Director - CMC

Isotopia USA; Town of Westfield (NY); On-site; USD 180,000 - 230,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Advancement opportunities

Job summary

Isotopia USA is seeking a Director, CMC to lead radiochemistry development and tech transfer for radiopharmaceutical products. You will oversee QC and analytical methods, ensuring cGMP compliance and high data integrity in a fast-paced environment.

Experience in radiochemistry, method validation, and regulatory compliance is required; advanced chemistry degrees are preferred. This leadership role offers opportunities for process improvements and strategic collaboration with production teams.

Qualifications

• Minimum of a Bachelor’s degree in Chemistry is required.
• Advanced degree(s) in chemistry is desired.
• Previous radiochemistry experience and scale-up/optimization required.
• Experience with compendial USP test methods, ICP-MS / ICP-OES, radio-TLC, and/or direct inoculation sterility testing is required.
• Strong GMP understanding and radiation safety practices required.

Responsibilities

• Lead and manage Chemistry and Manufacturing development projects including scale-up and optimization of radiopharmaceutical drug products.
• Support tech transfer of radiopharmaceutical drug products into GMP manufacturing operations.
• Serve as SME for radiochemistry and radiolabeling of drug products.
• Oversee QC operations, including staff, method development, transfers, and routine testing.
• Oversee analytical method development and validations for test specifications.

Skills

Radiochemistry

Leadership

GMP knowledge

Analytical testing

Regulatory compliance

Quality control

Data recording

Safety protocols

Education

Bachelor in Chemistry

Advanced degree in Chemistry

Tools

ICP-MS

ICP-OES

Radio-TLC

Direct inoculation sterility testing

Job description

Isotopia is a global biotech company manufacturing drug products and API for radio-pharmaceutical cancer drugs. At our US headquarters in Indianapolis, we will be next door to our key customers, delivering our products just in time, each day, every day. We are seeking a highly motivated and detail-oriented Director, CMC (Chemistry, Manufacturing and Controls) to join our dynamic team. You will play a crucial role in ensuring the safe and efficient production of our products. You will be part of a family, a team, dedicated to our mission to deliver on our covenant with our customers.

Responsibilities:

• Lead and manage Chemistry and Manufacturing development projects including scale-up and optimization of radiopharmaceutical drug products

• Support the tech transfer of radiopharmaceutical drug products into GMP manufacturing operations within the Isotopia operations

• Serve as the Subject Matter Expert for radiochemistry and radiolabeling of drug products

• Oversee the Quality Control operations, including staff, method development, method transfers, and routine QC testing

• Oversee, manage, and lead if necessary analytical method development and validations for the various test specifications required for Isotopia products

• Execute stability protocols and generate reports

• Comply with cGMP requirements for recording of data

• Oversee the chemical and physical testing of raw materials, in-process materials and finished products, using established test methods to provide accurate and reliable data to ensure their strength, identity, and purity.

• Train quality control staff to properly execute analytical tests

• Oversee and ensure success of the technology transfer of product chemistry and manufacturing processes, as well as process improvements to these systems

• Lead product and process chemistry development projects

• Coordinate with third party equipment vendors to schedule routine equipment requalification

• Work with radioactive materials using safe protocols

• Coordinate with production personnel to ensure timely testing and release of intermediate materials and final product

• Coordinate sampling plans and shipment of samples to third party labs for any necessary third-party testing

• Complete technical review of routine test documents, method validation protocols / reports, and method development protocols / reports

• Adhere to all applicable procedures, GMPs, company policies and any other quality or regulatory requirements

• Perform any other tasks as assigned

• Minimum of a Bachelor’s degree in Chemistry is required

• Advanced degree(s) in chemistry is desired

• Previous experience in radiochemistry and radiopharmaceutical product scale-up and optimization is required

• Previous experience with compendial USP test methods, ICP-MS / ICP-OES, radio-TLC, and/or direct inoculation sterility testing is required

• Previous experience in pharmaceutical / radiopharmaceutical quality control is desired

• Strong understanding of GMP requirements and radiation safety practices is required

• Detail-oriented mindset with excellent organizational and record-keeping skills

• Ability to work in a regulated and fast-paced environment while maintaining a high level of accuracy

• Flexibility to work nights / be on call as required and handle time-sensitive processes

• Strong commitment to safety, ethical conduct, and compliance with regulations

• Physical ability to stand for extended periods, lift moderately heavy objects up to 50 pounds, and to handle frequent stooping and crouching, and wear appropriate PPE

• Manual dexterity for manipulating small items

We offer a competitive salary, a comprehensive benefits package and advancement opportunity.

As an Equal Opportunity Employer, we are committed to a diverse workforce.