E: P:
Location : 35500 West 91st Street, DeSoto, KS
Pay: $30.50 / HR on W2
Must have:
• Lab experience in either Academic or industry
• Scientific experiments-In-vitro tests mainly ELISA
• Analytical tests within R&D and quality control environment
• USD experience is good to have but not required.
• Chemist background is not a right fit for the job.
Education
Bachelor's degree/Master's degree in a relevant biological area (Bacteriology, Biology, Microbiology, Virology).
Required Experience and Skills
• 1-3 years laboratory experience, preferably in Animal Health
• Detail-oriented with good documentation skills
• Ability to conduct scientific experiments, interpret results, and communicate with relevant team members and stakeholders.
• Effective written and oral communication
• Experience with Microsoft Office programs: Excel, PowerPoint, and Word
Preferred Experience and Skills
• Ability to independently design scientific experiments.
• Experience working in an R&D or Quality Control laboratory.
• Experience developing, working with, and troubleshooting in vitro analytical tests.
• Knowledgeable of USDA regulations for biological products
Note :
• This is an Onsite role at De Soto, KS for 40 hrs/week. Flexible work schedule: 8am-5pm/9am-6pm/8am-4pm/6am-2pm/7am-3pm.
• The possibility of conversion to permanent employee or extension depending upon the performance.
• Managers are open to non-local candidates who are comfortable relocating at their expense.
• Panel interviews will be conducted for this role for approximately 60 minutes.
Responsibilities:
• Assists in the maintenance of the reference management program for US biologics sites.
• Maintains compliance according to USDA guidelines and requirements for reference standards and in vitro potency tests.
• Conducts in vitro testing for stability of reference standards of pre- and post-licensure products.
• Prepares and tests small-scale vaccines to support formulation of new reference standards.
• Supports the formulation, dispense and testing of new reference standards as part of the reference qualification process.
• Participates and collaborates in cross-functional teams with colleagues from R&D, Biotechnology Solutions-Analytics, Production, Quality Control, and Regulatory Affairs to support qualification of new reference standards.
• May assist in the preparation of protocols or reports for submission to USDA.
• May participate in critical reagent qualification studies.
• May provide technical support for approved Quality Control assays.
• May support local, regional, and global program initiatives.
Interested, kindly share resume with following answers
1-How many years of exp in Lab in either Academic or industry
2-How many years of exp in Scientific experiments-In-vitro tests mainly ELISA
3-Analytical tests within R&D and quality control environment
4-how far you live from 35500 West 91st Street, DeSoto, KS and how will you commute daily