QC Lab Analyst - Radiopharma Testing & Compliance

Lantheus Medical Imaging Inc

Billerica (MA)

In loco

USD 72.000 - 107.000

Tempo pieno

4 giorni fa
Candidati tra i primi
Generatore di candidature

Una candidatura su misura per questa offerta di lavoro — un curriculum e una lettera di presentazione personalizzati, perfettamente in linea con l'annuncio.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Health benefits package
401(k) with company contribution
Paid time off

Descrizione del lavoro

Lantheus Medical Imaging Inc in Massachusetts is seeking a QC Laboratory professional to perform routine and advanced testing on incoming materials, reference standards, solutions, finished product release and stability in a cGMP environment. This is an onsite role based in Billerica, MA requiring 5 days on site each week.

You will operate analytical instruments, verify data, participate in audits, keep compliant with SOPs and CAPAs, and support continuous improvement while ensuring safety and

Competenze

  • Requires an Associate’s degree and typically 5 years of related experience; or a BS degree and 3 years related experience.
  • Vision acuity capable of particulate detection; color vision testing may be required.
  • Experience in GMP/pharmaceutical environment is highly preferred.

Mansioni

  • Perform routine QC testing per SOPs and cGMP guidelines; troubleshoot with minimal supervision.
  • Utilize lab equipment such as calipers, microscope, Raman Spectrometer; sample materials.
  • Verify data accuracy and approve per supervisor discretion; participate in audits and CAPAs.

Conoscenze

Analytical instrumentation experience
Good communication skills
Team player

Formazione

Associate’s degree or BS in scientific discipline
Equivalent combination of education and experience

Strumenti

LabVantage LIMS
SAP

Descrizione del lavoro

Lantheus Medical Imaging Inc in Massachusetts is seeking a QC Laboratory professional to perform routine and advanced testing on incoming materials, reference standards, solutions, finished product release and stability in a cGMP environment. This is an onsite role based in Billerica, MA requiring 5 days on site each week.

You will operate analytical instruments, verify data, participate in audits, keep compliant with SOPs and CAPAs, and support continuous improvement while ensuring safety and

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