**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.

- Bachelors 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.