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QC Production Associate (Chemist)
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England
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Job summary
An established industry player is looking for a Quality Control Production Associate (Chemist) to join their team. In this full-time role, you will operate radiosynthesizers and utilize analytical instruments for quality control analysis of drug products. The position requires a keen eye for detail and the ability to work flexible shifts, including weekends. If you are passionate about ensuring the quality of pharmaceutical products and thrive in a dynamic environment, this opportunity could be a perfect fit. Join a dedicated team committed to excellence in drug production and quality assurance!
Qualifications
- Bachelor’s degree in chemistry or related field is essential.
- Experience with analytical instrumentation is a plus.
Responsibilities
- Operate radiosynthesizers for drug product production.
- Perform quality control testing on finished drug products.
- Assist with inventory management and environmental monitoring.
Skills
Detail oriented
Accountable
Organized
Flexible with shifts
Education
Bachelor’s degree in chemistry
Degree in a related science field
Tools
HPLC
GC-MS
Microsoft Office Suites
Job description
Job Description
Kelly Science is seeking a Quality Control Production Associate (Chemist) opportunity with a leading company located in Somerset, NJ.
Pay: $27/hour
Shift: Monday- Friday 2:00am-10am and rotating weekends (required to work 1-2 weekends per month)
Employment Type: Full Time; Direct Hire
Summary:
As a Quality Control Production Associate (Chemist), you will be operating the radiosynthesizers for the production of drug products as well utilizing analytical instrumentation for quality control analysis of the drug products.
Job Duties Include:
- Perform FDG and NaF synthesis utilizing radiosynthesizers according to company Standard Operating Procedures.
- Perform Quality Control testing on finished drug products according to Standard Operating Procedures.
- Ensure all materials/reagents are accepted according to SOPs and within expiry.
- Ensure all equipment is appropriately qualified prior to use.
- Ensure completion of applicable cGMP documentation.
- Assist with inventory management.
- Perform environmental monitoring of classified areas according to SOPs.
- Report manufacturing metrics into data repository as required.
- Participate in any QA investigations for any change controls, deviations, OOS etc.
Requirements:
- Bachelor’s degree in chemistry or a related science field.
- Experience with analytical instrumentation such as HPLC or GC-MS is a plus.
- Detail oriented, accountable, and organized.
- Flexible with shifts and able to adapt well.
- Proficient with Microsoft Office Suites.
APPLY NOW! For immediate consideration!
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