QA Technician (2nd & 3rd Shift)

Job Description

Job Description

Description : Job Summary

The QA technician ensures compliance with cGMP and internal policies, procedures and specifications. This position is responsible for performing inspections, batch record review, and quality system functions in accordance with cGMP and related company SOP’s, state, federal and local laws as applicable.

Principle Accountabilities

JOB DUTIES & RESPONSIBILITIES

• Manage and maintain company document control and archival systems (hardcopy and electronic) in compliance with internal procedures and policies as well as regulatory requirements.
• Collaborate with team members and site customers to ensure timely deliverables for documentation.
• Track controlled documents through the issuance of Document Control numbers, logbooks, change requests, and document status reports.
• Management of quality documentation which includes but is not limited to number issuance, logbooks and spreadsheets.
• Review of batch records and equipment logbooks.
• Issue batch records, SOP’s. and protocols as needed.
• Assist in scanning of documents as needed.
• Collect purified water and environmental samples and trend results.
• Perform weekly floor audits for manufacturing.
• Perform swab sampling or cleaning validation and or verification.
• Ability to be flexible with working hours and weekend coverage when needed.
• Any other activity as assigned by the Supervisor

Reports to

QA Lead / Manager

Physical Requirements / Working Environment

While performing the duties of this job, the employee is regularly required to, stand, sit, talk, hear, and use hands and fingers to operate a computer and telephone keyboard.

Specific vision abilities required by this job include close vision requirements due to computer work.

Ability to sit at a computer terminal for an extended period of time.

Light to moderate lifting up to 10-15 lbs. is required.

Ability to work in a confined area.

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

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 rekated discipline