QC supervisor

Thermo Fisher Scientific•Florence, SC

8d•Hybrid

About The Position

This position will oversee a team responsible for one of three functions: Day shift, Chromatography group, or Wet chemistry group. These groups support raw material release, API (drug substance) release, in-process reaction completion testing and intermediate release, and stability testing in order to support the site’s fast-paced manufacturing needs. A key opportunity in this role will be the development of staff to grow into future roles within the site.

Requirements

Bachelor’s degree in physical science, preferably in Chemistry. Other science degrees, with experience in a pharmaceutical analytical laboratory, will be considered.
Requires a minimum of 5 years’ experience in quality/analytical/pharmaceutical industry or similar experience with a minimum of one year supervisory/ team lead experience within the pharmaceutical industry in a QA/QC leadership role, preferably with a plant manufacturing focus preferred.
Knowledge of QC analytical techniques is required (for example, HPLC, GC, KF, IR, optical rotation, etc.)
Excellent knowledge and understanding of chemistry and analytical instrumental technologies.
Excellent knowledge of qualitative and quantitative chemical analysis.
Excellent understanding of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs and descriptive organic chemistry.
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.
Excellent interpersonal and communication skills (both oral and written).
Good presentation skills to present information to customers, clients, and other employees.
Good leadership skills.
Ability to read, analyze, and interpret technical procedures and governmental regulations.
Ability to write standard operating procedures and policy manuals.
Ability to apply mathematical operations, to such tasks as determination of test reliability, analysis of variance, and correlation techniques.

Nice To Haves

Empower 3 experience for IPC and Chromatography group roles is preferred.

Responsibilities

Provide day to day leadership to a team of approximately 3-8 analysts by performing the following: leading organizational change; developing and empowering staff; cultivating relationships; putting staff in a position to succeed, meeting their personal career goals while also achieving organizational goals; building effective teams that apply their diverse skills and perspectives to achieve common goals; driving engagement and creating a climate where staff are motivated to do their best.
Revise/review specifications, SOPs, and other documents regarding QC and assay execution.
Train and supervise staff in order to perform QC tasks by ensuring completion of technique-related training, SOPs, OJT, and knowledge assessments, as well as ensuring on-going compliance to training and site SOPs.
Participate in the discrepancy management process.
Drive closure of deviations/ investigations/ CAPA.
Interact with auditors/clients during visits and tours.
Oversee daily activity for the group to ensure quality results
Performance management for direct reports.
Prepare and Assist in the Writing of Procedures (Standard Operating Procedures, Equipment Operating Procedures, Department Procedures, and Laboratory Investigations) 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.