Work Schedule

Other

Environmental Conditions

Able to lift 40 lbs. without assistance, Cold Room/Freezers -22degrees, Loud Noises (Equipment/Machinery), No eye contacts allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

Job Description

Thermo Fisher Scientific Inc. is seeking a Supervisor, QC to oversee a team responsible for one of three functions: Day shift IPC (2 shifts), Chromatography group, or Wet chemistry group. These groups play a crucial role in supporting the site's fast-paced manufacturing needs by conducting raw material release, API release, in-process reaction completion testing, intermediate release, and stability testing. As a Supervisor, you will have the unique opportunity to develop and empower your staff, fostering their growth into future roles within the site.

Excellent Benefits Package

Review our company’s Total Rewards

Medical, Dental, & Vision benefits-effective Day 1

Paid Time Off & Holidays

401K Company Match up to 6%

Tuition Reimbursement – eligible after 90 days!

Employee Referral Bonus

Employee Discount Program

Recognition Program

Charitable Gift Matching

Company Paid Parental Leave

Career Advancement Opportunities

Essential Functions:

Provide day-to-day leadership to a team of approximately 3-8 analysts, ensuring they are positioned to succeed and achieve both personal career goals and organizational objectives.Lead organizational change and build effective teams that apply their diverse skills and perspectives to achieve common goals.Revise and review specifications, SOPs, and other documents regarding QC and assay execution.Train and supervise staff in QC tasks, including technique-related training, SOPs, OJT, and knowledge assessments.Drive closure of deviations, investigations, and CAPA by actively participating in the discrepancy management process.Interact with auditors and clients during visits and tours.Oversee daily activities to ensure quality results.Perform performance management for direct reports.Prepare and assist in the writing of procedures in accordance with established standard lead times.Effectively communicate with peers, manufacturing, AD and QC staff to resolve technical issues and direct activities.Provide support to site Safety initiatives.Other job duties as assigned.

Education:

Bachelor's degree in physical science, preferably in Chemistry. Other science degrees, with experience in a pharmaceutical analytical laboratory, will be considered.

Experience:Minimum of 5 years' experience in quality/analytical/pharmaceutical industry or similar experience.Minimum of 1 year supervisory/team lead experience within the pharmaceutical industry in a QA/QC leadership role, preferably with a plant manufacturing focus.Knowledge of QC analytical techniques (e.g., HPLC, GC, KF, IR, optical rotation, etc.).Empower 3 experience for IPC and Chromatography group roles is preferred.

Competencies:Excellent knowledge and understanding of chemistry and analytical instrumental technologies.Excellent problem-solving skills and logical approach to solving scientific problems.Excellent proficiency with HPLC, GC, LC/MS KF, FTIR, and other wet chemistry methodology.Demonstrated proficiency in building relationships and exchanging information efficiently, both verbally and in writing.Good presentation skills.Good leadership skills.