About this role
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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. |
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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.
Primary 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.
Additional Responsibilities:
- 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.
- 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.
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.
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : NC-Clayton:USNC0002 - Clayton
Other facts
About GRIFOLS, S.A.
Grifols is a global healthcare company founded in Barcelona in 1909 committed to improving the health and well-being of people all over the world.
A leader in essential plasma-derived medicines and transfusion medicine, we develop, produce and provide innovative healthcare services and solutions in more than 110 countries.
Patient needs and our ever-growing knowledge of many chronic, rare and prevalent diseases, sometimes life-threatening, drive our innovation in plasma-based therapies and other biopharmaceuticals to enhance quality of life.
Grifols is focused on treating conditions across a broad range of therapeutic areas: immunology, hepatology and intensive care, pulmonology, hematology, neurology and infectious diseases.
With a workforce of over 23,000 employees in more than 30 countries and regions, we are committed to a sustainable business model that sets the standard for continuous innovation, quality, safety and ethical leadership in the industry. Our work has a positive social and economic impact in the countries where we operate, creating jobs and generating wealth.
People are at the heart of what we do, and we strive to create an inclusive, diverse, fair and equal society. Maintaining and promoting a workforce that reflects this reality leads to enhanced professional relationships and helps us to give our best to patients, donors and customers.
In 2024, Grifols was named one of TIME’s ‘World’s Best Companies’ for the second year in a row, reaffirming our commitment to excellence. We were also recognized by Forbes as one of the "Best Employers for Women 2023," reflecting our dedication to fostering an inclusive and supportive workplace for all.
To maintain a positive community and overall respectful communication, please keep our community guidelines in mind.
What you'll do
- The Senior Supervisor is responsible for supervising employees performing Quality Control tasks and ensuring compliance with company policies. They provide technical support and guidance on quality-related matters and consult with senior management on key decisions.
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