Overview
QC Validation Area Specialist – Computer Software Systems Jobs in Petersburg, Virginia, USA at BioSpace
QC Validation Area Specialist – Computer Software Systems
Join us as a QC Validation Area Specialist – Computer Software Systems at Bio Space.
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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Title: QC Validation Area Specialist – Computer Software Systems
Company: BioSpace
Location: Petersburg, Virginia, USA
Category: Quality Assurance – QA/QC, Healthcare (Data Scientist)
