Apex Systems QC Supervisor- Project Leads in St. Louis, Missouri
QC Supervisor- Project Leads in St. Louis, MO at APEX Systems
Date Posted: 1/5/2019
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- Employee Type:
St. Louis, MO
- Job Type:
Sci: Lab Mgmt
- Date Posted:
Job Description Job #: 915438
Supervisor, Quality Control (Project Leads and Technical Writers)
The Project Supervisor is the leader of the QC Analytical client relations, and will have overall operational management responsibility in completing the successful transfer of client processes and will serve as its primary spokesperson for QC Analytical.
This individual will manage the activities of all members of the Project and Technical Writers team and will be responsible for attending new client meetings as well as working with Program Managers to determine Timelines and Budgets for FTE Resources.
Provide leadership to assigned staff by performing the following:
Leading organizational change;
Developing and empowering staff;
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.
Lead activities of each client project to ensure that goals, objectives and ensure all elements of the QC process are accomplished within the prescribed period.
Review FTE assessments to determine time period, limitations, procedures for accomplishing project, staffing requirements, and allotment of available resources to various phases of project.
Establish work plan and staffing for each phase of project, and arrange for assignment of project personnel.
Supervision of all QC Project Leads and Technical writers assigned to each client project and ensures tasks are on schedule.
Recognize and solve potential problems and evaluate project/program effectiveness.
Interact with auditors/clients during visits and tours.
Bachelor’s Degree in a Biological Science related field and 5+ years related experience in biopharmaceutical or pharmaceutical industry.
At least 3 years supervisory/team lead experience within the pharmaceutical industry.
Extensive knowledge of GMP regulations in cGMP manufacturing environment.
Knowledge of scientific principles for wide range of analytical techniques strongly preferred. HPLC and ELISA experience with large molecules is preferred.
Apex is an Equal Employment Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at 844-463-6178