QC Analyst (Pharmaceutical Manufacturing)

Location: Liverpool, Merseyside, United Kingdom. Full-time onsite role. Working hours are Monday to Friday, 9:00am to 5:00pm, with flexibility where required.

Company

hirify.global develops vital organ therapies, digital solutions, and advanced services, with a focus on improving kidney care and patient outcomes.

What you will do

• Perform analytical testing of raw materials, in-process samples, finished products, and stability studies.
• Use SEC-HPLC, Atomic Absorption, pH, Conductivity, and TOC testing techniques.
• Manage laboratory samples from receipt and logging through storage and disposal.
• Review analytical data and laboratory records for accuracy and compliance.
• Support investigations, deviations, CAPAs, root cause analysis, method validation, and procedure reviews.
• Contribute to workload planning, colleague training, laboratory operations, regulatory readiness, and continuous improvement initiatives.

Requirements

• Degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related discipline, or significant relevant QC laboratory experience.
• Experience in a regulated pharmaceutical, medical device, healthcare, or manufacturing environment.
• Knowledge of SEC-HPLC, Atomic Absorption, pH, Conductivity, and TOC testing, including weighing, sample preparation, and dilution.
• Understanding of GMP, GLP, and GDP requirements and the ability to interpret pharmacopeial methods and laboratory procedures.
• Strong problem-solving, troubleshooting, attention-to-detail, and organisational skills.
• Ability to work independently and contribute effectively within a team.

Culture & Benefits

• Competitive salary and benefits package.
• Professional development and career progression opportunities.
• Collaborative and inclusive workplace culture.
• Commitment to work-life balance and employee wellbeing.
• Opportunity to work on products that positively impact patients' lives.