Company:
Integrated Resources, Inc
Location: St. Louis
Closing Date: 18/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Title: Analytical Data Specialist
M-F 8am-5pm
9 months, with potential to extend
2 positions
Candidates must have 3-5 years experience in an analytical role
Bachelor s degree required (science or analytical/technical background)
Heavy data entry
Lab Vantage preferred
Job Description -
Role responsibilities:
Responsible for creating, review, and approve product/master builds in LIMS per 21CFR Part 11 & EU Annex 11 guidelines and regulations including appropriate data integrity.
Included in the introduction of product/master builds, the individual will support by reviewing applicable documentation and make revisions and changes as required.
Additionally, the individual will act as a software administrator for LIMS software when requested, not including management of user accounts and roles. The individual will also assist in the investigation of deviations as needed.
Education requirements:
BS or MS degree, life sciences
Work experience requirements:
3-5 years of GMP experience in pharmaceutical, biopharmaceutical or chemical industry
Prior experience with analytical testing preferred.
Prior data entry experience recommended.
Role Specific Competencies & Skills:
Familiarity with general laboratory instrumentation and documentation.
Working knowledge of laboratory management systems, LabVantage LIMS preferred.
Prior Instrumentation testing experience is preferred
Able to excel in a team setting in a dynamic environment where shifting priorities are common.
Strong verbal and written communication skills.
Ability to work independently.
M-F 8am-5pm
9 months, with potential to extend
2 positions
Candidates must have 3-5 years experience in an analytical role
Bachelor s degree required (science or analytical/technical background)
Heavy data entry
Lab Vantage preferred
Job Description -
Role responsibilities:
Responsible for creating, review, and approve product/master builds in LIMS per 21CFR Part 11 & EU Annex 11 guidelines and regulations including appropriate data integrity.
Included in the introduction of product/master builds, the individual will support by reviewing applicable documentation and make revisions and changes as required.
Additionally, the individual will act as a software administrator for LIMS software when requested, not including management of user accounts and roles. The individual will also assist in the investigation of deviations as needed.
Education requirements:
BS or MS degree, life sciences
Work experience requirements:
3-5 years of GMP experience in pharmaceutical, biopharmaceutical or chemical industry
Prior experience with analytical testing preferred.
Prior data entry experience recommended.
Role Specific Competencies & Skills:
Familiarity with general laboratory instrumentation and documentation.
Working knowledge of laboratory management systems, LabVantage LIMS preferred.
Prior Instrumentation testing experience is preferred
Able to excel in a team setting in a dynamic environment where shifting priorities are common.
Strong verbal and written communication skills.
Ability to work independently.
Share this job