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Senior Engineer - Capital Projects

BioPharma Consulting JAD Group

Posted 4 days ago

The Senior Engineer independently leads and directs process optimization, troubleshooting, and system improvement initiatives across operations, manufacturing, pilot plant, and capital project environments. This role applies advanced and diverse engineering principles to design and implement major system modifications, experiments, and capital projects. The Senior Engineer develops, analyzes, and presents technical interpretations for operational issues or engineering projects of significant scope and complexity, while providing leadership, technical expertise, and cross‑functional coordination.

FUNCTIONS

  • Complete complex or novel engineering assignments requiring development of new or improved techniques and procedures.
  • Develop engineering policies and procedures impacting multiple organizational units.
  • Supervise, coordinate, and review the work of engineers, associates, and technicians on both ongoing and project‑specific bases.
  • Apply advanced engineering techniques and adapt specialized methods within area of expertise.
  • Apply engineering principles outside primary discipline to support a broad range of assignments.
  • Serve as a peer‑recognized technical specialist with responsibility for determining methodologies in at least one engineering area.
  • Utilize mature engineering judgment in planning and conducting projects.
  • Perform additional duties as assigned.
  • Develop innovative technical solutions to complex problems requiring creativity and strong analytical capability.
  • Collaborate with Research, Manufacturing, Process Development, Utilities, Facilities, Quality Assurance, and Validation to define requirements for large or highly complex system/facility modifications.
  • Work with Project Managers to deliver engineering and design projects within scope, schedule, budget, and quality expectations.
  • Coordinate work with consultants, architects, and engineering firms to develop standard design documentation.
  • Develop departmental or project budgets involving multiple engineering disciplines.

SKILLS

  • Working knowledge of pharmaceutical/biotech processes.
  • Familiarity with validation processes and documentation in highly regulated environments.
  • Ability to operate specialized laboratory equipment and computer systems.
  • Ability to interpret and apply GLPs, GMPs, and engineering science to production.
  • In‑depth knowledge of validation requirements for new equipment installations.
  • Expertise in at least three engineering technology areas.
  • Ability to provide solutions to a wide range of technical problems of moderate to large complexity.
  • Strong analytical problem‑solving skills requiring scientific and engineering theory, calculations, and creative hypothesis development.
  • Ability to determine when internal or external resources are required to resolve issues.
  • Advanced data interpretation and technical decision‑making.
  • Ability to manage multiple projects simultaneously.
  • Experience in schedule development, facilitation, and project follow‑up.
  • Working knowledge of financial analysis tools and project cost development.
  • Ability to delegate and manage project work of others.
  • Experience managing contractors and vendors.
  • Strong verbal communication and technical report writing.
  • Effective in technical presentations and cross‑functional collaboration.
  • Skilled in negotiation, persuasion, conflict resolution, and team‑building.
  • Ability to work effectively with diverse communication and working styles.
  • Ability to manage change and drive alignment across teams.

Requirements

EDUCATION & EXPERIENCE REQUIREMENTS

  • Doctorate OR
  • Master’s + 2 years of engineering experience OR
  • Bachelor’s in Engineering + 4 years of engineering experience

Preferred:

  • Bachelor’s in Engineering + 4 years of engineering experience.

PREFERRED QUALIFICATIONS

  • Experience in Commissioning & Qualification (C&Q) processes.
  • Experience with validation and packaging equipment.
  • Strong background in troubleshooting equipment and process systems in regulated environments.
  • Excellent communication and presentation skills in English and Spanish.
  • Strong organizational skills and ability to lead cross‑functional initiatives.

Benefits

  • Administrative Shift
  • 1-year contract with possible extension

Job details

Workplace

Office

Location

Juncos, Juncos, Puerto Rico

Experience

SE

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BioPharma Consulting JAD Group logo

BioPharma Consulting JAD Group

About

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.

Key Team Members

Peter G. Mescia, MBA, PMP

Peter G. Mescia, MBA, PMP

Zuleimy Torres

Zuleimy Torres

Carlos Rosado

Carlos Rosado

Jorge Torres

Jorge Torres

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