Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
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.
DESCRIPTION:
Join our high-performing team at Thermo Fisher Scientific, where you'll ensure quality compliance across manufacturing operations while advancing our mission to make the world healthier, cleaner, and safer. As a Quality Specialist I, you'll provide essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams. You'll help maintain GMP compliance, investigate quality events, and drive continuous improvement initiatives while working in a collaborative environment focused on delivering life-changing products to our customers.
REQUIREMENTS:
Bachelor's Degree required, preferred Fields of Study: Chemistry, Biology, Engineering, Life Sciences, or related scientific field
Additional relevant certifications (e.g. ISO auditor, Six Sigma) are advantageous
Fluency in English required; additional language skills beneficial
Proficiency with quality systems software and Microsoft Office applications
Strong analytical and problem-solving abilities with keen attention to detail
Outstanding verbal and written communication skills
Commitment to maintaining a quality-focused culture and driving continuous improvement
Collaborate with the Quality System Department to review SOPs
Conduct and manage departmental training
Prepare and present compliance documents and procedures
Manage internal, customer, and regulatory audits
Support continuous improvement initiatives
Provide documentary support to the production department
Proven ability to review and approve GMP documentation, batch records, and quality records