Job Description

• Provide support to clients on quality issues such as OOS results, deviations and non-conformances.
• Provides Mirco EM Plate Verification
• Provides Sample submission verification along with raw material releases 
• Provides Quality oversight of operations and data review for accuracy, completeness, and conformance to current Good Manufacturing Practices (cGMP) and company quality standards.
• Provide training, executing audits, document creation, communication, and oversight to meet the established quality goals of the client and applicable regulations.
• Provide assistance in performing CAPA metrics reporting, review of cleaning logs and process enchancements

Qualifications

• Qualified candidates will possess a Bachelor’s degree in scientific or engineering discipline along with 5 plus years related industry experience.
• Proficient in Microsoft Word, Excel, Power Point and Project.
• Required: QC Mirco experience;  Environmental Monitoring (EM),
• General knowledge of quality system elements and cGMP regulations.
• Experience providing support to clients with quality issues such as OOS results, deviations and non-conformances arise. Also, provide advisement for the implementation of proper CAPA to resolve deviations and non-conformances.
• Ability to write and revise Standard Operating Procedures.
• Effective written and oral communication skills; ability to write, type, express or exchange ideas; ability to convey information/instructions accurately.
• Carry out duties and responsibilities with limited supervision.

Additional Information

All candidates must be legally eligible to work in the United States.

We are an equal opportunity employer. M/F/D/V

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.