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Clinical Manufacturing Associate - Contract - Cranbury, NJ

Step into the future of medicine-manufacture viral vector therapies that power the next generation of gene treatments.

À±½·ÊÓƵ 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.

À±½·ÊÓƵ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓƵ is acting as an Employment Agency in relation to this vacancy.

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