Quality Control Technician
ElancoWant to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.
Role Summary
Quality Control Technician
As a Quality Control Technician, you will be part of the Clinton Laboratories Quality organization supporting laboratory testing activities for oral solid dose medications. In this role, you’ll assist with sample handling, routine lab testing, and documentation to ensure products meet quality and regulatory standards. You’ll also help maintain lab equipment, follow standard operating procedures, and contribute to continuous improvement efforts within the lab. Experience with dissolution or solid oral dose testing is beneficial but not required; training will be provided.
Responsibilities
- Prepare, handle, and label samples to support quality control testing activities in accordance with GMP requirements.
- Perform basic laboratory tasks such as weighing, measuring, and recording data following written procedures.
- Maintain and clean laboratory equipment and work areas to ensure readiness and compliance.
- Document test data and observations accurately and promptly in accordance with company procedures.
- Support laboratory investigations and contribute to process and safety improvement initiatives.
Qualifications
- Education: High School Diploma or equivalent required; Associate’s degree in a scientific field preferred.
- Required Experience: Hands-on laboratory or manufacturing experience, ideally within a GMP or quality-focused environment.
- Top 2 skills: Strong attention to detail and comfort working in a laboratory setting following written procedures.
Preferred Qualifications
- Experience with oral solid dose testing methods such as dissolution or disintegration.
- Proficiency with Microsoft Word, Excel, and laboratory informatics systems.
- Strong written and verbal communication skills.
- Ability to handle multiple priorities while maintaining accuracy and compliance.
- Experience working in a GMP or manufacturing environment.
Additional Requirements
- Location: Clinton Laboratories – Clinton, IN – Onsite manufacturing laboratory environment (PPE required; exposure to allergens possible).
- Shifts: Rotation 12-Hour Day Shift (5:45-6:00 likely shift).
- Contract: This position is a fixed duration employee with a one-year contract, annually renewable for up to 4 years with a potential for a full-time position, based on individual performance and business needs.