Responsibilities include, but may not be limited to:
- Ensures that assigned studies have appropriately trained staff, necessary supplies, and necessary forms or electronic systems for data collection.
- Performs and trains staff on technical procedures on animals, including; injections, blood draws, collection of urine samples, catherizations, surgical preparation, restraining, anesthesia, tissue collection, animal disposal.
- Monitors progress of studies during the In-Life phases to verify adherence to study guidelines and time lines.
- Attends and participates in meetings regarding study planning.
- Creates, reviews, and revises Standard Operating Procedures (SOP) relating to animals, technical procedures and facility issues.
- Monitors and reports changes in animal behavior or health and problems with animal room.
- Monitors and maintains animals and facilities in accordance to applicable laws and regulations.
- Monitors and reports problems with data collection or equipment. Sets up equipment for studies.
- Records and enters raw study data into templates for use by Study Directors.
- Operates and maintains selected laboratory equipment. Ensures equipment is GLP compliant.
- Maintains general organization and cleanliness of work area, including; cleaning and disinfecting procedure rooms and preparation areas.
- Provides technical knowledge to TPM group in developing training manuals and guidelines.
- Ensures animals are housed in accordance with federal and established guidelines.
- Ensures study conduct as described in study protocol. (e.g., dosing, treatments, surgery schedule, necropsy schedule).
- Documents study procedures and results in study notebooks in accordance with Good Laboratory Practices (GLP) regulations (e.g., animal assignment records, anesthesia records, treatment sheets, study events summaries, euthanasia records, necropsy records).
- Performs QC review study and facility data in a timely manner.
- Completes daily research data (e.g., protocols, schedules for projects).
- Assigns and oversees duties to personnel necessary to complete daily schedules.
- Schedules and assigns appropriate animal species for studies in consultation with the Study Scientist or Director. Schedules animal and procedure rooms and surgery suites.
- Reports information regarding clinical problems with the animals, data collection or equipment to project scientist.
- Assists staff supervisors in developing and completing training plans for functional team members. Meets regularly with functional team members and communicates study needs and goals.
JOB REQUIREMENTS
- Bachelor's degree, specializing in science and/or equivalent experience
- At least 3 years working in a research environment
- LATG certification preferred
- Previous GLP experience a plus
- Communicates effectively with all levels of individuals throughout the company.
- Strong attention to detail with the ability to multi-task and maintain organization in a fast paced, changing environment.
- Demonstrated performance in delivering results.
- Bring logical resolutions to conflicting interests and priorities.
- Regarded as objective, open-minded and an “out-of-the-box" thinker.
- Strives for continuous improvement of processes.
- The language skills required include, but are not limited to: the ability to read and interpret documents such as safety rules, operating and maintenance instructions, software manuals, study documents, and procedure manuals; the ability to write routine reports and correspondence; and the ability to speak effectively before groups of customers or employees of the organization.
- Proficient using Microsoft Word, Excel, Project, Info Path, Access, Outlook, and Powerpoint. Able to adapt easily to new software programs.
- Continual GLP training and training on applicable procedures and SOPs within the department.
- Wears appropriate PPE in accordance with policies and procedures.
- Ability to lift up to 26-50 pounds
- Handles and disposes biological and/or chemical substances and wastes in accordance with applicable policies and procedures
For consideration, send cover letter, resume and salary requirements to: [Click Here to Email Your Resumé]. For more information about SNBL USA, Ltd. please visit our website atwww.snblusa.com.
SNBL USA, Ltd. offers a competitive compensation and benefits package including company paid health, dental, vision, pharmaceutical, life, and disability insurances, company 401(k), Section 125, and a generous PTO package.
About SNBL:
For more than 55 years, SNBL (Shin Nippon Biomedical Laboratories, Ltd) has been a leader in helping biopharmaceutical companies generate high quality data with the exceptional precision needed to rapidly advance new medical therapies and innovations that improve patients’ lives, SNBL has facilities in Japan, the United States, China, and Cambodia. Our international footprint enables us to meet the research needs of clients around the globe. We are committed to providing our customers with fast and precise results across the entire drug development spectrum, from early discovery research to late-stage clinical trials.
The SNBL team is dedicated as a company and as individuals in working with our clients to improve patient care and treatment outcomes. This is a cornerstone in our drive for excellence across all aspects of our business.
JOB SNAPSHOT
Employment TypeFull-Time
Job TypeScience, Health Care, Research
EducationNot Specified
ExperienceAt least 3 year(s)
Manages OthersNot Specified
IndustryScience & Technology, Research & Development, Other
Required TravelNot Specified
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