In this role, you will support continuous daily operations by executing troubleshooting activities, process optimization strategies, equipment upgrades, replacements, and system modifications. You will ensure all activities comply with corporate policies, industry standards, and applicable regulatory requirements. This position supports non‑standard shift operations, including nights and weekends.
Functions
- 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.
- Provide engineering solutions to technical problems of moderate complexity.
- Apply standard engineering principles, techniques, and procedures under general supervision.
- Act as a technical expert during troubleshooting and cross‑functional discussions.
- Participate in daily operations when needed to meet production goals or resolve complex issues.
- Monitor manufacturing processes for performance indicators; recommend corrective actions and provide troubleshooting guidance.
- Support manufacturing and quality systems, including deviations, equipment qualification, process validation, procedures, training, and new product introductions.
- Apply scientific, operational, and compliance knowledge to support manufacturing operations.
- Analyze and present results for operational issues or engineering projects.
- Implement system modifications, experiments, and capital project activities.
- Support 24/7 operations, including extended hours and weekend coverage as required.
Requirements
- Master’s degree in Engineering OR
- Bachelor’s degree in Engineering + 2 years of engineering experience
Preferred Qualifications
- Working knowledge of pharmaceutical or biotech 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.
- Ability to apply engineering science to production environments.
- Strong problem‑solving and applied engineering skills.
- Basic technical report writing and presentation skills.
- Effective verbal communication skills.
- 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 Information
- 2nd Shift
- 3rd Shift
- 1‑year contract with possible extension
Skills Required
- Master's degree in Engineering
- Bachelor's degree in Engineering and 2 years of engineering experience
- Working knowledge of pharmaceutical or biotech 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
- Ability to apply engineering science to production environments
- Strong problem-solving and applied engineering skills
- Basic technical report writing and presentation skills
- Effective verbal communication skills
- Solid 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.
