Engineer at BioPharma Consulting JAD Group

Juncos, , Puerto Rico -

Full Time

Start Date

Immediate

Expiry Date

24 Jan, 26

Salary

0.0

Posted On

26 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Optimization, Troubleshooting, Technical Problem Solving, Engineering Techniques, Technical Expertise, Operational Performance, Regulatory Compliance, Cross-Functional Collaboration, Project Management Support, Cost Estimation, Manufacturing Operations, Automation Systems, Continuous Improvement, Technical Report Writing, Verbal Communication, Computer Systems

Industry

Biotechnology Research

Description

Under general supervision, this role supports process optimization and troubleshooting across manufacturing, pilot plant, and capital project environments. The engineer applies foundational principles to system modifications, experiments, and project execution, while analyzing and presenting results for operational issues of moderate scope and complexity. Key Responsibilities: Provide solutions to technical problems of moderate complexity Evaluate, select, and apply standard engineering techniques and procedures Perform assignments with clear objectives and limited variables Initiate and complete routine technical tasks Serve as technical expert for equipment and systems troubleshooting Actively support daily operations to meet schedules or resolve complex issues Audit operational performance and regulatory compliance of equipment and systems Collaborate with cross-functional teams (research, manufacturing, maintenance, process development, utilities, facilities, QA, validation) to define system requirements and recommend modifications Support project managers in design, engineering, and construction projects 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 Education Requirements: Master’s degree in Engineering Bachelor’s degree in Engineering + 2 years of engineering experience Preferred Background: Degree in Chemical Engineering, Industrial Engineering, Biotechnology, or related technical discipline Preferred Qualifications: Hands-on experience in manufacturing operations within regulated environments (biotech, pharmaceutical, or similar) Familiarity with automation systems, process equipment, and continuous improvement methodologies (Lean Six Sigma, Kaizen, root cause analysis) Demonstrated ability to troubleshoot manufacturing issues and implement CAPAs Experience collaborating with operations, quality, and maintenance teams Understanding of cGMP, compliance, and documentation practices Working knowledge of validation processes and protocol execution Ability to interpret and apply GLPs and GMPs Skilled in technical report writing, presentations, and equipment-specific problem solving Strong verbal communication, adaptability to change, and personal organization Proficient in computer systems and specialized laboratory equipment 6-months contract Administrative Shift

Responsibilities

The engineer supports process optimization and troubleshooting across various environments, providing solutions to technical problems of moderate complexity. They collaborate with cross-functional teams and audit operational performance to ensure compliance and efficiency.