Quality Control Intern - Bioanalytical

The Quality Control Intern - Bioanalytical - is responsible for supporting the QC laboratory by assisting in routine analytical testing and assisting with general laboratory operations. Working under the direct supervision of laboratory management, this role includes sample preparation, data recording, and maintaining a clean and compliant laboratory environment. The Quality Control Intern - Bioanalytical operates under current Good Manufacturing Practices (cGMP) and/or Good Laboratory Practices (GLP), ensures adherence to established procedures, and maintains accurate, timely documentation.

• Assist with performance of routine QC analytical procedures on raw materials, drug products, and stability samples using established procedures and validated analytical methods.
• Accurately document all experimental procedures, raw data, observations, and results in compliance with cGMP, GLP, and internal SOPs.
• Maintain a clean, organized, and safe working environment.
• Comply with environmental monitoring requirements and lab safety policies, including proper aseptic handling and personal protective equipment (PPE) use.
• Work effectively within the QC Team, supporting shared goals and timelines. Communicate clearly with team members and QC management regarding status updates, issues, or delays.

• Pursuing Bachelor’s degree in relevant scientific field;
  Preference given to 3rd or 4th year undergraduate students
• Excellent attention to detail to ensure accurate testing, documentation, and compliance with strict regulatory standards.
• Strong written and verbal communication skills and the ability to effectively interact with others across the organization as well as the ability to effectively present information in one‑on‑one and small groups.
• Demonstrated proficiency in Microsoft Office software (Word, Excel, PowerPoint and Outlook)
• Basic mathematical skills including addition, subtraction, multiplication and division, calculating concentrations, dilutions, molarity and basic statistical analysis.
• Exhibit high level of service orientation, confidentiality and professionalism
• Ability to follow instructions and work with general supervision to deliver work product
• High attention to detail and deliver work of expected quality in a timely manner
• High level of interest in learning and applying skills in a business environment

Duties will be performed in normal laboratory and occasionally in BSL2 laboratory.

Travel is not typical for this position.

Ability to regularly move up to 10 pounds. Specific vision abilities required by this individual include close vision, peripheral vision, and the ability to adjust focus. The employee will view a computer monitor for long periods of time.

The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

SAB BIO is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. SAB BIO is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non‑disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets