Analytical Development Chemist

Job title:

Analytical Development Chemist

Company:

Complete Laboratory Solutions

Job description

Overview:CLS is currently going through an unprecedented and exciting period of growth and development and is looking for dynamic, dedicated and solutions driven team members, who want to be part of the company’s continued success.Founded in 1994, Complete Laboratory Solutions (CLS) is the highest accredited contract laboratory in Ireland and the leading provider of sampling, analysis, and analysts to the pharmaceutical, medical device, food, and environmental industries.As well as analysis and testing at our commercial laboratories, CLS builds strategic partnerships with its clients to deliver a flexible and managed quality solution (FlexiQ) by supplying organisations with highly skilled, work-ready quality professionals on a temporary, project-specific, or long-term basis. This service can be provided at a CLS site or directly at the client’s location.Job Title:
Analytical Development ChemistJob Responsibilities:
As an Analytical Development Chemist, you will support product development and clinical supply through the troubleshooting, development, transfer, and validation of analytical test methods. Your key responsibilities will include:Transferring and validating robust, reliable analytical methods.Drafting and reviewing test methods, validation protocols, and reports.Preparing submission documentation to support license applications.Leading or participating in laboratory investigations.Liaising with customers and contract laboratories, including participation in conference calls.Attending internal project review meetings.Supporting customer and regulatory inspections.Identifying and recommending improvements to enhance quality and efficiency.Analyzing raw materials, in-process samples, and finished products to ensure quality and efficacy.Ensuring all work complies with cGxP, company SOPs, regulatory guidelines, and safety/environmental standards.Completing all documentation accurately in line with data integrity and GMP requirements, including peer review duties.Supporting laboratory functions and contributing to the effective running of the business.Promoting a strong safety culture by following and supporting the company’s Safety Statement.Who You Are:
You are a detail-oriented and adaptable professional with strong analytical and communication skills. You enjoy working in a collaborative environment and are motivated by continuous improvement and problem-solving. You bring planning, multi-tasking, and time management skills to your work and take pride in maintaining high quality standards.Where You Come From:
You hold a minimum of a degree in Analytical Chemistry, Pharmaceutical Science, or a related discipline, and you have at least two years’ experience in a technical or analytical lab environment. You have strong competency in analytical methods, including HPLC and dissolution testing, and are familiar with cGMP and regulatory compliance.Ideally, you also have:Experience with Empower chromatography software and electronic documentation systems.A working knowledge of regulatory requirements for dossier submissions across various markets (EU, USA, Japan, etc.).Project management skills and experience in method validation and technical report writing.What We Offer:A dynamic and collaborative work environment where your contributions matter.Opportunities to work on a variety of innovative pharmaceutical development projects.Continuous learning and career development opportunities.Exposure to regulatory and customer-facing activities.A culture that promotes safety, quality, and continuous improvement.

Expected salary

Location

Waterford

Job date

Wed, 02 Jul 2025 22:42:03 GMT

To help us track our recruitment effort, please indicate in your email/cover letter where (vacanciesin.eu) you saw this job posting.