Porton Pharma Solutions Ltd.
Sr. Research Scientist (Analytical DS &DP)
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
Cranbury, NJ, USA
Work mode:
Onsite
Published on:
12 September 2026
What they need
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).
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