Manufacturing Analyst, Continuous Improvement

Adare Pharma Solutions Recruiting Team • Vandalia, OH

2d

About The Position

This position supports manufacturing operations by analyzing production data, monitoring key performance metrics, and identifying opportunities for continuous improvement. This role assists with quality deviation investigations, root cause analysis, and operational error tracking to improve right-first-time performance. The Manufacturing Analyst also supports documentation management, internal audits, and compliance initiatives while providing data insights that help drive operational efficiency and reduce risk.

Requirements

• Bachelor’s Degree in Business Administration or a sufficient combination of work experience and training.
• Ability to perform mathematical calculations.
• Knowledge of cGMPs compliance.
• Must be capable of effectively communicating in both oral and written manner
• Must be able to provide accurate and affirmative instructions and reports to employees and management.
• Must be able to organize, plan, and control.
• Must have flexibility to work any shift or schedule with short notice.
• Proficient writing and speaking English

Responsibilities

• Complete trending data for each production batch for future analysis.
• Assist in monitoring and reporting department metrics on a continual basis.
• Assists in quality deviation investigations and supports root cause analysis.
• Develop and maintain a system for monitoring and reporting department metrics on a continual basis. Including a right the first-time matrix to track operational errors and develop recommendations for reduction in errors.
• Develop and maintain QA trending spreadsheets, review trending for potential issues or future OpEx initiatives.
• Provide documentation services to the Manufacturing department including writing, revising, formatting, processing, filing, and maintaining documents, including electronic files.
• Support Production Manager in reducing compliance risk by aiding in performing internal audits and developing action items to correct risks.
• Support and promote Safety and cGMP programs, ensuring strict conformance to all current FDA and cGMP guidance’s and guidelines.
• Support all Continuous Improvement efforts within the department.
• Perform other tasks as required.

Benefits

• Medical/dental/vision/life – low employee premiums
• 401k with a highly competitive match
• Generous PTO, including floating holidays
• Career growth and internal opportunities
• Tuition reimbursement
• Relocation assistance
• Performance-based bonus
• Employee Recognition Programs

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 11-50 employees