Validation Technician
GRIFOLS, S.A.
Summary
Principal responsibility is to support validation engineers through assistance with testing and protocol execution, and data analysis.
Job description
Primary responsibilities for role:
- Support validation engineers through assistance with testing and protocol execution, and data analysis
- Perform pre and post calibrations of thermal monitoring equipment, place probes, and generate reports and graphs of data
- Maintain calibrated state of thermal mapping equipment
- Monitor use and age battery life of wireless loggers
- Collect samples during cleaning, testing and validation, as well as generate test forms and submit samples to QC
- Perform documentation during protocol execution in support of validation engineer protocols, as assigned
- Assist with ensuring paperwork from other departments is available and complete when required
Requirements
- Associates degree or equivalent in a technical or scientific discipline
- Experience in an FDA regulated manufacturing facility - pharmaceutical, biologics, biotech, or medical device industry is preferred
- Any relevant experience in Validation is preferred
- Knowledge of cGMPs, FDA regulations, and industry guidelines is preferred
- Must be able to read, write, and speak English
- Self-starter with the ability to work independently with minimum supervision and use good judgment
- Proactive, results oriented, with a strong attention to detail
- Ability to keep neat, accurate and complete records and logs
- Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner
- Ability to meet deadlines, and handle an ever-changing, fast-paced critical work environment
- Strong organizational, analytical and problem-solving skills
- Ability to analyze details and perform structured decision-making on a daily basis
- Familiarity with Excel, Word and experience with creating reports in these software types
- Experience in a technical workplace environment
- Demonstrate responsibility and accountability in a team environment
Benefits
- Medical, Dental & Vision
- Life insurance
- Paid time off
- Paid holidays
- 401(k) match
- Tuition reimbursement
- Bonus pool up to 5%
Company overview
Grifols, S.A. is a global healthcare company and leading producer of plasma-derived medicines, founded in Barcelona, Spain in 1909. As the European leader and third largest plasma-derived medicine manufacturer worldwide, Grifols specializes in developing, producing, and marketing essential plasma-derived protein therapies for patients suffering from rare, chronic, and life-threatening conditions. The company operates across four main business units: Biopharma (plasma-derived medicines), Diagnostic (transfusion medicine and clinical diagnostics), Bio Supplies (biological materials for research), and Healthcare Solutions for Hospitals. With over 23,800 employees serving more than 110 countries, Grifols maintains 15 industrial facilities across seven countries and operates approximately 400 plasma donation centers globally. The company focuses on therapeutic areas including immunology, infectious diseases, pulmonology, hematology, hepatology, intensive care, and neurology, with more than 1,200 researchers working across 12 R&D centers worldwide. Grifols is publicly traded on both the Madrid Stock Exchange (GRF) and NASDAQ (GRFS), generating approximately €7.2 billion in annual revenue.