Pharmacist
Massachusetts General Hospital(MGH)
Charlestown, MA
5x8 hrs, Days

At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. When determining base pay, we take a comprehensive approach that considers your skills, relevant experience, education, certifications, and other critical factors. The pay information provided offers an estimate based on the minimum job qualifications, but it does not encompass all the elements that contribute to your total compensation package.

EDUCATION: Required: Bachelor's Degree Preferred: Doctoral Degree Field of Study/Additional Specialized Training: B. S. or higher in a pharmacy program is required. EXPERIENCE: Direct experience working with radiopharmaceuticals is required. Preferred to have 3-5 years of prior directly related experience. SUPERVISORY RESPONSIBILITY Direct: 2 (Laboratory Assistants, Technicians and Technologists) WORKING CONDITIONS: · Work is performed in the radiopharmaceutical facility of the Institute for Innovation in Imaging. Laboratory and office setting. · Must be able to lift 50 pounds. GENERAL SUMMARY/ OVERVIEW STATEMENT: Under the direct supervision of the Director of the Institute for Innovation in Imaging, the Nuclear Pharmacist will be part of our growing radiopharmaceutical production program. In alignment with existing facilities, this radiopharmaceutical production facility focuses on fluorine-18, gallium-68 and copper-64 based radiopharmaceuticals, and also developing new theranostics. The Nuclear Pharmacist will lead this facility and collaborate with existing facilities across the MGB network. PRINCIPAL DUTIES AND RESPONSIBILITIES: · Ensure compliance with all local and Federal, State, and Local regulations, USP <823> and <825> guidelines, Company Policies, Corporate Standards and Health and Safety rules related to area of responsibility. · Supervise and assist with radiotracer preparation, aseptic manipulation, and quality control. · Work with the Quality Assurance team to monitor overall integrity of the cGMP manufacturing process. · Coordinate cGMP documentation review and facilitate process documentation · Assist in documentation for IND and RDRC regulatory reviews. · Oversee inventory management for all chemicals, materials, supplies and equipment necessary to meet cGMP criteria. · Adjust par value inventory levels as necessary to meet future facility needs · Proactively identify backorder situations early enough in order to validate replacement components and as necessary, submit associated documentation to appropriate regulatory bodies if necessary. · Monitor all certified cleanroom ISO parameters required for daily aseptic operations. · Notify Engineering Department of any facility issues that are not meeting specifications and notify appropriate regulatory groups if necessary. · Oversee annual calibrations, preventative maintenance, certifications, and repairs of all analytical and associated equipment involve with the preparation of radiopharmaceuticals. · Facilitate, organize and document all daily temperature, humidity, differential pressure, and equipment checks to meet specifications. · Initiate, review, and complete all documented deviations, investigations (General or Out of Specification), and CAPAs to insure quality assurance. · Provide training and supervision to employees to assure all lab activities are performed in compliance with regulations and initiatives, Company Policies and Health and Safety rules. · Supervise and maintain cleanliness of lab in accordance with the facility housekeeping schedules. · Supervise and/or perform daily radiation wipes and surveys on outgoing shipping containers, pharmacy supplies, incoming RAM packages, work spaces, and equipment. · Identify and report any quality or compliance concerns and take immediate corrective action as required · Actively participate in maintaining a safe work environment by completing required training, providing suggestions for improving the health and safety program and bringing unsafe acts and/or conditions to the attention of management. · Work with Institute for Innovation in Imaging leadership in establishing research relationships with biopharma SKILLS & COMPETENCIES REQUIRED: · Ability to accommodate schedule changes based on user needs. · Ability to communicate effectively and in a professional manner, both with co-workers and study staff. · Ability to cultivate a positive and inclusive work environment. · Ability to prioritize job duties (i.e. successfully balances proactive versus reactive tasks). · Handles multiple tasks quickly without forfeiting quality. · Excellent command of underlying theory (e.g. chromatography method development and radiotracer synthesis optimization). · Strong organizational and communication skills. · Excellent judgment and ability to interpret information and protocol requirements. · Aptitude for technical problem solving. · Ability to supervise and train staff effectively. · Ability to make independentand effective decisions that are in the best interest of the lab. · Ability to adapt to shifting priorities in response to changing deadlines and work requirements. · Flexibility to deal positively with organizational changes. · Ability to anticipate problems and develop contingency plans to deal with them. · Ability to maintain high productivity in stressful situations. · Ability to challenge proposed actions in a way that facilitates constructive discussion. · Willingness to become an authorized user of radioactive materials. LICENSES, CERTIFICATIONS, and/or REGISTRATIONS: Licenses: Nuclear Pharmacist in MA or eligible for reciprocation Certifications: Preferred: Quality Assurance / Board certification in nuclear pharmacy

Recruiter: Hinton, Shayla