Supervisor, QC Sterility & Microbiology
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. The selected candidate will responsible for job assignments and supervising employees engaged in performing various Quality Control (QC) tasks (i.e. laboratory testing, documentation review, laboratory investigations & CAPA, test release, etc.). Participates in employee relations matters and is responsible for performance management in area of responsibility. May participates in technical and non-technical training, and other duties as assigned.
Requirements
- Excellent communication skills (written and verbal)
- Basic knowledge/understanding of domestic (i.e. Food and Drug Administration) and applicable foreign regulatory agency requirements/guidelines.
- BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 3 yrs of relevant experience or an equivalent combination of education and experience. Experience managing, leading, and coaching employees, projects, teams, etc. is recommended
- BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 5 yrs of relevant experience or an equivalent combination of education and experience. Experience managing, leading, and coaching employees, projects, teams, etc. is recommended
- BA/BS - preferably in a STEM (science, technology, engineering, or mathematics) curriculum and 6 yrs of relevant experience or an equivalent combination of education and experience. 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.
- 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.
- 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 area of responsibility.
- Apply expertise in testing to develop, validate and troubleshoot analytical methods.
- Serve as SME for laboratory assays and act as a resource for laboratory staff.
- Perform investigations and write reports.
- Author SOPs and other laboratory documents.
- Collaborate with production and Quality Assurance and Compliance on projects, incident investigations, and annual product reviews.
- Evaluate data and perform statistical analysis for various projects.
- Serve as system administrator and SME for various laboratory information systems and applications as required
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Manager
