Validation Specialist I​/Validation Specialist II

Position: Validation Specialist I / Validation Specialist II
Location: Clayton

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.

Location:

Clayton NC

Overview:

Validation Specialist I / Validation Specialist II position to support commissioning and validation for Fibrinogen Building and other future capital projects. This position is responsible for assigned qualification and validation related activities related to supporting the Clayton NC site.

Primary responsibilities for role include but are not limited to the following:

* Actively manages and completes all phases of assigned equipment, facilities, utilities and process qualification and validation activities.

* Facilitates cross functional problem-solving involving Quality Operations, Regulatory Affairs, Engineering and Manufacturing.

* Makes independent decisions within defined areas of responsibility.

* Write protocols, reports and validation master plans and assembles final validation report packets as required to meet qualification/validation objectives.

* Authors, reviews, and executes qualification and validation documents within a defined Quality system.

* Schedule and perform qualification and validation studies to meet timelines.

* Evaluate and analyze qualification/validation data collected, while verifying acceptability of the data and compliance with the protocol.

* Conducts discrepancy investigations and identifies and implements effective root cause corrective actions (CAPAs).

* Reviews engineering drawings (P&IDs, construction, as-built, flow diagrams) for compliance to GMP/Validation principles and provides feedback to project team for any noted deficiencies or improvements.

* Participates in meetings as the validation representative for assigned projects involving project planning, scope development, design, construction, startup, qualification, validation and administration.

* Interacts regularly with project team members and influences overall scope development and communicates with all levels of employees within and outside the team.

* Reviews qualification/validation turn-over packages for completeness and accuracy, compliance with policies and procedures and accurate data analysis.

* Prepare, program, maintain and use various data acquisition systems including Kaye Validators and Kaye Valprobes.

* Use other test equipment such as tachometers, thermometers, hygrometers and differential pressure monitoring devices as required for qualification protocols.

Skills/Qualifications/

Education Requirements:

(To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions)

Specialist I - Requires a BS/BA degree in STEM (Science, Technology, Engineering, and Mathematics). An equivalent combination of education and experience may be considered. The job requires a minimum of 2 years' experience in the pharmaceutical industry.

Specialist II - Requires a BS/BA degree in STEM (Science, Technology, Engineering, and Mathematics). An equivalent combination of education and experience may be considered. The job requires a minimum of 4 years' experience in the pharmaceutical industry.

* A technical background encompassing engineering, instrumentation, biology, chemistry, microbiology, statistics, and thermodynamics is desirable.

* Familiarity with plasma fractionation and purification, aseptic processing, filling, sterilization, GMP regulations, and Quality Operations is desirable.

* Must have knowledge of the principles of equipment design/operation and validation of at least 2 of the following:
Utilities (HVAC, WFI, clean steam, compressed process air and nitrogen), Filtration (Sterile, depth, filter presses), Purification (chromatography, ultrafiltration, nanofiltration), steam sterilization, Clean-In-Place systems and processing vessels.

* Large capital project validation experience preferred.

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. Example:
If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience.

Work is performed in an office and a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure to infectious…