QA Technician

Engramec; Town of Florida (NY); On-site; USD 65,000 - 90,000; Full time

Job summary

Engramec in New York is seeking a Quality Assurance professional to support production and validation activities. You will submit samples daily, inspect production areas and equipment, verify labeling and QC status, and review batch records and validation protocols to ensure compliance.

The role requires 2 years of QA or production experience in pharma or dietary supplements, and proficiency with Excel and Word. Attendance and reliability are essential for success in this position.

Qualifications

• Two years’ experience in Quality Assurance or production preferably in the pharmaceutical and/or dietary supplements industry.
• Proficient with Excel and Word for data entry and documentation.
• Strong attendance and reliability are required.

Responsibilities

• Submit samples on a daily basis for finished goods and validation studies.
• Inspect production areas before production starts on a product.
• Inspect equipment before production starts and sign the cleaning log books.
• Inspect labels of products in production for correct label, expiration date and lot number as compared to the Batch Production Record.
• Inspect finished goods in the shipping area for correct QC Status (e.g. Quality Hold).
• Review test results and place with the Batch Production Record and Validation Protocol as required.
• Review Batch Production Records in production for completeness.
• Review Validation Protocols so that they are ready when production starts.
• Audit Batch Production Records to assure they are complete before giving to the QA Supervisor.
• Conduct training as needed for validation protocols.
• Understand, review, and participate in cGMP training.

Skills

Quality Assurance experience

Attention to detail

Tools

Excel

Word

Job description

Responsibilities

• Submit samples on a daily basis for finished goods and validation studies.

Inspections

• Inspect production areas before production starts on a product.


• Inspect equipment before production starts and sign the cleaning log books.


• Inspect labels of products in production for correct label, expiration date and lot number as compared to the Batch Production Record.


• Inspect finished goods in the shipping area for correct QC Status (e.g. Quality Hold)

Review

• Review test results and place with the Batch Production Record and Validation Protocol as required.


• Review Batch Production Records in production for completeness.


• Review Validation Protocols so that they are ready when production starts.

Auditing

• Audit Batch Production Records to assure they are complete before giving to the QA Supervisor.

Training

• Conduct training as needed for validation protocols.


• Understand, review, and participate in cGMP training.

Job Qualifications

• Must have great attendance.


• Two years’ experience in Quality Assurance or production preferably in the pharmaceutical and/or dietary supplements industry


• Working knowledge of spreadsheet and word processing software such as Excel and Word