Work Schedule
Weekend days

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Unique Opportunity

Work Schedule 10 hour shifts Friday-Monday

At Thermo Fisher Scientific, you will be part of a global leader that makes a significant impact on the world. As a Supervisor, QC, you'll contribute to our mission of enabling our customers to make the world healthier, cleaner, and safer. This position offers the chance to lead a dynamic team within a rapidly growing site, surrounded by collaborative colleagues and supported by an exceptional organizational strategy.

Key Responsibilities

• Supervise the Quality Control Chemistry team, ensuring timely and scientifically sound output.
• Coordinate the implementation of sophisticated biological and physical characterization techniques such as capillary electrophoresis, UPLC/HPLC, ELISA, and PCR, ensuring compliance with quality standards.
• Establish and monitor employee goals, ensuring high analytical quality.
• Support customer-focused outcomes in stability study samples, method transfer, and validation studies.
• Assist the Engineering and Validation Team with equipment/system upgrades and qualifications.
• Perform peer and technical review of analyses for completeness and cGMP compliance.
• Drive performance by setting and tracking critical metrics, targets, and goals.
• Ensure compliance with EH&S guidelines and Quality Standards in the QC Chemistry Lab.
• Lead and mentor team members, encouraging a culture of continuous improvement.
• Maintain scientific integrity, working closely with the data integrity officer.
• Facilitate swift resolution of atypical, out-of-specification, or out-of-trend investigations.
• Select, develop, and evaluate staff for efficient QC Chemistry operations.
• Perform other duties as directed by the Manager, QC Operations.

• Bachelor of Science in Biotechnology, Chemistry, or a related field.
• 1+ years leadership experience (preferred)
• 2+ years of experience in the pharmaceutical industry, with a focus on Analytical and Quality Control fields.
• Expertise in method transfer and qualification/validation.
• Understanding of cGMP practices.
• Strong background in analytical theory and proficiency in laboratory analysis.
• Effective communication skills across multiple modalities.
• Proficiency in Microsoft applications and Laboratory Information Management Systems.

• Adaptability to daily business requirements.
• Collaborative skills to work with diverse departments and colleagues.
• Strive for continuous improvement.
• Quality orientation with strong attention to detail and accurate test record completion.
• Dedication to providing exceptional customer experiences and improving product value.