Quality Technician

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll 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 worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

Position Summary
In this role you will focus on reviewing batch documentation and test results in accordance with established procedures and Quality standards. You will play an important role in ensuring compliance and maintaining the high quality of our products.

This position supports QC operations in Quality related matters including handling deviations supporting investigations and updating addition you will contribute to continuous improvement initiatives participate in cross-functional projects and help maintain and develop our Quality processes.

You will also support training activities and contribute to building and maintaining a strong Quality awareness within the team. This is a great opportunity to grow in a dynamic and collaborative environment working closely with QC QA and other key stakeholders.

Key Responsibilities

• Review batch records and protocols to ensure compliance with procedures and quality standards
• Evaluate test results and ensure accurate and complete documentation
• Support deviation handling non-conformance reporting and investigations
• Maintain and update quality documentation in line with regulatory requirements
• Participate in continuous improvement initiatives and cross-functional projects
• Support training activities and contribute to knowledge sharing within the team
• Collaborate closely with QC QA and other stakeholders to ensure high quality standards

Qualifications & Experience

• Bachelors degree in Chemistry Biochemistry Molecular Biology or a related scientific field
• 12 years of experience in a similar role or within a regulated environment (e.g. ISO 13485 or GxP)
• Experience with batch record review test result evaluation or quality documentation is highly desirable
• Experience with deviation handling non-conformance reporting and investigations
• Familiarity with quality management systems and regulatory requirements
• Experience working with ERP systems and good proficiency in Microsoft Office
• Fluency in Swedish and English both written and spoken

Personal Competencies

• Strong attention to detail and a quality-focused mindset
• Structured thorough and able to work independently
• Strong communication and collaboration skills
• Proactive self-motivated and adaptable with a willingness to learn