Quality Control Lab Technician

Kindeva Drug Delivery Company; California (MO); On-site; USD 50,000 - 70,000; Full time

Job summary

Kindeva Drug Delivery Company is seeking a Quality Control Lab Technician responsible for ensuring the quality of materials and products through thorough inspection and testing. The position requires adherence to strict regulatory standards, including cGMP and FDA guidelines. Ideal candidates will have 3+ years of experience in a regulated environment and a high school diploma or GED. This role offers a chance to contribute to life-saving products in a collaborative environment.

Qualifications

• 3+ years related quality control experience in a highly regulated industry.
• Knowledge of cGMP regulations and documentation principles.
• Experience in using measurement and testing equipment.

Responsibilities

• Inspects components, assemblies, drug product containers, and packaging for conformance.
• Performs physical testing of assemblies and finished devices.
• Follows GMP documentation practices on labeling and test records.

Skills

cGMP regulations

quality control

documentation principles

measurement and testing equipment

Education

High School/General Education Development (GED)

Job description

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Quality Control Lab Technician engages in statistical sampling, inspection and physical testing of incoming materials for conformance to approved written specifications, Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), and Food and Drug Administration (FDA) regulations.

Typical hours for this role are: Monday - Thursday: 5:30 am- 2:00pm and Friday: 5:30 am- 2:00 pm with the option of working 2:30 am -11:00am

Role Responsibilities

• Inspects components, assemblies, drug product containers, packaging and labeling according to approved written material specifications.
• Performs physical testing of assemblies and finished devices according to approved written material specifications, test records and batch records.
• Creates in-process and carton labeling according to approved bill of material documents.
• Follows GMP documentation practices on labeling, logbooks, test records, batch records and other controlled documentation.
• Understands and utilizes American National Standards Institute (ANSI) sampling plans.

Basic Qualifications

• High School/General Education Development (GED)
• 3+ years related quality control experience in a highly regulated industry.
• Knowledge of cGMP regulations and documentation principles.
• Experience in use of measurement and testing equipment.

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!