Lab Tech I

Actalent; Texas; On-site; USD 25,000 - 28,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability benefits

HSA

Transportation benefits

Employee Assistance Program

PTO / Vacation

Job summary

Actalent is seeking a Lab Tech I to support quality control activities in a GMP laboratory, coordinating sample receipt and testing, entering data, and performing routine analytical testing of pharmaceutical products.

The role involves operating basic instrumentation, interpreting test data, and maintaining accuracy and reliability of QC results. Candidates should have 0–3 years of lab experience and a relevant degree.

Qualifications

• The candidate has 0–3 years of laboratory experience, preferably in a GMP setting.
• Bachelor’s degree in chemistry or biochemistry or related science is required.
• Attention to detail and accurate data entry are essential.
• Ability to work on-site in a GMP lab and follow SOPs.

Responsibilities

• Coordinate receipt, labeling, and tracking of samples for timely processing.
• Perform routine analytical testing on pharmaceutical products.
• Operate basic lab instruments: balances, carbon analyzers, spectrophotometers, pH meters.
• Enter test data into laboratory systems accurately and securely.
• Interpret data to identify potential issues and deviations.
• Follow GMP procedures and maintain proper documentation.
• Keep workspace clean, organized, and safe.
• Troubleshoot basic instrumentation and escalate when needed.
• Communicate results and sample status to team members.

Skills

Lab experience

Analytical instruments

Data entry

GMP familiarity

Communication

Education

Bachelor’s degree in chemistry or biochemistry

Tools

Laboratory software

Job description

Job Description

Job Title: Lab Tech I

Job Description

The Lab Tech I 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. This role involves operating basic laboratory instrumentation, interpreting test data, and contributing to the accuracy and reliability of quality control results 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 elevate 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.

Essential Skills

• 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 Skills & 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 is a 6-month contract and involves working with pharmaceutical products and standard analytical instrumentation such as analytical balances, total carbon analyzers, spectrophotometers, and pH meters. The work is performed in a controlled laboratory environment that requires adherence to safety protocols and quality standards. The schedule is 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. Laboratory attire such as appropriate clothing and any required personal protective equipment is expected to maintain safety and compliance.

Job Type & Location

This is a Contract position based out of Waco, TX.

Pay and Benefits

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

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms.

If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 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)

Workplace Type

This is a fully onsite position in Waco,TX.

Application Deadline

This position is anticipated to close on Aug 13,