**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **About Thermo Fisher Scientific** At Thermo Fisher Scientific, your work **builds real impact** . Every day, teams help make the world **healthier, cleaner, and safer** —by advancing treatments, ensuring food safety, and protecting the environment. We provide the **resources, training, and career growth opportunities** you need to succeed. **Location/Division Specific Information** As part of the **Microbiology Division (MBD)** within the **Specialty Diagnostics Group** , this role supports solutions that **diagnose infectious diseases and detect bacterial contamination** . Our work impacts **public health, clinical labs, food safety, environmental screening, and pharmaceuticals** —ensuring quality and accuracy in critical industries. **How Will You Make an Impact?** As a **Quality Technician** , you will ensure that our products meet the highest **quality and compliance standards** . You will review manufacturing records, collaborate with teams, and support continuous improvement efforts in a regulated environment. **A Day in the Life** In this role, you will: + Review **Batch Manufacturing Records (BMRs)** for **accuracy and completeness** before product release. + Ensure compliance with **Standard Operating Procedures (SOPs)** and support **training programs** . + Identify and resolve documentation issues, initiate **incident reports** , and support **root cause analysis** . + Promote **best documentation practices** and provide training on **quality standards** . + Work with **Operations, R&D, and Manufacturing Sciences** to improve workflows and reduce material waste. + Maintain documentation and ensure **audit readiness** by aligning records with regulatory and safety standards. _Additional responsibilities may be assigned as needed within the scope of the role._ **What You Need to Succeed** **Education** + **Required:** High School Diploma, Secondary Education, Advanced Certificate, or equivalent. **Experience** + **Preferred:** At least **1 year** of experience in **Quality Assurance (QA), Quality Control (QC), or a related field** (including office administration). + **Bonus:** Experience working in a **cGMP-regulated** environment. **Key Skills & Abilities** + **Attention to detail** – Accuracy is critical when reviewing documentation. + **Strong communication skills** – Ability to convey **clear, precise information** in writing and speaking. + **Problem-solving mindset** – Ability to **identify issues, suggest solutions, and improve processes** . + **Self-starter and organized** – Ability to **manage multiple priorities, work independently, and meet deadlines** . + **Technical skills** – Comfortable using **Microsoft Word, Excel, PowerPoint, and digital quality systems** . **What We Offer** + Competitive Annual Salary + Performance-Based Bonus + Annual Merit Pay Increase (based on performance) + Flexible Benefits Plan + Life Assurance & Health Support (including income protection and Employee Assistance Program) + Pension Scheme + Career Growth & Development Opportunities + Employee Referral Bonus (where eligible) **Why Join Us?** At Thermo Fisher Scientific, **your contributions matter** . Here, you will have the opportunity to **learn, grow, and innovate** in an environment that values **teamwork, impact, and continuous improvement** . Whether you are supporting scientific advancements, improving quality processes, or ensuring compliance, **your work makes a difference** . **Ready to take the next step? Apply today!** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.