BioPharma Consulting JAD Group

Engineer

BioPharma Consulting JAD Group  •  Juncos, PR (Onsite)  •  6 hours ago
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Job Description

Under general supervision, the Engineer supports process optimization, equipment troubleshooting, and operational improvements across manufacturing, operations, pilot plant, and capital project environments. Applies fundamental engineering principles to design and implement system modifications, experiments, and capital projects. Organizes, analyzes, and presents technical interpretations for operational issues or engineering projects of minor to moderate scope and complexity.

KEY RESPONSIBILITIES

  • Provide solutions to technical problems of moderate scope and complexity.
  • Evaluate, select, and apply standard engineering techniques, principles, and procedures; seek guidance for unusual or complex problems.
  • Perform assignments with clear objectives requiring investigation of a limited number of variables.
  • Initiate and complete routine technical tasks with accuracy and attention to detail.
  • Serve as a technical expert for equipment, process, and system troubleshooting.
  • Actively engage in daily operations when needed to meet schedules or resolve sophisticated issues.
  • Routinely audit operational performance and regulatory compliance of equipment and systems.
  • Supervise manufacturing processes for performance indicators; recommend solutions and provide troubleshooting mentorship.
  • Collaborate with Manufacturing, Maintenance, Process Development, Utilities, Facilities, Quality Assurance, and Validation to develop requirements and recommendations for system or process modifications.
  • Work under the supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints.
  • Collaborate with consultants, architects, and engineering firms to develop standard design documents.
  • Obtain and evaluate quotes for equipment modifications or installations.
  • Generate basic project cost estimates and schedules.
  • Support execution of manufacturing/quality systems such as deviations, equipment qualification, process validation, procedures, training, and new product introductions.
  • Apply process, operational, scientific, and compliance knowledge to support manufacturing operations.
  • Organize, analyze, and present interpretation of results for operational issues or engineering projects of moderate scope.
  • Apply engineering principles to design and implement system modifications, experiments, and capital projects.

CORE COMPETENCIES & SKILLS

  • Working knowledge of pharmaceutical/biotech processes.
  • Familiarity with validation processes and documentation in regulated environments.
  • Ability to interpret and apply GLPs, GMPs, and engineering science to production.
  • Ability to operate specialized laboratory and manufacturing equipment.
  • Strong analytical and troubleshooting skills.
  • Ability to develop solutions to routine technical problems of limited scope.
  • Excellent verbal communication and technical report writing skills.
  • Proficiency in:
    • Technical presentations
    • Personal organization
    • Validation protocol writing
    • Managing change
    • Equipment‑specific technical knowledge
    • Analytical problem solving
    • Computer literacy
  • Strong organizational and technical writing skills.
  • Effective communication skills in English and Spanish.

Requirements

EDUCATION REQUIREMENTS

One of the following is required:

  • Master’s degree, OR
  • Bachelor’s degree in Engineering + 2 years of Engineering experience.

Preferred Academic Background: Mechanical, Electrical, Chemical Engineering, or related discipline.

PREFERRED QUALIFICATIONS

  • Experience with equipment or process troubleshooting in regulated environments.
  • Knowledge of GMP production operations and biotech/pharma manufacturing.
  • Experience supporting deviations, equipment qualification, process validation, and new product introductions.
  • Hands‑on experience in biotechnology purification operations.
  • Knowledge of chromatography and UF/DF techniques.
  • Ability to lead troubleshooting discussions across multifunctional teams.
  • Experience supervising or mentoring operators during process troubleshooting.
  • Strong analytical skills for interpreting performance data and recommending improvements.
  • Ability to work extended hours and adapt to changing operational priorities.

Benefits

  • Contract position
  • Non standard shift
BioPharma Consulting JAD Group

About BioPharma Consulting JAD Group

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.

Industry
Biotech & Life Sciences
Company Size
11-50 employees
Headquarters
Cambridge, MASSACHUSETTS
Year Founded
2010
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