Job Description


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  • Ref: 283053
  • Type: Long Term Contract
  • Location: Ridgefield, CT
  • Industry: Pharmaceuticals
  • Job Level: Experienced Non-Manager
  • Pay: $33.00 - $36.00/hr.

Opportunity Description

Our client is currently in need of an experienced Scientist to support their Research and Development team.

Company Information

Our client is a global pharmaceutical firm with a philosophy rooted in impacting people's lives in a meaningful way. With a focus on driving innovation, their organization strives to challenge and inspire its employees, offering an environment that promotes diversity and collaboration among colleagues and the community. Excellent benefits, work-life balance, and a tremendous opportunity for growth for the right individual.

Job Duties

  • Initiate and complete routine purification strategies of biotherapeutics and reagent proteins in an independent and efficient manner, with minimal supervision; Independently operates and is responsible for lab equipment
  • Demonstrates technical ability to design and execute non-routine experiments with minimal supervision
  • Perform literature searches and extracts relevant information from published protocols; Facilitates training of others as requested
  • Demonstrate the ability to independently analyze results, interpret outcome of experiments and to propose appropriate follow-up
  • Communicate own work effectively orally and in writing; Contributes to writing protocols, procedures, and technical reports; provide input for scientific reports
  • Maintain proper records in accordance with SOPs and policies

Experience & Skills Required

  • Bachelor’s Degree with 3+ years’ experience in related scientific discipline or Master’s Degree in related scientific discipline or equivalent experience in related field
  • Experience with protein purification a must.
  • Apply knowledge of basic theory and scientific principle
  • An Analytical thinker with the ability to multi-task
  • Able to draft portions of technical reports
  • Concise and accurate reporting of technical data and information
  • Written and verbal communication skills
  • Appropriate level of understanding of applicable regulations
  • Knowledge of Pharmaceutical Life Cycle Process
  • Knowledge of Regulatory Requirements & Compliance
  • Knowledge of Technology Trends
  • Project/Program Management experience