JMD Technologies Inc.
Quality Systems & Investigations Specialist
JMD Technologies Inc., Boston, Massachusetts, us, 02298
Quality Systems & Investigations Specialist
Title:
Quality Systems & Investigations Specialist
Employment Type:
Contract
Status:
Accepting Candidates
About the role This position plays a key role in supporting daily manufacturing activities by resolving operational issues and driving high-quality investigations. The role ensures process reliability through strong technical oversight and collaboration with critical operations teams.
Key Responsibilities
Lead real-time floor support, triaging deviations and initiating
root cause investigations .
Produce thorough, compliant
quality documentation
for deviations, CAPAs, and impact assessments.
Partner with manufacturing, QC, facilities, and materials teams to define corrective and preventive actions.
Apply structured scientific thinking to evaluate data and support operational decisions.
Contribute to process improvement by identifying trends and proposing optimized workflows.
Qualifications
6+ years experience in pharma/biotech manufacturing environments.
Proven background in
investigations, RCA, QC analytics, and GxP documentation .
Skilled in cross‑functional coordination and rapid issue assessment.
Strong analytical mindset with the ability to interpret complex data sets.
Experience supporting manufacturing operations in fast‑paced, regulated environments.
Compensation (MA Pay Transparency)
Estimated hourly range: $50–$58/hr (W-2).
Final rate within this range will be based on skills, experience, and interview results.
Seniority level Mid‑Senior level
Employment type Contract
Job function Manufacturing and Quality Assurance
Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at JMD Technologies Inc. by 2x
Get notified about new Quality Specialist jobs in
Boston, MA .
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Quality Systems & Investigations Specialist
Employment Type:
Contract
Status:
Accepting Candidates
About the role This position plays a key role in supporting daily manufacturing activities by resolving operational issues and driving high-quality investigations. The role ensures process reliability through strong technical oversight and collaboration with critical operations teams.
Key Responsibilities
Lead real-time floor support, triaging deviations and initiating
root cause investigations .
Produce thorough, compliant
quality documentation
for deviations, CAPAs, and impact assessments.
Partner with manufacturing, QC, facilities, and materials teams to define corrective and preventive actions.
Apply structured scientific thinking to evaluate data and support operational decisions.
Contribute to process improvement by identifying trends and proposing optimized workflows.
Qualifications
6+ years experience in pharma/biotech manufacturing environments.
Proven background in
investigations, RCA, QC analytics, and GxP documentation .
Skilled in cross‑functional coordination and rapid issue assessment.
Strong analytical mindset with the ability to interpret complex data sets.
Experience supporting manufacturing operations in fast‑paced, regulated environments.
Compensation (MA Pay Transparency)
Estimated hourly range: $50–$58/hr (W-2).
Final rate within this range will be based on skills, experience, and interview results.
Seniority level Mid‑Senior level
Employment type Contract
Job function Manufacturing and Quality Assurance
Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at JMD Technologies Inc. by 2x
Get notified about new Quality Specialist jobs in
Boston, MA .
#J-18808-Ljbffr