Clinical Manufacturing Associate - Contract - Cranbury, NJ
Step into the future of medicine-manufacture viral vector therapies that power the next generation of gene treatments.
Proclinical is seeking a Clinical Manufacturing Associate to join a dynamic team in NJ, US. If you are passionate about science and gene therapy and thrive in a fast-paced environment, this role offers an exciting opportunity to make a meaningful impact.
Primary Responsibilities:
The successful candidate will contribute to the start-up of a cleanroom facility and support the cGMP manufacturing of viral vector therapies for clinical trials. This position involves hands-on process operations, equipment setup and maintenance, inventory management, and technical documentation.
Skills & Requirements:
- Academic background in Life Sciences, Biotechnology, Chemical Engineering, or a related field.
- Familiarity with mammalian/microbial cell culture techniques, filtration, purification, and aseptic techniques.
- Experience in clinical manufacturing, with the ability to execute production based on established procedures.
- Strong attention to detail and a commitment to completing tasks accurately and efficiently.
- Ability to work flexible hours, including early mornings, late evenings, nights, or weekends as needed.
- Effective communication and collaboration skills to work with diverse teams and escalate issues when necessary.
- Problem-solving mindset with the ability to assess options and take proactive action.
The Clinical Manufacturing Associate's responsibilities will be:
- Perform hands-on operations to manufacture viral vector therapies following established protocols.
- Set up, operate, and clean equipment while maintaining cleanrooms and equipment in an inspection-ready state.
- Monitor and troubleshoot processes and equipment to ensure smooth operations.
- Receive, process, and store materials and supplies in coordination with Materials Management-Warehouse personnel.
- Author and update Standard Operating Procedures (SOPs) and other technical documents.
- Complete batch documentation, including Batch Records, Forms, Logbooks, Sample Requests, and Test Results.
- Proactively identify and resolve potential issues with equipment, supplies, or processes.
- Collaborate with cross-functional teams and stakeholders to address challenges and implement improvements.
- Follow all safety, regulatory, and compliance requirements.
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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