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Job description

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:

• Complete complex or novel assignments requiring development of new and/or improved engineering techniques and procedures.
• 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.
• Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining methodologies in that area.
• Develop technical solutions to complex problems requiring the regular use of ingenuity and creativity.
• 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.

Qualifications:

• Bachelor Degree in Engineering (Mechanical, Electrical, Chemical or Industrial)
• Five (5) years of experience
• • Knowledge and experience working with Change Controls on trackwise. (Prefer experience that we are looking)
• • Knowledge in Packaging equipment.
• • Knowledge in Design of new equipment process.
• • Knowledge in Engineering Project
• • Knowledge in Validations and Commissioning
• • Experience in Medical Device or Pharma
• • Knowledge in CAPA and Compliance
• 1st and 2nd shift availability

Job Types: Full-time, Contract, Temporary

Schedule:

• 8 hour shift

Ability to commute/relocate:

• Juncos, PR: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Trackwise: 3 years (Required)
• CAPA: 3 years (Required)

Work Location: In person