Manufacturing Equipment Operator B and C Shifts

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Join to apply for the Manufacturing Associate - A, B and C Shifts role at Unither Pharmaceuticals

Who we are?

We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients’ lives to as many people as possible.

Who we are?

We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients’ lives to as many people as possible.

With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 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 280 employees.



Your role

Reporting to the Manufacturing Supervisor,

The Manufacturing Associate 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 Aseptic Manufacturing Associate 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 compliant 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 maintain aseptic standards at all times. 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 for 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.

WORK HOURS:

A

- Shift: 7:00am-3:30pm

B

- Shift: 3:00pm - 11:30pm with a 10% shift differential

C

- Shift: 11:00pm - 7:30 am with a 15% shift differential

ESSENTIAL

DUTIES / RESPONSIBILITIES:

Room & Process Ready for Production Run (25%)

Prepares for production by reviewing the production schedule, understanding deliverables, and reviewing applicable SOP’s, and any procedure changes.

Ensures that supplies, materials and documents are available as required to meet the production schedule.

Works with other departments to ensure adherence to production schedule.

Receives and distributes supplies into production area as necessary.

Executes equipment qualification protocols and validation protocols.

Product Ready for Further Processing (25%)

Operates general production equipment ensuring its proper operation, and adhering to production procedures.

Monitors and records critical process parameters.

Documents production by completing forms, reports, logs and records of equipment and batches.

Keeps equipment operating by following operating instructions, troubleshooting breakdowns, and placing work orders for repairs.

Elevates issues when work orders are placed.

Provides input regarding opportunities for improvement, waste reduction, etc. to supervision and/or during team meetings.

Support…