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:

• This position is responsible for inspecting products during the manufacturing process and directing and conducting routine final inspection of medical devices and related documentation as specified by priority or special request according to methods established.
• Perform periodic audits of manufacturing operators to ensure that they are able to self-inspect their work (Operator Sefl Inspection – OSI).
• Performs and documents final inspections to established procedures.
• Conducts device history review processes to established procedures.
• Performs product identification measurements to established print requirements.
• Verifies product label information and contents to appropriate specifications.
• Organizes and reports Final Inspection results.
• Exercises assigned responsibility for on-the-job training of less qualified personnel.
• Communicates with manufacturing cell members, manufacturing management and engineers concerning product & documentation defects.

Qualifications:

• High School Diploma or associate degree preferred.
• Must be able to read and understand blueprints, work instructions, engineering specifications and inspection documents.
• Quality Control Inspection experience MUST
• Must be able to communicate technical information, both verbal and written
• Must have vision correctable to 20/20
• Must be able to lift in the 40-pound range.
• Must be able to work in Clean Room environment.
• Must have demonstrated ability to use micrometers and calipers.
• Must have demonstrated ability to use shop math techniques (addition, subtraction, multiplication, division of decimals and fractions).
• Must have the following demonstrated computer skills-JDE, Synquest, MS Excel, MS Word
• Availability for 1st shift (Monday to Friday)

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.

Job Types: Full-time, Temporary

Experience level:

• 3 years

Schedule:

• 8 hour shift

Work setting:

• In-person
• Manufacturing facility
• Warehouse

Ability to commute/relocate:

• Palm Beach Gardens, FL: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Manufacturing: 2 years (Preferred)
• Quality inspection: 2 years (Required)

Shift availability:

• Day Shift (Required)

Work Location: One location

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