Analytical Chemistry

Tipperary, Ireland | Posted on 02/20/2026

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.

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.

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development through 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.

This role provides analytical testing support for all late stage clinical and marketed drug product manufactured at the Ballydine site. Following MMD approved methods or pharmacopoeia methods testing will cover raw materials, intermediates and finished product associated with the Drug Product facility.

Responsibilities will also include, documenting all work in a compliant manner, participating in laboratory investigations, training staff, reviewing analytical results to ensure accuracy and compliance to test methods, preparation of all laboratory documentation and participate in continuous improvement programs.

Core Competencies

This position requires a

B.Sc. (or equivalent experience) in analytical chemistry, pharmaceutical science or a related science discipline. The incumbent must have demonstrated problem solving, and communication skills. Strong scientific understanding of analytical methodology and knowledge of relevant regulatory requirements, including cGMPs, is important.

• The ability to work in partnership with all plant departments in areas related to analytical chemistry and related validation.
• Must be able to demonstrate the ability:
  Identify the Business competencies required of the role.
• To perform precise and constant analyses in support of various projects.
• To communicate technical information both verbally and written in a concise manner.
• To analytically evaluate projects, suggest appropriate options, solutions and timelines.
• To complete assignments in a timely manner and communicate progress at internals.

• Must be able to demonstrate skills in the following areas:
  Expertise in analytical laboratory techniques.
• Skills in leading defined projects.
• Computer skills – Excel, Word, Outlook, scheduler.
• Project Management Skills.
• Interpersonal Skills.
• Written & verbal presentation and communication skills.
• Time Management.

• Minimum of BSc in Chemistry or related discipline.