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. This position will require working in various Controlled/Non-Classified areas.
Requirements
- Perform the duties of operating assigned machinery consisting of servicing machines with materials, monitoring equipment status, reintroduction of materials, manually palletizing finished materials, and assuring a smooth flow of product.
- Perform manual packaging tasks as required including hand packaging and rework of in-process and finished material.
- Perform visual quality inspection and sampling of in-process materials. Promptly escalate concerns to Lead and Process Facilitator as needed.
- Perform minor troubleshooting including clearing minor jams and identifying equipment defects.
- Work collaboratively with technical resources to resolve equipment issues as needed.
- Perform inventory control and reconciliation activities, which may require the use of SAP and WES in a limited role.
- Perform cleaning, housekeeping and line clearance activities for assigned areas to maintain a cGMP environment.
- Perform batch record and GMP documentation entries.
- Be familiar with job-related safety procedures and hazards including PPEs, ergonomics, LOTO, human safety, material handling, chemical handling, and spill controls. Report all discrepancies to process facilitator.
- Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety and quality procedures.
- Support lean activities and process improvement work such as performing 5S in the work area, participating in problem-solving, and manual tracking of performance data for OEE and process improvement analysis.
- Act as a certified OJT trainer on the team on assigned equipment and process tasks.
- Review process documents such as operational SOPs, forms, and batch records for accuracy.
- Identify and provide suggestions for process improvement while maintaining quality and cGMP compliance as opportunities arise.
- Execute protocols as required as a part of equipment qualification and process validation work.
- Be flexible and support other work areas within the Manufacturing Team as needed.
- Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee as needed.
- Acquire and maintain all required certifications and qualifications for the assigned work area.
- Capable and motivated to learn new skills and develop new capabilities on an on-going basis to contribute to the success of the Process Execution Team.
- Ability to work effectively in a team environment.
- Candidate should possess the ability to work in and adapt to a changing/demanding environment.
Benefits
- Annual cash bonus program
- 401(k) plan with a generous company match
- Healthcare (including medical, dental and vision)
- Family building benefits
- Life and disability insurance
- Flexible time off
- Paid holidays
- Other paid leaves of absence
- Tuition reimbursement
- Support for caregiving needs
