Now Hiring - Quality Assurance (QA) Specialist I | $21-$24/hour at CLENE NANOMEDICINE INC

North East, Maryland, United States -

Full Time

Start Date

Immediate

Expiry Date

10 Jul, 26

Salary

24.0

Posted On

11 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality assurance, Compliance, Standard operating procedures, Good manufacturing practices, Good laboratory practices, Cgmp principles, Attention to detail, Problem solving, Accountability, Time management, Ms office, Communication skills, Data analysis, Pharmaceutical industry knowledge, Biotech industry knowledge, Cgxp

Industry

Pharmaceutical Manufacturing

Description

Description Are you passionate about quality, compliance, and making a real difference in healthcare? Step into a role that will assist in the oversight of quality systems and support the Analytics and Operations groups for the manufacturing and testing of non-clinical and clinical products. As a Q/A Specialist I, you’ll help ensure our products and processes meet the highest standards of quality and compliance. You’ll thrive in a fast-paced environment where precision and accountability matter every day. Excellent benefits package, including, but not limited to: - Up to 4 weeks paid vacation. - Paid holidays. - Comprehensive health coverage – medical, dental, vision, and prescription for you and your family. - 401(k) with employer match – plan your future with confidence. Requirements Essential Duties and Responsibilities Key responsibilities include: - Follow all Standard Operating Procedures (SOPs) and internal quality processes - Understand Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). - Apply working knowledge of cGMP principles to daily tasks. - Maintain attention to detail and focus on accuracy, organization, and thoroughness. - Analyzie and resolve moderate to complex quality issues independently. - Demonstrate initiative and accountability in a dynamic, deadline-driven setting. - Manage multiple priorities effectively. - Perform additional quality-related duties as assigned Position Requirements - Associate or bachelor's degree in a related science-related field preferred but not required. - 2+ years' experience in the pharmaceutical or biotech industry in a GMP-compliant environment, preferred but not required. - Experience with cGxP (Current Good X Practices). - Strong computer skills, including MS Office. - Clear, professional communication skills, both verbal and written. - Ability to lift up to 50 pounds as needed. Salary - Competitive pay: $21-$24/hour (based on experience). - Consistent schedule, Monday to Thursday, 3pm to 1am. Apply Today Submit your resume with your online application to be considered.

Responsibilities

The QA Specialist will assist in the oversight of quality systems and support analytics and operations groups for product manufacturing and testing. Responsibilities include following SOPs, maintaining GMP/GLP compliance, and resolving quality issues.