Vice President, Quality

Summary:

The Vice President of Quality manages all quality assurance quality control and quality compliance functions at the Grifols Therapeutics (GT) site. The VP Quality will oversee the development of all policies practices procedures and specifications applicable to Grifols products manufactured in accordance with companys policies; and interface with other members of the senior management team at their respective sites as well at other Grifols locations technical departments customers suppliers and regulatory agencies in the review of issues and data.

Primary Responsibilites:
Oversees all Quality functions for Grifols Therapeutics.
Ensures that all biological products which are manufactured or distributed any GT location are manufactured and tested in compliance with company specifications and regulatory requirements.
Directs the establishment of Quality policies systems procedures and specifications for raw materials in-process product and finished products.
Establishes Quality systems and practices to assure compliance with state-of-the-art standards current GMP regulations (domestic and international) and corporatecrequirements.
Directs analytical method validations and QC execution to assure that appropriate information is collected specifications developed and methods established to assure the approval of IND/NDAs for all biotech compounds researched at GT or any other licenser that will be manufactured.
Directs Quality activities to insure that clinical supplies meet FDA requirements for Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) that are being used by Grifols clinical investigators to receive approved IND/NDAs on compounds to be marketed.
Participates in the technical review process and approves all new or modified products to be manufactured by GT before submission to the FDA for approval and/or release to the market.
Approves all Quality and Manufacturing procedures to ensure that all phases of operations conform to current GMP regulations. Assures that contract manufacturers of GT are in compliance with appropriate manufacturing practices and that product contract manufacturers meet the desired quality attributes as verified in GT laboratories.
Responsible for the establishment of appropriate quality policies standards and practices for manufacturing warehousing testing training release valiation documentation maintenance etc. at the GT facility.

Additional Responsibilities:
Coordinates activities of various GT departments whenever the recall of released products sold by the company and manufactured at the facility is required; Ensures Quality representation at appropriate industry associations by the Quality team in order to stay abreast of industry trends and new regulations in the areas of compliance/quality assurance/control and manufacturing practices; Actively participates in site and Grifols BioScience Group (BIG) Committees; Assist in establishing GT Quality Policies and Procedures; Maintains and updates manuals as necessary; Recommends staffing needs and organizes the activities of the various Quality functions for effective and economical operation; Provides for the timely and proper testing and release of raw materials components and finished products including new products for clinical trials; Makes final decision on discrepant materials and products; Prepares as well as approves budgets for Qualitys operating and capital expenses; and Makes final recommendations on major expenditures requested by the GT Quality organization.

Requirements Knowledge Skills and Abilities:
Requires a Ph.D. plus 15 years experience or an equivalent combination of education and experience. Advanced college degree level knowledge in chemistry biology and/or microbiology is required or equivalent experience to perform at a decision making level for Grifols Therapeutics. (MS plus 18 years)

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

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