QA Technician- Warehouse Operations/IPQA for Documentation Granules Consumer Health, LLC is a subsidiary of Granules India LTD, a vertically integrated pharmaceutical company with headquarters in Hyderabad, India. Granules Consumer Health, LLC is located in Manassas, Virginia. We have over 106 employees and annual revenue of $76.64 million. We serve as Granules' packaging facility and front-end division for private label over the counter (OTC) products in the US. We offer OTC generics that meet the highest level of quality at an affordable cost. As such, we are well-established on bulk supply through efficiencies garnered through manufacturing, integration and a high level of regulatory compliance. We are dedicated to excellence in manufacturing, quality, and customer service.
Job Duties & Responsibilities:
The QA Warehouse Operations is responsible for quality activities supporting Warehouse Operations in accordance with Granules policies, standards, procedures and Global cGMPs.
Perform in-process checks during packaging activities.
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
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
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
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
Compliance of the facility.
Any other activity as assigned by the Supervisor.
Reports to QA Manager
Requirements:
Knowledge & SkillscGMP compliance within the pharmaceutical manufacturing industry. Writing and maintaining cGMP 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 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.)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.
- We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.
