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Mgr, Manufacturing Cyclotron
$106k-132k (estimate)
Full Time 0 Months Ago
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Jubilant DraxImage, Inc. dba Jubilant Radiopharma is Hiring a Mgr, Manufacturing Cyclotron Near Atlanta, GA

Jubilant DraxImage, Inc., a nationwide radiopharmaceutical company, is dedicated to nuclear medicine. We use our 25 years of experience in Nuclear Pharmacy to provide our customers with the best service and safest products. The Jubilant Radiopharmacies Network of facilities positions us to serve national GPO’s, regional systems, as well as standalone clinics and hospitals. Through our open formulary, we provide choice by giving our customers access to all radiopharmaceuticals available, allowing them to better serve their patients. Jubilant Radiopharmacies provides the strength of national coverage while remaining connected to our local community. We are patient-focused and community-driven to ensure that we are intimate with our healthcare partners’ needs.

We are currently seeking a Manager, Manufacturing Cyclotron to support our pharmacy inAtlanta, GA.

RESPONSIBILITIES:

  • Assist in the development and communication of goals for PET Manufacturing Facility (PMF) and individual staff that support the organization’s mission and performance goals; Ensure facility is meeting the outlined goals and objectives;
  • Administer the PET operations budget; Monitor current revenues and expenses and analyze and report on variances from plan; Oversee accounts payable and receivable; Provide corporate accounting with weekly statistics reports, monthly operations and financial statements, and assist Accounts Receivable in collections;
  • Interview, select, recommend hire, train and supervise assigned staff; Provide leadership and direction to staff and assist in the investigation and resolution of problems; Evaluate performance and provide counseling and coaching to team members; Assist in personnel actions, such as promotions, transfers, terminations, or disciplinary measures; Determine current and future staffing levels; Develop and implement staffing plans and related budgets;
  • Collaborate with Sales Director to maintain customer relationships and develop service contracts; Provide recommendations for pricing and terms; Respond to customer inquiries and complaints; take appropriate steps to ensure customer satisfaction;
  • Collaborate with legal department to review contracts, provide input as to the content and terms of the contract, and abide by terms of contracts;
  • Collaborate with the Director, Manufacturing Compliance, the PET Quality Group (PQG) and the PET QM (if not designated the QM) to ensure an environment conducive to manufacturing & releasing PET radiopharmaceuticals per established procedures and regulatory criteria.
  • Work with local vendors for services and equipment to ensure product reliability and to maintain facility so that it meets applicable manufacturing standards; Monitor and supervise facility maintenance and alteration under guidance;
  • Maintain and ensure accuracy of perpetual inventory records; Supervise the taking of periodic physical inventory; Investigate and reconcile inventory discrepancies; May requisition, order or report on items that have become depleted or are at inventory order points;
  • Prepare and provide reports as required by Home Office;
  • Ensure that the facility’s business is conducted at all times with the highest standards of personal, professional and ethical conduct;
  • Perform or assist with any operations, as required;
  • Maintain safe work area and comply with safety procedures and equipment operating rules keeping work area in a clean and orderly condition
  • The PET Operations Manager (POM) can also have the role of Quality Manager for the facility; The role of Quality Manager is described in the Quality Manager Role Description;
  • In the Quality Manager Role the POM would oversee the Quality Program at the Triad PET manufacturing facility; ensuring that the Triad manufactured PET drugs are manufactured and released according to established procedures and regulatory criteria;
  • Oversee cyclotron operators to maintain workflow so as to meet production schedules and quality requirements; Notify regulatory personnel and operations management of unusual equipment or operating problems;
  • Serve as the liaison to the government regulatory agencies concerned with organization’s services; Work with RSO and/or QM to maintain awareness of regulatory changes or enactments and translate to staff to ensure compliance;
  • The PET Operations Manager (POM) may have the responsibility of being the Radiation Safety Officer (RSO) for the facility; In the RSO role the POM would be responsible for compliance with regulations, and licensure requirements related to the handling of radioactive material;
  • In the RSO role the POM would manage the facilities Radiation Safety Program; Ensure that the manufacturing facility remains in compliance with state and federal laws and regulations for radiation safety as well as those outlined internally by Quality and Safety Department; The facility RSO also conducts quarterly radiation safety audits and ensures deliveries to end-user follow DOT guidelines and maintains the security of radioactive materials;
  • The RSO can designate an authorized user of radioactive materials in the RSO’s absence;
  • The POM may be required to supervise the maintenance of local fleet operations depending on needs of facility; Monitor staff mileage reports for company vehicles and ensure that periodic maintenance procedures are being performed as required; Ensure staff maintains valid driver’s license and qualifications for insurance;
  • Manage the proper handling and disposal of radioactive and bio-hazardous waste; Ensure facility meets department of public health and hazardous material regulations, and remain prepared for annual and unannounced inspections; Ensure safety of personnel through training, periodic review of policies and procedures, and the monitoring of radiation exposure levels;
  • Ensure that all instruments and equipment are maintained, properly calibrated and meet requirements set forth by regulatory requirements and internal policy;
  • Participate in any variety of meetings and work groups to integrate activities, communicate issues, obtain approvals, resolve problems and maintain specified level of knowledge pertaining to new developments, requirements, policies, and regulatory guidelines;
  • Perform other related duties as assigned.

REQUIREMENTS:

  • Associates Degree in or equivalent experience preferred
  • Must be able to successfully pass company’s background check and pre-employment drug test;
  • Ability to operate a vehicle and maintain a valid driver’s license also required;
  • Comprehensive knowledge of the theories and operation of cyclotrons;
  • Two (2) plus years experience in management of operations and teams;
  • Four (4) plus years experience in a PET manufacturing environment preferred;
  • Demonstrated leadership skills in motivating team members and meeting performance goals, preferably in a medical environment;
  • Ability to analyze and resolve complex issues, both logical and interpersonal;
  • Highly organized and very effective time management skills;
  • Strong written and verbal communication skills;
  • Ability to negotiate and defuse conflict;
  • Self-motivator, independent, cooperative, flexible, creative;
  • Customer focused; team oriented

Qualified candidates, please begin the application process by clicking the “apply” button. Jubilant Radiopharmacies offers a competitive salary and benefits package, non-nuclear pharmacist training, relocation assistance and the opportunity to work for the fastest growing radiopharmaceutical company in the nation.

If qualified individuals with a disability need assistance in applying for this position, call Human Resources at 407-455-6700 informing us regarding the nature of your request and providing your contact information.

Until the final policy is released, the following guidance is in place for Jubilant Radiopharma employees:

1. If your Customer currently requires that you be vaccinated to enter their establishment, you must show proof of full vaccination.

2. If your Customer requires that you be vaccinated to enter their establishment, sometime in the future, you will be required to show proof of full vaccination by the effective date established by the Customer.

AA/DFWP/EOE –M/F/Individuals with Disabilities/Protected Veteran

Job Type: Full-time

EEO Notice of Rights

Equal Employment Opportunity is the Law.

View Notice

Salary Range $130,000 -$150,000

Job Summary

JOB TYPE

Full Time

SALARY

$106k-132k (estimate)

POST DATE

05/12/2023

EXPIRATION DATE

05/22/2024

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