Visual Inspection Lead - Multi-Site GMP Oversight

PCI Pharma Services

Bedford (NH)

On-site

USD 65,000 - 90,000

Full time

8 days ago

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Job summary

PCI Pharma Services in Bedford, NH is seeking a Lead Inspector to supervise visual inspection, labeling and packaging of sterile vials. You will ensure compliance with GMPs, SOPs, and regulatory requirements while guiding a team across multiple sites.

You will review batch records, monitor KPIs related to defect rate and throughput, and drive continuous improvement. Travel between facilities is expected as part of the role.

Qualifications

  • 3-5 years of experience with inspection and manufacturing equipment and processes that comply with regulatory requirements.
  • Experience with Visual Inspection and/or labeling and packaging of pharmaceutical final products, medical devices, and/or combination products a plus.
  • Proficient with MS Office (Word / Excel / Access).
  • Excellent math skills and strong attention to detail.

Responsibilities

  • Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practice.
  • Supports Visual Inspection, Packaging and Labeling of product as needed across multiple sites with minimal supervision.
  • Follows written procedures and documents results in a neat and precise manner according to GMP standards.
  • Motivate workers to enhance production quantity while maintaining high standards.
  • Review protocols and manufacturing batch records; provide insight for process improvements.

Skills

Visual inspection
Labeling
Packaging
MS Office
Regulatory compliance
Team leadership
Communication

Education

High school diploma or equivalent

Tools

Master Control system
Inspection equipment

Job description

PCI Pharma Services in Bedford, NH is seeking a Lead Inspector to supervise visual inspection, labeling and packaging of sterile vials. You will ensure compliance with GMPs, SOPs, and regulatory requirements while guiding a team across multiple sites.

You will review batch records, monitor KPIs related to defect rate and throughput, and drive continuous improvement. Travel between facilities is expected as part of the role.

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