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Radiochemist
1 month ago
Wilmington, United States Masis Professional Group Full timeGMP RADIOCHEMISTOur client has a production facility for the contract manufacturing of radiopharmaceuticals. This cGMP clean room suite is a 21 CFR 211 compliant, radiopharmaceutical manufacturing facility dedicated to late stage investigational and commercial stage radiopharmaceuticalsCurrently they are looking to add another GMP Radiochemist to join there...
Radiochemist
1 month ago
We are seeking a highly skilled Radiochemist to join our team at Masis Professional Group. As a Radiochemist, you will be responsible for performing and developing all processes and procedures used in the GMP Clean Rooms for contract manufacturing.
Key Responsibilities:- Support production by performing GMP radiochemistry processes in a safe, efficient, and timely manner.
- Support irradiation program through the preparation of targets and radiochemical processing of the targets after irradiation.
- Maintain physical inventory of all material assigned to GMP Suites.
- Develop and document new procedures as assigned.
- Support Inventory management, sales, and other production departments through technical assistance and estimation of time/labor.
- Develop new products in coordination with contracted companies.
- In-depth understanding and experience with analysis and interpretation of research data, and the ability to recognize and resolve irregularities and invalid results.
- Ability to provide technical leadership and coordinate major installation, materials, tooling, supplies, and scheduling of work crews; ability to work with scientific or research staff in developing/supporting technical procedures.
- Ability to communicate effectively, both verbally and in writing, and to contribute to the development of the research plan.
- Proficient in the use of MS Office Suite required.
- Ability to be detail-oriented, accountable, patient, organized, and work in a team environment with minimum supervision required.
- Strong technical writing skills required.
- Experience in a GMP manufacturing environment.
- Expertise in laboratory procedures and techniques required (thin layer chromatography, GC, HPLC, preparative HPLC, Radiometric Detectors, endotoxin, etc.).
- Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals required.
- Knowledge of cGMP requirements, aseptic process (cleanroom environment), and equipment qualification required.
- Must have the ability to work safely using concentrated solutions of radioactivity.
- Must have the ability to operate a hot-cell safely and without contaminating the equipment.
BS degree in Chemistry, Radiochemistry, or Chemical Engineering and 5+ years' experience. Will also consider MS in Chemistry/Radiochemistry with 3+ years' experience or PhD with 1-2 years.