QCD Analyst II- 2nd Shift

Kindeva Drug Delivery

Kindeva Drug Delivery (Legacy Meridian Medical Technologies) is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows.

ROLE SUMMARY

The QC Analyst 2 is a second level position with training 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.  This opening is on 2^nd Shift (1:45pm- 10:15pm).

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) with three years related experience and/or successful completion of a job-specific training program or equivalent combination of education and experience.
• Knowledge of cGMP regulations and documentation principles.
• Experience in use of measurement and testing equipment. 

California residents should review our Notice for California Employees and Applicants before applying. 
 
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