Job Title: Quality Specialist I Duration: 2 year contract Location: Hybrid Role - 3 days onsite - 770 Sumneytown Pike, West Point, PA 19486 Pay Range: $35- $39.92/hr. **Notes/requirements:** + Prefer quality experience(QA/QC) in batch record deposition. + Operations in packaging clinical supplies. + Previous SAP is nice to have. + Veeva is nice to have. **Qualifications:** **Education:** + Bachelor's Degree or higher in engineering, science, or related discipline. **Required skills and experience:** + **Minimum 2 years of experience in the pharmaceutical or equivalent industry, Good Manufacturing Practice (GMP) related field including Technical, Engineering, Quality or Operations.** + **Familiarity with batch disposition activities** + Strong problem-solving, and written and oral communication skills + Ability to manage multiple priorities + Demonstrated teamwork skills and ability to work independently + Proficiency in the use and maintenance of Microsoft applications (Excel, Outlook, and/or MS Access, Teams) + Attention to detail, flexibility and an awareness of production and quality control problems. **Preferred skills and experience:** + Proven ability to work independently and collaborate effectively as part of a team. + Strong organizational, interactive, and time management skills. + Computer skills; knowledge and competency in ERP/MES, SAP **Responsibilities:** + Our client's department supports the release of clinical supply to global clinical trials. Primary duties may include but are not limited to the following: + Evaluation and disposition of clinical supply materials with the assurance that the materials were produced in conformance to all applicable policies/procedures of our Company and compliance with all governing regulations. + Coordinate and/or support the preparation of procedures, processes and quality improvements. + Completing projects to improve the performance of our processes, including continuous process improvements, and value capture projects that seek to improve yield, reduce cost, or lower our processing cycle times. + Assists in the coordination of significant quality events including fact finding, investigation support + Actively using and championing the use of Lean Six Sigma and our company's Production System (MPS) tools, both in problem solving and day-to-day operational activities. ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.