Micro Quality Control (Q/C) & Biology Analyst I or II (based on experience) at CLENE NANOMEDICINE INC

North East, Maryland, United States -

Full Time

Start Date

Immediate

Expiry Date

11 Jun, 26

Salary

0.0

Posted On

13 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, Biology, Testing Activities, Media Preparation, Technician Qualification, Product Validation, SOPs, GMP, GLP, Data Analysis, Equipment Calibration, Research Procedures, Microbiology Testing, Analytical Skill Set, Attention To Detail, Computer Skills

Industry

Pharmaceutical Manufacturing

Description

Description The Micro Quality Control (Q/C) & Biology Analyst I or II position will organize and perform testing activities with accuracy and precision while minimizing workloads. This position provides support for the team through hands-on training, activity oversight (when needed), preparation of media, cleaning lab areas, technician qualification, and product validation. Excellent benefits package, including, but not limited to: - Up to 4 weeks paid leave. - Paid holidays. - Eligible for medical, dental, vision, and prescription coverage (employee & family). - 401(k) retirement plan with employer match. Requirements Essential Duties and Responsibilities This position is required to follow all Standard Operating Procedures (SOPs), Test Methods (TSMs), Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal processes. Duties will include, but not limited to: - Perform and monitor testing activities. - Review and update work schedules to effectively maintain the testing schedule. - Review testing results to ensure report accuracy. - Coordinate testing plans to ensure materials are testing according to schedule. - Plan usage of laboratory materials to ensure optimal testing levels. - Work with management to address issues regarding testing, quality, and production. - Manage deadlines based on project expectations. - Track production and research to help predict future scheduling needs. - Gather, process, analyze, and share research and product test data. - Work with management to establish SOPs for testing, equipment, and laboratory procedures. - Work with management to establish test methods, validate products, and qualify technicians. - Ensure GMP/GLP equipment calibration and IOPQ (mapping) are current. - Assist in the acquisition and/or production, if required, of research-related materials. - Work with management to design and enact research procedures. - Participate in research and/or microbiology testing. - Analyze and present research data. - Perform other duties as assigned. Education and/or Experience This position requires the following: - Bachelor's degree in microbiology/biology, or related science field. - One (1) to four (4) years' experience in a related field. - Exceptional analytical skill set and attention to detail. - Knowledge of USP testing procedures and FDS regulations. - Excellent computer skills, including, but not limited to, MS Office. - Excellent verbal and written communication skills with all levels. Physical Demands The physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Required to stand, walk, and talk or hear. - Ability to lift up to 50 pounds. - Ability to read and interpret documents such as, operating, maintenance, and procedure manuals. Work is normally performed Monday through Friday during normal business hours. Resume must accompany online application to be considered to this position.

Responsibilities

This role involves organizing and executing accurate and precise testing activities while supporting the team through training, oversight, media preparation, and lab cleaning. Key duties include performing and monitoring tests, reviewing results for accuracy, managing schedules, and ensuring compliance with SOPs and regulatory practices.