JT070 - MANUFACTURING ASSOCIATE

Quality Consulting Group, LLC; Thousand Oaks (CA); On-site; USD 45,000 - 75,000; Full time

Job summary

Join a forward-thinking company in the pharmaceutical and biotech industry as a key player in their manufacturing team. This exciting role involves hands-on operations in a dynamic environment, focusing on purification processes while adhering to GMP standards. You'll have the opportunity to contribute to crucial development and clinical activities, all while working alongside a passionate team. If you thrive in fast-paced settings and are eager to make a difference in the manufacturing landscape, this position is perfect for you. Embrace the chance to grow and excel in a supportive and innovative workplace.

Qualifications

• Bachelor’s degree in a science-related field preferred.
• Experience with large-scale purification processes is preferred.

Responsibilities

• Support development, clinical, and launch activities in a dynamic production environment.
• Perform operations in the Manufacturing area, specifically for Purification processes.
• Monitor and perform critical processes with the ability to troubleshoot basic issues.

Skills

Chromatography

Filtration

Purification Processes

GMP Documentation

Troubleshooting

Education

Bachelor's degree in a science-related field

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. Work in a dynamic production environment at the client's Drug Substance plant supporting development, clinical, and launch activities.
2. Under general supervision, perform operations in the Manufacturing area, specifically for Purification processes.
3. Operate according to Standard Operating Procedures (SOPs) while complying with GMP standards in a safe manner.
4. Perform hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment.
5. Prepare buffers/media per defined manufacturing procedures (MPs) and SOPs.
6. Follow GMP documents (SOPs, MPs) with strict adherence to safety and compliance.
7. Monitor and perform critical processes with the ability to troubleshoot basic issues.
8. Initiate quality deviation reports.
9. Draft and revise documents (SOPs, MPs).
10. Identify, recommend, and implement improvements related to routine functions.
11. Review documentation for assigned functions (equipment logs, batch records).
12. Perform in-process sampling of equipment and operate analytical equipment.
13. Work around high-pressure systems and heavy equipment.

Qualifications:

• Bachelor’s degree in a science-related field is preferred; relevant manufacturing experience will also be considered.
• Highly adaptable team player capable of working in a structured, fast-paced manufacturing environment.
• Experience with large-scale purification processes, including chromatography, filtration, and pressurized equipment, is preferred.
• Detail-oriented, open to feedback, and able to follow strict GMP documentation procedures.
• Primary Shift: 7:00 AM – 8:00 PM to start.
• Rotating Shift: 7:00 AM – 8:00 PM and 7:00 PM – 8:00 AM (6-month rotations).
• Weekend work required at least one day per shift.
• Holidays required.
• Availability to work various shifts (day, swing, graveyard, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs).

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.