Join a global leader in mRNA innovation – now hiring a Manufacturing Associate.
About the Client
Our client is a pioneer in mRNA technology, focusing on vaccine and therapeutic development. They are establishing a state-of-the-art research, development, and manufacturing facility dedicated to onshore mRNA vaccine production for respiratory diseases, with a growing global presence and a commitment to public health.
The Opportunity
We are looking for a skilled, digitally proficient Manufacturing Associate to operate advanced manufacturing equipment within a high-tech production environment, ensuring compliance with cGMP and health & safety standards, and contributing to the production of vital vaccines.
Responsibilities
* Operate production equipment in a cleanroom environment, adhering to cGMP and safety protocols.
* Support QA teams with batch documentation and release processes.
* Participate in investigations and CAPA processes to address deviations.
* Troubleshoot equipment and digital systems to ensure continuous operation.
* Perform routine maintenance and maintain training records.
* Contribute to continuous improvement initiatives and cross-functional projects.
Qualifications and Skills
* Minimum of 3 years’ experience in a GMP manufacturing environment.
* Degree in Pharmaceutical Production Technology or a related field.
* Strong technical and scientific skills.
* Experience with filtration, chromatography, and cold chain management is advantageous.
* Knowledge of regulatory guidelines and audit readiness.
* Excellent communication, organizational, and teamwork skills.
* Proactive, detail-oriented, with a passion for innovation.
Work Schedule
This is a site-based role at the client’s facility. The work pattern during manufacturing campaigns is a 2-2-3 (Panama) shift pattern:
* 12-hour shifts
* 2 days on, 2 days off, 3 days on, rotating every 28 days.
About Planet Pharma
Planet Pharma is an American-owned employment agency providing global staffing solutions. Headquartered in Chicago with a regional office in London, we operate in over 30 countries, supporting 2500+ contractors worldwide. We specialize in regulatory affairs, pharmacovigilance, QA, QC, clinical development, and more.
We are committed to equal opportunity employment and welcome applications from all qualified candidates regardless of race, gender, disability, religion, sexual orientation, or age.
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