Quality Assurance Technician

We are seeking a QA Technician to join our team. In this role, you will help support our mission by ensuring high-quality execution of daily responsibilities, maintaining accuracy, and contributing to a collaborative environment focused on patient care and continuous improvement.

The role is responsible for performing quality activities in a sterile pharmaceutical manufacturing facility. The candidate should understand pharmaceutical cGMP requirements. The position requires an individual who works independently and in a team environment, with attention to detail, and maintains communication with other functional areas and sites.

Location:

Albany, OH
Job Type: Onsite, Full Time Permanent

Schedule:

Monday-Friday, 8:00 AM-4:30 PM
Compensation: $22/hour

• Release all components, drug product containers, closures, packaging, labeling, in-process materials, and finished products.
• Monitor storage conditions of the manufacturing environment, materials, and products.
• Maintain document control through review, approval and issuance of SOPs, batch records, labels and other controlled documents.
• Review and retain all records associated with batch issuance, work instructions, release of product and all quality management data
• Review laboratory data of the finished drug product, environmental monitoring, microbiological testing, chemical testing, in-process testing and stability testing.
• Identify adverse trends and recommend improvements.
• Communicate with Production and Shipping/Receiving to ensure appropriate materials and supplies inventory are appropriately qualified, documented, and suitable for intended use in manufacturing.
• Investigate, review and trend deviations, OOS results and customer complaints.
• Support equipment calibration, equipment/utility/facility validation, and preventive maintenance.
• Participate in reviews of process qualification and product quality.
• Manual QMS, including document control of SOPs, batch records, controlled documents, training module, and all quality activities.

• 1+ years' experience in a quality position at a cGMP facility. Fundamental knowledge of cGMP regulations as well as quality management systems.
• High School Diploma required, Bachelor's Degree preferred
• Experience in investigating and writing customer complaints
• Excellent written, verbal communication and presentation skills
• Ability to think and act independently while knowing when to include others in decisions
• Ability to work in a dynamic, fast paced and timeline-driven environment with shifting priorities
• Strong understanding of Microsoft Office and Excel software
• Strong problem solving and decision making skills

• Competitive compensation and benefits
• Opportunities for growth and career development
• A supportive, team-first culture where your work matters
• The ability to make a real impact on animal health every day

Wedgewood Pharmacy is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where everyone can thrive.

Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.