Work Schedule Rotational shift days Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials Job Description Working shift pattern : 4 days on - 4 days off - Day Shifts only As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Position Summary : Join our team at Thermo Fisher Scientific as a QC Technician, where you'll help make the world healthier, cleaner and safer. In this important role, you'll ensure quality standards are met through testing and inspection of products in a cGMP environment. You'll perform quality control activities, work with a team of QC technicians, and collaborate with cross-functional teams to maintain the highest quality standards. You'll perform analytical testing, document results, and support continuous improvement initiatives. Key Responsibilities: To perform routine laboratory procedures, and to perform project work within the department. To carry out projects within the Department and at international level, as required. To prepare technical documentation within the Department, as required. To assist in the development and validation of laboratory procedures within the team, as required. To train others as required. To assist with training and assessment of cleanroom operators. To review analytical and laboratory data within the Department for accuracy, completeness and compliance with documented procedures. To communicate effectively with others on site and internationally, and to participate with them in problem solving activities, as required. To assist in the development and validation of laboratory procedures within the team and with other organisations internationally, as required. This includes but is not limited to purchase & qualification of equipment. Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business. To carry out any other tasks which may be required from time to time Additional Responsibilities: Ensure equipment status and readiness are effectively monitored and maintained - this will include that any faults or issues are reported. Assure timely review of the data for the delivery of the batch. Managing change control or CAPA actions OOS investigations and deviation investigation handling Ensure that all equipment is maintained in accordance with GMP Timely escalation of all issues that cannot be resolved. Tracking of progress and downtime reporting, escalating issues as appropriate. Accurate and timely completion of the analytical activities within the team. Ensure Continuous improvements - Identify and support PPI initiatives to eliminate or/and reduce waste and non-value adding activities within the Lab EH&S: Understand emergency procedures and comply with safe systems of work. Ensure compliance with environment, health and safety rules, signage and instructions at all times. Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules. Qualifications/Experience: Degree in Microbiology or strongly related scientific discipline. Experience of instrumental and traditional analytical techniques. Experience of GLP/GMP environment. Effective communication skills at all internal and external levels. Excellent attention to detail. Excellent organisational skills. Ability to coach others.