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Manager Radiochemistry Jobs in Indiana (NOW HIRING)

You will work closely with the Production Lead and Manager to ensure production is executed in a ... Training in radiochemistry or radio pharmacy is preferred. * Knowledge of cGMP regulations and FDA ...

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Manager Radiochemistry information

What is a manager radiochemistry?

A Manager Radiochemistry is a professional responsible for overseeing radiochemistry laboratories and teams that handle radioactive materials for research, medical, or industrial purposes. They ensure the safe and compliant handling, analysis, and disposal of radioactive substances, manage staff, and often coordinate research or production projects involving radiochemistry techniques. Their role also includes maintaining regulatory compliance, developing protocols, and providing training to laboratory personnel. This position typically requires a strong background in chemistry or physics, with specialized knowledge in radiochemistry and relevant safety regulations.

What are some typical challenges a manager radiochemistry might face when leading a laboratory team?

A Manager Radiochemistry often encounters challenges related to maintaining strict safety protocols, ensuring regulatory compliance, and managing complex workflows under tight deadlines. Balancing administrative duties with hands-on scientific oversight requires strong organizational skills and clear communication with both technical staff and upper management. Additionally, staying updated on evolving industry standards and training team members on new techniques are essential to ensure both safety and research quality.

What are the key skills and qualifications needed to thrive as a manager radiochemistry, and why are they important?

To thrive as a Manager Radiochemistry, you need in-depth knowledge of radiochemistry, laboratory management experience, and at least a master's or doctoral degree in chemistry or a related field. Familiarity with radiation detection instruments, quality control systems, and regulatory compliance (such as GMP or NRC guidelines) is essential. Leadership, strong organizational abilities, and effective communication are standout soft skills for this role. These competencies ensure safe, compliant operations, effective team management, and reliable production of high-quality radiochemical products.

What is the difference between Manager Radiochemistry vs Radiochemist?

AspectManager RadiochemistryRadiochemist
CredentialsTypically requires advanced degrees (MS/PhD) and management experienceRequires degrees in chemistry, radiochemistry, or related fields; certifications vary
Work EnvironmentLeads teams in laboratories, oversees projects, manages compliancePerforms laboratory experiments, develops radiochemical processes
Employer & Industry UsageFound in nuclear facilities, research institutions, pharmaceutical companiesWorks in research labs, nuclear medicine, radiopharmaceuticals

The main difference is that a Manager Radiochemistry oversees radiochemistry teams and projects, focusing on management and compliance, while a Radiochemist conducts hands-on research and laboratory work. Both roles require relevant education, but the Manager typically has additional leadership responsibilities.

What are the most commonly searched types of Radiochemistry jobs in Indiana?

The most popular types of Radiochemistry jobs in Indiana are:

What are popular job titles related to Manager Radiochemistry jobs in Indiana?

For Manager Radiochemistry jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Manager Radiochemistry jobs in Indiana look for?

The top searched job categories for Manager Radiochemistry jobs in Indiana are:

Production Technician

Novartis

Indianapolis, IN

$27.40 - $43.22/hr

Full-time

Medical, Retirement, PTO

Re-posted 15 days ago


Key responsibilities

  • Execute activities related to the manufacturing of radioligand therapy (RLT) isotope products, including operating and maintaining grade C isolators.

  • Support all technical aspects related to production readiness, including cleaning and sterilization of isolators, and perform environmental monitoring.

  • Prepare materials, maintain documentation such as batch records and shipping documents, and participate in qualification/validation activities.


Novartis rating

7.8

Company rating: 7.8 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical


Job description

Job Description Summary

At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for an experienced pharmaceutical production professional to help us reach our ambitious goals.
As the Production Technician, you will play an active role in daily production of radioactive isotopes as well as setup and preparation of instruments and equipment. You will adhere to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Your responsibilities will be performed within a team and according to an assigned production shift schedule. You will work closely with the Production Lead and Manager to ensure production is executed in a safe and timely manner.
NOTE: This role will support our new Isotopes Manufacturing facility. Shift hours and schedule will evolve as we move from start up to business as usual.


Job Description

Key responsibilities:

  • Execute all activities related to the manufacturing of radioligand therapy (RLT) isotope products, including operating and maintaining grade C isolators, focusing on KPI goals and ensuring adherence to all state, federal and Novartis radiation safety guidelines.
  • Successful on time completion of required training curriculum comprising necessary Standard Operating Procedures (SOPs) and Techniques, Gowning Qualifications and other relevant training including role-specific Health, Safety & Environment training.
  • Support all technical aspects related to production readiness including manually cleaning the cell and performing sterilization of the isolators.
  • Conduct routine and dynamic environmental monitoring as required.
  • Prepare all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure.
  • Participate in assigned qualification/validation activities.
  • Facilitate a “speak up” culture. Ensure all cGMP compliance activities are followed.
  • Prepares applicable documents and records such as batch records, shipping documents, and training materials.
  • Participates in periodic mandatory overtime to ensure process continuity and completion.

Essential Requirements:

  • Bachelor of Science degree is strongly preferred. In lieu of degree, a minimum of 2 years of experience in a cGMP or aseptic environment can be substituted.
  • 2+ years of experience in pharmaceutical manufacturing, with low bioburden manufacturing preferred.
  • Good understanding of manufacturing and validation requirements and activities
  • Ability to utilize new technology and techniques to eliminate non-value adding activities and improve productivity / performance through new processes.
  • Proficient in MS Office applications.

Desirable Requirements:

  • Training in radiochemistry or radio pharmacy is preferred.
  • Knowledge of cGMP regulations and FDA guidance applicable to radioligand therapy or isotope manufacturing.

#LI-Onsite

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: novartis-life-handbook.pdf​.

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

The pay range for this position at commencement of employment is expected to be between $27.40 and $43.22 per hour; however, while salary ranges are effective from 1/1/24 through 12/31/24 fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$57,000.00 - $85,600.00


Skills Desired

Assembly Language, Cooperation, Efficiency, Electronic Components, Flexibility, General Hse Knowledge , Good Documentation Practice, Installations (Computer Programs), Iso (International Organization For Standardization), Job Description, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Nuclear Medicine, Physics, Product Distribution, Production Line, Scheduler

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