Only the job description changed.
| Previous Job Description | Current Job Description | ||||
|---|---|---|---|---|---|
| t | 1 | Job Description: | t | ||
| 2 | The Quality Control Manager applies extensive knowledge of clinical radiopharmaceuticals to ensure t | 1 | The Quality Control Manager applies extensive knowledge of clinical radiopharmaceuticals to ensure t | ||
| > | he quality of investigational radiopharmaceuticals specified by the standards stated in the USP Chap | > | he quality of investigational radiopharmaceuticals specified by the standards stated in the USP Chap | ||
| > | ter <823> and the laboratory requirements of 21 CFR 212. This position will report to the Director o | > | ter and the laboratory requirements of 21 CFR 212. This position will report to the Director of the | ||
| > | f the Radiopharmaceutical Facility in the development of quality control standard operating procedur | > | Radiopharmaceutical Facility in the development of quality control standard operating procedures for | ||
| > | es for the investigational PET drugs such that the facilities, equipment, and inventory control meet | > | the investigational PET drugs such that the facilities, equipment, and inventory control meet the a | ||
| > | the associated regulatory requirements. This position will also assist in creating new approaches | > | ssociated regulatory requirements. This position will also assist in creating new approaches in the | ||
| > | in the quality control of novel radiopharmaceuticals for clinical use, and in working with the direc | > | quality control of novel radiopharmaceuticals for clinical use, and in working with the director in | ||
| > | tor in writing investigational drug applications (IND) and Abbreviated New Drug Applications (ANDA). | > | writing investigational drug applications (IND) and Abbreviated New Drug Applications (ANDA). The ba | ||
| > | The background for this position requires a minimum of a BS in chemistry or related subject with at | > | ckground for this position requires a minimum of a BS in chemistry or related subject with at least | ||
| > | least 5 years experience in a GMP radiopharmaceutical facility. | > | 5 years experience in a GMP radiopharmaceutical facility. | ||
| 3 | |||||
| 4 | Qualifications: | ||||
| 5 | Required Qualifications - Bachelor's degree in chemistry or related area - Minimum of 5+ years of re | ||||
| > | lated experience - 3 years’ experience in quality control of cGMP PET Radiopharmaceuticals - Advance | ||||
| > | d ability to effectively lead one or more projects with competing to meet the demands of a fast-pace | ||||
| > | d and dynamic work environment. Adaptable to quickly changing priorities - In depth critical thinkin | ||||
| > | g skills to evaluate issues and identify a potential solution. Creatively addresses complex or new p | ||||
| > | roblems - Advanced interpersonal skills, including but not limited to: problem-solving, teamwork dev | ||||
| > | elopment, leadership with other team members. Works well with others to achieve common goals Preferr | ||||
| > | ed Qualifications - Master’s degree in chemistry or related area - Knowledge of 21CFR212 and USP 823 | ||||
| > | regulatory requirements | ||||