Our performance is measured by the way we serve donor families and recipients. To be successful in this endeavor is our ultimate mission. By mobilizing the power of people and the potential of technology, we are honored to extend the reach of each donor’s gift and share the importance of the gift of life.
With the help of our employee-led strategy team, we will ensure that all communities feel welcome and safe with us because we are a model for fairness, belonging, and forward thinking.
Key responsibilities this position will perform include
Assist in creation of engineering and validation protocols for new products/processes
Assist in development of SOP’s and Work Instructions for new formulations, products and product improvements
Assist in sourcing, installing, and developing maintenance programs for manufacturing equipment
Support process validation and equipment qualification activities.
Support process scale-up, technology transfer, and manufacturing readiness activities.
Analyze process data to identify trends and opportunities for process improvement.
Participate in root cause investigations and implementation of corrective actions.
Develop process metrics and dashboards to monitor manufacturing performance.
Assist with capacity planning and efficiency improvement initiatives.
Support project activities and complete assigned deliverables to help ensure timely completion.
Support investigations, deviations, CAPAs, and change controls related to manufacturing processes.
Support manufacturing floor activities and provide day-to-day process engineering support.
Represent R&D and collaborates with other functions such as Manufacturing, Quality, and Regulatory
Act as a role model for DCIDS by supporting, reinforcing, and exhibiting behaviors consistent with the DCIDS core values, which are: selfless, hardworking, passionate, and dependable
Perform other related duties as assigned
Detail the job responsibilities in each step below
The ideal candidate will have
Bachelor’s Degree in Biomedical, Mechanical, Chemical Engineering, or related degree. Master’s degree preferred
0 – 2 years of biotech research, process engineering or product development experience. Direct experience with regulated environments (FDA, OSHA, EPA, etc.) and/or with cGMP procedures and engineering practices on tissue banking / pharmaceutical /biotech production processes, clean utilities, facilities, instruments, and equipment preferred.
LEAN/Six Sigma certification preferred
Microsoft Office Suite (Word, Excel, etc.), SolidWorks (or equivalent CAD software) and computer software programs relevant to the engineering discipline and project management.
We offer a competitive compensation package including
Up to 184 hours of PTO your first year
Up to 72 hours of Sick Time your first year
Two Medical Plans (your choice of a PPO or HDHP), Dental, and Vision Coverage
403(b) plan with matching contribution
Company provided term life, AD&D, and long-term disability insurance
Wellness Program
Supplemental insurance benefits such as accident coverage and short-term disability
Discounts on home/auto/renter/pet insurance
Cell phone discounts through Verizon
DCIDS is an EOE/AA employer – M/F/Vet/Disability.
You will receive a confirmation e-mail upon successful submission of your application. The next step of the selection process will be to complete a video screening. Instructions to complete the video screening will be contained in the confirmation e-mail. Please note - you must complete the video screening within 5 days from submission of your application to be considered for the position.
