The Sr. Manufacturing Associate I/II Upstream is responsible for the execution of production activities for early and late phase Cell Culture programs within a GMP environment. The Sr. Manufacturing Associate I/II Upstream must follow the instructions depicted in SR's, EPR's, BR's, SOP's and forms. Additionally, must ensure all work is conducted following Good Manufacturi

The Manufacturing Specialist I/II is responsible for supporting equipment and cGMP operations for the Downstream team in a large scale biopharmaceutical facility. The manufacturing specialist has experience in downstream unit operations (UF/DF, chromatography techniques, purification, viral inactivation), and a working knowledge of other downstream equipment. The incumben

Manages all activities related to the planning, purchase, receipt, warehousing, and distribution of supplies and materials used in the company's development, production, and administrative support functions. Position Responsibilities Execute the daily operations of inventory planning and procurement areas in the development and execution of short and long range production

The specialist has responsibility for the implementation of the environmental, health, safety, and sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous improvement. EHS&S supports operations of biologic contract development and manufacturing organization. Responsibilities include incident response, reporting and investigatio

Identifies, evaluates, develops and closes new customers and expands business at existing customers. Identifies and assists in progressing biopharmaceutical business opportunities including new scientific and strategic partnerships, collaborations, licensing opportunities, joint ventures and alliances. Establishes and implements appropriate development strategies to suppo

The calibration technician works within a team environment that actively supports, participates, and embraces an empowered team culture including significant interaction with Quality Assurance, Manufacturing Operations, Engineering, and other support groups. Perform calibration to instrumentation that includes but is not limited to temperature, relative humidity (RH), tim

This position operates on a 2 2 3 day shift schedule. The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleaning of equipment, prepares buffers/medias, glass wash of misc. parts, assembles setups and filters, autoclaves media/materials, tests filter integrity, manages

This position operates on a 2 2 3 day shift schedule. The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing. This position performs all routine/non routine cleaning of equipment, prepares buffers/medias, glass wash of misc. parts, assembles setups and filters, autoclaves media/materials, tests filter integrity, manages

Responsible for directing and overseeing microbiological programs and methods activities for processes, instruments and equipment. Ensures the effective use of material, equipment and personnel while developing products and processes at high quality levels. This person is responsible for the aspects of the following programs as directed by management Environmental Monitor

This position is on 2 2 3 shifts, 7p 7a. MFG Support Associate I/II is responsible for the execution of production activities of Media and Buffer preparation within a GMP environment. The Manufacturing Associate I/II Support must follow the instructions depicted in SR's (Media / Buffer Solution Records), SOP's and forms. Additionally, must ensure all work is conducted fol

Perform the day to day management and distribution of samples and materials. Will be primarily responsible for logging samples and reference materials in and out and performing stability activities in compliance with standard operating procedures, safety, and cGMP regulations. Responsible for all associated documentation and for maintenance of stability/sample coordinatio

The incumbent will support GMP manufacturing operations for late phase and commercial mammalian Cell Culture programs and oversee compliance activities for the department. The individual will support operations during the planning stages by releasing electronic manufacturing logbooks and records, as needed. The employee will support operations during the execution stage b

We are looking for a Lab Systems Support Analyst for our new, state of the art manufacturing facility being built in Geneva. In this role you would be joining a small, rapidly growing and highly motivated team setting up the busines in Geneva while drawing on the support of your colleagues in the US and Europe. What you’ll do You are excited at the prospect of joini

Oversees the management of all areas of Upstream manufacturing (media preparation, cell culture and harvest steps) and related Specialist support teams involved in producing drug substances with the aim of achieving schedule, quality and cost objectives. JOB RESPONSIBILITIES Lead Upstream staff hiring, oversee training and lead staff evaluations. Develop an engaged and hi

The manufacturing support manager will oversee the management of the manufacturing support activities in support of the startup and production at a new clinical GMP biopharmaceutical manufacturing facility. The individual will lead the manufacturing support team with the aim of achieving superior quality, safety, productivity and cost objectives. The individual will lead