QA Technician

Rippling, Inc.; Youngtown (AZ); Sur place; USD 60 000 - 90 000; Plein temps

Avantages offerts par ce poste

Health coverage

401(k) with 5% match

Paid time off

Referral bonuses

Prescription benefits

Résumé du poste

Belmar Pharma Solutions, a leader in compounded medications, invites applications for a Quality Assurance position in a fast-paced FDA-regulated environment.

You will apply cGMP and cGDP, manage batch records, issue records, and support batch release while maintaining high attention to detail and clear communication.

Qualifications

• Bachelor’s degree or higher (preferred) in science, or similar.
• High school diploma required.
• At least two years of practical experience in a Quality role in an FDA regulated company.
• Experience working to cGMP guidelines and demonstrates expertise in a variety of the field’s concepts, practices, and procedures.
• Experience working with Production or Manufacturing (preferred).

Responsabilités

• Applies cGMP and 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.

Connaissances

cGMP guidelines

Quality assurance

Attention to detail

Communication skills

Teamwork

Formation

Bachelor’s degree or higher in science

High school diploma

Description du poste

Since our beginning in 1985, Belmar Pharma Solutions has emerged as an industry pioneer, creating compounded medications tailored to meet individual patient needs. Today, we operate trusted Compounding Centers of Excellence across the country. Our 503A pharmacies serve healthcare providers and patients in all 50 states, Washington D.C. and Puerto Rico. Our two 503B outsourcing facilities compound manufacture hormones to meet the needs of clinical practices, delivering to 48 states.

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 positionis responsible forperforming 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,guidelinesand practices.
• Printing primary product labelsandinprocesslabels.
• 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,professionalverbal and email communications.
• Author and/or initiate deviations asappropriate.
• ProvidecGDPtraining 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 berequiredas 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 technologydevices asassigned).
• Special projects and other duties as assigned by Management.

Qualifications

• Bachelor’s degree or higher (preferred) in science, or similar.
• High school diplomarequired.
• At least two years (preferred) of practicalexperience ofin a Quality role in an FDA regulated company.
• Experience workingtocGMP guidelines anddemonstratesexpertiseinvarietyof the field’s concepts, practices, and procedures.
• Experience working with Production or Manufacturing (preferred)
• Ability to work as part of a small team in a fast-paced environment.
• Excellent communication skills and attention to detail.