Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
true
Target PR Range: 20-30/hr
*Depending on experience
Responsibilities:
• Monitor critical laboratory instruments and equipment to ensure compliance with qualification, maintenance and calibration schedules, initiation of service requests and escorting vendors.
• Assist with coordination of set up and qualification activities for new assets.
• Assist with OOT investigations in the Asset Management System.
• Assist with maintenance and monitoring of stability environmental chambers, including routine visual inspection, temperature monitoring trending and coordination of cleaning and maintenance.
• Assist with stability inventory and initialization activities including receiving, storage, distributing and disposal of samples for stability studies.
Required Skills:
• Strong working knowledge of cGMP, FDA and EMA GMP regulation and ICH guidance documents.
• Experienced in GMP regulated drug development environment.
• Must possess a BS in molecular biology, biochemistry, or related field with at least three years of relevant experience.
Lab Tech III
Posted: 03/13/2025
2025-03-13
2025-04-24
Employment Type:
Contract
Job Category: Scientific
Job Number: 618203
Is job remote?: No
Country: United States
Job Description
Target PR Range: 20-30/hr
*Depending on experience
Responsibilities:
• Monitor critical laboratory instruments and equipment to ensure compliance with qualification, maintenance and calibration schedules, initiation of service requests and escorting vendors.
• Assist with coordination of set up and qualification activities for new assets.
• Assist with OOT investigations in the Asset Management System.
• Assist with maintenance and monitoring of stability environmental chambers, including routine visual inspection, temperature monitoring trending and coordination of cleaning and maintenance.
• Assist with stability inventory and initialization activities including receiving, storage, distributing and disposal of samples for stability studies.
Required Skills:
• Strong working knowledge of cGMP, FDA and EMA GMP regulation and ICH guidance documents.
• Experienced in GMP regulated drug development environment.
• Must possess a BS in molecular biology, biochemistry, or related field with at least three years of relevant experience.
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