What are the responsibilities and job description for the Quality Control 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 Control 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 QC Technician, you will:
- Perform analytical testing of Asteria Health products to support finished goods product release.
- Perform analytical testing to support cleaning validation activities.
- Identify and document Out of Specification (OOS) events as related to laboratory testing. Initiate Corrective and Preventative actions (CAPA) and conduct effectiveness checks.
- Communicate any OOS results immediately and effectively across departments.
- Review laboratory standard operating procedures and conduct change controls to revise and improve documents as necessary.
- Assist in the dissolution testing program. This includes building a sampling schedule and submitting samples to a third-party laboratory in a timely manner.
- Assist in laboratory method transfer work and setup of laboratory space at the new Asteria Health site.
- Ability to identify and initiate continuous improvement projects in the laboratory.
- Sample incoming raw materials for routine and full compendial testing.
- Perform other Quality Control tasks as assigned by the Quality Unit, such as reviewing continuous room monitoring data.
- Ability to troubleshoot and maintain UHPLC instruments.
- Assist with inventory of laboratory consumables, spare parts and equipment.
As the QC Technician, your background should include:
- Bachelor degree in the sciences, preferably with a Chemistry focus.
- At least three years (preferred) of practical experience in an analytical laboratory role.
- Experience working with cGMP guidelines and demonstrate expertise in a variety of the field’s concepts, practices, and procedures.
- Assumes responsibility for the accuracy of one’s work.
- Must exhibit excellent verbal and written communication skills.
- Must exhibit exceptional attention to detail.
- Multitasking skills and ability to meet deadlines in a fast-paced environment.
- Ability to work independently but in a team environment.
- Exceptional computer skills (data entry, Microsoft Office products, Adobe, eQMS).
- Excellent work ethic and reliability.
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!
