Study Director - Microbiology (Day Shift) presso Sterigenics
Sterigenics · Salt Lake City, Stati Uniti d'America · Onsite
- Professional
- Ufficio in Salt Lake City
Job Description
Study Director I
Classification:
Schedule:
Traditional
Job Summary:
The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study director is the single point of study control. The study director ensures all assigned studies are completed on time.
Essential Duties:
Scientific/General
- Ensure reports are compliant with current procedures.
- Ensure final reports accurately reflect the data, results, and conclusions of the testing.
- Act as a final signature for assigned studies.
- Collaborate on Customer Specification Sheets (CSS) etc. as assigned.
- Ensure sample and data traceability are maintained throughout testing.
- Ensure calculations and statistics accurately reflect the raw data.
- Ensure accuracy of raw data.
- Ensure test controls and monitors are accurately recorded and reviewed.
- Collaborate within the Quality Event (QE) process.
- Read and maintain an understanding of validation procedures.
- Collaborate with document owners on Standard Test Procedures (STP) as assigned.
Regulatory Compliance
- Know and follow applicable regulatory requirements (GMP, GLP, ISO, etc.).
- Know and follow company policies and procedures.
- Ensure that test procedures are approved, communicated to, and followed by analysts.
- Ensure all data are accurately and concurrently recorded.
- Ensure unforeseen circumstances or events are recorded and that corrective action is taken.
- Complete required training on time.
Customer Service
- Uphold the NL service standard.
- Communicate regularly with sponsors as needed to relay study updates and CSS details.
- Collaborate with the Sales department on testing quotes.
- Maintain a general understanding of company pricing and credit policies.
- Review and update study information in CRM and/or other laboratory systems.
Project Management
- Coordinate workflow to ensure sponsor expectations are met.
Work Environment:
This job operates in a professional laboratory environment. This role routinely uses standard office equipment and lab equipment including but not limited to computers keyboards, computer mouse, telephones, photocopiers, file cabinets, microscopes, micropipettes, pipette aids, various hand tools, and analytical equipment.
The possibility exists for exposure to biological and chemical hazards, exposure to carcinogenic compounds and other environmental aspects which may be considered unfavorable. Employees are expected to follow Biosafety and Chemical Hygiene policies, practices and procedures.
Physical requirements:
The physical demands described here are a representative of those that must be met to perform the essential job functions.
- Requirements to stand and traverse to various office and lab locations and sit at a computer workstation will vary.
- Bending, stooping, and crouching.
- Occasional push and pull tasks with one or both hands.
- Must be able to work while wearing personal protective equipment such as safety glasses, goggles, face shields, gloves, lab coats and personal protective equipment deemed necessary to protect testing and to protect employees from various solutions, wastes, etc.
- Must be able to lift up to 45lbs.
Education and experience requirements:
- B.S. degree (life science strongly preferred)
About Company
Safeguarding Global Health® - with every test we complete.
