Labcorp Drug Development is a global, world-leading Life Science Contract Research Organization that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical industry.
At Labcorp, we offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. We put our trust in science and in one another. This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner, as Labcorp Drug Development has helped pharmaceutical and biotech companies develop one-third of all prescription medicines on the market today.
Essential Job Duties:
- Conducts routine and non-routine sample analysis in compliance with GLP, applicable methods, protocols, SOPs, and regulatory agency guidelines.
- Documents work and maintains study documentation and laboratory records.
- Performs routine and non-routine maintenance on general equipment.
- Provides input and participates in project meetings.
- Performs QC review of data.
- Reports any difficulties, unexpected findings and/or deviations that may affect the integrity of the data to Study Director/Manager, Principal Investigator/Contributing Scientist and/or management of and participates in corrective action of problems.
- Displays understanding of theory and ability to set up and perform practical requirements for routine and non-routine assays and for the instruments used
- Develops working knowledge to assist in performing validations of various Immunotoxicology assays.
- Maintains awareness and compliance with all safety directives and safety procedures in accordance with the regulations.
- Accepts responsibility in ensuring clean and safe laboratory work environment.
- Support training and assists less experienced staff, prioritize workloads on a daily basis contributing to a team environment and culture of care.
- Ensures that chemicals and reagents in use, are correctly labelled and associated documentation is available.
- Participates in process improvement initiatives.
- Participates in client visits/audits as required.
- Builds competency in a comprehensive range of I&I procedures.
- Develops knowledge to assist in writing text for methods or protocols.
- Fully participate in Performance Management Systems
- Performs other related duties as assigned.
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Requirements:
- Bachelor's degree in biology, chemistry, or related life science
- Benchwork with pipetting experience preferred but full training will be provided.
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. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.
Labcorp is proud to be an Equal Opportunity Employer:
Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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