Granules Pharmaceuticals, Inc. · 3 months ago
QA Technician- Warehouse Operations
Manassas, VA
Full-time
Onsite
Entry Level
2+ years expGranules Pharmaceuticals, Inc. is focused on ensuring compliance with cGMP and internal policies in their Warehouse Operations. The QA Technician is responsible for performing quality assurance inspections, sampling, and maintaining compliance with applicable regulations and procedures.
Pharmaceuticals
Responsibilities
The QA Warehouse Operations is responsible for quality activities supporting Warehouse Operations in accordance with Granules policies, standards, procedures and Global cGMPs
Responsible for inspection of bulk, packaging components, packaged finished product, raw materials, and outgoing product
Responsible for sampling of bulk, packaging components, printed packaging components, finished products and raw materials
Responsible for ensuring GMP warehouse compliance with applicable procedures, providing real-time review of warehouse records and logbooks, and working with Warehouse Operations to resolve issues
Ability to follow data that affects quality of materials, such as environmental/temperature tracking
Archive and maintain hardcopy and electronic copies of label files and change history files
Responsible for issuance, control and management of printed packaging components
Responsible for Control and management of stability, retain and reject materials
Assist in copying and scanning of documents as needed
Build and maintain relationships with Warehouse Operations, Supply Chain and other departments to effectively accomplish responsibilities, make improvements and resolve issues
Ensure compliance with GMPs, Good Documentation Practices, applicable procedures and warehouse requirements for storage, documentation, material handling, safe equipment operation, etc
Ensure standard operating procedures are periodically reviewed for relevance and accuracy in compliance with company policies and procedures
Collaborate with team members to ensure timely deliverables for documentation
Perform and support maintenance and closure activities of documents such as reports, protocols exceptions/deviations, CAPAs, change controls and complaints
Must be flexible with working hours and able to work weekends and off hours as needed to support the patient
CGMP Compliance of the facility
Any other activity as assigned by the Supervisor
Qualification
Required
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
At least two (2) years' experience in a quality assurance role in a cGMP-regulated environment
A college Degree preferably in Sciences (i.e. Pharmacy, Biology, Chemistry etc.)
Ability 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
Company
Granules Pharmaceuticals, Inc.
Granules Pharmaceuticals, Inc. is a pharmaceuticals company based out of 3701 CONCORDE PKY, Chantilly, Virginia, United States.
Founded in 2014Chantilly, Virginia, US
51-200 employeesH1B Sponsorship
Granules Pharmaceuticals, Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (49)
2024 (7)
2023 (22)
2022 (24)
2021 (10)
2020 (19)
Funding
Current Stage
Growth StageLeadership Team
Gregory B. Reeves
Chief Human Resources Officer
Company data provided by crunchbase