In this role, you will integrate safety and health requirements into complex project planning, design, and operations to reduce the potential for adverse impacts. You will perform risk assessments, provide input on bid decisions, lead meetings and communications, and track and monitor performance trends. Your recommendations will contribute to enhanced quality of safety procedures and work processes.

Under general direction of the Lead, the Customer Integration Specialist works directly with the divisional and regional management team to provide data integrity, consistency, and reliability throughout the region. This critical role is responsible for all regional customer maintenance on the information technology system within the assigned region, contributing to the profitability of the customer.

• Group is involved in a combination of research and system engineering/application efforts focused on the goals of enhancing the capacity and the flexibility of future generations of communications satellites. A major focus of Group is to develop proof-of-concept test beds for the US Air Force to be used at government and contractor facilities within the United States..

Billing Specialist I will be responsible for qualifying, preparing and submitting claims to major medical. Will be working with billing and reimbursement staff. This position requires work within several different operating systems and web-based programs to retrieve document images, collect supporting or additional information on files and work claims through to resolution to ensure compliant, timely and accurate billing practices.

Print Center responsible for assisting with printing and finishing jobs. They need to have print center experience. Standing to fulfill print work and bindery equipment. Lifting things like cases of paper to use for printing. Walking within the Hospital to deliver some of the print jobs.

The contingent worker chosen for this role will provide customer service, mail, print, and general office support. This role will also require shipping and receiving. They receive equipment packages that they open, clean and test equipment (monitors, mice, etc.) and then repackage and ship out

Performs review of documents, records and procedures supporting release of clinical and commercial GMP products and participates in development of GMP operations, as assigned. Performs review of validation documentation, periodic reviews of validated systems, and/or procedures, as assigned.

You will be part of a multi-disciplinary team responsible for cGMP production of phase I/II clinical drug substance supporting the Biotherapeutics portfolio. Your initial focus will be as part of the manufacturing team focused on mammalian bio-processing. This includes and not limited to supporting the manufacturing operations team, reviewing Standard Operating Procedures, reviewing batch records, and standard work. As part of technical operations, you will be a team member who is relied to have a good understanding of procedures, techniques, tools, materials and equipment. Your decision making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, some of which may vary in scope, sequence, complexity and timing. You will contribute to the team’s success by sharing of previously acquired knowledge. It is your hard work and focus that will help in making ready to achieve new milestones and help patients across the globe.

Performs a variety of support functions to support the department. Handles multiple projects and may assist in compiling data and generating reports. Requires 1-4 years of experience in the field or in a related area. Familiar with standard concepts, practices, and procedures within a particular field. Location: Position is hybrid with the requirement to be in the office 1x per week on Wednesdays. It can be located near the office, but there is a strong preference that the candidate be local to the Houston/Kinder Morgan location.