JT078 - MANUFACTURING ASSOCIATE

Quality Consulting Group, LLC; Thousand Oaks (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

Quality Consulting Group, LLC is seeking a motivated individual for a role in chemical engineering. You'll be involved in manufacturing activities, including sampling cell cultures and cleaning equipment. The ideal candidate should hold a Bachelor's degree in chemical engineering or related fields and have at least one year of relevant experience in manufacturing.

Qualifications

• Minimum 1 year of related experience.
• Experience in manufacturing equipment setup and sanitization.
• Knowledge of GMP documents with adherence to safety standards.

Responsibilities

• Sample and analyze cell cultures and clean equipment.
• Perform operations in the manufacturing area under supervision.
• Draft and revise SOPs and maintain organized workspace.

Skills

Mechanical inclination

Cleanliness

Teamwork

Problem solving

Education

Bachelor's degree in chemical engineering

Bachelor's degree in engineering

Bachelor's degree in biology

Bachelor's degree in chemistry

Job description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated, and enthusiastic individual to join our team. In this role, you’ll work with a highly enthusiastic team, contributing to a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

1. Sample and analyze cell culture, review reactor trends, passage cell culture from one stage to the next sterilely, clean the plant, edit documents.
2. Work in a dynamic production environment on-site supporting development, clinical, and launch activities.
3. Perform operations in the Manufacturing area under general supervision.
4. Follow Standard Operating Procedures (SOPs) during operations.
5. Perform in-process sampling of equipment and operate analytical equipment.
6. Conduct washroom activities: clean small- and large-scale equipment used in production activities.
7. Maintain an organized and clean workspace.
8. Initiate quality reports.
9. Draft and revise documents (SOPs, MPs).
10. Assist in reviewing documentation for assigned functions (equipment logs, batch records).
11. Work around high-pressure systems and occasionally handle heavy equipment.

Qualifications:

1. Bachelor's degree in chemical engineering, engineering, biology, or chemistry.
2. At least 1 year of related experience.
3. Experience in setup, cleaning, and sanitization of manufacturing equipment.
4. Experience in preparing buffers/media according to manufacturing procedures (MPs) and SOPs.
5. Knowledge of GMP documents (SOPs, MPs) with strict safety and compliance adherence.
6. Ability to work in a manufacturing environment wearing steel toe shoes, lab coat, safety glasses, and gloves.
7. Mechanically inclined.
8. Comfortable with physical labor, standing for extended periods (this is an on-your-feet role).
9. Day shift: 8 am - 4:30 pm, Sunday to Thursday or Tuesday to Saturday.
10. Flexible and available for weekend and holiday work.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.