Under general supervision, this role provides engineering support across operations, manufacturing, pilot plant, and capital project environments. Responsibilities include process optimization, troubleshooting operational issues, and applying engineering principles to system modifications, experiments, and small‑scope projects. The role requires strong analytical skills to organize, interpret, and present results for operational or engineering activities.
Responsibilities:
- Provide solutions to technical problems of moderate scope and complexity.
- Evaluate, select, and apply standard engineering techniques and procedures; seek guidance for unusual or complex issues.
- Perform assignments with clear objectives requiring investigation of a limited number of variables.
- Initiate and complete routine technical tasks independently.
- Serve as a technical expert for equipment and systems during troubleshooting activities.
- Engage directly in daily operations when needed to meet production schedules or resolve complex issues.
- Conduct routine audits of equipment performance and regulatory compliance for systems of significant complexity.
- Collaborate with cross‑functional teams (Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance, Validation) to define requirements and recommendations for system or process modifications.
- Support project managers in completing design, engineering, and construction projects within established timelines and budgets.
- Partner with consultants, architects, and engineering firms to develop standard design documentation.
- Obtain and evaluate quotes for equipment modifications or installations.
- Prepare basic project cost estimates and schedules.
- Perform additional engineering duties as assigned.
Requirements
- Master’s degree in Engineering OR
- Bachelor’s degree in Engineering + 2 years of engineering experience
Preferred Qualifications
- Working knowledge of pharmaceutical, biotech, or medical device processes.
- Familiarity with validation processes and documentation in regulated environments.
- Ability to operate specialized laboratory equipment and relevant software.
- Understanding and application of GLPs and GMPs.
- Strong problem‑solving and applied engineering skills.
- Technical report writing proficiency.
- Experience identifying and managing CAPAs.
- Proficiency in statistical analysis and Design of Experiments (DOE).
- Experience with packaging equipment, process characterization, validation, monitoring, and optimization.
- Solid understanding of validation protocol execution.
- Skills in:
- Technical presentations
- Personal organization
- Validation protocol writing
- Change management
- Equipment‑specific technical knowledge
- Analytical problem solving
- Computer literacy
Benefits
Shift & Contract Details
- 1st Shift
- 2nd Shift
- 6‑month contract with possible extension
- Availability to support non‑standard shifts, extended hours, nights, weekends, and holidays.
Skills Required
- Master's degree in Engineering
- Bachelor's degree in Engineering plus 2 years of engineering experience
- Working knowledge of pharmaceutical, biotech, or medical device processes
- Familiarity with validation processes and documentation in regulated environments
- Ability to operate specialized laboratory equipment and relevant software
- Understanding and application of GLPs and GMPs
- Strong problem-solving and applied engineering skills
- Technical report writing proficiency
- Experience identifying and managing CAPAs
- Proficiency in statistical analysis and Design of Experiments (DOE)
- Experience with packaging equipment, process characterization, validation, monitoring, and optimization
- Understanding of validation protocol execution
- Technical presentation skills
- Personal organization skills
- Validation protocol writing skills
- Change management skills
- Equipment-specific technical knowledge
- Analytical problem-solving skills
- Computer literacy
What We Do
BioPharma Consulting JAD Group provides a complete portfolio of technical support and solutions for the FDA regulated industry. We deliver solutions with a flexible cost effective approach to meet your company’s needs. BPC JAD group is a company created to help our customers bridge the gap between their business strategy and results. Our mission is to help our clients succeed by partnering with them and providing value added business solutions on the validation, engineering and compliance fields. We will carry out our mission by creating a long-term partnership with our customers and provide reliable and cost effective technical solutions. BPC JAD Group objective is to deliver reliable tailored solutions; from providing consultation to becoming part of your staff. We will develop customized frameworks to help our customers unlock the hidden value in their plants, facilities, equipment and people with an optimal integration of resources regulations and technology.
