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Medical Writer/Clinical Scientist @ Remote
Company | Intellectt Inc |
Address | United States |
Employment type | CONTRACTOR |
Salary | |
Category | Medical Equipment Manufacturing |
Expires | 2023-11-11 |
Posted at | 1 year ago |
Role: Associate Scientist II
Location: Abbott Park, IL 60064-3537 (Remote)
Duration: 10+ Months on W2
Shift Timings: 8 AM to 5 PM
Support Reagent manufacturing.
Conduct investigations on internal nonconformances and customer complaints related to Reagents.
Assist in developing/ improving Reagent manufacturing processes and/or products.
Major Responsibilities: Design experiments and testing schemes, analyze data, write protocols and reports and present results to a cross-functional team.
Must demonstrate strong problem solving and analytical skills and be a team player.
Must possess a BS in molecular biology, biochemistry, or related field with at least 2-4 years relevant experience.
Knowledge of GMP, ISO, and FDA regulations and audits a plus.
Familiar with process and test method validations.
Excellent communication skills.
Shall be able to perform under pressure to meet project deadlines.
Note
Experience in Regulatory Affairs can be considered but a person with Clinical Background is preferred.
Location: Abbott Park, IL 60064-3537 (Remote)
Duration: 10+ Months on W2
Shift Timings: 8 AM to 5 PM
Support Reagent manufacturing.
Conduct investigations on internal nonconformances and customer complaints related to Reagents.
Assist in developing/ improving Reagent manufacturing processes and/or products.
Major Responsibilities: Design experiments and testing schemes, analyze data, write protocols and reports and present results to a cross-functional team.
Must demonstrate strong problem solving and analytical skills and be a team player.
Must possess a BS in molecular biology, biochemistry, or related field with at least 2-4 years relevant experience.
Knowledge of GMP, ISO, and FDA regulations and audits a plus.
Familiar with process and test method validations.
Excellent communication skills.
Shall be able to perform under pressure to meet project deadlines.
Note
Experience in Regulatory Affairs can be considered but a person with Clinical Background is preferred.
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