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MCS Manufacturing Senior Associate, Biopharma (JP11845)
Thousand Oaks, CA · Biotech/PharmaceuticalJob Title: MCS Manufacturing Senior Associate, Biopharma (JP10845)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Manufacturing Systems
Duration: 18 months
Rate: $32-37/Hr W2
Posting Date: 10/03/2023
3 Key Consulting is hiring MCS (Manufacturing and Clinical Supply) Manufacturing Sr. Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
In this vital role you will be part of the Manufacturing Systems team which is responsible for supporting manufacturing activities through new product introduction, new technology and equipment introduction, continual improvement projects, supporting the multiproduct facility operation program, CAPA ownership, and optimization/implementation of single use technologies. The position is within the drug substance supply organization in ATO Building 23 which is a dynamic environment and an important launch point for Amgen’s pipeline products. The plant manufactures drug substance at all phases of clinical trials through commercial production.
Responsibilities include:
Basic Qualifications:
Master’s degree OR
Bachelor’s degree and 2 years of experience OR
Associate’s degree and 6 years of experience
Top Must Have Skills:
Interview process:
Webex interviews. Potential for in-person follow-up.
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: Manufacturing Systems
Duration: 18 months
Rate: $32-37/Hr W2
Posting Date: 10/03/2023
3 Key Consulting is hiring MCS (Manufacturing and Clinical Supply) Manufacturing Sr. Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
In this vital role you will be part of the Manufacturing Systems team which is responsible for supporting manufacturing activities through new product introduction, new technology and equipment introduction, continual improvement projects, supporting the multiproduct facility operation program, CAPA ownership, and optimization/implementation of single use technologies. The position is within the drug substance supply organization in ATO Building 23 which is a dynamic environment and an important launch point for Amgen’s pipeline products. The plant manufactures drug substance at all phases of clinical trials through commercial production.
Responsibilities include:
- Support manufacturing by providing subject-matter expertise for drug substance upstream and downstream processes as process owner (PPO) or Single-use SME.
- Lead projects using project management skills.
- Resolve quick issues and execute function tests to troubleshoot and optimize process.
- Write protocols and reports in support of validation, function testing, equipment commissioning and qualification, and change management.
- Own Quality Records, such as CAPA, and CAPA-EV.
- Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs) as instructed by the production schedule to execute function-testing and project tasks with minimal disruption to operations.
- Available to work on site.
- Must be able to work in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work while following GMP documents (SOPs) with strict adherence to safety and compliance.
- Apply technical process, scientific, operational, and compliance knowledge with analytical troubleshooting skills to support the implementation of new technologies into the plant.
- Demonstrate strategic problem-solving skills and champion continual improvement.
- As Process owner:
o Support operational readiness of new technologies, equipment, or processes by applying technical process, scientific, operational, and compliance knowledge with project management skills
o Develop/own drug substance manufacturing processes and procedures. Draft and revise GMP manufacturing documents (SOPs, Forms). Draft and develop user requirements for new technologies. - As Single-use SME:
o Support New Product introduction and projects through SUS mapping
o Support manufacturing and quality through the SUS defect/leak triage process – perform troubleshooting on the floor, initiate investigation and bring leaks and defects to triage
o Initiate EN/SICAR records and follow process to conclusion, including working with vendors on investigation.
o Maintain up-to-date EN/SICAR/EE trackers and manage or lead small to medium projects
o Understand single-use material capabilities and user requirements for new technologies.
Basic Qualifications:
Master’s degree OR
Bachelor’s degree and 2 years of experience OR
Associate’s degree and 6 years of experience
Top Must Have Skills:
- Degree in Engineering or Life Sciences (if not, then at least 5 years’ experience)
- Experience in Drug substance GMP technical support roles, GMP manufacturing, Engineering, Process Development, or equivalent.
- Ability to learn quickly, self-monitor, and prioritize.
- Previous biopharma industry experience highly preferable
Interview process:
Webex interviews. Potential for in-person follow-up.
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at the other positions on our website www.3keyconsulting.com/careers. You are welcome to also share this opportunity with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team