Manufacturing Associate Level III - Portsmouth, NH

We are looking for a skilled · Manufacturing Associate III to lead end-to-end manufacturing · (Bioreactors, Chromatography, · CIP/SIP) in a cGMP environment. · Lead end-to-end manufacturing (Bioreactors, · Chromatography, CIP/SIP) · Maintain a 6S-ready facility. · ...

The HVAC Maintenance Mechanic Level III is responsible for preventive maintenance of Air Handlers Walk-in Cold Room and Freezer systems periodic inspections of HVAC systems to ensure proper operation and perform daily checks repairs in compliance with company departmental Standar ...

The Manufacturing Associate III is responsible for manufacturing therapeutic proteins under cGMP conditions. · Set up operate equipment monitor production processes including clean-in-place (CIP) steam-in-place (SIP) operations report production in written electronic documents in ...

The Manufacturing Associate III is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. · ...

+Supports Engineering Services group by performing daily checks & operating Direct & Indirect Maintenance equipment. · +Perform all work safely following GMP guidelines SOPs & work instructions. · ...

The State of New Hampshire Department of Health and Human Services Division for Children Youth & Families has a full-time vacancy for Child Protective Service Worker I-IV. · This role involves assessing reports of alleged abuse/neglect of children under RSA 169-C providing for th ...

The Manufacturing Associate III is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. · Executing process recipes · FOLLOWING WRITTEN PROCEDURES (SOPs) · MONITORING EQUIPMENT AND PROCESSES · ...

The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. They are expected to be fully proficient in executing process recipes, following written procedures (SOPs), monitoring equipment and processes, · Set up, operate eq ...

The Manufacturing Associate III is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. · An agile career and dynamic working culture. · An inclusive and ethical workplace. · ...

The Equipment Validation Specialist ensures all critical GMP equipment and systems are validated and maintained. · Ensure validation of all critical GMP equipment and systems · ...

The Manufacturing Associate III is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. · ...

The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. · Set up, operate equipment, and monitor production processes, · Demonstrate proficiency and understanding of suite specific production activities and laboratory ta ...

The Equipment Validation Specialist (Levels III & IV) ensures all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters, and global regulatory guidelines. · Ensure validation of all critical GMP equipment and syst ...

The Equipment Validation Specialist ensures all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters, and global regulatory guidelines. · Ensure validation of all critical GMP equipment and systems in accordance ...

The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. They are expected to be fully proficient in executing process recipes, following written procedures (SOPs), monitoring equipment and processes, independently perfor ...

We are seeking a skilled Quality Control Technical Transfer Analyst III to join our team in Portsmouth. · We need someone who will act as key member of Quality department supporting production by driving technical transfers activities participating critical quality testing,This i ...

We are seeking a fully proficient Biotechnologist III to join our full-time, on-site production team in Portsmouth, NH. · ...

The Logistics Specialist will be responsible for dispensing raw materials liquids and powders under cGMP conditions to support the manufacture of therapeutic proteins. They will perform tasks such as weighing, monitoring equipment processes, and preparing materials for transport. ...

We are seeking a fully proficient Biotechnologist III to join our full-time, on-site production team in Portsmouth, NH. · High school diploma or equivalent is required. · An AS/BS in a Science-related field is preferred. · ...

We are seeking a fully proficient Biotechnologist III to join our full-time production team in Portsmouth, NH working on rotational night shift (7 PM – 7 AM). This intermediate-level role is responsible for the cGMP manufacture of therapeutic proteins focusing heavily on upstream ...