Process Development Associate Scientist — HPLC/UPLC Troubleshooter

Aequor

Cambridge (MA)

On-site

USD 90,000 - 120,000

Full time

4 hours ago
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Job summary

Aequor in Cambridge, MA seeks a Process Development Associate Scientist for onsite 12‑month contract to support analytical method development and protein-based biotherapeutics. The role focuses on HPLC/UPLC, troubleshooting, and data documentation.

You will work in a cross‑functional team, perform analyses with capillary electrophoresis and LC methods, maintain instruments, and contribute to regulatory filings.

Qualifications

  • Master's degree with 2 years scientific/pharmaceutical experience or Bachelor's with 4 years experience.
  • 2+ years laboratory experience in industry
  • Analytical chemistry/biochemistry experience
  • Biopharmaceutical industry experience

Responsibilities

  • Work in a cross-functional team environment to advance therapies in late-stage development.
  • Analyze late-stage protein-based therapies with analytical techniques such as capillary electrophoresis, liquid chromatography, and compendial methods (pH, visual appearance, turbidity).
  • Support development, optimization, and troubleshooting of analytical methods.
  • Data analysis, electronic notebook records, drafting protocols and reports, presenting results at team meetings, and regulatory filing support as needed.
  • Expert level troubleshooting and maintenance of HPLC/UPLC instruments.
  • Expertise in Empower software for instrument methods and data handling.

Skills

Analytical chemistry
Biochemistry
Laboratory skills
Biopharma industry

Education

Master's degree
Bachelor's degree

Job description

Aequor in Cambridge, MA seeks a Process Development Associate Scientist for onsite 12‑month contract to support analytical method development and protein-based biotherapeutics. The role focuses on HPLC/UPLC, troubleshooting, and data documentation.

You will work in a cross‑functional team, perform analyses with capillary electrophoresis and LC methods, maintain instruments, and contribute to regulatory filings.

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