Senior QA Specialist
Piper Companies, Eagleville, PA, United States
Piper Companies is seeking a Senior QA Specialist to join a healthcare company located in Audubon, PA through a 5-month, temporary position with the potential for conversion to a permanent role. The Senior QA Specialist will focus primarily on supporting quality investigations and compliance activities.
Responsibilities of the Senior QA Specialist include:
Investigate GMP deviations and write investigation reports
Ensure investigations comply with SOPs and regulations
Review/investigate customer complaints and document investigation outcomes
Ensure compliance with industry and company regulatory standards
Offer CAPA support by identifying root causes and recommending effective preventative action
Qualifications for the Senior QA Specialist include:
Bachelor’s degree with 3 years' of professional experience in the field
OR
High School Diploma with 5 years' of professional experience in the field
Pharmaceutical QA experience with strong knowledge of GMP compliance, deviation investigations, root cause analysis, and CAPA processes.
Ability to review and assess investigations to ensure compliance with regulatory requirements and quality standards.
Comfortability and/or familiarity working in a regulated GMP environment supporting commercial pharmaceutical products.
Compensation/Schedule for the Senior QA Specialist includes:
Pay Rate Range: $40-43/hour
This is a full-time, onsite position with a flexible start time – either 7am-3pm or 8am-4pm
The role is slated to begin training in April and last until September, with strong potential for the role to convert to permanent placement
Comprehensive Benefits: Medical, Dental, Vision, 401k, 6 Paid Holidays, Paid Sick Leave as required by law
This job opens for applications on 03/10/2026. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: quality assurance, quality assurance specialist, QA, QA specialist, healthcare, onsite, deviation investigations, GMP deviations, regulatory, compliance, investigation reports, SOPs, CAPA, pharmaceutical, pharma, GMP compliance, root cause analysis, commercial pharmaceutical products
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Responsibilities of the Senior QA Specialist include:
Investigate GMP deviations and write investigation reports
Ensure investigations comply with SOPs and regulations
Review/investigate customer complaints and document investigation outcomes
Ensure compliance with industry and company regulatory standards
Offer CAPA support by identifying root causes and recommending effective preventative action
Qualifications for the Senior QA Specialist include:
Bachelor’s degree with 3 years' of professional experience in the field
OR
High School Diploma with 5 years' of professional experience in the field
Pharmaceutical QA experience with strong knowledge of GMP compliance, deviation investigations, root cause analysis, and CAPA processes.
Ability to review and assess investigations to ensure compliance with regulatory requirements and quality standards.
Comfortability and/or familiarity working in a regulated GMP environment supporting commercial pharmaceutical products.
Compensation/Schedule for the Senior QA Specialist includes:
Pay Rate Range: $40-43/hour
This is a full-time, onsite position with a flexible start time – either 7am-3pm or 8am-4pm
The role is slated to begin training in April and last until September, with strong potential for the role to convert to permanent placement
Comprehensive Benefits: Medical, Dental, Vision, 401k, 6 Paid Holidays, Paid Sick Leave as required by law
This job opens for applications on 03/10/2026. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: quality assurance, quality assurance specialist, QA, QA specialist, healthcare, onsite, deviation investigations, GMP deviations, regulatory, compliance, investigation reports, SOPs, CAPA, pharmaceutical, pharma, GMP compliance, root cause analysis, commercial pharmaceutical products
#J-18808-Ljbffr