IN-Process Quality Assurance Technician(2nd & 3rd Shift)

Granules Pharmaceuticals, Inc.; Chantilly (VA); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

401(k)

401(k) matching

Health insurance

Dental insurance

Vision insurance

Paid time off

Job summary

A leading pharmaceutical company in Chantilly, Virginia is looking for a QA Technician to ensure compliance with cGMP and SOPs in daily operations. Responsibilities include performing line clearance, collecting water samples, and maintaining training records. The ideal candidate should have 2-3 years of experience in quality assurance, a strong attention to detail, and a background in the pharmaceutical industry. This full-time position offers various benefits.

Qualifications

• 2-3 years of experience in quality assurance in a cGMP-regulated environment.
• Experience in pharmaceutical manufacturing industry required.
• Ability to manage multiple priorities.

Responsibilities

• Perform line clearance and material verifications.
• Collect water samples for testing and coordinate environmental monitoring.
• Review and maintain documentation of SOPs and Batch records.

Skills

cGMP compliance

Documentation management

Communication skills

Data analysis

Attention to detail

Education

High School diploma or Associate degree

College Degree in sciences (Biology, Chemistry)

Job 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 Type: Full-time

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