Associate Lead Scientist - BioA (LC-MS)
About The Position
Associate Lead Scientist – BioA LC/MS in Madison, WI Work Schedule: Monday - Friday (Day Shift) Job Responsibilities: You will support the Study Director, Responsible Scientist, or Principal Investigator for non-regulated, GLP-regulated, and GCP-regulated bioanalysis studies Lead and direct scientific work to support internal methods and experiments Develop and review protocols and sample analysis plans Review data with the method development team to ensure methods are ready for validation Approve validation methods and reviews sample analysis methods Independently review and approve raw data Evaluate data and tables to ensure regulatory guidelines and expectations are met Review reports for scientific accuracy and completeness Provide technical support as needed Assist with efforts to troubleshoot and solve assay problems Assist with client communications regarding scientific direction Work with the client to determine project requirements Assist with scientific directives for the study team Identify scientific issues or scope changes within the study Communicate and monitor scientific expectations with scientific staff and clients Promote quality within the study team Provide a technical resource for less experienced team members
Requirements
- Bachelor's Degree (e.g. Chemistry, Biology )
- 2 years or more experience in method and experimental work in a GLP environment
- 1 year or more using regulatory agency guidelines
- Excellent communication and interpersonal skills
- Proven ability to prioritize and manage time
- Excellent attention to detail
- Able to utilize word processing, database, spreadsheet, and specialized software
Nice To Haves
- Masters (MS) degree in science related field
- 4 years or more experience experience in method and experimental work in a GLP environment
- 1 year or more experience Watson, Nautilus, and Analyst software
Responsibilities
- Support the Study Director, Responsible Scientist, or Principal Investigator for non-regulated, GLP-regulated, and GCP-regulated bioanalysis studies
- Lead and direct scientific work to support internal methods and experiments
- Develop and review protocols and sample analysis plans
- Review data with the method development team to ensure methods are ready for validation
- Approve validation methods and reviews sample analysis methods
- Independently review and approve raw data
- Evaluate data and tables to ensure regulatory guidelines and expectations are met
- Review reports for scientific accuracy and completeness
- Provide technical support as needed
- Assist with efforts to troubleshoot and solve assay problems
- Assist with client communications regarding scientific direction
- Work with the client to determine project requirements
- Assist with scientific directives for the study team
- Identify scientific issues or scope changes within the study
- Communicate and monitor scientific expectations with scientific staff and clients
- Promote quality within the study team
- Provide a technical resource for less experienced team members
Benefits
- Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.
- Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
1-10 employees
