We are looking for a remarkable QA Specialist I to join our cohesive team at Varite, Inc in Frederick, MD.
Growing your career as a Full-Time QA Specialist I is an outstanding opportunity to develop competitive skills.
If you are strong in presentation, adaptability and have the right personality for the job, then apply for the position of QA Specialist I at Varite, Inc today!
Specific Job Responsibilities: - Performs a variety of activities to ensure compliance with applicable regulatory requirements.
- Maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs).
- Supports site Quality Systems programs (Deviation, CAPA, CC, etc...)
- Works with operating entities with guidance from senior colleagues to ensure that inspections, statistical process control analyses and audits are conducted on a continuing basis as specified to enforce requirements and meet specifications.
- May support root cause analysis investigations and corrective actions
- Provides visibility on key site metrics to site leadership and escalation issues as needed.
- Normally receives general instruction on routine work, detailed instructions on new assignments.
Knowledge: - Demonstrates basic knowledge of current Good Manufacturing Practices (GMPs) and/or Good Laboratory Practices (GLPs).
- Demonstrates basic knowledge of FDA / EMEA standards and quality systems.
- Demonstrates good verbal, written, and interpersonal communication skills.
- Demonstrates working knowledge in Microsoft Office applications.
Specific Education & Experience Requirements:- 2+ years of relevant experience in a GMP environment related field and a BS.
- 3+ years of relevant experience and an AA degree.
- Prior experience in regulated industry is required.
- Pharmaceutical industry experience is beneficial.
Benefits of working as a QA Specialist I in Frederick, MD:
● Excellent benefits
● Professional Development Opportunities
● Generous Compensation
No CV Required
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