Mid-Senior level
Posted March 29, 2026
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Responsibilities
Commitments
Responsibilities
- Primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.
- Reads and follows Standard Operating procedures with attention to details
- Successfully trains on 1-2 methods and/or techniques mentioned above and performs ad hoc sample testing activities under cGMP as required
- Applies basic scientific and laboratory concepts and theories related to specific testing in the group
- Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance.
- Supports drafting of simple methods, method forms and result reports.
- Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner
- Hiring 3 different skills within molecular biology (in-vitro assays, PCR, ELISA, potency assays, flow cytometry), chemistry (Compendial assays, pH, viscosity, Karl Fischer, UV-Vis, HPLC, FTIR, etc.), and laboratory operations (labeling, stocking, maintaining data and documentation, inventory, etc.)
Commitments
6-month temp to perm position (Hiring 7 people!)
Onsite, M-F, 8am-4pm
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Not Met Priorities
What still needs stronger evidence
Requirements
- Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance.
- Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner
- Hiring 3 different skills within molecular biology (in-vitro assays, PCR, ELISA, potency assays, flow cytometry), chemistry (Compendial assays, pH, viscosity, Karl Fischer, UV-Vis, HPLC, FTIR, etc.), and laboratory operations (labeling, stocking, maintaining data and documentation, inventory, etc.)
- 6-month temp to perm position (Hiring 7 people!)
Preferred Skills
- Hiring 3 different skills within molecular biology (in-vitro assays, PCR, ELISA, potency assays, flow cytometry), chemistry (Compendial assays, pH, viscosity, Karl Fischer, UV-Vis, HPLC, FTIR, etc.), and laboratory operations (labeling, stocking, maintaining data and documentation, inventory, etc.)
Currently I have an opening for an Associate Scientist located in Kansas City, MO. Details for the position are as follows:
Job Description:
Primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.
Reads and follows Standard Operating procedures with attention to details
Successfully trains on 1-2 methods and/or techniques mentioned above and performs ad hoc sample testing activities under cGMP as required
Applies basic scientific and laboratory concepts and theories related to specific testing in the group
Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports.
Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner
Hiring 3 different skills within molecular biology (in-vitro assays, PCR, ELISA, potency assays, flow cytometry), chemistry (Compendial assays, pH, viscosity, Karl Fischer, UV-Vis, HPLC, FTIR, etc.), and laboratory operations (labeling, stocking, maintaining data and documentation, inventory, etc.)
Technical Information:
6-month temp to perm position (Hiring 7 people!)
Pay: $26 hourly (W2)
Onsite, M-F, 8am-4pm
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy
Job Description:
Primarily responsible for testing samples, drafting methods and reporting data under cGMP regulatory guidance for Large Molecules/Biologics product development and related stability studies.
Reads and follows Standard Operating procedures with attention to details
Successfully trains on 1-2 methods and/or techniques mentioned above and performs ad hoc sample testing activities under cGMP as required
Applies basic scientific and laboratory concepts and theories related to specific testing in the group
Follow cGMP requirements for legible, accurate and thorough documentation to meet regulatory compliance. Supports drafting of simple methods, method forms and result reports.
Adheres to policies, processes, and procedures for operating laboratory equipment in a safe and compliant manner
Hiring 3 different skills within molecular biology (in-vitro assays, PCR, ELISA, potency assays, flow cytometry), chemistry (Compendial assays, pH, viscosity, Karl Fischer, UV-Vis, HPLC, FTIR, etc.), and laboratory operations (labeling, stocking, maintaining data and documentation, inventory, etc.)
Technical Information:
6-month temp to perm position (Hiring 7 people!)
Pay: $26 hourly (W2)
Onsite, M-F, 8am-4pm
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy