Associate Research Scientist

Smithers

$75K — $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BA/BS in Biological or Physical Sciences with 3-5 years experience, or MS with 1-2 years experience
  • Expertise in bioanalytical assays design and platforms
  • Experience in method validation and assay troubleshooting
  • Ability to mentor and guide junior scientists
  • Familiarity with CRO operations, GLP, GCP, and/or CLIA
  • Experience with automated lab systems and SOP drafting is a plus

Responsibilities

  • Design and develop new bioanalytical assays
  • Ensure feasibility assessments for assay development
  • Support method validation and assist troubleshooting
  • Train and provide technical guidance to junior scientists
  • Ensure compliance with health and safety procedures in the lab
  • Maintain equipment and materials as per lab standards
  • Report non-compliance with regulations and SOPs

Benefits

  • Comprehensive health insurance with multiple plan options
  • Dental and vision coverage
  • 401K retirement plan
  • Paid time off (PTO)
  • Opportunity for professional development and training
Full Job Description
Smithers is seeking a talented Associate Research Scientist with expertise in bioanalytical assays (PK, ADA, Nab). The individual will be responsible for design, development and feasibility of new assays.

This position is salaried and is classified as an exempt position. Exempt employees typically work 40 hours or more to adequately perform their responsibilities. Extended work hours may be necessary to support the business in meeting client deliverable commitments.

The salary range for the role is $75,000 - $100,000 per year commensurate with experience and qualifications. Smithers PDS has a comprehensive health insurance package including a choice of 3 medical plans, dental, vision, 401K retirement plan and PTO.

The qualifications for this role are:

  • BA/BS in Biological or Physical Sciences and at least 3 - 5 years of relevant experience, MS in relevant field and at least 1-2 years of experience
  • Understanding of bioanalytical assays (various design and platforms)
  • Experience supporting method validation studies
  • Experience with assay troubleshooting
  • Ability to assist with training and provide technical guidance to more junior scientists as needed
  • Prior CRO and GLP, GCP, and/or CLIA experience a plus
  • Experience with automated laboratory systems a plus
  • Experience in drafting SOPs a plus


Corporate Responsibilities:

  • Adherence to laboratory health and safety procedures
  • Adherence to Standard Operating Procedures (SOPs)
  • Adherence to applicable company policies and guidelines
  • Adherence to federal and/or local regulations, as applicable
  • Ensures appropriate reporting when there is reason to believe compliance with regulations, policies, guidelines, SOPs, quality, or other criteria are not being observed or enforced
  • Ensure materials and equipment are maintained


Standard Requirements:

  • Excellent oral and written communication skills
  • Proficient in advanced computer applications including MS Word, Excel, statistical programs, and Watson LIMS database
  • Able to work independently and manage priorities, as well as operate as a team member
  • Must be solution oriented and open to input
  • Must be able to comfortably and successfully operate in a dynamic environment with shifting priorities
  • Must be able to collaborate and partner at all levels of the organization to accomplish deliverables and meet quality standards


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