Scientist

Title: Quality Control Laboratory & Clinical Animal Operations Scientist

Pay Rate: $21 hr.

Benefits include health, dental, and vision (following 60 days of employment)

Employment Type: Contract

Est. Start Date: 09/07/2026



Est. End Date: 09/05/2027



Schedule: Monday-Friday, 6AM-2:30PM

Location: Charles City, IA 50616



Job Code: JPC-12561

Tekberry is looking for a highly qualified and motivated Quality Control Laboratory & Clinical Animal Operations Scientist to work on-site with our client, the world's largest producer of vaccines and medicine for pets and livestock. As a W2 employee you will have access to health benefits.

Responsibilities:

First half of contract: Bacteriology/Immunology QC laboratory supporting product testing and GMP-compliant operations.

Second half of contract: Clinical/animal-side operations supporting product release studies and laboratory animal handling in a regulated environment.

The technician will perform routine testing and support activities under supervision while following company quality systems, regulatory requirements, and safety and animal welfare standards.

Bacteriology/Immunology Laboratory (first half of contract):

• Test samples from manufacturing to ensure quality and compliance using applicable assays and good aseptic practices.

• Perform pipetting and other routine bench techniques to support assay execution.

• Prepare media and reagents; support media fill inspections.

• Maintain testing schedules and assist with reagent/supply planning to ensure uninterrupted workflow.

• Complete documentation in accordance with cGMP and data integrity expectations.

• Clean and maintain laboratory equipment, instrumentation, and facility areas; support routine equipment monitoring.

• Follow all applicable quality standards, policies, and procedures.

• Provide minimal input/support for laboratory investigations (LIR) and other assigned project support.

• Develop working knowledge of QC software used in routine work, including MODA EM and zLIMS/SAP.

• Follow established safety practices at all times.

Clinical/Animal-Side Operations (second half of contract):

• Perform product release safety and potency testing under supervision, following established regulatory and company standards.

• Maintain laboratory animal care by adhering to best practices and ethical responsibilities consistent with IACUC, AAALAC, and other regulatory guidelines.

• Accurately record laboratory observations and test results; promptly report deviations or concerns to senior team members.

• Assist with monitoring and maintaining inventory levels of animal/lab supplies and equipment to support consistent workflow and compliance.

• Support upkeep, cleanliness, and routine maintenance of work areas to maintain a safe, organized, and compliant environment.

• Build understanding of assigned testing requirements to communicate effectively with senior staff and the team leader regarding testing schedules and animal distribution.

• Contribute to a collaborative, solutions-focused team culture that supports continuous improvement and ethical conduct.

• Develop knowledge of the on-site IACUC, its expectations, and the application of Animal Usage Protocols (AUPs).

• Participate in laboratory investigations as directed, assisting with data collection and reporting when needed.

Qualifications:

• High school diploma or equivalent required; Associate's or Bachelor's degree in Biology, Microbiology, Immunology, Animal Science, or related field preferred.

• Ability to follow written procedures (SOPs), work instructions, and quality documentation requirements.

• Demonstrated attention to detail and ability to maintain accurate records.

• Comfort working in a regulated environment with strict adherence to GMP/GLP, safety, and animal welfare standards.

• Willingness to work across both laboratory and animal/clinical environments during the contract term.

Preferred Qualifications:

• Experience with aseptic technique, media preparation, and routine microbiology/immunology testing.

• Familiarity with cGMP documentation practices and deviation/investigation support.

• Experience using laboratory/QC systems such as MODA EM, LIMS, and/or SAP (or comparable platforms).

• Prior experience working with laboratory animals and understanding of IACUC/AUP expectations.

We need hard-working, reliable employees.

Tekberry Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected categories under all applicable laws.

Tekberry, Inc is a Certified Minority Business Enterprise (MBE) and Certified Disadvantaged Business Enterprise (DBE).

By submitting your resume, you are explicitly consenting to receive communications from our organization via text message. Rest assured all our texts are sent by real people and we look forward to a conversation with you about this job!

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