Herd Mundy Richardson Limited, an independent analytical testing facility specialising in pharmaceutical analysis, is seeking an Analytical Chemist to join our laboratories in Stockport. The company provides analytical testing services for pharmaceutical grade materials and finished drug products across all stages of the product lifecycle, from early-stage development through to QC release testing. Key Responsibilities Follow approved written procedures to perform analytical testing on raw materials, intermediates, and finished pharmaceutical products. Conduct analysis of pharmaceutical samples using validated methods and appropriate analytical techniques. Work effectively with Technical Management (TM)and Quality Assurance (QA) to generate accurate and compliant analytical data to support batch review and product release. Identify potential non-conforming quality events, supporting QA in investigation and resolution in accordance with current Good Manufacturing Practice (cGMP) requirements. Assist Technical Management in the delivery of method transfer and staff training programmes. Maintain high standards of laboratory housekeeping, safety, and compliance to ensure a safe and efficient working environment. Skills and Knowledge The successful candidate should have experience in several of the following analytical areas. Additional training will be provided where required. Chromatographic techniques (e.g. HPLC, UPLC, GC) Spectroscopic techniques (e.g. FT-IR, UV-Vis, AA, ICP-MS) Wet chemistry and compendial techniques Dissolution testing Inhaled product analysis Candidates should also demonstrate: Working knowledge of pharmaceutical regulatory standards and GMP requirements Good computer literacy, including experience with laboratory data systems where applicable Personal Attributes The successful candidate will demonstrate Excellent attention to detail and a thorough approach to analytical work Strong laboratory problem-solving and decision-making skills Ability to analyse, interpret, and report analytical data clearly and accurately Strong communication and interpersonal skills, with the ability to work collaboratively Good organisation and time management skills to meet client and project deadlines Experience Experience working within a cGMP pharmaceutical laboratory environment is preferred. Hands-on experience with HPLC and/or UPLC analysis would be particularly advantageous. Education Minimum of a BSc in Chemistry, Pharmaceutical Sciences, or a related scientific discipline, or equivalent qualification. The position is available for an initial 12-month term, with the possibility for extending this subject to project demands.