At Safecor Health, we pride ourselves on creating a culture built on Care, Commitment, and Excellence. These core values guide every interaction, decision, and relationship within our organization.
As we continue to grow, we are seeking a dedicated and experienced Part Time Weekend Shift Quality Associate to join our dynamic team. In this role, you will be responsible for a variety of tasks related to quality assurance, documentation, training, and compliance within the pharmaceutical industry. You will work closely with multiple departments to ensure Safecor Health's high standards for quality, safety, and regulatory compliance are consistently met. This position is an exciting opportunity for someone passionate about quality assurance and pharmaceutical operations. The Quality Associate is responsible for ensuring that products and processes meet established quality standards and regulatory requirements.
Days/Hours: Saturdays/Sundays ONLY, 7:00am-5:30pm
Key Responsibilities:
- Ensure compliance with industry regulations, standards, and internal quality procedures.
- Provide training and support regarding quality assurance practices and standards.
- Stay up to date with changes in industry regulations and best practices.
- Create and manage labels for all Safecor Health business segments.
- Facilitate end-of-day processes for documentation filing and QAD updates.
- Track and document controlled substance samples and manage DEA 222 forms.
- Investigate and document unplanned deviations and incidents in collaboration with Operations.
- Lead and execute Quality Audits, including data assembly and report writing.
- Participate in incoming inspections for repackaging components or drugs.
- Conduct final quality checks on delineated repackaging formats.
- Ensure timely communication with customers regarding quality-related issues.
- Perform in-process quality checks and final inspections on commercial lots.
- Conduct daily and monthly control retain sample audits.
- Facilitate the destruction of Rx and OTC drugs quarterly, at year-end, and as needed.
- Communicate effectively with management and peers about inspection results or deviations.
- Collaborate with drug manufacturers to obtain necessary product-related information.
- Monitor adherence to Good Manufacturing Practices (GMP) across all operations.
- Lead by example and embody Safecor Health’s Core Values of Care, Commitment, and Excellence in every aspect of your work.