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Grifols Shared Services North America, Inc Supervisor I/II/III, Quality, QC in Clayton, North Carolina

Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic, Hospital and Bio Supplies - develop, produce and market innovative medicines, solutions and services in more than 100 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, investigations, 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.

ESSENTIAL DUTIES and RESPONSIBILITIES include the following. Other duties may be assigned.

  • 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

Required Skills:

  • Excellent communication skills (written and verbal)

  • Basic knowledge/understanding of domestic (i.e. Food and Drug Administration) and applicable foreign regulatory agency requirements/guidelines.

Education and Experience Requirements by Level:

Supervisor I, Quality, QC - 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

Supervisor II, Quality, QC - 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

Supervisor III, Quality, QC - 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

Shift: 3rd Shift Sunday-Thursday 10:00PM-6:30AM

Work is performed in an office and/or a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office equipment. Exposure to extreme cold below 32

  • , miscellaneous production chemicals, moving machinery and production equipment. Exposure to high levels of noise on production floor. Personal protective equipment required such as protective eyewear, garments and gloves. Frequently sits for 4-6 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Occasionally walks. Often performs duties standing. Frequently bends and twists neck and waist. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Frequently drives to other facilities. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Frequently interacts with others, relates sensitive information to diverse groups.

EEO Minorities/Women/Disabled/Veterans

Req ID: 280627

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