R&D Researcher - Expert in Boulder, CO at Volt

Date Posted: 6/25/2018

Job Snapshot

  • Employee Type:
    Contingent
  • Location:
    Boulder, CO
  • Job Type:
    Computer Industry
  • Duration:
    48 weeks
  • Date Posted:
    6/25/2018
  • Job ID:
    117248
  • Contact Name
    Volt Branch
  • Phone
    913-201-4928

Job Description

Volt Workforce Solutions is seeking a Technical Writer for our customer in Boulder for their  Acids Solutions Division.  The  Technical Writer is for their high-performance Process Validation team working at their new state-of-the-art facility that specializes in Nucleic Acid Chemistries.

Job Description As a technical writer in the chemical development department of the  Nucleic Acid Solutions Division,  the candidate will be responsible for assisting the department in document creation across multiple aspects of process development, process transfer and process validation.

Essential duties and responsibilities include but are not limited to:

* Strong understanding of synthetic chemistry and downstream purification technologies used in modern API manufacturing settings.

  • Ability to write process chemistry technical documents including process development and validation protocols, reports and procedures.
  • Ability to edit documents for data integrity, completeness and documentation formatting standards and adherence to document SOP's
  • Interface and collaborate with cross-functional departments (process chemists, manufacturing, engineering) to fully understand procedures and processes as well as equipment to generate the protocols, SOPs and change controls.
  • Work independently on assigned tasks and is highly productive
  • Bachelor's degree in chemistry or a related science field and/ or equivalent combination of education and experience.
  • 5 years of related professional experience * Prior experience and/or training in a process development or API manufacturing environment with responsibility for authoring of related documents is required. 
  • Knowledge of GMP guidelines as well as international regulations pertaining to the production of APIs and drug products.
  • Knowledge and understanding of the oligonucleotide manufacturing or related synthetic pharmaceutical manufacturing processes is desired.
  • Strong written and verbal communication skills.
  • Proficient using MS Word and MS Excel and other document applications. Must be able to provide advanced formatting for controlled documents.

Volt is an Equal Opportunity Employer