Mogi I/O : OTT/Podcast/Short Video Apps for you
Production Quality Inspector - Overnight
Mogi I/O : OTT/Podcast/Short Video Apps for you, Boston, Massachusetts, us, 02298
Production Quality Inspector - Overnight
Location:
USA – Fall River, MA (Onsite)
Work Type:
Full Time
Experience Required:
3 – 15 Years
Compensation:
USD $21 – $26 per hour
Visa Status:
US Citizen / Green Card Holder
Shifts:
Third Shift (11:00 PM – 07:30 AM) – May vary based on business needs
Job Overview:
The QA Inspector I is responsible for ensuring product quality throughout all stages of pharmaceutical manufacturing. This role performs on-the-floor in-process inspections, AQL checks, equipment and room verifications, and documentation review in compliance with cGMP, SOPs, and batch record requirements. The position requires strong attention to detail, understanding of quality systems, and strict adherence to regulatory and safety standards. This is an onsite, 3rd-shift role supporting high-volume manufacturing operations.
Key Responsibilities
Perform in-process testing as per batch record instructions (weight, thickness, hardness, disintegration, friability, etc.).
Conduct room and equipment checks prior to each stage of manufacturing following established SOPs.
Execute AQL sampling and inspections as required.
Inspect in-process and finished product samples for the QC Lab and document results accurately.
Maintain standard weight records and perform daily balance verification.
Ensure proper isolation and documentation of rejected materials.
Monitor environmental and facility operating conditions.
Review engineering records (temperature/humidity calibration, PM data, pest control logs, contractor records).
Assess batch records for completeness, reconciliation, signatures, and yield accuracy before releasing for next steps.
Must-Have Qualifications
High School Diploma (minimum requirement).
Minimum 3 years of QA experience in a GMP pharmaceutical manufacturing environment.
Strong chemistry background (mandatory).
Experience performing quality checks in pharmaceutical manufacturing (excluding biopharmaceutical experience).
Understanding of cGMP, QA principles, and documentation compliance.
Proficiency in English—written, verbal, and documentation clarity.
Basic computer proficiency (Microsoft Office, SAP, and similar applications).
Ability to identify quality issues, follow SOPs, and maintain accurate records.
Seniority level:
Mid‑Senior level
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USA – Fall River, MA (Onsite)
Work Type:
Full Time
Experience Required:
3 – 15 Years
Compensation:
USD $21 – $26 per hour
Visa Status:
US Citizen / Green Card Holder
Shifts:
Third Shift (11:00 PM – 07:30 AM) – May vary based on business needs
Job Overview:
The QA Inspector I is responsible for ensuring product quality throughout all stages of pharmaceutical manufacturing. This role performs on-the-floor in-process inspections, AQL checks, equipment and room verifications, and documentation review in compliance with cGMP, SOPs, and batch record requirements. The position requires strong attention to detail, understanding of quality systems, and strict adherence to regulatory and safety standards. This is an onsite, 3rd-shift role supporting high-volume manufacturing operations.
Key Responsibilities
Perform in-process testing as per batch record instructions (weight, thickness, hardness, disintegration, friability, etc.).
Conduct room and equipment checks prior to each stage of manufacturing following established SOPs.
Execute AQL sampling and inspections as required.
Inspect in-process and finished product samples for the QC Lab and document results accurately.
Maintain standard weight records and perform daily balance verification.
Ensure proper isolation and documentation of rejected materials.
Monitor environmental and facility operating conditions.
Review engineering records (temperature/humidity calibration, PM data, pest control logs, contractor records).
Assess batch records for completeness, reconciliation, signatures, and yield accuracy before releasing for next steps.
Must-Have Qualifications
High School Diploma (minimum requirement).
Minimum 3 years of QA experience in a GMP pharmaceutical manufacturing environment.
Strong chemistry background (mandatory).
Experience performing quality checks in pharmaceutical manufacturing (excluding biopharmaceutical experience).
Understanding of cGMP, QA principles, and documentation compliance.
Proficiency in English—written, verbal, and documentation clarity.
Basic computer proficiency (Microsoft Office, SAP, and similar applications).
Ability to identify quality issues, follow SOPs, and maintain accurate records.
Seniority level:
Mid‑Senior level
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