Product Development Specialist
Company: SOFIE
Location: Sanford
Posted on: May 28, 2023
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Job Description:
Title - Product Development Specialist Location - Open to any
SOFIE locationsDepartment - Radiopharmaceutical Contract
Manufacturing (RCM)Reports To - Director, Radiopharmaceutical
Contract Manufacturing (RCM)OVERVIEWThe Product Development
Specialist will lead the development, implementation, and
validation of manufacturing and analytical methods of new
diagnostic and therapeutic radiopharmaceuticals for SOFIE within
the Radiopharmaceutical Contract Manufacturing Division. Working
closely with SOFIE's pharmaceutical partners, they will ensure that
these radiopharmaceuticals are in full compliance with all
regulatory requirements (specifically, 21 CFR 211 and
212).ESSENTIAL DUTIES AND RESPONSIBILITIESDevelop protocols for the
production and analysis of clinical-grade radiopharmaceuticals,
validate these methodologies against quality requirements, and
implement them for regular production of radiopharmaceuticals for
preclinical or clinical use according to cGMP standards.It is
expected that the development of these protocols will involve both
the application of scientific principles and rationales and
adherence to regulatory requirements.Write clear Standard Operating
Protocols (SOPs) for these protocols.Review existing SOPs and
suggest logical modifications based on either scientific rationales
and/or regulatory requirements.Provide technical support and/or
training for production staff at SOFIE sites, either remotely or
on-site.Write corporate exception reports and other regulatory
documents, such as risk assessments, change controls, etc.Conduct
production or quality control analytical tests for regular
production of radiopharmaceuticals for preclinical or clinical use
according to cGMP standards.Install, qualify, and maintain
laboratory equipment on site.Validate existing production or
analytical methods on existing or new equipment.Collaborate with
other production radiochemists and quality control chemists as
required to ensure successful protocol development and
radiopharmaceutical production.Perform release testing, according
to SOPs, on other materials (e.g. raw materials for
radiopharmaceutical production).Maintain all qualification and
validation requirements for entering ISO classified areas.Maintain
a clean and safe working environment and perform radiation safety
duties in compliance with safety and pharmaceutical regulations.
Maintain accurate radiopharmaceutical production records and
test/validation results.Write reports, presentations, and other
documentation summarizing experimental/production data.Coordinate
with the Radiopharmaceutical Contract Manufacturing team's
activities to reach defined objectives.Liaise with our contract
partners (e.g. biotech and pharma).Other duties as
assigned.QUALIFICATIONSDegree in chemistry, engineering or natural
sciences preferred but will entertain applicants with relevant
education and work experience.3-years' experience in
radiopharmaceutical manufacturing and QC in a GMP environment
required.Expertise in laboratory procedures and analytical
chemistry techniques required (thin layer chromatography, GC, HPLC,
preparative HPLC, Radiometric Detectors, endotoxin, etc.).
Experience with the use of automated synthesis modules and
maintenance of automated modules is preferred.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.Efficient 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.Excellent
organizational skills required.Ability to work various shifts and
weekends required.Travel: up to 40%
domestically.PDN-993d610d-51c9-4e3a-bfbc-d84b7d7f210d
Keywords: SOFIE, Sanford , Product Development Specialist, Other , Sanford, Florida
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