytical sciences or related field.
  • 2–5 years in pharma/biotech GMP lab experience.
  • Experience with method validation, transfer, and testing.
  • Proficient in analytical data review and documentation.
  • Knowledge of GMP and data integrity practices.

Responsibilities

  • Support analytical method transfers and validations.
  • Perform lab-based testing and technical studies.
  • Generate and review analytical data and docs.
  • Support lifecycle management of analytical methods.
  • Assist with troubleshooting lab methods and equipment.
  • Participate in investigations and CAPAs.
  • Collaborate with QC, Manufacturing, and Global teams.
  • Ensure compliance with cGMP and data integrity.
  • Support digital method development.

Skills

Analytical thinking
Attention to detail
Teamwork
Communication
Problem solving

Education

Bachelor's Degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related field

Tools

HPLC/UHPLC
CE-SDS
icIEF
Empower
ELISA
Laboratory instrumentation

Job description

Who are we?

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

About PSC Biotech

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

‘Take your Career to a new Level’

PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.

Employee Value Proposition

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

Overview:

The Site Analytical Sciences Associate Specialist/Specialist role is responsible for supporting Analytical Procedure Life Cycle through end-to-end method lifecycle management including introduction of new analytical methods, analytical transfers, SME assessment for all analytical method & equipment performance qualification, investigations, product testing and technical rationale. This work will support pipeline and commercial products by utilizing expertise in the analytical areas of separations and biochemistry.

Requirements
Key Responsibilities:
  • Support/Lead analytical method transfers, validations, and compendial method verifications.
  • Perform laboratory-based analytical testing and technical studies using a variety of analytical techniques and instrumentation.
  • Generate, review, interpret, and verify analytical data and technical documentation.
  • Support lifecycle management and continuous improvement of analytical methods.
  • Assist with troubleshooting of analytical methods and laboratory equipment.
  • Support equipment performance qualification activities (PQ).
  • Participate in laboratory investigations, deviations, CAPAs, and change controls.
  • Collaborate with Quality Control, Manufacturing, Validation, Technical Operations, and Global Analytical teams.
  • Ensure compliance with cGMP, data integrity, safety, and regulatory requirements.
  • Supporting digital method development.
Qualifications & Experience:
Education:
  • Bachelor's Degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline.
  • Experience:
  • Minimum 2-5 years' experience within the pharmaceutical, biotechnology, or vaccine industry.
  • Experience working in a GMP-regulated laboratory environment.
  • Experience with analytical testing, data review, and technical documentation.
  • Experience with method validation, method transfer, compendial testing, chromatography, electrophoresis, ELISA or analytical troubleshooting is advantageous.
Desired Technical Skills
  • HPLC/UHPLC (Agilent/ Waters)
  • CE-SDS (AB Sciex instruments)
  • icIEF (Maurice, Biotechne)
  • Empower Software Competency
  • Solo VPE
  • ELISA
  • Cell Based Assay
  • Compendial testing and Method Verifications
  • Data analysis and technical report writing
  • Laboratory investigations and root cause analysis
  • GMP documentation and data integrity practices
What We Are Looking For
  • Strong analytical and problem-solving skills.
  • Excellent attention to detail and commitment to quality.
  • Effective communication and teamwork skills.
  • Ability to manage multiple priorities in a fast-paced environment.
  • A proactive approach to learning, innovation, and continuous improvement.
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