QC DATA AND DOCUMENT REVIEWER DEPARTMENT: QUALITY REPORTING TO: QUALITY CONTROL MANAGER HOURS 40 hours per week Monday to Friday MAIN DUTIES AND RESPONSIBILITIES: The post holder will review data and documents within the Quality Control department. JOB PURPOSE: The purpose of this job is to ensure the quality, accuracy, and regulatory compliance of analytical data within GMP/GLP environments. GENERAL DUTIES Ensure the quality, accuracy, and regulatory compliance of analytical data within GMP/GLP environments. Check and review laboratory data, raw chromatographic data, laboratory notebooks, equipment logbooks to ensure compliance with analytical methods, specifications and SOPs. Evaluate and approve standard operating procedures (SOPs), analytical protocols and reports. Manage equipment calibration and qualification schedules, associated master plans and summary reports. Identify data gaps or documentation errors and communicate directly with laboratory staff to address issues. Review testing datasets, including (but not limited to) HPLC / UHPLC / GCHS, Karl Fischer water determination, spectroscopic data and reference standard certification. Manage and plan daily activities to meet strict project timelines and ensure clear, concise record-keeping. Manage their time so as to accommodate the tasks allocated to them on a daily basis. Undertake any other duties, which may be assigned by Management. ESSENTIAL CRITERIA: Chemistry (or closely related) degree HPLC /UHPLC / GC methodology and techniques Knowledge and understanding of GMP aspects of laboratory software applications. Proficiency in Microsoft Office, particularly?Word and Excel Must be able to work individually and as part of a team. Right to work in the UK. DESIRABLE CRITERIA: Previous experience in a quality control laboratory (pharmaceutical preferred) Knowledge and understanding of the development and validation of HPLC and GC methods. Good interpersonal skills. BENEFITS: Company sick pay Length of service awards Discretionary bonus scheme Health care plan On site parking Cycle to work scheme 34 day leave per year inclusive of public holidays (FTE) Wedding leave Competitive salary Applicants must have the right to work in the UK TPBN1_NI
QC Data and Document Reviewer in Larne employer: Millicent Pharma Ni
Millicent Pharma is an exceptional employer that prioritises the well-being and growth of its employees in the vibrant location of Milbrook, Larne. With a strong commitment to innovation in women's health, the company fosters a collaborative work culture where team members are encouraged to develop their skills and advance their careers while contributing to meaningful projects that improve patient lives. Employees enjoy competitive benefits and a supportive environment that values quality and compliance, making it a rewarding place to build a career in the pharmaceutical industry.
