Quality Associate/ Sr. Quality Associate Materials Evaluation Coordinator

Grifols, S.A; Clayton (NC); On-site; USD 40,000 - 80,000; Full time

Job summary

Join an innovative healthcare company dedicated to improving lives worldwide. As a Quality Associate/Sr. Quality Associate, you will play a crucial role in ensuring product quality through rigorous inspections and audits. Your expertise in quality assurance and compliance will directly impact the safety and efficacy of life-saving products. This position offers a dynamic work environment where you can leverage your skills and knowledge in a meaningful way. If you are passionate about quality and healthcare, this is an exciting opportunity to contribute to a global leader in the industry.

Qualifications

• Minimum of an Associates degree in sciences or mathematics or equivalent experience.
• Prior inspection experience in manufacturing components or packaged goods.

Responsibilities

• Perform quality audits of materials and packaging at the facility.
• Evaluate quality attributes of unlabeled final containers and finished products.
• Train new employees and serve as a Subject Matter Expert.

Skills

Assessment Skills

Effective Communication

Computer Skills

Knowledge of cGMP

Technical Drawing Interpretation

Education

Associates degree in sciences or mathematics

Tools

SAP

Job description

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Quality Associate/ Sr. Quality Associate Materials Evaluation Coordinator

Location:

NC-Clayton, US

Contract Type: Regular Full-Time

Area: Quality

Would you like to join an international team working to improve the future of healthcare? 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.

Position Summary:

The Quality Associate/Sr. Quality Associate Materials Evaluation Coordinator performs in the Packaging area as a Quality representative for sampling, auditing, and making Quality decisions. In this area, the Quality Associate/Sr. Quality Associate Materials Evaluation Coordinator audits unlabeled final container vials, media, syringes and finished product batches using designated ANSI sampling plans. Additionally, the responsibilities include reserve sampling, post-pack identity sampling, packaging commodity verification and reconciliation, line clearance verification, and stability sample inspection. The Quality Associate/Sr. Quality Associate Materials Evaluation Coordinator inspects product final container reserve samples according to approved standard operating procedures. Decisions made by Quality Associate/Sr. Quality Associate Materials Evaluation Coordinators have major compliance and monetary implications for Grifols.

Primary Responsibilities:

• Evaluate critical quality attributes (visual, dimensional, functional) of unlabeled final containers and finished product, and execute required SAP transactions on all quality audits of material inspected and packaged at the facility.
• Stay abreast of the rapidly changing requirements of various regulatory agencies, as new policy changes have immediate impacts on Materials Evaluation responsibilities and release of material to production.
• Perform quality verification of component issuance, vial etch, production order picklists of products packaged at the Clayton site. Non-verification of primary and secondary packaging components could lead to material or plasma product recall and will impact product market availability.
• Possess extensive knowledge of cGMP, company specifications, and packaging operating procedures.
• Serve as trainers to new employees in all aspects of this position and are considered to be a Subject Matter Expert (SME).

Knowledge, Skills & Abilities:

The incumbent must possess keen assessment skills and the ability to distinguish insignificant deviations from significant deviations that jeopardize the integrity of the product to be released. The incumbent must be able to learn and understand the concepts of statistical sampling used in daily activities. Computer skills are required. Must be able to read and understand technical drawings. Effective communication skills, including proper grammar, are essential in order to report (both in writing and verbally) data and product impact. Must keep neat, accurate, and complete records of material evaluations and release activities performed. Tactful human relations skills are essential to achieve cooperation between business partners and customers.

Incumbent must have prior inspection experience (i.e. manufacturing components, packaged goods, etc.)

Education:

Requires minimum of an Associates degree with an emphasis in sciences or mathematics or an equivalent combination of education and experience is acceptable.

Experience:

A minimum of one year of related experience, preferably as a packaging inspector or in Materials Evaluation, is required for the Quality Associate/ Sr. Quality Associate Materials Evaluation position.

Equivalency:

Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements.

Occupational Demands:

When working with raw material chemicals and product, the incumbent must be able to wear all required safety equipment such as protective eyewear, garments and gloves and able to work with limited supervision. Must demonstrate initiative and have the ability to defend a decision based on specifications and procedures. In addition, the incumbent must have near vision correctable to at least 20/20 in one eye and 20/40 in the other eye, have no color blindness, excellent color and depth discrimination, and be able to lift up to 50 lbs. The incumbent must be able to successfully pass the certification requirement for product final container visual inspection.

Work is performed in an office and a manufacturing environment or warehouse. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to occasional extreme cold below 32* in production areas. Personal protective equipment required such as protective eyewear, garments and gloves. Work is performed sitting or standing for 10 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements of the fingers to grasp and manipulate objects. Light to moderate lifting and carrying objects with a maximum lift of 35lbs. Occasionally walks, bends and twists neck and waist, may reach above or below shoulder height. Frequent foot movements. Color perception/discrimination and near vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate complex 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. Performs tasks by following a set of written or oral instructions/procedures.

Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws.