Location: Research Triangle Park, NC 27709 (Onsite) Responsible for performing testing and sampling of bulk gases, monitoring utility parameters, inspecting raw materials, and collaborating with cross-functional teams including Microbiology and Manufacturing to ensure quality and compliance in research and production activities.

Location : Portsmouth NH 03801. The Dispensing Technician Level 1 supports the manufacturing of therapeutic proteins (API) by dispensing raw materials, including liquids, powders, acids, and bases, under cGMP conditions. This night-shift role requires attention to detail, adherence to cGMP and SOPs, and active participation in safety and quality processes within a controlled Class C environment.

Location (mandatory): Portsmouth NH Looking for a candidate with science degree and some manufacturing experience

Location (mandatory): Portsmouth NH The Quality Microbial Control Analyst V will be part of the Quality Microbial Control team, supporting the production of in-process and final product drug lots for customers. The role involves quality testing for customer stability studies, providing timely, high-quality results to meet Manufacturing demands. The Analyst will apply job skills, follow company policies, and contribute to projects and tasks of increasing scope. The role also provides technical support within the department and across the facility, potentially acting as a subject matter expert (SME) and supporting the supervisor in their absence.

Location- Westborough, MA 01581. The QC Scientist I Raw Materials will be responsible for executing and troubleshooting a variety of laboratory test methods, defining the requirements for implementation of procedures, processes and assays within QC, and identifying and implementing continuous improvement initiatives related to overall laboratory functionality. This role will work closely with the assay transfer technical lead. This role will mentor junior analysts and develop and facilitate training initiatives within the labs. Preferred: • Experience in a Biotech/Pharmaceutical company with a high growth, fast-paced environment. • Experience in qualification of analytical equipment, including those with computerized systems. • Experience in method validation/qualification/verification/transfer. Working Conditions: • This role frequently requires long periods of sitting, standing and use of hands and regular motion to include bending, stooping, and lifting up to 20lbs. • This is an on-site role working in a cGMP regulated manufacturing facility.

Location: Cambridge, MA 02139 Description: The primary role of the Media Prep Technician is to prepare pharmaceutical buffers, agar plates, and tissue culture media for Client’s lab operations in Cambridge, MA. Formulating buffers, plates and media for the PRD community allows our scientists to focus their time and skills on developing Breakthroughs That Change Patients’ Lives

A QA Specialist II (Quality Operations) ensures that manufacturing and related processes comply with regulatory and quality standards such as GMP and ISO. The role involves supporting production activities, reviewing documentation, overseeing compliance, and contributing to continuous improvement in a biopharmaceutical or life sciences environment.

This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsibilities include preparation and compilation of submission/documentation for specific projects working as or working with the Regulatory CMC Lead and key stakeholders, primary contact for affiliates on Regulatory CMC activities in the assigned regions and managing of routine and non-routine Health Authority interactions as delegated. Depending on the stage of development and complexity of the program, this role can be a Regulatory CMC Lead for early stage development programs or working with the Regulatory CMC Lead for late stage development or commercial programs. The Regulatory CMC Lead is the primary global contact for Regulatory CMC activities, as delegated. This candidate must have proven leadership and abilities to work cross-functionally and across cultures. Strong communication, Regulatory CMC knowledge and interpersonal skills are required. 100% Remote or hybrid (Cambridge, MA or RTP)

Location: Portsmouth NH. Looking for a candidate with science degree and some manufacturing experience