Senior Supervisor, Quality, QC

GRIFOLS, S.A.•Clayton, NC

5d•Onsite

About The Position

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Shift: Day Summary: Responsible for job assignments and supervising employees engaged in performing various Quality Control tasks (i.e. documentation review, product and laboratory investigations, product release, internal and external audit support) within Quality Control Environmental Assurance Laboratory. Participates in employee relations matters and is responsible for performance management in area of responsibility. May facilitate technical and non-technical training. (M10) level may occasionally be assigned the role of interim or acting Quality Manager, and other duties as assigned.

Requirements

Sr. Supervisor, Quality, QC: PHD in a Life Sciences or relevant degree with minimum of 4 years relevant experience. MS in a Life Sciences or relevant degree with minimum of 6 years relevant experience. BS in a Life Sciences or relevant degree with minimum of 8 years relevant experience.

Nice To Haves

Excellent communication skills (written and verbal) with demonstrated use of domestic and applicable foreign regulatory agency requirements/guidelines.
Demonstrated ability to influence decision makers in other departments.
Experience with SAP-QM, EXCEL, Word is preferred.
Experience managing, leading, and coaching employees, projects, teams, etc. is recommended.

Responsibilities

Directly supervise employees engaged in various QC related tasks as well as assign job duties or projects.
Ensures compliance with company policies and procedures and is responsible for optimum use of staff and technical capabilities within defined areas.
Provides technical/non-technical support on quality related matters.
Provides guidance or may consult with manufacturing and internal regulatory departments on GXP matters.
Follows cGMP and department safety practices.
Provides effective leadership to employees in Quality Control.
Demonstrates high levels of value and integrity.
Consults with QC Sr. Management regarding key decisions which need to be made within his/her defined areas of responsibility.
Apply expertise in testing to data analysis and reporting of data.
Serves as SME for laboratory assays and act as a resource for laboratory staff. Perform investigations and writing reports.
Author SOPs and other laboratory documents.
Collaborate with production and QA on projects, incident investigations, and annual product reviews.
Evaluate data and perform statistical analysis for various projects and reports.
Serve as system administrator and SME for various laboratory information systems and applications as required.