St. Louis, Missouri, USA
6 days ago
Supervisor, QC - Weekends

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 ResponsibilitiesSupervise 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.

Minimum Requirements/Qualifications

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.

Skills & Attributes

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.

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.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process.

Confirm your E-mail: Send Email