Micro Quality Control (Q/C) & Biology Analyst I or II

CLENE NANOMEDICINE INC; Maryland; On-site; USD 25,000 - 41,000; Full time

Benefits offered by this job

4 weeks paid leave

Paid holidays

Medical, dental, vision, and affordable

401(k) with employer match

Mon-Fri schedule

Job summary

CLENE NANOMEDICINE INC. is seeking a detail-oriented Micro Quality Control (Q/C) & Biology Analyst I or II to organize and perform testing activities with accuracy while managing workloads.

The role requires a bachelor’s degree in microbiology/biology and 1–4 years of related experience. You will follow SOPs, GMP/GLP, and internal processes, ensuring timely, precise test data and collaboration with management on production issues.

Qualifications

• Bachelor's degree in microbiology or related science.
• 1–4 years of related lab experience.
• Knowledge of USP testing procedures.
• Ability to follow SOPs and GMP/GLP guidelines.

Responsibilities

• Perform and monitor testing activities.
• Review and update work schedules to maintain testing cadence.
• Review testing results for report accuracy.
• Coordinate testing plans to ensure timely testing.
• Plan usage of laboratory materials to optimize testing levels.
• Collaborate with management on testing, quality, and production issues.
• Track deadlines based on project expectations.
• Gather, process, and analyze research and product data.
• Assist in establishing SOPs for testing and equipment.
• Help validate products and qualify technicians.
• Ensure GMP/GLP equipment calibration and IOPQ is current.
• Assist in acquisition/production of research-related materials.
• Participate in research and microbiology testing.
• Analyze and present research data.
• Perform other duties as assigned.

Skills

Analytical skills

Attention to detail

MS Office

Verbal & written communication

Education

Bachelor's degree in microbiology/biology

Tools

MS Office

Job description

Description

Join Our Team

We are seeking a detail-oriented and motivated Micro Quality Control (Q/C) & Biology Analyst I or II to join our team. In this role, you will organize and perform testing activities with accuracy and precision while minimizing workloads.

Benefits include:

• Up to 4 weeks paid leave
• Paid holidays
• Medical, dental, vision, and prescription insurance for employees and eligible dependents
• 401(k) retirement plan with employer match
• Monday-Friday schedule with normal business hours
• Opportunities for professional grown and continued learning

Requirements

Position Summary

The Micro Quality Control (Q/C) & Biology Analyst I or II follows all Standard Operating Procedures (SOPs), Test Methods (TSMs), Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal processes.

Essential Responsibilities

• 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.

Qualifications:

Education

• Bachelor's degree in microbiology/biology, or another related science field preferred.

Experience

• One (1) to four (4) years' experience in a related field.

Equivalent combinations of education and relevant laboratory experience will be considered.

Knowledge, Skills & Abilities

• 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 Requirements

• 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.

Compensation

$23 - $30 per hour, based on qualifications and experience.

Schedule

Monday through Friday

Normal business hours