Company:
LanceSoft Inc
Location: St. Louis
Closing Date: 18/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Title: Analytical Data Specialist
Location : St. Louis, MO
Duration : 9 Months Contract
Shift : Monday - Friday 8:00-AM - 5:00-PM
Pay Range : $30.00 - $38.00 USD hourly on W2
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.
Location : St. Louis, MO
Duration : 9 Months Contract
Shift : Monday - Friday 8:00-AM - 5:00-PM
Pay Range : $30.00 - $38.00 USD hourly on W2
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.
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