Manufacturing Associate III, Buffer Media Services

## Manufacturing Associate III, Buffer Media Services (3-6 Month Contract)
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Milford, MA, United States:
Full time:
Posted 2 Days Ago:
JR2812
** Advancing medicine to save lives. Together.
** Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.  Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals.

As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions – together with our clients.

Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.  As an independent family-owned company, we live by the motto:
Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.

The Manufacturing Associate III serves as a senior subject matter expert within biologics manufacturing operations, providing strategic and operational leadership across all manufacturing teams. This role is responsible for overseeing the execution of complex manufacturing processes, ensuring consistent compliance with cGMP requirements, environmental health and safety (EHS) standards, and all applicable regulatory expectations.
In addition to advanced process execution and troubleshooting, the Lead drives operational excellence by proactively identifying and mitigating risks, leading deviation investigations, and ensuring timely and effective CAPA implementation. This role is accountable for coordinating cross-functional activities, optimizing workflows, and supporting continuous improvement initiatives to enhance efficiency, compliance, and overall process robustness.
The Manufacturing III provides direct guidance, mentorship, and training to associates, fostering technical development and reinforcing a culture of compliance and accountability. They serve as a key point of contact during critical operations, escalations, and audits, ensuring clear communication and alignment across departments.
This role maintains full ownership of production readiness and execution, ensuring that all manufacturing teams are consistently equipped with qualified materials, components, and equipment, while driving adherence to production schedules and minimizing operational disruptions.
** Duties and Responsibilities
*** Perform operations of the following (may be applicable to commercial scale product, development studies, clinical scale, or validation activities).
* Prepare buffers and media, perform weigh-and-dispense activities, and support manufacturing teams as needed.
* Perform applicable operations for commercial-scale products, development studies, clinical materials, or validation activities.
* Supports monitoring and documentation of batch-related activities, including data entry in electronic systems, and completes required documentation in accordance with GDP and cGMP guidelines.
* Communicates effectively with external stakeholders (e.g., auditors and global colleagues) and collaborates with cross-functional groups to support manufacturing operations
* Familiar…