Business Services & Consulting • all cities, WY 51
Life Sciences GxP Validation Engineer (51)
all cities, WY 51On-sitePosted 20 hours ago
Business Services & Consulting
About the Role
Life Sciences GxP Validation Engineer
Rate: $60 Duration: 9-12 months Location: Remote Must have Veeva QRM validation experience Conduct thorough Functional Validation for MES recipes used in manufacturing, ensuring compliance with GxP and other regulatory standards.Guide and review the work of other team members, providing expertise in protocol execution and validation documentation.Collaborate with IT and manufacturing teams to digitize production processes, enhancing efficiency and compliance.Utilize basic programming skills to understand and validate formulas and transitions within the MES environment.
Participate in automation testing processes when necessary, contributing to the overall quality assurance of the MES system.Qualifications Proven experience with MES systems such as Rockwell Automation, Siemens, Aveva, or similar platforms within the pharmaceutical industry.Strong understanding of GxP, USDA regulations, and healthcare validation processes, with the ability to apply this knowledge practically.Diligent and detail-oriented approach to work, with a commitment to maintaining high-quality standards.Excellent communication skills, with the ability to clearly convey complex information to team members and stakeholders.
Basic programming knowledge is preferred to facilitate understanding of MES functionalities; automation testing knowledge is an advantage but not mandatory.
Life Sciences GxP Validation Engineer
Rate: $60 Duration: 9-12 months Location: Remote Must have Veeva QRM validation experience Conduct thorough Functional Validation for MES recipes used in manufacturing, ensuring compliance with GxP and other regulatory standards.Guide and review the work of other team members, providing expertise in protocol execution and validation documentation.Collaborate with IT and manufacturing teams to digitize production processes, enhancing efficiency and compliance.Utilize basic programming skills to understand and validate formulas and transitions within the MES environment.
Participate in automation testing processes when necessary, contributing to the overall quality assurance of the MES system.Qualifications Proven experience with MES systems such as Rockwell Automation, Siemens, Aveva, or similar platforms within the pharmaceutical industry.Strong understanding of GxP, USDA regulations, and healthcare validation processes, with the ability to apply this knowledge practically.Diligent and detail-oriented approach to work, with a commitment to maintaining high-quality standards.Excellent communication skills, with the ability to clearly convey complex information to team members and stakeholders.
Basic programming knowledge is preferred to facilitate understanding of MES functionalities; automation testing knowledge is an advantage but not mandatory.
What You'll Do
Life Sciences GxP Validation Engineer Rate: $60 Duration: 9-12 months Location: Remote Must have Veeva QRM validation experience Conduct thorough Functional Validation for MES recipes used in manufacturing, ensuring compliance with GxP and other regulatory standards.
Guide and review the work of other team members, providing expertise in protocol execution and validation documentation.
Collaborate with IT and manufacturing teams to digitize production processes, enhancing efficiency and compliance.
Utilize basic programming skills to understand and validate formulas and transitions within the MES environment.
