JMD Technologies Inc.
JMD Technologies Inc. provided pay range
This range is provided by JMD Technologies Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
$50.00/hr - $55.00/hr
Title:
QC Investigations Specialist
Employment Type:
Contract
Status:
Accepting Candidates
About the role This role supports real-time manufacturing operations by leading investigations, resolving on‑floor issues, and ensuring high‑quality documentation. You’ll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance.
Key Responsibilities
Triage manufacturing issues and lead
analytical investigations
and
root cause analysis .
Write clear, compliant
quality documentation
including deviations and CAPAs.
Coordinate with SMEs to determine immediate actions, containment, and impact assessments.
Interpret data to support structured problem‑solving and continuous improvement.
Provide technical operations support across manufacturing and QC functions.
Qualifications
6+ years pharmaceutical or biotech manufacturing experience.
4+ years analytical investigation and QC‑focused experience.
Strong background in
RCA, deviation management, and GxP documentation .
Ability to interpret analytical data and think scientifically under time‑sensitive conditions.
Experience partnering cross‑functionally with manufacturing, QC, materials, and facilities teams.
Compensation (MA Pay Transparency)
Estimated hourly range: $50–$55/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
#J-18808-Ljbffr
This range is provided by JMD Technologies Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
$50.00/hr - $55.00/hr
Title:
QC Investigations Specialist
Employment Type:
Contract
Status:
Accepting Candidates
About the role This role supports real-time manufacturing operations by leading investigations, resolving on‑floor issues, and ensuring high‑quality documentation. You’ll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance.
Key Responsibilities
Triage manufacturing issues and lead
analytical investigations
and
root cause analysis .
Write clear, compliant
quality documentation
including deviations and CAPAs.
Coordinate with SMEs to determine immediate actions, containment, and impact assessments.
Interpret data to support structured problem‑solving and continuous improvement.
Provide technical operations support across manufacturing and QC functions.
Qualifications
6+ years pharmaceutical or biotech manufacturing experience.
4+ years analytical investigation and QC‑focused experience.
Strong background in
RCA, deviation management, and GxP documentation .
Ability to interpret analytical data and think scientifically under time‑sensitive conditions.
Experience partnering cross‑functionally with manufacturing, QC, materials, and facilities teams.
Compensation (MA Pay Transparency)
Estimated hourly range: $50–$55/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
#J-18808-Ljbffr