Skip to main content

This job has expired

You will need to login before you can apply for a job.

SR. Associate Scientist

Employer
Inotiv
Location
Rockville, MD
Start date
Aug 3, 2022

View more

Discipline
Science/R&D, Biotechnology
Required Education
Associate Degree
Position Type
Full time

Job Title:

      Senior Associate Scientist (SAS)

Qualifications:

Master’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) with 3+ years experience working in a research laboratory

- OR – 

Bachelor’s degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) with 5+ years experience working in a research laboratory

– OR - Associate degree in a scientific discipline (i.e., Biology, Chemistry, Biochemistry, etc.) with 7+ years experience working in a research laboratory

 

Preferred Qualifications:

  • Working knowledge of a research laboratory
  • Knowledge and understanding of GLP regulations 
  • Experience in cell/tissue culture and aseptic technique
  • Possess good interpersonal and strong written/verbal communication skills
  • Highly motivated and detail oriented with good organizational skills
  • Possess the ability to multitask and work independently or in a team environment with minimum supervision
  • Good computer skills in word processing, spreadsheets and database software applications, specifically MS Office (Word and Excel)

 

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

 

Position Responsibilities:

  • Perform a wide variety of assays or tests required to characterize a product or material safety
  • Maintain sterile and good cell/tissue culture techniques
  • Prepare study reagents in accordance with SOPs and study instructions
  • Use and maintain scientific equipment, instrumentation and computer systems
  • Conduct pre-designed or custom assays using laboratory techniques and skills
  • Make scientific observations, maintain detailed data books/documentation, and ensure all documentation fulfills generally accepted professional/industry standards and GLP regulations
  • Follow Study Protocol, SOPs and relevant compliance regulations in regard to assay procedures, safety procedures, scientific responsibility and following GLP documentation, as applicable
  • Independently analyze data and interpret results
  • Ensure all testing guidelines are followed for assays performed
  • Perform peer review of study data and lab support records
  • Keep the next level manager and Study Director informed of study status, technical problems and other issues which impact the lab/study
  • Address quality audit findings and generate deviations in the quality system, as needed 
  • Maintain an understanding of scientific guidelines, technological principles and applications of the organization’s services  
  • Receive instructions on new assignments from the Laboratory Manager or designee and Study Directors
  • Must be able to work with no direct supervision on routine tasks and receive minimal supervision while performing new assigned assays
  • Assist in training new staff members in the performance of routine lab tasks 
  • Serve as a mentor to junior staff members and acts as a leader in the lab by demonstrating correct behavior and work ethics
  • Write and review SOPs
  • Contribute ideas to improve standard laboratory techniques, protocols, processes and equipment, and lead such process improvements  
  • Attend pre-planning, or operational team meetings, as needed
  • Demonstrate consistent good communication and interpersonal skills with employees, management and clients, as applicable
  • Conduct R&D projects as assigned
  • Perform other job duties, as assigned

 

Professional Responsibilities:

  • Attend continuing education courses or webinars, as appropriate

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert