Scientific Search
Location:
Rochester, MN
Be the force behind the quality of tomorrow’s targeted therapies. My client is seeking a
Quality Engineer
to help maintain excellence in the production of radiopharmaceuticals. This role blends regulatory compliance, process validation, and technical problem‑solving in a dynamic manufacturing environment where science meets safety and precision. If you’re detail-oriented and thrive in cross‑functional, regulated teams—this opportunity offers impact and growth.
Why You Should Apply
Work at the forefront of nuclear medicine and advanced biologics
Collaborate with QA, MSAT, and Supply Chain on high-impact products
Competitive full‑time role with comprehensive benefits: health, dental, vision, paid holidays, PTO, life & disability coverage, Simple IRA match
Contribute to global regulatory submissions and inspection readiness
What You’ll Be Doing
Ensuring compliance with cGMP, FDA, ISO, NRC, and DOT standards
Supporting validation, process optimization, and equipment qualification
Managing CAPAs, deviations, and root cause investigations
Authoring SOPs and training programs across radiopharma operations
Overseeing supplier quality, material review, and tech transfer documentation
About You
2–5 years of quality experience in pharmaceutical or radiopharma environments
Strong knowledge of 21 CFR 210/211/212, ISO 13485, and risk management tools (FMEA)
Proficient in root cause analysis, validation, and statistical methodologies
Background in radiation safety and automated synthesis platforms is a plus
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to emily@scientificsearch.com and tell us why you’re interested. Or, feel free to email your resume. Please include Job#19569A
#J-18808-Ljbffr
Rochester, MN
Be the force behind the quality of tomorrow’s targeted therapies. My client is seeking a
Quality Engineer
to help maintain excellence in the production of radiopharmaceuticals. This role blends regulatory compliance, process validation, and technical problem‑solving in a dynamic manufacturing environment where science meets safety and precision. If you’re detail-oriented and thrive in cross‑functional, regulated teams—this opportunity offers impact and growth.
Why You Should Apply
Work at the forefront of nuclear medicine and advanced biologics
Collaborate with QA, MSAT, and Supply Chain on high-impact products
Competitive full‑time role with comprehensive benefits: health, dental, vision, paid holidays, PTO, life & disability coverage, Simple IRA match
Contribute to global regulatory submissions and inspection readiness
What You’ll Be Doing
Ensuring compliance with cGMP, FDA, ISO, NRC, and DOT standards
Supporting validation, process optimization, and equipment qualification
Managing CAPAs, deviations, and root cause investigations
Authoring SOPs and training programs across radiopharma operations
Overseeing supplier quality, material review, and tech transfer documentation
About You
2–5 years of quality experience in pharmaceutical or radiopharma environments
Strong knowledge of 21 CFR 210/211/212, ISO 13485, and risk management tools (FMEA)
Proficient in root cause analysis, validation, and statistical methodologies
Background in radiation safety and automated synthesis platforms is a plus
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to emily@scientificsearch.com and tell us why you’re interested. Or, feel free to email your resume. Please include Job#19569A
#J-18808-Ljbffr