BioSpace
QC Validation Area Specialist - Computer Software Systems
BioSpace, Virginia State University, Virginia, us, 23806
QC Validation Area Specialist - Computer Software Systems
Join us as a
QC Validation Area Specialist - Computer Software Systems
at
BioSpace . Position Overview
This role involves planning, managing, and performing laboratory validation activities on computer software systems. Responsibilities include troubleshooting software issues, conducting system audits, and ensuring compliance with validation protocols. The role requires collaboration with IT, metrology, and other stakeholders to ensure quality and timely completion of deliverables. Key Responsibilities
Validate QC equipment and instrumentation Manage change control activities for QC systems and equipment Review validation procedures and protocols for accuracy and completeness Ensure compliance with GMP and corporate requirements Collaborate with cross-functional teams to support validation activities Qualifications
Bachelor’s Degree in Life Sciences, Chemistry, Engineering, or related field; or an associate’s degree with 4+ years of relevant experience Minimum of 2 years of experience in laboratory validation or engineering in the pharmaceutical industry Experience with validation protocols, electronic validation systems, and GMP knowledge Physical and Other Requirements
Ability to lift up to 33 pounds, perform close work with hands, and work at heights occasionally. Must follow safety protocols. Join Us
At Novo Nordisk, we offer competitive pay, comprehensive benefits, and opportunities for career growth. Be part of a diverse and inclusive team dedicated to making a difference in healthcare.
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Join us as a
QC Validation Area Specialist - Computer Software Systems
at
BioSpace . Position Overview
This role involves planning, managing, and performing laboratory validation activities on computer software systems. Responsibilities include troubleshooting software issues, conducting system audits, and ensuring compliance with validation protocols. The role requires collaboration with IT, metrology, and other stakeholders to ensure quality and timely completion of deliverables. Key Responsibilities
Validate QC equipment and instrumentation Manage change control activities for QC systems and equipment Review validation procedures and protocols for accuracy and completeness Ensure compliance with GMP and corporate requirements Collaborate with cross-functional teams to support validation activities Qualifications
Bachelor’s Degree in Life Sciences, Chemistry, Engineering, or related field; or an associate’s degree with 4+ years of relevant experience Minimum of 2 years of experience in laboratory validation or engineering in the pharmaceutical industry Experience with validation protocols, electronic validation systems, and GMP knowledge Physical and Other Requirements
Ability to lift up to 33 pounds, perform close work with hands, and work at heights occasionally. Must follow safety protocols. Join Us
At Novo Nordisk, we offer competitive pay, comprehensive benefits, and opportunities for career growth. Be part of a diverse and inclusive team dedicated to making a difference in healthcare.
#J-18808-Ljbffr