Senior Engineer - Packaging

Biopharma-Consulting-Jad-Group; Juncos (PR); On-site; USD 90,000 - 130,000; Full time

Job summary

Biopharma-Consulting-Jad-Group seeks a Senior Engineer - Packaging for a 12‑month on-site role in Juncos, Puerto Rico. Lead complex packaging initiatives, write protocols and drive process improvements for final product manufacture in a regulated biopharma environment.

You will mentor technicians, coordinate with QA, validation, facilities and contractors, and ensure adherence to GMP/GDP standards while optimizing packaging materials and processes.

Qualifications

• Experience in final product packaging within pharma/biotech is preferred.
• Strong understanding of GMP and GDP principles in regulated environments.
• Ability to read and interpret technical specifications and standards.

Responsibilities

• Lead complex packaging projects from concept to implementation.
• Develop and enforce packaging procedures and policies across units.
• Supervise a small team of engineers and technicians on projects.
• Collaborate with manufacturing, QA, validation and facilities teams.

Skills

Process optimization

GMP/GDP knowledge

Documentation

Project management

Vendor/contractor management

Team leadership

Education

Doctorate degree

Master's degree

Bachelor's degree in Engineering

Job description

We are seeking a Senior Engineer - Packaging to support packaging and final product manufacturing operations at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. This role independently provides and directs process optimization strategies and troubleshooting of operational issues in operations, manufacturing, pilot plant or capital project environments, applying advanced engineering principles to the design and implementation of major system modifications, experiments, process and capital projects.

Key Responsibilities

• Complete complex or novel assignments requiring the development of new or improved engineering techniques and procedures.
• Develop engineering policies and procedures that affect multiple organizational units.
• Supervise, coordinate and review the work of a small team of engineers, associates and/or technicians on an ongoing and project basis.
• Serve as a peer-recognized technology specialist, responsible for determining methodologies in your area of expertise.
• Develop technical solutions to complex problems requiring ingenuity and creativity.
• Partner with manufacturing, process development, utilities, facilities, quality assurance and validation to define requirements and recommendations for large or highly complex system/facility modifications.
• Work with project managers to complete design and engineering projects within schedule, budget and quality constraints.
• Coordinate the work of consultants, architects and engineering firms on standard design documents.
• Develop project budgets encompassing multiple disciplines.
• Write test protocols and perform technical evaluations and testing to support reports justifying selected packaging materials and components.
• Develop, organize, analyze and present results for engineering projects of significant scope and complexity.

Education (one of the following)

• Doctorate degree; OR
• Master's degree + 2 years of engineering experience; OR
• Bachelor's degree in Engineering + 4 years of engineering experience

Preferred Qualifications

• Packaging/engineering experience in final product manufacturing within the pharmaceutical/biotech industry
• Excellent understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
• Strong knowledge of primary and secondary packaging materials (bottles, labels, trays, lidding material, leaflets, paperboard, sterile barrier packaging, corrugate, etc.)
• Familiarity with distribution testing per ASTM D4169 and ASTM, ISO, TAPPI, USP and EP testing standards
• Experience writing test protocols, performing technical evaluations and testing to support material/component selection reports

Key Skills

• Working knowledge of pharmaceutical/biotech processes and validation (protocol writing and execution, new equipment installations)
• Documentation in a highly regulated environment; ability to interpret and apply GMPs/GLPs
• Strong interpersonal, project management, technical problem-solving and written/verbal communication skills
• Schedule development, project cost development and working knowledge of financial analysis tools
• Leadership, team building, negotiation, conflict resolution and management of contractors and vendors
• Ability to handle multiple projects and adapt to a continuously evolving environment

• Contract position: 12 months (October 2026 - October 2027), with possible extension
• Shift: Administrative shift
• Days: Monday to Friday, 8 hours/day (40 hours/week)
• 100% on-site in Juncos, Puerto Rico