Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:- Review and verify all manufacturing batch documentation, production records, and ensure the documentation complies with regulations and internal quality control practices.- Assist in reviewing and writing Standard Operating Procedures for manufacturing, and protocols for development, Installation Qualification (IQ) and Operational Qualification (OQ) and validations- Assist in routine internal audits, review deviations and investigations- Ensure compliance with Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's)Working hours: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Meticulous organizational skills and demonstrating meticulous documentation and record review practices- Technical writing experienceEducation:BachelorsExperience:1-4 yearsQualifications:- Associate's degree and/or one to three years of relevant experience- Must have previous technical writing experience- Experience working in a GMP facility or pharmaceutical environment is preferred- Experience with microbiology techniques is preferred Apply today at www.spherion.com/applySpherion 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.