Senior Scientist

ClinLab Staffing; Cranbury Township (NJ); On-site; USD 100,000 - 150,000; Full time

Job summary

ClinLab Staffing is looking for a Senior Scientist specialized in LC-MS Platforms to join their team in Cranbury, NJ. This role involves conducting method development for biologics and managing client interactions. Candidates should possess a Ph.D. in Chemistry or Biochemistry and extensive experience in CRO or Pharma settings. The position offers the opportunity to lead laboratory operations and mentor junior staff while ensuring high-quality analytical services.

Qualifications

• Ph.D. or M.S. in Chemistry, Biochemistry or a related field.
• 4+ years experience for Ph.D. or 9+ years for M.S. in CRO/Pharma/Biotech.
• Hands-on experience with LCMS method development.

Responsibilities

• Independently conduct LC-MS method development for biologics in support of various assessments.
• Serve as Subject Matter Expert (SME) for LCMS platform and Principal Investigator for client interactions.
• Mentor junior staff and improve operational excellence.

Skills

LC-MS method development

Analytical techniques

Project management

Client interaction

Education

Ph.D. in Chemistry or Biochemistry

Job description

Direct message the job poster from ClinLab Staffing

Scientific Recruiter focusing in NJ, PA, and DE

Sr. Scientist, LCMS Platforms – Cranbury, NJ

Position Summary:

My client is a CRO providing advanced analytical services for biological drug discovery and development area. Our clients include multinational pharmaceutical companies and biotech companies.

The company focuses on analytical and bioanalytical services for biologics in CMC development with further extension to support pre-clinical and clinical analysis. The team has successfully supported non-GLP, GLP (non-clinical) and GCLP (clinical) projects. The role is responsible for supporting lab operation in non-GLP area.

Key Responsibilities:

• Independently conduct LC-MS method development for biologics (e.g., ADC, mAb, protein, peptide, oligonucleotide, etc.) in support of developability assessment, comparability assessment, in-depth characterization, biotransformation, and CQA related analysis.
• Present and interpret data internally and/or externally as needed.
• Serve as Subject Matter Expert (SME) for LCMS platform.
• Serve as the Principal Investigator responsible for interaction with the client from the study design to scheduling, conducting, reporting, and transferring data. Ensure responsiveness to the client, timely delivery, and overall customer satisfaction.
• Provide oversight of the laboratory, mentor junior staff, and collaborate to keep improving operational excellence.
• Assist in establishing and improving policies, procedures, work instructions and SOPs.
• Understand and adhere to corporate standards regarding code of conduct and Environment Health & Safety (EHS).
• Perform other related duties as assigned.

Qualifications:

• Ph.D., M.S., in Chemistry, Biochemistry or related scientific fields required, including a minimum of 4+(Ph.D.) or 9+(Master’s) years of CRO/Pharma/Biotech experience.
• Hands-on experience with high-resolution LCMS method development and in-depth characterization.
• Supervisory experience in both project and talent (people) management is preferred.
• Ability to work independently and pay good attention to details.
• Ability to achieve objectives/timelines through collaborative efforts with co-workers, managers, and clients.
• Must be goal-oriented, compliance-ensured, quality-conscientious, and client-focused.
• Effective writing and communication skills.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science and Research

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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