Job Openings

We are seeking a curious, determined professional with an interest in continuous improvement and/or project management within the pharmaceutical/biotech industry. As a junior consultant, you will have the opportunity to support the execution of large capital projects and gain invaluable experience in the industry along the way.

The Sr. Process Engineer is responsible for ensuring the proper design, reliability approach and modification of process equipment such that it has the capability to consistently meet customer expectations. They will serve as the SME on process equipment and have an understanding associated with process use.

Responsible for overseeing the packaging team producing quality products in a safe and cost effective environment on multiple shifts to meet production plans.

We are seeking a Continuous Improvement Lead responsible to develop, initiate, lead and drive continuous improvement projects such as process changes to improve operating costs.  You will be responsible for facilitating key continuous improvement activities in areas such as waste reduction, cost savings, production efficiency, maintenance reliability, quality, safety, environmental, people development, business systems, business technology and business development initiatives. The scope is limitless!

We're seeking a Validation Engineer to perform the functions for validation of product and cleaning of in-house manufacturing and packaging systems. This includes IQ/OQ/PQ, process validation and cleaning validation. This person will develop company validation standards, and support quality programs such as change control, calibration and technical releases.

We are looking for a Process Engineer that supports a wide variety of Batching, Manufacturing and Packaging equipment that utilize programmable systems including PLCs, machine vision, HMI, process controls, and instrumentation for the manufacturing facility.

Ensures plant systems are compliant with applicable regulations. Oversees and coordinates daily process and activities of QA Specialists to assure objectives are met. Coordinate plant Quality training activities as well as departmental training for QA Specialist. Assist departments in corrective actions and quality improvement initiatives.

The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of area management or designee, the Aseptic Operator is responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products.

The contents contained in this job description are the minimum requirements required to be met for the aforementioned position. Under the direction of the Sterile Operations Manager or designee, the Sterile Operations supervisor responsible for performing all necessary tasks both in and outside of the classified manufacturing suites in support of manufacture of safe and effective sterile (injectable) pharmaceutical products. 

Focusing primarily on the pharmaceutical industry, our client company provides for improvement programs, management consulting, project management, R&D support, supply chain planning and training for leading companies worldwide. 

Qualified candidates must implement, and insure the regulatory compliance of the validation program for the facility. - Writes and executes protocols for IQ, OQ, and PQ validation for plant processes and utility support; process validation; cleaning validation; process cycle development and process development; and computer validation.

In this role, you will be responsible for oversight of manufacturing engineering projects including: programming modifications of machinery and equipment, specification and procurement of new equipment and tooling, equipment installation and start-up, and supervision of team members.

Seeking an experienced Process Engineer to join our team. This position will provide support and assistance in the manufacture of pharmaceutical products for commercial and clinical supplies.

This position is responsible for packaging related projects to include package design and specifications and packaging materials specifications. This role will work in conjunction with purchasing, quality assurance, and suppliers to reduce packaging material rejects, and to implement packaging material cost reduction projects.