Quality Support
Bethlehem PA
1st Shift $18/hour Full-Time
About the Role
HTSS is seeking a Quality Support team member to assist with training programs procedural documents and the daily operation of our electronic Quality Management System. This role helps ensure compliance with cGMP standards and supports key Quality System activities. We will need support to help offset the workload on a temporary basis.
Responsibilities
Support daily QualityOne system activities and user access management
Track and manage Quality System records (NCRs CAPAs Change Controls)
Assist with quality metrics trending document updates and training
Help prepare for inspections and audits (FDA DEA partner companies)
Maintain quality records retention and documentation accuracy
Participate in cross-functional projects and inspection readiness activities
Qualifications
BA/BS in a scientific field preferred
Bachelors Degree Associates Degree or equivalent in science related field accepted
4 years of Quality Assurance/Quality Systems experience
Experience with Veeva or validated electronic QMS systems a plus
Knowledge of cGMP Part 11 compliance and pharmaceutical regulations
Strong communication organization and computer skills
Schedule & Pay
Apply today and text Support to .
Quality SupportBethlehem PA1st Shift $18/hour Full-TimeAbout the RoleHTSS is seeking a Quality Support team member to assist with training programs procedural documents and the daily operation of our electronic Quality Management System. This role helps ensure compliance with cGMP standards and su...
Quality Support
Bethlehem PA
1st Shift $18/hour Full-Time
About the Role
HTSS is seeking a Quality Support team member to assist with training programs procedural documents and the daily operation of our electronic Quality Management System. This role helps ensure compliance with cGMP standards and supports key Quality System activities. We will need support to help offset the workload on a temporary basis.
Responsibilities
Support daily QualityOne system activities and user access management
Track and manage Quality System records (NCRs CAPAs Change Controls)
Assist with quality metrics trending document updates and training
Help prepare for inspections and audits (FDA DEA partner companies)
Maintain quality records retention and documentation accuracy
Participate in cross-functional projects and inspection readiness activities
Qualifications
BA/BS in a scientific field preferred
Bachelors Degree Associates Degree or equivalent in science related field accepted
4 years of Quality Assurance/Quality Systems experience
Experience with Veeva or validated electronic QMS systems a plus
Knowledge of cGMP Part 11 compliance and pharmaceutical regulations
Strong communication organization and computer skills
Schedule & Pay
Apply today and text Support to .
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