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
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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
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