What are the responsibilities and job description for the Quality Assurance Technician position at Biote?
Biote is the world leader in hormone optimization and we are adding to our team! We partner with providers to take a complete approach to healthier aging through patient-specific bioidentical hormone replacement therapy and the only nutraceutical line created specifically to support hormone health.
We are looking to add a Quality Assurance Tech to our Birmingham team. You must reside in the Greater Birmingham area to be considered as this will be an in-office position.
As the QA Technician, you will:
- Ensure training documentation for all Asteria personnel is complete and up to date.
- Ensure documentation for group and individual training is assigned as part of change control activities.
- Shadow all departments at Asteria Health to learn tasks and roles. Be able to provide training and qualifications and assist with the development of new training materials as part of continuous improvement.
- Print off and review cleaning logs, equipment logs, and room usage logs.
- Assist the Quality Assurance Specialist with batch record review and communicating any issues to the appropriate personnel.
- Review standard operating procedures and conduct change controls to revise and improve documents as necessary.
- Applies current Good Manufacturing Practice (cGMP) requirements, guidelines and practices.
- Review product labels prior to printing.
- Documentation of minor complaints and deviations.
- Attend all required meetings and provide clear, professional verbal and email communications.
- Complete special projects assigned by Quality Unit such as filing, scanning and data entry.
- Assist the Quality Unit with change control activities.
As the QA Technician, your background should include:
- Continued education in science, or similar.
- At least two years (preferred) of practical experience of in a Quality role in an FDA regulated company.
- Experience working with cGMP guidelines and demonstrate expertise in a variety of the field’s concepts, practices, and procedures.
- Experience working with Production or Manufacturing.
- Must exhibit excellent verbal and written communication skills.
- Must exhibit excellent attention to detail.
- Ability to work well independently and in a team environment.
- Good computer skills (data entry, Microsoft Office products, email, internet, eQMS, and inventory management software systems).
Additional Notes
- Must be able to gown for ISO 8 area.
- Must be able to work in a variety of positions and locations such as sitting, standing, squatting, kneeling, reaching, and walking, for prolonged periods of time.
- Must be able to use necessary equipment such as computers, scanners, phone/headset, or other technological devices as assigned.
If you would like to learn more about this opportunity, please consider applying today and let's connect!
