Specialist I, Quality Assurance - Quality Operations

Abeona Therapeutics; Cleveland (OH); On-site; USD 60,500 - 71,500; Full time

Benefits offered by this job

Medical insurance

Dental and vision coverage

401(k) match plan

Lifestyle spending account

Job summary

A biopharmaceutical company in Cleveland is seeking a Specialist I in Quality Assurance to ensure compliance with cGMP guidelines and support manufacturing operations. The ideal candidate will hold a Bachelor's degree and have at least one year of experience in a regulated manufacturing environment. Responsibilities include documentation review and quality control processes. Competitive annual salary ranges from $60,500 to $71,500, with a comprehensive benefits package.

Qualifications

• 1 year of experience in quality or manufacturing in a cGMP regulated environment.
• Knowledge of cGMPs and relevant ISO standards.
• Experience in aseptic manufacturing processes.

Responsibilities

• Perform routine quality assurance activities for cell and gene therapies.
• Ensure compliance with regulatory and cGMP guidelines.
• Review and reconcile batch-related documentation.

Skills

Organizational skills

Attention to detail

Communication skills

Interpersonal skills

Education

Bachelor's degree in related field

Tools

MS Word

Excel

Power Point

Job description

Specialist I, Quality Assurance - Quality Operations

3 weeks ago Be among the first 25 applicants

Our Values: Patient First | Innovation | Integrity | Determination | Trust

Join us in making cure the new standard of care. At Abeona Therapeutics, we exist for our patients and their caregivers; their needs guide our decision‑making. We challenge ourselves to think differently, move quickly, and deliver solutions. We hold ourselves to the highest ethical and quality standards. We persevere with resilience and focus to achieve our mission. We build trust through humility, mutual appreciation, openness, and respect.

Company Description

Abeona Therapeutics Inc. is a commercial‑stage biopharmaceutical company focused on developing cell and gene therapies for serious diseases. Notably, Abeona's ZEVASKYN™ (prademagene zamikeracel) is the first autologous cell‑based gene therapy treating wounds in adults and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB). The company's cGMP manufacturing facility in Cleveland, Ohio, is dedicated to producing ZEVASKYN™. Abeona's portfolio includes adeno‑associated virus (AAV)-based gene therapies for ophthalmic diseases with unmet medical needs, and their novel AAV capsids aim to improve treatment outcomes for various debilitating conditions.

Position Overview

The Specialist I, Quality Assurance performs routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the maintenance of the quality systems in support of a cGMP Operation for Manufacturing logistics processes relating to Abeona Manufactured Media batch record review and release from start to end of manufacturing activities, in‑process sampling / testing, autoclave, and document management ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist I, Quality Assurance will report to the Associate Manager, Quality Assurance or above and will support manufacturing and quality control as the production area Quality Assurance representative.

Essential Duties and Responsibilities

• Position is on a Day Shift with occasional weekends (as needed).
• Process document control requests and issue‑controlled forms, logbooks, notebooks, master production records, labels, and protocols.
• Reconcile issued controlled forms, logbooks, notebooks, master production records, and protocols.
• Coordinate and facilitate QA‑related production and production‑related activities.
• Review batch‑related documentation and ensure resolution of issues to release product.
• Ensure that products are manufactured in compliance with site procedures, regulatory and cGMP guidelines.
• Compile and verify all batch‑related documents into a final product lot disposition package.
• Communicate lot disposition pending issues to management.
• Gather metric information for use in continuous improvement of areas of responsibility. Report to management as needed.
• Work with Manufacturing and Quality Control as a production area Quality Assurance representative. Key areas of collaboration include but are not limited to; calibration and preventive maintenance, process monitoring, and inventory control monitoring.
• Support site inspections and inspection readiness activities.
• Enhance skills via regular training and continuing education, including professional society membership/participation.
• Completion of gowning qualification and maintaining status for entry into Aseptic processing area. Must be able to demonstrate a sound knowledge of aseptic gowning practices.
• Author, Approve or Authorize documents as assigned. Documents include but are not limited to: Master Production Records, Quality Control test methods/forms, etc. Authorization includes a review of the content for applicability in connection with customer audit/inspections as well as GMP compliance.
• Perform other duties as required.

Qualifications

• Minimum of a Bachelor's degree in related field and/or equivalent experience.
• Minimum of 1 year of experience in quality and/or manufacturing in a pharmaceutical, biotech, or biologics cGMP regulated manufacturing environment preferred.
• Working knowledge of quality operations and ability to apply cGMPs in conformance to U.S. standards, and where appropriate, other regulatory authority standards.
• Working knowledge of GCP, GDP, GLP and cGMP regulations and their relevant ISO counterparts and ICH Guidelines.
• Thorough knowledge of aseptic manufacturing processes.
• Excellent organizational skills, attention to detail, and Good Documentation Practices.
• Proficiency in MS Word, Excel, Power Point, Microsoft Office 365 and other applications.
• Ability to communicate and work independently with scientific and/or technical personnel.
• Must possess effective interpersonal, verbal, and writing skills, patience, professionalism, and the ability to effectively interact and communicate with internal staff and management.
• Ability to thrive in a fast‑paced, patient‑focused manufacturing environment with minimal direction and able to adjust workload based on changing priorities.

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to experience prolonged sitting, some bending, stooping, and stretching. Hand‑eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required. A normal range of hearing and vision correctable to 20/20 is required. Occasional lifting up to 20 pounds is required.

Benefits and Compensation

We strive to offer a competitive benefits package that includes:

• Medical insurance coverage (multiple options to meet our employees' and their families' needs)
• Dental and vision coverage
• 401(k) match plan
• Lifestyle spending account
• Compensation (annual): $60,500 - $71,500

Visa Sponsorship Not Currently Available

IMPORTANT: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.