QA Associate - Laboratory
Montrose Environmental Group•Richmond, VA
•Onsite
About The Position
As a QA Associate, you’ll be responsible for assisting multiple projects where you will have increasing interaction with our multi-disciplinary staff, regulatory agencies and clients. You will be part of a strong team of committed professionals. The hourly compensation range for this role is $20.00 to $23.00, commensurate with experience, skills, and geographic location. Schedule: Monday - Friday
Requirements
- Bachelor’s degree or equivalent in a scientific field, or a combination of education, training, and experience.
- 1+ years of relevant experience working in a laboratory or quality assurance role (or equivalent).
- Strong understanding of scientific terminology, analytical laboratory procedures, and lab safety.
- Understanding of physical and chemical principles underlying why procedures are specified the way they are for each method with which they work.
- Good written and verbal communication, with sharp editorial and proofreading abilities.
- Ability to collaborate with lab teams to gather, interpret, and document data.
- Good organization, time management, and communication skills and able to facilitate priorities in an effective manner.
- Proficiency in Microsoft Office (e.g., Word, Excel, SharePoint, and PowerPoint).
- Conflict resolution skills and removes/breakdowns organizational communication barriers.
- Assertion skills-problem diagnosis, assess corrective action, not blame.
- Ability to handle multiple tasks simultaneously while maintaining composure.
- A team player who can work independently and thrives in a collaborative, fast-paced, quality-driven environment.
Nice To Haves
- Familiarity with TNI 2016, ISO 17025 standards, GDP, CAPA, or RCA is a plus.
- Experience with LIMS.
- Proficiency using and data visualization tools for reports and graphs.
Responsibilities
- Track or perform verifications of laboratory supply equipment to ensure operational reliability per SOP and manufacturer specifications.
- Perform daily/weekly reviews of appropriate logbooks, bench sheets, or data for Good Documentation Practices (GDP) compliance.
- Initiate and address non-conformances for corrective actions.
- Collect and interpret quality control data, create control charts, and audit sample reports to track lab performance and identify trends.
- Track CAPA and perform or assist with Root Cause Analysis (RCA).
- Conduct routine internal audits of laboratory processes, documentation, and facilities.
- Prepare audit checklists, reports, and follow-up on findings.
- Accurate and timely communication with internal and external clients.
- Draft, review, and/or revise SOPs, work instructions, forms, or other controlled documents.
- Review and enter Proficiency Testing (PT) data and results.
- Troubleshooting and problem-solving.
- Develop and deliver in-laboratory GDP, ethics, data integrity, safety, and technical training.
- Maintain training records and competency assessments.
- Archive documents in accordance with SOPs.
- Review laboratory data, workflows, and procedures to ensure accuracy and compliance with TNI 2016, ISO 17025, client requirements, and our robust quality system.
- Support external audits.
- Communicating relevant updates to applicable people in a timely manner.
- Adhere to documented quality manual, policies, and health and safety practices and protocols (i.e., use of PPE, chemical hygiene, and waste handling).
- Take on additional duties and responsibilities as needed to support our dynamic lab team.
Benefits
- We are committed to providing access and reasonable accommodation in its employment for individuals with disabilities.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
