Chemist - Quality Control

Chemist - Quality Control Our global pharmaceutical client based in Milton Keynes is recruiting a Chemist to join their busy Quality Control team reporting to the QC Project Lead. This is a contract role initially signed off for 1 year with a possible extension offering an hourly rate of up to £23.50 per hour, plus 25 days holiday pro rata and other benefits. Hours are Mon- Friday 37.5 hours per week. Company / Division Overview Our Client is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, they are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Their ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, they strive to create an environment of mutual respect, encouragement and teamwork. As part of their global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. Purpose of Role Currently QC is looking for an enthusiastic and dedicated analyst to - Support activities in the areas of qualification of standards/controls used in in-process and final product testing within Analytical Chemistry lab. To support analytical method validation / improvements and method transfers between sites. Key Accountabilities & Duties: Expertise in Analytical Chemistry techniques is essential. Validation of standards/controls used in in-process and final product testing. Analytical Chemistry method validation / improvements and test transfer between labs/sites. Drive change management for introduction of new / improved methods and validation of new equipment. Be able to produce technical documents such as protocols, testing and execution plans and final reports. Ability to work on several projects simultaneously and be able to prioritise. Reporting and communication of results to stakeholders. Liaise with several departments - technical support groups, QA, Regulatory to drive project completion and deliver on milestones. The candidate will be required to report all laboratory activities in a clear, organised manner, in the form of reports, following the standard operating procedures. Good understanding and ability to perform efficient lab investigations arising from deviations or invalid/atypical results. The candidate should be able to provide training to staff on Analytical methods and equipment usage. Additionally, the candidate may be required to support laboratory investigations, perform troubleshooting exercises and participate in proof of principle studies. Reporting and investigation of OOS and OOT results, determine root causes and implementing effective CAPA actions. Perform project related literature searches. Interact closely with fellow scientists and global/regional colleagues within own and other departments. Work in a multi-disciplinary and international team and environment. Other responsibilities Comply with Standard Operational Procedures (SOP’s), GMP, ESH procedures and Company corporate policies and process improvements. Maintain all documentation and training records as per GMP requirements. To comply with company’s health and safety practices and procedures. Ensure positive, timely and effective communication with team members and internal customers. The above list of duties is not exhaustive and is subject to change. The post holder may be required to undertake other duties within the scope and grading of the post. Person Specification Knowledge: Spectrophotometric Analyses (FTIR, UV/VIS), TOC Wet Chemistry techniques including titrations, digestions, full metal analysis GMP Compliance Experience: Minimum 5 years background in Pharmaceutical QA/Analytical Lead Raw Materials testing including pharmacopoeia Laboratory investigations Validation and method development Skills & Abilities: MS Word and Excel Protocol and Report writing Ability to troubleshoot to resolve Basic Statistical understanding such as Minitab Statistical software (desirable) Personal Attributes: Able to communicate at all levels and across all functions Ability to communicate concise technical information with clarity Ideal candidate should be self-motivated, be able to work under pressure to deliver success within set timelines and hold a positive mind-set Able to assist in Fact finding discussions Flexible approach to changing priorities Attention to detail Qualifications: Degree in Applied Chemistry Other requirements: Fluent in English Speaking/writing Full Drivers Licence Cross functional work experience