QA Technician
Belmar Pharma Solutions
Summary
This position is responsible for performing Quality assurance functions that will support Belmar Pharma Solutions in carrying out the mission of the company.
Job description
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.
Requirements
- High school diploma required
- Bachelor's degree or higher (preferred) in science, or similar
- At least two years (preferred) of practical experience in a Quality role in an FDA regulated company
- Experience working to cGMP guidelines
- 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
Benefits
- Health coverage
- 401(k) with 5% match
- Paid time off
- Holidays
- Referral bonuses
- Free or reduced-cost prescriptions
Company overview
Belmar Pharma Solutions is a leading national compounding pharmacy organization specializing in personalized hormone therapies and compounded medications. Founded in 1985 in Golden, Colorado, the company has grown from a single family-owned compounding pharmacy into a comprehensive network of Compounding Centers of Excellence across the United States. Belmar operates both 503A patient-specific compounding pharmacies and 503B FDA-registered outsourcing facilities dedicated to sterile manufacturing, particularly hormone pellets. The company focuses on women's and men's hormone health, sexual wellness, and age-related health changes, providing customized medications that mainstream pharmaceutical companies cannot offer. With facilities in Colorado, Florida, Wisconsin, Arizona, Kansas, and Utah, Belmar serves patients and healthcare providers in all 50 states, maintaining strict compliance with FDA regulations and industry standards while pioneering innovative compounding solutions for personalized healthcare.