Actively engage in site safety culture. Read, understand, and comply with cGMPs (Good Manufacturing Practices) and SOPs (Standard Operating Procedures), including general safety, lock outs, etc. Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities. Train/guide others on systems, software, equipment, procedures, and/or

Member of the Engineering Dept and perform the functions of a Responsible System Engineer (RSE) for assigned systems. Lead, plan and execute the design, installation, qualification, operation, maintenance, and continuous improvement of mechanical systems as applied to BioPharma manufacturing facility (e.g. HVAC systems, Boilers, Heat exchangers, Compressors, Processes ves

The Integration Manager manages the design, development, implementation and support of frontend and backend APIs/Messaging solutions using middleware integration tools and platform(s) to integrate disparate business systems in multi tier environments across Resilience. Key responsibilities include General description of the role Collaborate with business stakeholders, IT

Support the preparation, planning, logistics, and execution of the activities related to client audits and inspections. Actively support the Logistics Center during an external audit/inspection. Participate in the established review cycle of QA controlled documents to assure practices reflect written procedures. Coordinate and support GxP Documentation Control Systems to

The Quality Technician II (Day Shift) should autonomously perform tasks related to environmental monitoring to support the regulatory requirements of a sterile manufacturing site. This position requires operating equipment in various classified/non classified areas up to a Class 100 aseptic environment and in a laboratory setting. NOTE This is a Day Shift position (12 hou

This position autonomously performs tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. This includes operating equipment in various classified/non classified areas up to a Grade A aseptic environment and in a laboratory setting and maintaining gowning qualification. In addition, the incumbent will perform tasks re

The Quality Technician II, Aseptic Control (Night Shift) should autonomously perform tasks related to environmental monitoring to support the regulatory requirements of a sterile manufacturing site. This position requires operating equipment in various classified/non classified areas up to a Class 100 aseptic environment and in a laboratory setting. NOTE This is a Night S

We seek an experienced Analyst, QC Bioassay / Biochemistry to support establishing new commercial level in house GMP testing laboratories performing release and stability testing for multiple stages of our gene therapy and immune oncology products. This includes performing analytical methods, data review and trending, and implementation of GMP operational support systems

The Analyst II , Quality Control, will be responsible for method development, transfer qualification, validation and performing various in vitro assays to support drugs and clinical product development. These products will include recombinant vaccines, viral based vaccines, antibodies and other therapeutic biopharmaceuticals. This position requires working with cross func

Provide direction to PET personnel in the efficient use of equipment and materials to produce quality products in accordance with the PET Plan or Rhythm Wheel Responsible for all PET activity to include coordination of support staff, scheduling, and improvement initiatives. This coordination may be across shifts and across Process Facilitators directly reporting to this r

This position is responsible for all QA activities that directly support execution of the process both within the Process Execution Team (PET) and in assigned areas outside of the PETs. These activities may include, but are not limited to, batch release, change control and documentation, equipment and process validation, deviation investigations, SOPs, supplier management

Prepare documentation of activities, actions, and/or results. Read SOPs (Standard Operating Procedures) and excerpts from technical documentation. Complete required training. Ensure proper documentation practices during job activities. Perform visual inspections. Conduct troubleshooting activities. Gather, organize, and communicate operational information to others. Lead

A career at Resilience is more than just a job it's an opportunity to change the future. Resilience is a technology focused biomanufacturing company that's changing the way medicine is made . We're building a sustainable network of high tech, end to end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For

A career at Resilience is more than just a job it's an opportunity to change the future. Resilience is a technology focused biomanufacturing company that's changing the way medicine is made . We're building a sustainable network of high tech, end to end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For

A career at Resilience is more than just a job it's an opportunity to change the future. Resilience is a technology focused biomanufacturing company that's changing the way medicine is made . We're building a sustainable network of high tech, end to end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For