What are the responsibilities and job description for the QA Technician position at Belmar Pharma Solutions?
RESPONSIBILITIES
- Applies current Good Manufacturing Practice (cGMP) and Good Documentation Practice (cGDP) requirements, guidelines and practices.
- Printing primary product labels and in process labels.
- Scan and file completed batch records.
- Perform batch record issuance activities.
- Support batch release activities as applicable, including review of batch records.
- Perform data entry for trending.
- Attend all required meetings and provide clear, professional verbal and email communications.
- Author and/or initiate deviations as appropriate.
- Provide cGDP training as needed.
- Must be able to read, understand SOPs and all guidelines as they relate to the process.
- Gowning for ISO classified cleanroom area may be required as part of training or special project.
- Must be able to work in a variety of positions and locations such as sitting, standing, squatting, kneeling, reaching, and walking, for prolonged periods of time.
- Must be able to use necessary equipment such as computers, scanners, printers, phone/headset, or other technology devices as assigned (data entry, Microsoft Office products, email, internet, and other software or technology devices as assigned).
- Special projects and other duties as assigned by Management.