Quality Control Technician I

Job Opening for Quality Control Technician I, Carmel, NY : Client: Lannett Company 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

Job Opening for Quality Control Technician I, Carmel, NY : Client: Lannett Company 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