QA Technician (2nd & 3rd Shift)

Job Description

Job Description

Description :

The QA Technician compliance with cGMP and SOP’s and systems. This position is responsible for daily floor monitoring., water sampling for testing, swab collection. In-process testing, line clearance. Monitor manufacturing personnel follow and adhere to SOP pertaining to Manufacturing floor activities.

Job Description / Responsibilities

• Perform line clearance, material verifications
• Collect purified water sample for testing, Trending the results
• Co-ordinate Environmental monitoring in GMP area.
• Log book and Batch record review
• Check the equipment cleanliness and Equipment Swab collection, Equipment release to the operations.
• In process QA testing.
• Archival of SOP’s, Batch documentation.
• Review the In-process SOP’s and identify the gaps
• Initiation of Change control / Incidents
• Maintain the employee training records
• Perform Any other activity as assigned by the Supervisor.

Minimum Requirements

A background in cGMP compliance within the pharmaceutical manufacturing industry is required.

Experience in maintaining cGMP documentation.

Ability to manage multiple priorities and re-prioritize tasks, as required.

Flexible and able to adapt to company growth and evolving responsibilities

Strong attention to detail and excellent organization

Minimum Education / Experience

High School diploma, or Associate degree.

At least 1 to 2 years’ experience in pharmaceutical / food industry.

Benefits :

401(k)

401(k) matching

Dental insurance

Disability insurance

Employee assistance program

Health insurance

Health savings account

Life insurance

Paid time off

Referral program

Vision insurance

Requirements :

Required Qualifications :

Quality assurance within Pharmaceutical Industry : 2 years highly preferred

Manufacturing : 2 years (Preferred)

Document management : 2 years (Preferred)

Knowledge & Skills

cGMP compliance within the pharmaceutical manufacturing industry.

Writing and maintaining cGMP documentation.

Analyze data / information and resolve complex issues.

Verbal and written communication skills.

Work and communicate with cross-functional teams.

Multiple priorities and re-prioritize tasks.

Experience & Education

At least 2 -3 years of experience in a quality assurance role in a cGMP-regulated environment.

A college Degree preferably in sciences (i.e., Biology, Chemistry etc.), or related discipline