Quality Control Laboratory Analyst

The Impact You Will Make:As a Quality Control Laboratory Analyst you will be responsible for the testing of pharmaceutical raw materials components and packaging supporting batch release stability programmes and customer complaint within established GMP EHS and laboratory procedures you will help ensure testing is completed accurately safely and within required timelines while championing data integrity and a right-first-time this role you will also provide technical guidance and training to colleagues and represent the department during regulatory and customer Responsibilities include but are not limited to:Providing technical expertise and support to help resolve laboratory and testing testing is completed accurately and within required timelines with a strong focus on right-first-time in accordance with GMP GLP ALCOA principles specifications test methods and laboratory physical and analytical testing including HPLC to support batch release stability studies and customer complaint laboratory investigations with minimal support and contributing to quality investigations and GMP deviations within your area of accurate complete and compliant laboratory laboratory documentation within your areas of technical continuous improvement initiatives and participating in wider team improvement responsibility for the maintenance and calibration of basic laboratory and training colleagues sharing technical knowledge and good laboratory the QC laboratory during customer and regulatory excellent laboratory housekeeping and consistently following site safety safety quality data integrity and continuous improvement in everything you & Experience:Were looking for someone who combines strong technical laboratory knowledge with a proactive and collaborative you will have:2 years experience in testing within a pharmaceutical QC or regulated laboratory environment.A BTEC HND or above in a science-based discipline or a similar relevant experience working within GMP and/or GLP knowledge of laboratory specifications and test with HPLC GC or related analytical understanding of pharmaceutical testing requirements and current analytical working with laboratory equipment and supporting calibration or maintenance computer skills including familiarity with Microsoft Capabilities:Has excellent written and verbal communication maintain focus and a high attention to detail while performing repetitive sharing technical knowledge and supporting less experienced work effectively both independently and as part of a cross-functional comfortable working with detailed technical information while understanding the wider business excellent organisational skills and attention to ownership and approaches problems with a positive solutions-focused manage changing priorities and demanding timelines without compromising consistently high standards of accuracy documentation and data passionate about creating a right-first-time We Offer:Attractive compensation pension scheme (up to 10% employer contribution).25 days holiday per year (plus bank holidays) plus service days after 5 Medical sick pay. Employee Assistance Program with 24/7 confidential helpline support for employee and immediate assurance of four times life cover working recognition on-site and cashback at many to work referral Information: Working Hours: 37.5hrs per weekLocation: Derby Road Loughborough All applicants must be eligible to work in the believe our people make the difference at Kindeva we look for skilled passionate and driven professionals to come and work with us to help us excel in manufacturing technologies and processes which bring lifesaving products to patients worldwide.#LI-AC1 #AC