Job Description

Reference # : 18-01443Title : Technical Writer
Location : Pennington, NJ
Experience Level : Start Date / End Date : 02/26/2018 / 08/25/2018
Assignment Detail
Industry:Biotech/PharmaJob Category:Scientific / Clinical
Position : Technical Writer
Location : Pennington, NJ
Duration : 6 months (Possible for extension or permanency)

Job Description:
  • Preparation of CMC elements of regulatory filings
  • Plan the authoring and review of CMC Regulatory documents
  • Working in collaboration with GRS CMC teams and Client technical experts. Creates final drafts of Regulatory documents for submission to GRS and onwards to global Health Authorities.
  • Author regional filings and amendments for approved products
  • Carries out integrated review process for documents. Set up system for collection of comments, support the operation of the review process and creates updated draft for next phase review.
  • Critically review documents for consistency and quality
  • Responsible for working very closely with various functional groups to develop content for CMC submissions.
Skills and Experience
  • Bachelors/ Masters in life-sciences
  • Experience in preparation of regulatory documentation
  • Experience in biotech product development and manufacturing in the pharmaceutical industry

If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • TransitChek Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
Interested in applying? Contact Karyn Suayan, at (201) 283.9627 or you may send your updated CV to now.

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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