Pharmaceutical Production Chemist I
Company: SOFIE
Location: Totowa
Posted on: April 25, 2025
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Job Description:
Title Pharmaceutical Production Chemist I
If you are interested in applying for this job, please make sure
you meet the following requirements as listed below.
Location NJ5-Totowa, New Jersey
Department Radiopharmaceutical Contract Manufacturing
Training Curriculum ID TCU.006
Overview: The Pharmaceutical Production Chemist I will support the
production of new 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).
Essential Duties and Responsibilities
--- Operate, maintain, and report process data from automated and
semi-automated radiopharmaceutical manufacturing equipment.
--- Prepare materials/consumables for manufacturing processes and
perform system checks on equipment before use in aseptic
processes.
--- Perform manufacturing activities in ISO-7 and ISO-5
environments.
--- Follow detailed instructions in Master Batch Records and
recognize and report any deviations from those instructions during
batch manufacturing.
--- Perform line clearance and pre-batch cleaning activities on the
production line.
--- Execute the qualification of manufacturing processes,
validation protocols, and manufacturing validations.
--- Assist in SOP preparation for manufacturing/production
activities and validation protocols for production processes and
equipment including final reports.
--- Contribute to the production of multiple radiopharmaceutical
products.
--- Initiate and author Investigations, CAPAs, Deviation, and
Change Control documentation as related to manufacturing of drug
product including samples generated for testing of
radiopharmaceuticals.
--- Follow and observe all radiation safety procedures in agreement
with regulatory licensing of radioactive material possession and
handling. Provide related training to other staff members as
required.
--- Participate in the qualification/validation campaign for new
radiopharmaceutical process implementation according to GMP
standards.
--- Maintain approved gowning validation and media fill
participation to allow access to classified manufacturing
areas.
--- Maintain a clean and safe working environment in compliance
with hazardous material safety and pharmaceutical regulation.
--- Perform radiation safety duties in compliance with
regulations.
--- Packages manufactured drug product for shipment to clinical
sites.
--- Efficiently comply with waste management rules and
regulations.
--- Attend internal and external meetings as required.
--- Other assigned duties as required.
--- May require over-time work.
Qualifications
--- High School Diploma required; Bachelor's degree in Chemistry,
Biological, or Physical Science preferred.
--- Experience in a GMP manufacturing environment highly
preferred.
--- Experience with the use of automated synthesis modules and
maintenance of automated modules highly 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 (cleanrooms
environment), and equipment qualification preferred.
--- Efficient in the use of MS Office Suite required.
--- Ability to be detail-oriented, accountable, patient, and work
in a team environment with minimum supervision required. Individual
must be capable of learning and understanding multiple disciplines.
Individual must have previous HAZMAT worker compliance and/or
Radiation Worker compliance experience, as occupational exposure to
ionizing radiation within ALARA is part of the position.
--- Ability to work multiple or staggered shifts required.
--- Ability to lift up to 50 lbs. preferred.
--- Travel 10% required
Keywords: SOFIE, Cherry Hill , Pharmaceutical Production Chemist I, Professions , Totowa, New Jersey
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