Quality Control Analyst - Middlesbrough, United Kingdom - AM Recruitment Ltd

    AM Recruitment Ltd
    AM Recruitment Ltd Middlesbrough, United Kingdom

    Found in: Appcast UK C C2 - 1 week ago

    Default job background
    Description

    Provides a comprehensive analytical service, testing intermediates, products and raw materials in line with customer demand and business requirements. Identify ways to improve material flow through the lab to aid reduction in turnaround times and reduce costs, whilst still adhering to corporate quality standards.

    Assist in coaching and developing other members of the team

    Main Tasks and Responsibilities

    n Follows approved methods and procedures in accordance with cGLP & GMP requirements.

    n Plan and prioritises own work with guidance from QC Senior Analyst/QC Manager

    n Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements

    n Maintain the flow of QC documents within the department ensuring they are complete, accurate and compliant with procedures or guidelines

    n Ensure that OOS/OOT investigations are performed in timely manner in accordance with the procedural requirements

    n Carry out minor analytical method development to improve analysis, including HPLC, GC, spectrophotometric techniques and titrations

    n Carry out basic equipment maintenance and calibration of laboratory equipment following approved methods and procedures on assigned pieces of equipment

    n Write and review SOPs, Work Instructions and testing procedures for raw materials, intermediates and finished products

    n Monitor and maintain stock levels of reagents and consumables

    n Ensure that all Health, Safety and Environmental requirements are met including (but not limited to) workplace organisation, work instructions, risk assessments, COSHH assessments, housekeeping standards in accordance with GLP and GMP

    n Demonstrable evidence of understanding the importance creating a safe environment

    n Working in a safe manner

    n Follow appropriate and relevant practices and procedures

    n Will and ability to work co-operatively and to encourage cooperation within and across departments

    n Supports the team

    n Build positive relationships, trust and respect with co-workers

    n Communicate and coordinated with production, supply chain and sales departments

    n Understands customers' needs

    n Participate in communication with customer if necessary and authorised

    n Follow Corporate Trade Secret Protection (TSP) regulations to maintain confidentiality on sensitive customer and corporate information

    n Participate in training on Business Secrets Protection regulations when issued by the corporate TSP office

    n

    n Undertake any other duties of which the responsibility, skill and experience required fall within a post holder's expected capability and commensurate with the post holder's position in the company

    Skills & Qualifications

    Education

    Chemistry (or very closely aligned subject) degree with experience as an analyst in a fine chemical or pharmaceutical industry role. HPLC and GC experience

    Experience of working in a GMP environment / method development experience / cleaning validation experience

    Key Skills

    Attention to detail

    Ability to Plan and organize workload

    Ability to think creatively and apply new and innovative ideas to bring business benefit

    Analytical aptitude and confidence in working in a multi-disciplinary laboratory

    Adapt to changing circumstances by accepting new and different ideas and approaches

    Enthusiasm and a desire to achieve high standards

    Data and computer literate, fluent user of typical office software application packages, especially Word and Excel

    Working knowledge of GMP/GLP

    Delivers on commitments as per timelines and quality standards

    Shows a positive attitude in difficult situations

    2 years working in an analytical laboratory environment

    Experience of working in a GMP environment / method development experience / OpenLab software experience