This primary purpose of the Validation Specialist will be to support production and product quality. Verification and validation of equipment and documentation and products to ensure products are in accordance with company requirements.Responsibilities:* Support validation by developing validation documentation protocols and executing them.* Compiling data and authoring reports*Support new products, optimize processes, and technology transfers.*Support Quality Control and validate assays.*Support Quality Control instrumentation.* Participate in team projects in order to implement product development. * Maintain process and validation schedules and filing to company standards.* Training of staff and team growth support. * Stay current of all process technology and recommend improvements as needed. * Report to Quality Assurance manager status of Operations.Working hours: 8:00 AM - 5:00 PMSkills:* Validation and re-Validation of Quality Control assays preferred. * Qualification and re-Qualification of Quality Control testing and instrumentation preferred. * GMP experience. * Experience in Pharmaceutical and Biologics preferred.Education:BachelorsExperience:1-4 yearsQualifications:* 1 - 3 years applicable experience.* Bachelor's degree in Life Sciences field, or experience or training in a Pharmaceutical or Biologics environment. www.spherion.comSpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.