Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to provide software validation and equipment calibration support to manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:BachelorsExperience:1-4 yearsQualifications:- Bachelor???s degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus Apply today!Spherion 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.