What are the responsibilities and job description for the Quality Control Lab Technician position at Kindeva Drug Delivery Careers?
Our Work Matters
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
Equal Opportunity Employer:
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!
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.
- 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.
Equal Opportunity Employer:
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!
