JT400 - PACKAGING ENGINEER

Juncos, Puerto Rico
Contracted
Biopharmaceutical
Mid Level

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

  • Under general supervision, provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
  • Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects. 
  • Responsible for enhancing system reliability focusing on equipment availability, downtime reduction and maintenance optimization.
  • Function as a technical expert to equipment or systems regarding troubleshooting operations.
  • Frequently become actively involved in daily operations when required to meet schedules or to resolve complex problems.
  • Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of significant complexity.
  • Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications.
  • Work under the direct supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints.
  • Work with consultants, architects and engineering firms on development of standard design documents.
  • Obtain and critique quotes for equipment modifications or installations.
  • Generate rudimentary project cost estimates and schedules.
Qualifications:
  • Bachelor's degree in engineering (Chemical Engineering, Mechanical Engineering, and Industrial engineering fields)
  • 2 years of Engineering experience
  • General packaging/engineering experience in final product manufacturing within the Pharma/Biotech Industry
  • Excellent understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
  • Strong knowledge of common materials used in pharmaceutical primary and secondary packaging (bottles, labels, trays, lidding material, leaflets, paperboard, sterile barrier packaging, corrugate, etc.).
  • Familiar with distribution testing per ASTM D4169 and ASTM, ISO, TAPPI, USP and EP testing standards.
  • Strong interpersonal, project management, technical problem solving and communication (written and verbal) skills.
  • Ability to work in teams and adapt to a continuously evolving environment.
  • Ability and experience writing test protocols, performing technical evaluations and testing to support reports used to uphold the use of selected materials and packaging components.
  • Available for administrative Shift (8am to 5pm)

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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