Radiopharmaceutical Product Development Manager — Transfer

RXinsider LTD.; Indianapolis (IN); Hybrid; USD 105,000 - 150,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

401k savings plan

HSA (Health Savings Account)

Job summary

Cardinal Health is seeking a Manager, Product Development reporting to the Director, Nuclear Manufacturing, to lead a team of Product Development scientists in technology transfer for clinical phase and commercial radiopharmaceuticals.

You will oversee transfer activities across a network of cGMP facilities, ensuring adherence to regulatory guidelines while coordinating resources and maintaining governance documentation.

Qualifications

• Bachelor’s degree in engineering or a physical science with at least five years of GMP experience in the pharmaceutical/biotech industry; R&D background preferred.

Responsibilities

• Plan and evaluate the transfer of manufacturing and testing procedures across cGMP facilities.
• Coordinate resources to generate study protocols and documentation for technology transfer and qualification.
• Administer, track and report manufacturing/testing activities for process qualification and method validation per SOPs.
• Collaborate on equipment qualification, computer system validation, and cleaning verification protocols with validations team.
• Lead and/or support investigations and document deviations during technology transfer.
• Train facility personnel on new manufacturing/testing procedures and provide routine production support.

Skills

Leadership

Communication

Interpersonal skills

Regulatory knowledge

GMP experience

Problem solving

Education

Bachelor’s degree in engineering or physical science

Tools

HPLC/GC/TLC

Chromatography data systems

Process equipment

Job description

Cardinal Health is seeking a Manager, Product Development reporting to the Director, Nuclear Manufacturing, to lead a team of Product Development scientists in technology transfer for clinical phase and commercial radiopharmaceuticals.

You will oversee transfer activities across a network of cGMP facilities, ensuring adherence to regulatory guidelines while coordinating resources and maintaining governance documentation.