Lab Tech I

About the role

This position supports quality control activities by coordinating the receipt and testing of samples, entering data into laboratory computer systems, and performing routine analytical testing of pharmaceutical products in a GMP laboratory setting.

Responsibilities

• Coordinate the receipt, labeling, and tracking of samples to ensure accurate and timely processing.
• Perform routine analytical testing on pharmaceutical products in support of quality control requirements.
• Operate basic laboratory instruments, including analytical balances, total carbon analyzers, spectrophotometers, and pH meters.
• Accurately input test data and sample information into laboratory computer applications and databases.
• Conduct preliminary data interpretation to assess test results and identify potential issues or inconsistencies.
• Follow established GMP laboratory procedures, protocols, and documentation practices.
• Maintain a clean, organized, and safe laboratory work area in accordance with internal standards.
• Apply problem-solving skills to troubleshoot basic instrumentation or testing issues and escalate when necessary.
• Communicate effectively with team members and other laboratory personnel regarding sample status, test results, and any observed deviations.
• Manage workload efficiently to meet testing timelines and support overall laboratory operations.

Requirements

• 0–3 years of laboratory experience, preferably in a GMP laboratory setting.
• Proficiency in basic lab instrumentation, including analytical balances, total carbon analyzers, spectrophotometers, and pH meters.
• Bachelor’s degree in chemistry or biochemistry, or an associate degree in a related scientific discipline.
• Strong attention to detail to ensure accurate testing, data entry, and documentation.
• Ability to stay well organized when handling multiple samples, tests, and data entries.
• Basic computer skills for data entry and use of laboratory software applications.
• Effective communication skills to collaborate with colleagues and report findings clearly.
• Demonstrated problem-solving abilities in a laboratory environment.

Additional Qualifications

• Experience with pharma or biotech quality control testing is preferred but not required.
• Familiarity with GMP laboratory practices and documentation standards.
• Ability to learn and follow detailed standard operating procedures.
• Capacity to work independently while also contributing to a collaborative team environment.

Work Environment

This position is based 100% on-site in a GMP laboratory setting in Waco, TX. The role involves working with pharmaceutical products and standard analytical instrumentation. The work is performed in a controlled laboratory environment that requires adherence to safety protocols and quality standards.

Laboratory attire such as appropriate clothing and any required personal protective equipment is expected to maintain safety and compliance.

Schedule

First shift, with typical hours of 8:00 a.m. to 4:30 p.m. The position may follow either a Tuesday–Saturday schedule or a Monday–Friday schedule, depending on operational needs.

Pay

The pay range for this position is $18.00 - $20.00/hr.

Benefits

Eligibility requirements apply to some benefits and may depend on job classification and length of employment. Benefits are subject to change and may include:

• Medical, dental, and vision
• Critical Illness, Accident, and Hospital insurance
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)