Technologist I – Qc
Company | Werfen |
---|---|
Location | San Diego, CA, USA |
Salary | $19 – $24 |
Type | Full-Time |
Degrees | Bachelor’s |
Experience Level | Entry Level/New Grad, Junior |
Requirements
- High school diploma required; Bachelor’s degree in Science or equivalent experience preferred.
- Phlebotomy certification required.
- Understanding of Good Laboratory Practices (GLP) preferred.
- Previous experience in a Quality Control (QC) lab and/or Quality Assurance (QA) role within regulated medical device manufacturing or In-Vitro Diagnostic device (IVD) manufacturing.
- Knowledge of FDA-GMP/QSR and ISO standards for quality a plus.
- Good written and verbal communication skills.
- Ability to work as part of a team.
- Basic skills with common laboratory techniques, such as pipetting and use of balances.
- Basic skills with Microsoft Office suite.
- Basic skills with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems a plus.
Responsibilities
- Operate as a phlebotomist.
- Perform testing finished goods per relevant SOP.
- Assist with testing as required for product validation and process validation on existing products.
- Maintain proper laboratory housekeeping and ensure adequacy of supply levels in the QC laboratory by informing appropriate personnel of low supply levels as required.
- Document all finished goods test results and maintain product release records (including electronic records).
- Document existing product/process validation test results (including electronic records).
- Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs.
- Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes.
- Other duties as assigned.
Preferred Qualifications
- Bachelor’s degree in Science or equivalent experience preferred.
- Understanding of Good Laboratory Practices (GLP) preferred.
- Knowledge of FDA-GMP/QSR and ISO standards for quality a plus.
- Basic skills with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems a plus.