Sr. Research Scientist (Analytical DS &DP) Job at Porton Pharma Solutions Ltd., Cranbury, NJ

  • Porton Pharma Solutions Ltd.
  • Cranbury, NJ

Job Description

Job Title: Sr. Research Scientist (ARD/QC)

Location: Onsite, Cranbury NJ

Position Type: Full-Time

Reports To: Director, Analytical R&D/QC


Job Summary

:We are seeking a highly motivated Sr. Research Scientist to join our Analytical R&D and QC department within the CDMO (Contract Development and Manufacturing Organization) industry. The ideal candidate will have a strong background in analytical chemistry and experience in method development, validation, and quality control testing

.
Key Responsibilitie

  • s:Conduct analytical method development and validation independentl
  • y.Troubleshoot analytical methods as needed and gain more experience in the related are
  • a.Conduct release testing for GMP regulatory starting materials, intermediates, and final API
  • s.Conduct testing for stability studies and cleaning verificatio
  • n.Review test data to ensure completion and accurac
  • y.Write raw material test procedures as needed under supervisio
  • n.Write SOPs and protocols as needed under supervisio
  • n.Write instrument operating, maintenance, and qualification/calibration procedures as neede
  • d.Participate in OOS and deviation investigations, as neede
  • d.Support Quality Assurance as needed during internal audits and audits by clients and regulatory agencies. Assist in the development and implementation of corrective actions related to QC/A
  • D.Troubleshoot and maintain analytical instruments. Ensure that instrument calibration and qualification intervals are curren

t.
Qualificatio

  • ns:BS, MS, or PhD in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or a related fie
  • ld.3+ years of experience in analytical R&D and/or QC within the pharmaceutical or CDMO indust
  • ry.Strong knowledge of analytical techniques, including HPLC, GC, UV-Vis spectroscopy, and dissolution testi
  • ng.Familiarity with method validation protocols and regulatory requiremen
  • ts.Excellent problem-solving skills and attention to deta
  • il.Strong communication and interpersonal skills, with the ability to work effectively in a team environme
  • nt.Proficient in data analysis software and laboratory information management systems (LIM

S).

Job Tags

Full time, Contract work

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