Quality Systems Engineer – GAMP5 / GMP

JMD Technologies Inc.; Boston (MA); On-site; USD 120,000 - 160,000; Part time

Job summary

A leading technology recruitment firm in Boston is seeking a Sr. Technical Recruiter with expertise in life sciences, biopharma, and IT hiring. The ideal candidate will provide quality oversight for computerized systems and possess over 5 years of experience in QA compliance, along with familiarity with platforms like Veeva and ServiceNow. This role focuses on collaborating with cross-functional teams to ensure regulatory adherence and data integrity. Contract employment type with a mid-senior level expectation.

Qualifications

• 5+ years of experience in computerized systems quality, compliance, or QA oversight (non-validation focused).
• Familiarity with ITIL, GAMP5, and Agile methodologies.
• Strong understanding of GxP compliance and data integrity principles.

Responsibilities

• Provide quality oversight for enterprise computerized systems.
• Lead reviews for new system implementations and upgrades.
• Support data integrity assessments and system testing oversight.
• Review and approve system documentation such as test plans, execution results, and quality reports.
• Identify and mitigate quality and compliance risks during system development and lifecycle management.
• Ensure adherence to regulatory and data integrity standards (GxP, GMP, GCP, GLP).

Skills

Quality oversight for computerized systems

Analytical skills

Communication skills

Collaboration with cross-functional teams

Data integrity

Analytical skills

Communication skills

Education

Bachelor’s degree in Computer Science or related discipline

Tools

Veeva

ServiceNow

ALM

Job description

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Sr. Technical Recruiter | Life Sciences, Biopharma & IT Hiring Expert | 12+ Yrs in Talent Acquisition | Boolean Search Pro | Pharma, Healthcare…

Key Responsibilities:

• Provide quality oversight for enterprise computerized systems, including Veeva, ServiceNow, and ALM.
• Lead reviews for new system implementations, upgrades, and releases, including deviation and CAPA management.
• Support data integrity assessments, change control, and system testing oversight.
• Review and approve system documentation such as test plans, execution results, and quality reports.
• Identify and mitigate quality and compliance risks during system development and lifecycle management.
• Ensure adherence to regulatory and data integrity standards (GxP, GMP, GCP, GLP).

Qualifications:

• Bachelor’s degree in Computer Science, Information Technology, or a related discipline.
• 5+ years of experience in computerized systems quality, compliance, or QA oversight (non-validation focused).
• Hands‑on experience with Veeva, ServiceNow, ALM, or similar enterprise platforms (QMS, ERP, or workflow management tools).
• Familiarity with ITIL, GAMP5, and Agile methodologies.
• Strong understanding of GxP compliance and data integrity principles.
• Excellent analytical and communication skills; able to collaborate across cross‑functional teams.

Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Information Technology

Industries

Pharmaceutical Manufacturing

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