Lannett company Details

Lannett company

splintpharma - Carmel, NY

Employment Type : Full-Time

Quality Control Technician I

Scientific Search client has an immediate need for a Quality Control Technician I. This is a 6+ month contract engagement with a potential transition to perm.The Quality Control Technician I reports directly to the Quality Control Supervisor and is responsible for performing routine and non-routine sampling of raw materials and packaging components.  The Quality Control Technician I is also responsible for ensuring that sampling activities are properly documented in the ERP system.  The Quality Control Technician I works independently and assists with inspections of Quality Assurance reserve sample inspections.  Assist with special projects and other tasks as deemed necessary.

Summary:

• Lab sample management including storage and destruction of lab samples, including raw material, packaging component and finished product testing samples.
• Manage shipment of lab samples to third party laboratories as needed.
• Sampling raw materials and packaging components per required procedures and methods.
• Ensure that all sample quantities are accurately performed and are completed in a timely manner.
• including sample labeling and SAP inventory deductions.
• Management of the reserve sample program for raw materials and packaging components.
• Assists with the monthly inspection of finished product reserve samples.
• Audit the reserve sample program to ensure that maintained records are accurate.
• Ordering of required laboratory reagents.
• Responsible for monitoring the laboratory reagents to ensure that expired or unusable samples or materials are destroyed in a timely manner.
• Ensures that adequate sampling materials are always available.
• High School Diploma (or GED) and 0 – 3 years of laboratory technician experience or an Associate’s  Degree in Chemistry, Life Sciences or related degree with 0 – 1 years of experience, preferably within a pharmaceutical or manufacturing environment
• Knowledge of cGMP and other regulatory requirements
• Basic understanding pharmaceutical development and manufacturing
• Ability to wear PPE, gown up for sampling area.
• Ability to perform general office tasks
• Ability to lift 40 pounds