JT334 - SR ENGINEER

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:

• Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment
• Work with research, manufacturing, process development, utilities, facilities, quality assurance and validation departments in developing requirements and recommendations for large and/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 development of standard design documents
• Develop departmental budgets or project budgets encompassing multiple disciplines for area within project or entirety of smaller project
• Develop engineering policies and procedures that affect multiple organizational units
• Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians on an ongoing basis as well as on a project basis
• Employ advanced engineering techniques and/or modifications of advanced techniques within area of engineering expertise
• Apply knowledge of engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields
• Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining methodologies in that area
  

Qualifications:

• Bachelor’s degree in mechanical engineering preferred
• +4 years of Engineering experience
• Experience in parenteral products, vision system, device assembly and packaging
• Working knowledge of pharmaceutical/biotech processes
• Familiarity with validation processes
• Familiarity with documentation in a highly regulated environment
• Ability to operate specialized laboratory equipment and computers as appropriate
• Ability to interpret and apply GLPs and GMPs
• Ability to apply engineering science to production
• Administrative Shift