Senior Engineer - Capital Projects & Process Design

Posted 5 Days Ago
Be an Early Applicant
Juncos, PRI
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Lead technical process optimization, equipment characterization, and troubleshooting across manufacturing, pilot plant, and capital projects. Design and implement major system modifications, develop engineering policies, coordinate cross‑functional teams and external consultants, manage project budgets/schedules, and supervise engineers and technicians. Support validation, regulatory documentation, and continuous improvement activities to deliver complex engineering solutions within regulated biotech/pharma environments.
Summary Generated by Built In

The Senior Engineer provides independent technical leadership in process optimization, equipment characterization, and troubleshooting across operations, manufacturing, pilot plant, and capital project environments. This role applies advanced engineering principles to design and implement major system modifications, experiments, and process improvements. The engineer develops, analyzes, and presents technical interpretations for projects and operational issues of significant scope and complexity.

RESPONSIBILITIES

  • Execute complex or novel engineering assignments requiring new or improved techniques.
  • Develop engineering policies and procedures impacting multiple organizational units.
  • Supervise, coordinate, and review the work of engineers, associates, and technicians.
  • Apply advanced engineering techniques and adapt specialized methods within area of expertise.
  • Support assignments outside primary discipline using broad engineering knowledge.
  • Serve as a peer‑recognized technical specialist, determining methodologies in at least one engineering area.
  • Apply mature engineering judgment in planning and executing 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.
  • Partner 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

  • Strong knowledge of pharmaceutical/biotech processes and regulated documentation.
  • Familiarity with validation processes, including protocol development and execution.
  • Ability to apply engineering science to production systems and process optimization.
  • Proficiency with specialized laboratory equipment, process systems, and computer tools.
  • Expertise in at least three engineering technology areas.
  • Ability to troubleshoot routine to highly complex technical issues using scientific and engineering theory.
  • Strong analytical problem‑solving skills, including hypothesis development and data‑driven decision‑making.
  • Ability to determine when internal or external resources are required.
  • Ability to manage multiple projects simultaneously.
  • Experience in scheduling, facilitation, cross‑functional collaboration, and project follow‑up.
  • Contractor and vendor management experience.
  • Working knowledge of financial analysis tools and project cost development.
  • Ability to delegate and oversee project work of others.
  • Strong verbal communication and technical report writing.
  • Effective in technical presentations and cross‑functional collaboration.
  • Skilled in negotiation, conflict resolution, leadership, and team‑building.
  • Ability to work effectively with diverse communication and working styles.
  • Adaptability to change and ability to drive alignment across teams.

Requirements

EDUCATION & EXPERIENCE REQUIREMENTS

  • Doctorate in Engineering OR
  • Master’s in Engineering + 2 years of engineering experience OR
  • Bachelor’s in Engineering + 4 years of engineering experience
  • Preferred academic backgrounds: Chemical, Mechanical, Industrial Engineering, or Biotechnology

PREFERRED QUALIFICATIONS

  • Engineering experience in manufacturing operations within biotech, pharmaceutical, or other regulated environments.
  • Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean, Six Sigma, Kaizen, RCA).
  • Experience supporting CAPA, deviation resolution, and process optimization initiatives.
  • Strong cross‑functional collaboration with Operations, Quality, and Maintenance.
  • Knowledge of vision systems (inspection system analysis).
  • Experience in Packaging operations or equipment.

Benefits
  • 6-month contract
  • Administrative Shift

Skills Required

  • Doctorate in Engineering OR Master's in Engineering + 2 years of engineering experience OR Bachelor's in Engineering + 4 years of engineering experience
  • Strong knowledge of pharmaceutical/biotech processes and regulated documentation
  • Familiarity with validation processes, including protocol development and execution
  • Ability to apply engineering science to production systems and process optimization
  • Proficiency with specialized laboratory equipment, process systems, and computer tools
  • Expertise in at least three engineering technology areas
  • Ability to troubleshoot routine to highly complex technical issues using scientific and engineering theory
  • Ability to manage multiple projects simultaneously, including scheduling, facilitation, and project follow-up
  • Contractor and vendor management experience
  • Working knowledge of financial analysis tools and project cost development
  • Strong verbal communication, technical report writing, and presentation skills
  • Leadership skills including delegation, negotiation, conflict resolution, and team-building
  • Engineering experience in manufacturing operations within biotech, pharmaceutical, or other regulated environments
  • Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean, Six Sigma, Kaizen, RCA)
  • Experience supporting CAPA, deviation resolution, and process optimization initiatives
  • Knowledge of vision systems (inspection system analysis)
  • Experience in Packaging operations or equipment
  • Preferred academic backgrounds: Chemical, Mechanical, Industrial Engineering, or Biotechnology
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The Company
HQ: Cambridge, MASSACHUSETTS
39 Employees
Year Founded: 2010

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.

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