Applies GMP/GLP in all areas of responsibility as appropriate
Applies the highest quality standard in all areas of responsibility
Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
Reviews and approves/rejects completed client laboratory reports and like records for accuracy traceability and completeness. Evaluates addressed deficiencies for clarification and for potential impact on compliance status. Works with staff to correct any noted deficiencies/inconsistencies.
Assist with implementation and monitoring of quality systems and procedures (e.g. CAPA change controls trainings etc.)
Reviews protocols procedures data reports and other documents to ensure accordance with specified regulatory requirements protocol and/or project plan methods and SOPs.
Keeps supervisor informed of significant issues or developments identified during quality assurance activities.
Learn new tasks and remember the processes associated with this role.
Ability to communicate with Scientific staff for resolving comments
Ability to complete tasks in situations that have a speed or productivity quota.
Communicates effectively with client staff members
Performs other duties as assigned
Qualifications :
Basic Minimum Qualifications :
- Bachelors degree is required. A degree in a relevant field such as chemistry biochemistry biology chemical engineering pharmaceutical science or other directly related field or degree with comparable coursework is preferred. In some cases experience in the relevant area may be used to substitute the Bachelors degree.
- Authorization to work in the United States indefinitely without restriction or sponsorship
Other Qualifications :
- Experience with reading and understandings protocols SOPs and technical guidelines.
- Ability to define and solve practical problems present solutions establish facts and draw valid conclusions
Additional Information :
Position is full-time Monday-Friday 8:00 a.m.-4:30 p.m. with additional hours as needed. Candidates currently living within a commutable distance of Columbia MO are encouraged to apply.
We offer excellent full-time benefits including:
- Comprehensive medical coverage
- Life and disability insurance
- 401(k) with company match
- Paid holidays and vacation
- Dental and vision options.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
Applies GMP/GLP in all areas of responsibility as appropriate Applies the highest quality standard in all areas of responsibility Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Reviews and approves/rejects completed client laboratory reports and like r...
Applies GMP/GLP in all areas of responsibility as appropriate
Applies the highest quality standard in all areas of responsibility
Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
Reviews and approves/rejects completed client laboratory reports and like records for accuracy traceability and completeness. Evaluates addressed deficiencies for clarification and for potential impact on compliance status. Works with staff to correct any noted deficiencies/inconsistencies.
Assist with implementation and monitoring of quality systems and procedures (e.g. CAPA change controls trainings etc.)
Reviews protocols procedures data reports and other documents to ensure accordance with specified regulatory requirements protocol and/or project plan methods and SOPs.
Keeps supervisor informed of significant issues or developments identified during quality assurance activities.
Learn new tasks and remember the processes associated with this role.
Ability to communicate with Scientific staff for resolving comments
Ability to complete tasks in situations that have a speed or productivity quota.
Communicates effectively with client staff members
Performs other duties as assigned
Qualifications :
Basic Minimum Qualifications :
- Bachelors degree is required. A degree in a relevant field such as chemistry biochemistry biology chemical engineering pharmaceutical science or other directly related field or degree with comparable coursework is preferred. In some cases experience in the relevant area may be used to substitute the Bachelors degree.
- Authorization to work in the United States indefinitely without restriction or sponsorship
Other Qualifications :
- Experience with reading and understandings protocols SOPs and technical guidelines.
- Ability to define and solve practical problems present solutions establish facts and draw valid conclusions
Additional Information :
Position is full-time Monday-Friday 8:00 a.m.-4:30 p.m. with additional hours as needed. Candidates currently living within a commutable distance of Columbia MO are encouraged to apply.
We offer excellent full-time benefits including:
- Comprehensive medical coverage
- Life and disability insurance
- 401(k) with company match
- Paid holidays and vacation
- Dental and vision options.
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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