Manufacturing Equipment Operator- C Shift

Manufacturing Equipment Operator- C Shift

Who we are?

As a French pharmaceutical industrial group, we strive to make healthcare solutions that improve and simplify patients' lives accessible to as many people as possible.

As a world leader in sterile single dose, we have 10 sites on 4 continents and more than 2400 employees.

Since 2013, our site Unither Manufacturing LLC. based in Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 360 employees.

Reporting to the Manufacturing Supervisor,

Monday
- Friday 11pm-7:30am

The Manufacturing Equipment Operator is responsible for manufacturing pharmaceutical batches by setting up, cleaning, operating, and maintaining equipment. Executes all Production processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Equipment Operator is expected to fully participate in both departmental projects and any quality working teams that may be applicable.

This position shall be responsible for the hands-on execution of activities as they relate to the manufacturing or packaging of products. Supports the leader and subject matter (SME) expert in their area(s) of responsibility. Supports production, operations projects and process improvements. Maintains accurate and complete documentation on all activities. Responsible for monitoring and maintaining quality of product and processes. Will require working with other Associates to minimize downtime during startup process.

Perform, and verify, integrity of sterilizing grade filters used in product transfers. Requires working in a classified area (ISO
7) while dressed in clean room gown for extended periods of time. Must be able to obtain, and maintain, clean room gowning certification. When manufacturing batch, manufacturing associates are to abide by good clean room techniques. Will use, and troubleshoot, Supervisory Control Systems during manufacture of batches; these are heavily automated systems used for batch processing and cleaning and steaming of tanks and transfer lines.

Ability to sample pH readings and perform titrations. Attention to detail is critical as an oversight can compromise the sterility of a batch. Performs integrity testing of sterilizing grade air and product filters using bubble point and diffusion testing methods.

• Prepares for production by reviewing the production schedule, understanding