JT303 - MANUFACTURING SR. ASSOCIATE
Quality Consulting Group, LLCThousand Oaks, California, United States
Posted May 22, 2026
Full Time
About the Company
Quality Consulting Group, LLC is a specialized consultancy firm providing comprehensive services to pharmaceutical, biotechnology, food, and medical device industries. With expertise in regulatory compliance, quality operations, validation, training, and technical support, the company helps clients implement industry standards such as Validation Guidance, ICH Guidelines, and Process Excellence tools. Quality Consulting Group stands out by offering a wide range of services including quality management, risk management, staffing, and human resources, ensuring clients achieve operational excellence and regulatory compliance.
Job Description
Quality Consulting Group is looking for a Senior Associate to join their team in the manufacturing industry. The ideal candidate will have experience in GMP technical support roles, GMP manufacturing, and downstream operations. The role will involve working with a highly enthusiastic team to contribute to a world-class manufacturing industry in Puerto Rico & USA.
Requirements
- Associate degree in engineering or Life Sciences
- 2 years or more experience in Drug substance GMP technical support roles, GMP manufacturing
- Technical knowledge of downstream operations
- Project management skills
- GMP knowledge and experience in a GMP environment
- Experience running functional test and writing protocols
- Ability to work in a clean room environment with proper attire
Benefits
- Equal opportunity employer