The Opportunity

We are looking for a Scientist II, working in the Pharmaceuticals & Medical Products industry in Cambridge, Massachusetts, United States.

  • Participates in design, manages and executes testing and studies pertaining to vaccine manufacturing, formulation and/or bioanalytics for vaccine products at all stages of development. 
  • Coordinates information exchange between both in-house and 3rd party vendors for testing. 
  • Participates in the development of and execute assays as needed. 
  • Participates in the creation and review of necessary SOPs and development reports. 
Details

The pay range we are offering is 30 to 50 per hour. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
EDUCATION AND EXPERIENCE:
  • PhD in a scientific discipline with a minimum of 4+ years industry experience (may include post doctoral experience), or 
  • MS with a minimum of 4 years industry experience, or 
  • BS with a minimum of 8+ years industry experience
KNOWLEDGE AND SKILLS:
  • Knowledge and skills in chemistry and biochemistry (e.g. medicinal chemistry, bioanalytical chemistry, protein chemistry, protein expression)
  • Training and experience in Design of Experiments and other statistical methodologies
  • Current knowledge in vaccine literature and basic science related to vaccine development
  • Strong math skills required
  • Working knowledge of statistical models for DOE, and familiarity with JMP is highly desirable
  • Remain well versed in regulatory requirements to assure appropriate design and execution of vaccine manufacture and toxicology studies via services of CMO and CROs
  • Excellent oral and written communication skills
  • Well organized and detail oriented, able to effectively prioritize, interact cooperatively and effectively with others in a team environment, and consistently demonstrate reliability and responsibility
  • Good time and project management skills, ability to oversee several projects simultaneously
  • Comply with safety practices and standard operating procedures
  • Exhibit and promote Core Competencies
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.

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