Demo

Scientist

Aequor Technologies LLC
Arvada, CO Full Time
POSTED ON 2/16/2025
AVAILABLE BEFORE 5/11/2025

This position can be 100% remote or EW can be aligned to an

  • office if they prefer;
  • Massachusetts or Thousand Oaks site.

EW will be supporting

  • core business hours, EW will be working a standard 8 hour day. No preference on time zone, but the ask is the EW may be required to support workload outside of their time zone on occasion.
  • Please put the candidate location at the top of resume and specify if they are requesting 100% remote work or prefer to be aligned to an
  • office / site
  • This position is 100% computer based and this scientist will be working on the document side. No hands on lab responsibilities
  • 3 years of pharma / biotech experience
  • Biotech / pharma experience required)
  • Analytical method validation and transfer experience
  • Ideal candidate with a bachelor's degree in Biochemistry, Analytical Chemistry, Physical or Life Sciences. Strong understanding of analytical methods within the following platforms Chromatography, Bioassay, PCR, Microbiology, Immunoassay, CE, Gel, Device, Viral, and General (compendia).

    Biopharmaceutical leader founded on discovering, developing, manufacturing, and delivering innovative human therapeutics. Attribute Sciences group within Process Development is seeking a Scientist.

    The Scientist role in Commercial Process Development will be part of the global method implementation team responsible for method transfer and method validation to Quality Control for pivotal and late stage programs. The role will provide technical support for critical large projects. Strong familiarity with the following method platforms is highly preferred : Chromatography, Bioassay, Device, PCR, Microbiology, Immunoassay, CE / Gel, Viral, and General. Protocol and report authoring according to regulatory and industry guidelines (i.e., ICH) and data analysis will be a core activity in this role. This individual may support clinical and commercial locations throughout the company under the guidance of project leads.

    Basic Qualifications : Pharma or Biotech

    Master s degree and 2 years of Operations or Scientific experience OR Bachelor s degree and 4 years of Operations or Scientific experience

    Preferred Qualifications :

    Bachelor's in Biochemistry, Analytical Chemistry, Physical or Life Sciences

    Strong understanding of methods within the following platforms Chromatography, Bioassay, PCR, Microbiology, Immunoassay, CE, Gel, Device, Viral, and General (compendia)

    Direct experience with method transfer and method validation processes from a Pharmaceutical or Biotechnology Company.

    Knowledge of analytical methods / technologies used in biologic and synthetic development and manufacturing

    Excellent written and oral communication skills for the timely coordination of scientific results in a fast-paced, multi-disciplinary, team-based environment

    Demonstrated ability to manage projects cross functionally

    Demonstrated ability to propose and drive new scientific initiatives

  • is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.
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