Quality Assurance Specialist II/III (Production/Manufacturing QA) (ADX-261-20)
Quality Assurance Specialist II/III (Production Manufacturing QA) (ADX-261-20)
THE COMPANY: ArcherDX, Inc. - www.ArcherDX.com
ArcherDX is advancing molecular diagnostics with a robust technology platform for genetic mutation detection by next-generation sequencing. By combining patented Anchored Multiplex PCR (AMP™) chemistry in an easy-to-use, lyophilized format and powerful bioinformatics software, the Archer® platform enhance genetic mutation identification. ArcherDX provides oncology-focused research products and is pursuing regulatory approval for multiple companion diagnostic assays. ArcherDX is headquartered in Boulder, Colorado. Learn more at www.archerdx.com and follow @ArcherDXInc on Twitter, Facebook and LinkedIn.
POSITION SUMMARY:
The Quality Assurance Specialist, reporting to a Quality Engineer, will support Production/Manufacturing processes by maintaining quality system compliance in a regulated environment on a day-to-day basis.
RESPONSIBILITIES:
- Assigned as direct QA support to production/manufacturing of ArcherDX assay components and processes.
- Support of other Production-related activities including raw materials receipt/transfer/release, labeling verification, kitting verification, QC report review, shipping verification, etc.
- Timely review of batch records (Travelers) and product release.
- May assist with validation activities (IQ/OQ/PQ) of processes, methods, and equipment.
- May assist in managing equipment, including installation and monitoring of maintenance and calibration.
- May assist Quality Engineers with audit response and follow up on required actions.
- May assist with the management of Nonconformance reports, and Corrective and Preventive Actions reports, and complaints.
- Maintain compliance with all company policies, quality systems, and procedures.
- Perform other duties as assigned by supervisor.
QUALIFICATIONS:
- 2+ years of experience within quality assurance in a medical device industry. (Pharma/biotech are acceptable).
- Experience with FDA 21 CFR 820 and ISO13485 regulations.
- Attention to detail and ability to follow directions in modifying the documentation
- Ability to interact and collaborate with multiple disciplines, and communicate clearly and effectively verbally and in writing
- Ability to work with minimal direction, and utilize good problem-solving skills
- Ability to multitask and work within a fast-paced dynamic team environment
EDUCATION:
- Bachelor’s Degree in a scientific field