TSR Consulting
About TSR:
TSR is a relationship-based, customer-focused IT and technical services staffing company.
For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.
Mission & Vision
We do not believe in building a vision around the company but building a company around our vision, which is simply;
Every employee's voice matters, their effort is appreciated, and their talent is rewarded.
We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.
Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.
Process Engineer
Job Description
Job ID: 83070
Work Location:
Warren, NJ - 100% on site
Summary:
Responsible for supporting the production of personalized cell therapy products for global clinical trials. Collaborates with SMEs from the Development Group, Global MSAT Group, Supply Chain Group, Manufacturing Group, and Quality Group while providing technical support for the resolution of process deviations, the evaluation and implementation of process changes and continuous improvement support to the production operations to ensure rapid, flawless, compliant, and cost-effective delivery of quality products.
Education/Experience:
Pay: $50-$52/hr
TSR is a relationship-based, customer-focused IT and technical services staffing company.
For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.
Mission & Vision
We do not believe in building a vision around the company but building a company around our vision, which is simply;
Every employee's voice matters, their effort is appreciated, and their talent is rewarded.
We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.
Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.
Process Engineer
Job Description
- Location: Warren, New Jersey
- Type: Contract
- Job #83070
Job ID: 83070
Work Location:
Warren, NJ - 100% on site
Summary:
Responsible for supporting the production of personalized cell therapy products for global clinical trials. Collaborates with SMEs from the Development Group, Global MSAT Group, Supply Chain Group, Manufacturing Group, and Quality Group while providing technical support for the resolution of process deviations, the evaluation and implementation of process changes and continuous improvement support to the production operations to ensure rapid, flawless, compliant, and cost-effective delivery of quality products.
Education/Experience:
- Bachelors Degree required in Engineering or Related Discipline (advanced degree is preferred)
- Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities
- 2 years of manufacturing support or related experience in the biopharmaceutical industry
- Experience in cell therapy/biologic/vaccine manufacturing support, tech transfer, and validation
- Basic knowledge of cGMPs and multi-national biopharmaceutical/cell therapy regulations
- Basic knowledge of facility/clean room design, process, equipment, automation, and validation
- Intermediate strong verbal/written communication skills and ability to influence at all levels
- Intermediate ability to think strategically and to translate strategy into actions
- Intermediate ability to prioritize and provide clear direction to team members in a highly dynamic environment
- Basic knowledge of quality by design and risk management
- Basic experience with Operational Excellence and Lean Manufacturing
- Ensure safe and compliant cGMP operations.
- Maintain permanent inspection readiness and actively support regulatory inspections.
- Interface with regulatory authorities as required to support Manufacturing Operations audits.
- Foster a culture of compliance and strong environmental, health, and safety performance.
- Stay current with industry trends and standards (e.g. PDA, ISPE) and participate in best practice forums consistent with function responsibilities.
- Provide technical input and investigation support for production related investigations, ensuring compliance with internal standards and regulatory requirements
- Design and execute test plans and other risk mitigation exercise as part of investigations (e.g. Root cause analysis and CAPAs)
- Sponsor and support the change initiatives and the implementation of process improvement initiatives
- Support Clinical Production Activities.
- Support production-related investigations, ensuring compliance with internal standards and regulatory requirements.
- Continuously monitor, anticipate and permanently resolve issues that may arise during production.
- Interface with operators and serve as process SME. Learn the procedures, analytics and document any known sensitivity.
- Provide technical input and investigation support for production related investigations, ensuring compliance with internal standards and regulatory requirements
- Work closely with Engineering /Maintenance on the design and implementation of new technology and new systems/facilities related to production process needs
- Review and revise the content of technical documentation (e.g. investigations, changes, SOPs and batch records)
- Interact with other teams including Validation, Development, Operations, QA and Regulatory
- Display Leadership Qualities.
- Create an environment of teamwork, open communication, and a sense of urgency
- Support the change agent in promoting flexibility, creativity, and accountability
- Support organizational strategic goals and objectives that are linked to the overall company strategy
- Drive strong collaboration within the plant and across the network
- Build trust and effective relationships with peers and stakeholders
- Deliver results through timely and quality decision making and advice
- Promote a mindset of continuous improvement, problem solving, and prevention
- Lead project teams, prepare project schedules, coordinate the execution of technical projects and develop presentations to disseminate results to project stakeholders and senior management
Pay: $50-$52/hr