Quality Control Technician

As a Pro Med employee, you will contribute to the manufacture of products that have a significant impact on people’s lives. Through honesty, integrity, and collaboration, we strive to be the very best as we hire the very best.

Pro Med was founded in 1989 addressing an industry need for cleanroom manufacturing of silicone components, specifically those having a medical application. We treat every component and finished device as though it will be used by a beloved family member or friend. We are dedicated to our customers and to our employees while helping to improve the health and well-being of people around the world.

Working as one to help many.

The Quality Technician is responsible for day-to-day administration and support as applicable to the organization’s environmental monitoring, preventative maintenance and calibration, facilities control, material management, pharmaceutical operations and cleaning verification/validation. This position operates under minimal guidance from management or senior staff. The Quality Technician ensures Pro Med’s brand, philosophy, systems, policies, and procedures are properly implemented and observed.

Position duties and responsibilities include, but are not limited to the following:

• Perform and document routine environmental monitoring of clean rooms and controlled areas and test/send samples to approved testing laboratories.
• Interpret sampling results, maintain trending spreadsheets, and complete data review forms.
• Author (annual) trend reports.
• Standardize/Assist with updating sampling maps in the event of room changeover.
• Coordinate with Facilities for scheduling of and accompany cleanroom certification/testing contractors.
• Maintain inventory of consumable testing supplies, submit purchase requisitions to restock.
• Monitor Dickson One and address/assist with any excursions.
• Review and trend preventative maintenance and calibrations.
• Review and trend pest control logs, vendor reports and issues.
• Perform cleaning verification/validation swabbing and submit samples to analytical lab for testing.
• Perform sampling of materials for QC testing, retains, and retesting.
• Assist with incoming material inspection records.
• Assist in updating or revision SOPs/forms/templates for clarity and accuracy.
• Review of logbooks.
• Assist with line clearance and checks.

• Identify and elevate gaps, inconsistencies, or potential compliance risks within the QMS to the QA Manager.
• Participate in internal audits and self-inspections as assigned; support corrective action follow‑up activities.
• Support the implementation of regulatory changes and quality system improvements as directed;
• Assist in preparing responses to audit observations or regulatory findings that involve document or records management.

This job also requires performing other duties as assigned.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Required:

• Bachelor’s degree in Life Sciences, Chemistry, Microbiology, or a related field.
• 0-3 years of experience in a regulated industry (pharmaceutical or biotech).
• Knowledge of GMP principles and FDA regulatory requirements (21 CFR Parts 210/211 and/or 820).
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
• Knowledge of ALCOA+ data integrity principles.

Preferred:

• Familiarity with eQMS platforms (e.g., Master Control, Veeva Vault, Agile, Track Wise) even if primary system is paper-based.
• Experience with EU GMP, ICH Q7, ICH Q2(R1), and/or ISO 13485 requirements.
• Ability to work autonomously, effectively manage time and deliver results on time.
• Attention to detail and commitment to data integrity and accuracy in all quality records.
• Effective written and verbal communication skills; ability to clearly document processes, decisions, and deviations.
• Strong organizational skills with the ability to manage multiple priorities,…