Grifols Shared Services North America, Inc Associate Director, Quality Assurance in San Diego, California
Grifols is a global healthcare company whose mission is to improve the health and well being of people. Our three divisions –Bioscience, Diagnostic and Hospital–develop, produce and market our innovative products and services to medical professionals in more than 100 countries.
We are committed to fostering an environment that creates continuous learning opportunities and encourages professional development and growth. As a company devoted to improving the health and well-being of people, we are looking for talented professionals worldwide. Make a difference and join us in this challenging and rewarding enterprise.
To direct the day to day to day activities of the Grifols Diagnostic Solutions Manufacturing QA consisting of: QA Technical, QA Validation, QA Lot release. Ensures that his/her QA organization units coordinate with Manufacturing, Engineering, Validation and Manufacturing Sciences (MS) groups to investigate product quality issues and ensure Quality oversight for Validation. Direct the QA managers and associates to examine Quality processes that can be streamlined and improved.
This is a full time position located in San Diego, CA, reporting to the Director of Quality (Technical Director), Grifols Diagnostic Solutions.
Primary responsibilities for role:
Direct the day to day activities of the Manufacturing QA – QA Technical, QA Validation and QA Lot release. Manage a staff of approximately fifteen (15) individuals responsible for the designated QA functions. The individual will also be responsible for being the Single Point Of Contact/Subject Matter Expert during all health authority (FDA, TUV) inspections for Manufacturing QA, ensuring that his/her QA team(s) investigates production non-conformities/deviations, ensuring that NCRs/DRs and CAPAs are reviewed and closed on time. Collaborate with Manufacturing, MS, Validation and Regulatory Affairs departments as necessary.
Owns the procedures that govern the Quality Assurance functions and ensures that all documents are approved and in alignment with the applicable Grifols Quality Standards
Ensure that his/her QA teams conduct thorough investigations and product impact assessments in accordance with local procedures
Cross-functional coordination with other Quality teams for deviations impacting multiple areas
Ensures that his/her QA Validation staff reviews/approves validation documents that are in alignment with site validation master plans and procedures
Ensure that his/her QA staff are trained and that training records within Grifols Training Platform (GTP) are up to date
Ensure that internal trending reports and Product Quality Indicators (PQIs) are completed and reported on time in Site Quality Committee (SQC) and Management Review (MR) meetings
Coordinate with the Engineering group to ensure that equipment utilized at the site is calibrated and maintained per the required schedule
Coordinate with Engineering to assess changes to Facilities, Utilities and Equipment
Coordinate with MS to ensure release testing methods are transferred per the approved SOP/protocols
Champions the continuous improvement of QA processes, defines process improvement/efficiency projects for QA,
Champions the risk assessement of Production and QA processes
Select, train and develop staff so that they realize their full potential and work in conformance to company policies relating to environmental protection, health and safety at work.
Work with Site Environmental Health & Safety (EH&S) representatives to ensure that the Process QA organization adheres to Grifols EH&S standards, requirements and best practices while working in the plant.
Key Performance Indicators / Measures for Success:
Completion of PQI reports within the required times
Completion of Product Quality Impact Assessments and Investigation and closure of NCRs/DRs and closure of CAPAs within the required time within his/her QA units
QA Single Point Of Contact (SPOC) and Subject Matter Expert (SME) during FDA and other health authority inspections for matters related to QA Technical, QA Validation, QA Lot release
The number of QA Validation/CPV and Facilities/Utilities/Equipment related DRs defended to regulatory agencies during product review or site inspections.
The number and severity of GMP issues identified during internal and external audits related to Quality Assurance oversight of QA Validation, CPV and Facilities/Utilities/Equipment QA.
Efficiency of QA operations.
No safety incidents or HSE related observations.
Bachelor’s degree in Biochemistry, Molecular Biology, Immunology or related science or MS/PhD degree in science related science or appropriate education and experience in Medical Device, IVD or biological/pharmaceutical manufacturing field
At least 10 years experience in a regulated GMP/ISO/QSR environment (biotechnology, blood banking, diagnostics, medical device or biopharmaceutical industries) and a minimum of 7 years management experience
Experience with Process, Cleaning, Facilities/Utilities/Equipment and Analytical Method Validation
Experience with technical investigation of deviations and performing product impact assessments and product complaints
Strong scientific analytical and writing skills, proficient in MS Word, MS Powerpoint and MS Excel software
Must be familiar with GMP's and Quality System Regulations (QS Regs) and practical judgment in the interpretation and application of regulations and standards specific to Quality Assurance
Experience working with FDA licensed biologics and performing as Quality Single Point Of Contact (SPOC) and Subject Matter Expert (SME) during FDA inspections for matters related to Technical QA, QA Validation.
Must be able to think abstractly about data and be able to work with a team toward shared goals.
Must have good planning and organizing skills, manage time effectively by prioritizing tasks, taking the initiative to solve problems quickly, and knowing when to obtain assistance.
Individual must work in an ethical manner and ensure employees follow Grifols ethics and compliance guidelines.
Must meet the six (6) mission critical competencies listed below
Specific Professional Competencies:
Six Mission Critical Competencies:
Is dedicated to meeting the expectations and requirements of internal and external customers; gets first-hand customer information and uses it for improvements in products and services; acts with customers in mind; establishes and maintains effective relationships with customers and gains their trust and respect.
Has the functional and technical knowledge and skills to do the job at a high level of accomplishment.
Is cool under pressure; does not become defensive or irritated when times are tough; is considered mature; can be counted on to hold things together during tough times; can handle stress; is not knocked off balance by the unexpected; doesn’t show frustration when resisted or blocked; is a settling influence in a crisis.
Is bright and intelligent; deals with concepts and complexity comfortably; described as intellectually sharp, capable, and agile.
Is effective in a variety of formal presentation settings: one-on-one, small and large groups, with peers, direct reports, and bosses; is effective both inside and outside the organization, on both cool data and hot and controversial topics; commands attention and can manage group process during the presentation; can change tactics midstream when something isn’t working.
Is easy to approach and talk to; spends the extra effort to put others at ease; can be warm, pleasant, and gracious; is sensitive to and patient with the interpersonal anxieties of others; builds rapport well; is a good listener; is an early knower; getting informal and incomplete information in time to do something about it.
Location: [[mfield6]] : [[cust_building]]
Learn more about Grifols at http://www.grifols.com/es/web/international/home