Associate, Manufacturing - Operations

Abeona; Cleveland (OH); On-site; USD 50,000 - 90,000; Full time

Job summary

An innovative firm is seeking a Manufacturing Operations Associate to join a dynamic team in Cleveland. This role involves supporting the production of cutting-edge gene therapies and requires expertise in aseptic techniques and cell culture. The successful candidate will execute cGMP processes, ensuring high-quality production while collaborating with a dedicated team. With a focus on process optimization and adherence to strict regulatory standards, this position offers a unique opportunity to contribute to groundbreaking advancements in the field of biotechnology. If you're passionate about making a difference in the healthcare landscape, this is the role for you.

Qualifications

• 2-4 years lab or GXP production experience required.
• Experience with mammalian/insect cell culture technology preferred.

Responsibilities

• Execute cGMP processes and maintain compliance with training.
• Perform cell culture techniques and retroviral vector production.

Skills

Aseptic technique

Cell culture techniques

Project management

Attention to detail

Communication skills

Education

BS in scientific discipline

MS in scientific discipline

Tools

Microsoft Office

Job description

Abeona is looking for a Manufacturing Operations Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector and autologous gene-corrected cell therapies. Responsibilities will include executing protocols and manufacturing clinical and commercial material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position.

Essential Duties and Responsibilities:

1. Performs cGMP processes within the manufacturing facility in conjunction with manufacturing production records (MPRs) and operates within written procedures.
2. Execute studies in support of process optimization and validation.
3. Performs cell culture techniques including cell passaging, microscopy, and cell observation.
4. Performs retroviral vector transduction and production of retroviral vector.
5. Maintains compliance by completing ongoing training.
6. Author, review, and provide technical support for manufacturing SOPs, MPRs, and other documents.
7. Maintains manufacturing and laboratory equipment through preventive maintenance and routine cleaning.
8. Identify, suggest, and manage projects in parallel with manufacturing activities to reach set goals.
9. Ability to collaborate with others while maintaining a strong capability in independent, critical thought.
10. Strong organizational skills required.
11. Must be able to work as part of a team.
12. Contribute to activities that support safety and/or lab infrastructure.

Qualifications:

1. BS or equivalent in scientific discipline and min of 2-4 years related lab or GXP production experience or MS or equivalent with 1-2 years of experience.
2. Experience with mammalian and/or insect cell culture technology.
3. Experience with production processes for cell therapies and/or viral vectors or vaccines is highly preferred.
4. Familiarity with aseptic technique and cell culture is strongly preferred.

Other Skills and Abilities:

1. Advanced communication and organizational skills.
2. Advanced interpersonal skills and the ability to work with individuals across all organizational levels.
3. Attention to detail and accuracy.
4. Detailed record keeping and data documentation.
5. Demonstrated project management skills.
6. Ability to read, analyze, and interpret technical procedures, publications, intellectual property and/or government documents.
7. Working knowledge of GLP, GDP, GCP, and GMP regulations and their ISO counterparts and ICH Guidelines.
8. High level of proficiency with Microsoft Office programs.
9. Less than 10% travel. Any travel will be reimbursed in accordance with company policy.

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 office equipment is required. A normal range of hearing and vision correctable to 20/20 is required. Occasional lifting of up to 50 pounds is required.