The Scientist II leads biotechnology projects, focusing on upstream processing with cell culture techniques, ensuring compliance with cGMP standards, and providing technical support and documentation for biopharmaceutical manufacturing.

The Process Engineer III leads technical support and improvement initiatives in biomanufacturing, focusing on process validation, compliance, and ensuring operational efficiency.

The Automation Engineer IV will lead automation efforts in manufacturing, involving equipment design, troubleshooting, process compliance, and staff training. Responsibilities include 24/7 support, documentation, and quality audits.

Lead the MSAT process transfer team, manage technology transfer activities, and ensure compliance with regulatory standards while collaborating with cross-functional teams.

The Process Engineer IV leads continuous improvement in a GMP environment, focusing on standardization, training, and performance enhancement while coaching teams to drive results.

The Senior Specialist, Technical Quality ensures operational excellence and compliance in biomanufacturing by leading quality oversight, investigations, and improvement initiatives.

The Process Engineer will oversee equipment design, project specifications, compliance with regulatory standards, and process optimization in biopharmaceutical manufacturing.

The Process Engineer III will lead and manage biomanufacturing projects, focusing on equipment design and operational compliance within a biomanufacturing facility.

The Director will lead Downstream Process Development for Biologics, Vaccines, and Gene Therapy, overseeing project execution, staff mentorship, and technical strategy implementation.

The Director of Sales & Business Development is responsible for driving revenue in a defined territory, building strategic relationships, and generating new business opportunities in biomanufacturing, specifically in Biologics, Vaccines, and Cell and Gene Therapy.

The Specialist Network Engineer will design, implement, and maintain network infrastructures, focusing on firewalls, routing, and data center networking using Cisco technologies.

The Senior Analyst II in Quality Control (Potency) will conduct testing, validate methods, mentor junior staff, and ensure compliance with GMP standards.

The Automation Engineer III manages projects related to inspection and packaging, ensuring asset operation, leading process improvements, and providing technical support in a cGMP environment.

The Aveva PI Engineer will design, troubleshoot, and enhance data historians, assist in process improvements, and provide technical guidance on manufacturing systems.

The Director of Sales and Business Development manages the sales strategy, builds customer relationships, drives revenue growth, and oversees lead generation within the biomanufacturing industry.

Oversee technical aspects of upstream biomanufacturing, including process design, GMP documentation, troubleshooting, and training staff. Lead cGMP runs and support continuous improvement initiatives.

Provide technical support for end-user devices, manage onboarding, handle conference room technology, and contribute to continuous improvement initiatives.

The analyst performs quality control testing and documentation for pharmaceutical products, supports microbiological testing, and aids in troubleshooting and process improvements.

The role supports technology transfer and manufacturing processes, assists senior specialists, and conducts technical analyses to optimize biomanufacturing activities.

The Senior Specialist, Technical Quality oversees QA activities for pharmaceutical manufacturing, ensuring regulatory compliance and driving process improvements across departments.