Shoolin Inc Jobs in United States

Seeking an experienced Manufacturing Engineer to support medical device manufacturing operations. · ...

Seeking a senior Project Manager with deep expertise in Commissioning & Qualification (C&Q) of dark utilities to lead construction and qualification activities for an automated warehouse in a regulated environment. · Lead and manage construction and C&Q activities for dark utilit ...

The Reliability Engineer will be responsible for driving equipment reliability, performance trending, · and continuous improvement initiatives within a regulated pharmaceutical manufacturing environment.Lead equipment reliability and performance monitoring programs. · Evaluate eq ...

This Chemical Operator role involves regenerating filtration resin and preparing mobile water treatment equipment for field use. · ...

We are seeking a CSV Engineer with hands-on experience in Computer System Validation and Commissioning, Qualification, and Validation (CQV) to support GMP-regulated pharmaceutical or biotech operations across multiple sites. · ...

Responsible for assisting in the fabrication of various components and/or whole parts to support the production and manufacturing of specialized water treatment equipment and associated systems. · ...

Seeking a CSV Engineer with hands-on experience in Computer System Validation and Commissioning, Qualification, and Validation (CQV) to support GMP-regulated pharmaceutical or biotech operations. · ...

Seeking a Validation Engineer to support pharmaceutical or biotech manufacturing operations with a strong focus on Vaporized Hydrogen Peroxide (VHP) decontamination processes. · ...

Maintenance Tech Provide preventative maintenance for the facilities equipment like printers scanners scales forklifts they will build and maintain racks and fixtures They need to be able to troubleshoot and repair the facilities equipment to keep the warehouse running Need to ha ...

The Calibration Technician will support calibration, maintenance, and compliance of GMP-critical equipment used in regulated pharmaceutical, biotechnology, or medical device manufacturing environments. · Perform calibration, verification, and maintenance of GMP-critical instrumen ...

This role involves leading complex projects related to utilities management. · Responsibilities include: · Managing multiple vendors · Coodinating with teams for scope alignment · ...

The Quality Program Manager will lead enterprise-level quality remediation programs with a primary focus on FDA 483 and Warning Letter remediation. · A leader for driving program governance, cross-functional alignment, and sustainable Quality Management System (QMS) improvements ...

Seeking a Mechanical Designer/Drafter to support fixture and tooling documentation for medical device manufacturing. · ...

+The client needs someone with Facilities CQV experience including EMPQ (environmental monitoring performance qualification), Vessel IQ/OQ/PQ including mixing and temp mapping. · ...

We are seeking a hands-on Sterilization Validation Engineer with strong expertise in lyophilization (freeze-drying) to support sterile pharmaceutical manufacturing operations. · ...

The Utilities Engineer will be responsible for supporting the operation maintenance and reliability of critical clean utility systems within a regulated pharmaceutical manufacturing environment. · The role will focus on ensuring compliant reliable and efficient operation of syste ...

As a Controls Engineer, you'll play a key role in designing and building cutting-edge automation and robotic systems for a world-class Powertrain facility. · This is an opportunity to work on innovative projects that push the boundaries of technology and efficiency in a high-perf ...

A hands-on Project Engineer is sought to support facilities and equipment capital projects within cleanroom and controlled manufacturing environments. · ...

The CQV Engineer will execute commissioning qualification validation testing activities in a GMP pharmaceutical manufacturing environment. · <li_Execute IQ OQ PQ protocols for pharmaceutical manufacturing equipment processes.<li_Perform hands-on test execution autoclaves parts wa ...

Sterilization Validation (Lyophilizer Specialist) performs lyophilization processes and equipment on the floor execution. Key responsibilities include Life Cycle Development, sterility and sterilization validation, IQ OQ PQ for lyophilizers. · Perform Life Cycle Development · ...