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

Chantilly, Virginia, United States -

Full Time

Start Date

Immediate

Expiry Date

28 May, 26

Salary

0.0

Posted On

27 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

cGMP Compliance, SOP Adherence, Floor Monitoring, Water Sampling, Swab Collection, In-Process Testing, Line Clearance, Material Verifications, Environmental Monitoring, Log Book Review, Batch Record Review, Equipment Cleanliness Check, Change Control Initiation, Incident Initiation, Training Record Maintenance, Attention To Detail

Industry

Pharmaceutical Manufacturing

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

Responsibilities

This position is responsible for daily floor monitoring, water sampling, swab collection, in-process testing, and ensuring manufacturing personnel adhere to SOPs pertaining to floor activities in compliance with cGMP.