Radiochemist

RadioMedix, Inc.; Houston (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

A biotechnology company in Houston, Texas, is seeking an experienced Radiochemist for its GMP radiopharmaceutical manufacturing facility. The role involves developing methodologies for chemical handling and supporting various projects aimed at clinical drug trials. The ideal candidate holds a Ph.D. with a strong background in radiochemistry and at least 10 years of pharma experience. This position offers significant growth potential within the rapidly evolving nuclear medicine sector.

Qualifications

• 10+ years of experience in pharma/laboratory management or related pharma experience.
• Radiochemistry experience preferred.
• Thorough knowledge of cGMPs and GLPs is required.

Responsibilities

• Provide technical expertise for radiochemical handling and manufacturing.
• Develop methodologies for radioisotope production.
• Support new product development and collaborate cross-functionally.

Skills

Technical writing

Problem solving

Communication

Team collaboration

Root cause analysis

Education

Ph.D. in Chemistry, Biology, Microbiology, and/or life sciences

Tools

ICP-MS

HPLC

LIMS

Job description

Radiochemist

RadioMedix Inc., a biotechnology company headquartered in Houston, Texas, is seeking an experienced Radiochemist to work in its newly constructed GMP radiopharmaceutical manufacturing facility. The successful candidate will play a key role in R&D, process development, radioisotope and radiopharmaceutical manufacturing, and life-cycle management of GMP products. This position will focus on high-priority projects at RadioMedix that will be integral to upcoming clinical drug trials. This is a newly created position with potential for significant growth.

We’re a growing company and we continue to add talent from a variety of fields. RadioMedix seeks to hire highly motivated and forward-thinking professionals interested in nuclear medicine research and development and influencing change within the nuclear medicine landscape.

Roles/Deliverables

The Radiochemist will provide technical expertise to support the development of methodologies and procedures for chemical and radiochemical handling, remote handling systems, and radiochemical separations. They will also support the development and validation of analytical and radioanalytical methods and procedures that will be used to demonstrate manufacturing and quality control (QC) over radioisotope and radiopharmaceutical production processes. The Radiochemist will support the implementation of Laboratory Information Management Systems (LIMS) and quality assurance procedures under 21 CFR 211, and ICH guidelines.

Research

• Develop radiopharmaceuticals to support RadioMedix’s new product pipeline
• Propose, develop, and conduct experiments to support design, scale‑up, start‑up, and ongoing production of radioisotopes
• Develop and optimize radiolabeling procedures and analytical/radioanalytical methods
• Utilize a broad spectrum of analytical techniques/instrumentation (ICP‑MS, ICP‑OES, HPLC, iTLC, alpha/beta spectroscopy, gamma spectroscopy, and wet chemistry techniques)
• Develop associated analytical methods for characterization of radiolabeled products
• Perform development and validation of RMX radiopharmaceuticals
• Troubleshoot radiochemical reactions, radiochemical separations, and automated systems
• Execute engineering runs and process validations
• Technical writer and reviewer of validation documentation, Standard Operating Procedures (SOPs), and other quality documents
• Train team members in laboratory procedures and equipment
• Supervise the work of team members and assign tasks as needed
• Provide leadership and mentoring to team members
• Supper new product development, assist in management multiple projects, and contribute to team based investigations
• Ensure compliance with environment, safety, health, and quality program requirements

Production/Manufacturing

• Proficient in utilizing manipulators during production
• Proficient in synthesizer machines (e.g., Trasis All‑in‑one, mini‑All‑in‑one) for new product development
• Provide training to team members in the use of synthesizer machines
• Manufacture radiopharmaceuticals including Ga68PSMA
• Calibrate manufacturing and quality control instrumentation
• Perform OOS investigations and CAPAs

Opportunity for growth

• Opportunity to grow the R&D team with room for advancement in the company
• Cross‑functional work to support current and new products as needed
• Potential to a drug product manufacturing team

Minimum Requirements

• Ph.D. in Chemistry, Biology, Microbiology, and/or life sciences
• Radiochemistry experience preferred
• Minimum 10 years’ experience in pharma/laboratory management and/or related pharma experience
• Thorough knowledge of cGMPs, GLPs, and pharma manufacturing
• Ability to collaborate with cross‑functional teams including research, process development, quality assurance, and quality control
• Demonstrated proficiency in root cause analysis as applied in a pharma environment
• Excellent problem solving, communication, and decision‑making skills
• Computer skills, and knowledge of document management/quality systems
• Experience working and communicating productively in a multidisciplinary team
• Perform all work in compliance with site safety and radiation protection guidelines
• Strong organizational and communication skills including technical writing, presentation, and interpersonal skills

Location: 19705 Aldine Westfield Rd., Humble, TX 77338