Process Engineer II, MSAT

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 more information, please visit www.resilience.com

Job Summary :

The Process Engineer will work in the Manufacturing Science and Technology (MSAT) group to provide technical support to CMP Manufacturing operations at the Philadelphia, PA site.

The responsibility of this role is to support cell therapy production. This is a site based role in East Norriton, PA.

Job Responsibilities :

Leading the introduction of new manufacturing processes to the facility for clinical and commercial manufacturing of cell therapy products.

Performing technology transfer from the development laboratory into all phases of GMP manufacturing.

Supporting the design, test, and qualification of MES recipes for electronic batch records.

Supporting process investigations, equipment and process troubleshooting.

Identifying and driving implementation of improvements to maximize throughput and capacity utilization.

Defining relevant operational / technical standards and practices for the site.

Providing support and content for regulatory submissions.

The primary objective is to ensure manufacturing processes are capable, compliant, in control, and continuously improved.

Provide technical support to GMP operations in a multi-product facility.

Function as a technical resource for the resolution of deviations, investigations, and process issues. Complete technical investigations and provide on the floor technical expertise.

Generate technical documents (memos, protocols, reports, plans, etc.,) related to technology transfer, process monitoring, process improvements, etc.

Actively participate in client meetings and serve as a technical SME.

Complete process monitoring tasks that require a variety of statistical and data analysis methods and techniques (e.g., excel, JMP, etc.).

Routinely troubleshoot operational issues for process related operations.

Be a technical resource in the evaluation and implementation of process improvements, policy changes, compliance improvements and optimization programs.

GMP Process Design :

Provide technical leadership for execution of engineering runs during technology transfer from development to manufacturing.

Monitor, track, evaluate, and report data from unit operations to support project / client communication and deliverables.

Perform statistical analysis.

Respond to and trouble-shoot process issues related to assigned work and areas of expertise.

Assess and select equipment to meet process needs.

Perform material assessments as required.

Develop scientific and technical understanding of unit operations and production processes.

Technology Transfer to GMP Production :

Participate in technology transfer activities and provide oversight of GMP runs to support technology transfer to production.

Perform key project deliverables for technology transfer activities for new client projects.

Define and justify critical and key process parameters.

Participate in the development of specifications, standard operating procedures, work instructions and forms to support implementation of new processes.

Collaborate with manufacturing as well as all support functions such as engineering, quality, and supply chain to provide robust and coordinated support.

Perform and / or support risk assessment activities including hazard and operability studies.

Train production staff to ensure they can perform duties involving new equipment and new processes.

Generate protocols and reports for engineering, and clinical GMP runs.

Prepare change controls and perform change control assessments according to internal procedures as required.

Comply with safety requirements and work to resolve any environmental, health and safety issues.

Optimize processes to effectively and efficiently produce product that meets clients' quality specifications.

Minimum Qualifications :

Understanding of biotechnology processes.

Embodies the Resilience phenotypes of grit, quality + rigor, service orientation, EQ+IQ, builder mentality, velocity, and ownership.

Demonstrated technical, operational, and / or hands-on equipment knowledge of cell / gene therapy, and process data analysis.

Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.

Understanding of quality, compliance, regulatory, and good manufacturing practices.

Demonstrated ability to successfully execute responsibilities in a fast-paced environment, collaborating across functions and multiple stakeholders.

Ability to influence others without direct authority and communicate with all levels of the organization.

Excellent communication (oral and written) and attention to detail; ability to present and defend technical and scientific approaches and decisions in both written and verbal form to internal and external partners.

Preferred Qualifications :

M.S. / B.S. in Life Sciences, Chemical or Biological Engineering, or related discipline with 3-5 years of relevant industry experience in process development, technology transfer, or GMP Manufacturing.

Experience in the scale up and operation of cell / gene therapy manufacturing practices.

Experience developing acceptance criteria for technology transfer.

Hands-on experience cell and / or gene therapy biotechnology unit operations.

Experience with single use technology and systems.

Experience working for or with contract manufacturing organizations.

Experience with digital Manufacturing Execution Systems (MES).

Experience owning, managing, and executing change controls and using management systems (ex. Veeva).

Additional Requirements :

On site work required for position.

Support 24 / 7 production / manufacturing activities, which may require off-shift work on occasion including weekends.

Ability to gown.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws.

Requests for reasonable accommodation can be made at any stage of the recruitment process.

Resilience offers employees a robust total rewards program including equity, an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great 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 and support for caregiving needs.

Our target base pay hiring range for this position is $75,000.00 - $101,250.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge.

Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.