Company:
The Fountain Group LLC
Location: St. Louis
Closing Date: 29/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Currently we have an opening for an Analytical Data Specialist located in St. Louis, MO. Details for the position are as follows:
Pay Range: $28-$38/hour
Job Description:
9-month contract with the possibility of extending or converting to permanent based on performance and budget.
Shift: M-F 8am-5pm
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.
Qualifications:
BS or MS degree, life sciences
3-5 years of GMP experience in pharmaceutical, biopharmaceutical or chemical industry
Prior experience with analytical testing preferred.
Prior data entry experience recommended.
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.
Pay Range: $28-$38/hour
Job Description:
9-month contract with the possibility of extending or converting to permanent based on performance and budget.
Shift: M-F 8am-5pm
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.
Qualifications:
BS or MS degree, life sciences
3-5 years of GMP experience in pharmaceutical, biopharmaceutical or chemical industry
Prior experience with analytical testing preferred.
Prior data entry experience recommended.
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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