Responsibilities :
- Ensure compliance with all company policies and procedures.
- Monitor project progress to ensure deadlines are met.
- Develop and implement IQC plans, ensuring timely completion.
- Collaborate with management to create new quality control processes and procedures.
- Participate in regular staff meetings to address quality issues and concerns.
- Act as a liaison between management and various departments, including manufacturing.
- Conduct training sessions on quality control methods to ensure best practices.
- Review internal audit and investigation data to identify issues or necessary corrective actions.
- Assist in supervising incoming quality control inspections and other quality management system requirements.
- Perform data entry tasks.
- Maintain effective communication with other departments as needed.
- Report quality findings to designated parties.
Requirements :
- Experience with FDA regulations and compliance, preferably within a medical device company.
- Bachelor’s degree preferred but not required.
- Experience with Quality Management Systems (QMS).
- Proficiency in Microsoft Office, including Word, PowerPoint, and Excel (database analysis, complex formulas, pivot tables, etc.).
- Demonstrated experience in process improvement.
- Self-starter with strong attention to detail and the ability to prioritize tasks.
- Ability to maintain confidentiality.
- Strong organizational and time management skills with the ability to meet deadlines.
- Effective communication skills.
- Strong organizational and analytical skills.
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