QA Production Analyst
POSITION SUMMARY
Responsible for compliance and continuous quality improvement within the production area. Responsible for monitoring production daily activities in regards to compliance to SOP’s and cGMP’s, follow through with appropriate actions needed. Follow all quality department SOP’s including any actions taken. Contribute to and support the company’s quality initiatives through individual and team contributions.
MINIMUM JOB QUALIFICATIONS AND REQUIREMENTS
· Two years of college with an emphasis in a science related field or minimum 3 years of work experience in a cGMP environment.
· Must possess good computer skills to be proficient in Microsoft office. Be able to learn quickly in house computer programs.
· Good working knowledge of cGMP’s.
· Strong written and communication skills to include the ability to be effective in working with production operators and supervision, writing of deviations and nonconformance’s.
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES
· Conducting detailed production audits and enforcing strict cGMPs. To ensure the highest quality is produced by continually striving to improve company and quality SOPs.
· Conduct daily production audits to monitor production performance within cleanliness, sanitization, dispense, blending, encapsulation, bottling, labeling and documentation accuracy and completeness.
· Inspect and monitor all in-process materials and finished goods.
· Create paperwork for any nonconformance issues, collect data, and report to QA management/production management for complete follow through.
· Audit all production electronic paperwork (PCLE) to include checklists, data reporting, releases and rejections for completeness.
· Recommend and initiate procedures to prevent errors or to improve quality in all areas of production and quality.
· Generate daily pass down for QA production auditors and QA supervisor.
· Workweek hours may extend as needed per production schedule.
· Assist in providing labels as needed to production staff.
· Perform other duties and responsibilities as assigned.
WORK ENVIRONMENT
· Daily work is on the production floor, standing/walking the majority of the time.
· Working around powders and odors.
ProCaps Laboratories is an Equal Opportunity Employer.
Pre-employment Drug Testing is a condition of employment.