Since 1985, Belmar Pharma Solutions has been the compounding pharmacy of choice for healthcare providers who refuse to compromise on quality, consistency, and clinical support. We have been leaders in Women’s Health since our inception and continue to offer unsurpassed educational resources for women’s and men’s hormones, along with a dedicated Women’s Health team. At Belmar, our benefits reflect our commitment to wellness, respect, and accountability. We offer comprehensive health coverage, a 401(k) with 5% match with no vesting period, paid time off and holidays, $500 referral bonuses, and access to free or reduced-cost prescriptions—because supporting our team enables us to deliver unmatched care. This position is responsible for performing Quality assurance functions that will support Belmar Pharma Solutions in carrying out the mission of the company. 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.
Qualifications - Bachelor’s degree or higher (preferred) in science, or similar.
- High school diploma required.
- At least two years (preferred) of practical experience of in a Quality role in an FDA regulated company.
- Experience working to cGMP guidelines and demonstrates expertise in variety of the field’s concepts, practices, and procedures.
- Experience working with Production or Manufacturing (preferred)
- Excellent multitasking skills.
- Good computer skills.
- Ability to work as part of a small team in a fast-paced environment.
- Excellent communication skills and attention to detail.
- Possesses a strong work ethic.
Pay Range: $22.90 - $25.70
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