Pharmaceutical Quality Control inspector

Computech Corporation • Franklin Township, NJ

386d • $72,800 - $85,280

About The Position

The Quality Control Specialist at Computech Corporation is responsible for supporting quality-related activities within the manufacturing department of a pharmaceutical facility. This role requires a detail-oriented individual with experience in GMP inspection and documentation review, ensuring compliance with regulatory standards and internal procedures. The position involves conducting audits, providing quality support during manufacturing, and ensuring adherence to safety and environmental responsibilities.

Requirements

• High school diploma or equivalent (GED) with 8+ years of relevant experience within the pharma industry in Quality Assurance, Compliance, or Manufacturing
• 5 years of experience in Quality Assurance
• Thorough knowledge of cGMPs and ability to evaluate facilities records, processes, procedures and practices for conformance to these requirements
• Full understanding of FDA, CGMP, and DEA regulations pertaining to Pharmaceutical manufacturing
• Good understanding of compliance regulations and audit techniques
• Good mathematical skills
• Ability to read and understand MSDS requirements and restrictions
• Understanding of procedures related to document control and Quality Assurance.

Nice To Haves

• Experience with HPLC, GC, UPLC, and Karl Fischer techniques (3 years preferred)
• Experience in GMP-regulated Labs (3 years preferred)

Responsibilities

• Conduct audits of Pharmaceutical Development Manufacturing Facility to ensure compliance with CGMP, DEA, Corporate and pharmaceutical development SOPs
• Perform QA Room Releases, line clearances, equipment releases and AQL inspections as required
• Provide Quality Floor support during batch manufacturing by performing routine Quality auditing
• Provide QA support to Manufacturing for clinical and commercial batches
• Audit executed Batch Records for compliance with CGMP and provide customer audit responses as required
• Audit raw materials, facility logs, and release data
• Facilitate interdepartmental communication for obtaining information and audit corrections
• Comply with and ensure compliance of the department with Health, Safety and Environmental responsibilities
• Assist with batch investigations as required
• Work over the weekend and stay outside business hours if required as directed by the department manager
• Assist with other duties assigned by the manager to support the department and business.

Benefits

• Competitive hourly pay ranging from $35.00 to $41.00 per hour
• Full-time contract position with expected hours of 40 per week
• On-site work environment

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Professional, Scientific, and Technical Services
• Education Level: High school or GED