What are the responsibilities and job description for the Quality Control Coordinator position at Katalyst Healthcares & Life Sciences?
Company Description
- Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
- We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description
Job Description:
The QC Coordinator I is responsible for receiving, verifying, documenting, distributing, and archiving QC test samples. Sample receipt and testing completions are tracked by the QC Coordinator to report status updates daily. The QC Coordinator also distributes and maintains the integrity and accuracy of QC sample inventories for in-coming samples. Other duties could include administrative functions such as filing, archiving QC data, and consumable monitoring.
Responsibilities:
- Receiving, verifying, labeling, distribution to test labs, documenting and archiving QC test samples.
- Manage all paperwork that accompanies each sample and verifies quantities and items received for correctness.
- Maintenance and report out of daily metrics.
- Verifies and distributes QC samples to each functional QC group.
- Maintain the integrity and accuracy of QC sample inventories.
- Requisition new samples, references, and consumables, managing receipt and distribution.
- Communicate with QC and MFG teams within Operations via e-mail and phone or in person to track material movements.
- Perform other related duties and assignments, as required.
- Follow Quality, ISO, and Environmental, Health & Safety requirements.
- Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
- Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements.
Requirements:
- High School diploma or equivalent experience in lab or QC environment is required.
- College coursework in biology or the life sciences is preferred.
- A minimum of one year in a manufacturing, laboratory, or inventory control environment is required.
- Experience with SAP preferred.
- Intermediate computer skills preferred: MS Windows, word processing, Excel, experience with database and information management systems.
- Knowledge of general laboratory safety, familiar with GMP preferred.
- Effective interpersonal, written and oral communication skills.
- Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs.
- Effective analytical and problem-solving skills.
Additional Information
All your information will be kept confidential according to EEO guidelines.
