QUALITY INSPECTOR -1st SHIFT

Primo Medical Group, Inc. is searching for a Quality Inspector to join our team! We are a leader in the development of medical devices and precision machined components. There are currently three locations with a fourth nearing completion. Primo is a dynamic, innovative company offering competitive salary, excellent benefits and has a strong focus on the training and professional advancement of its employees.

Summary: Perform all aspects of Incoming, In-process and Final Inspection of materials, components and finished medical products. The QC Inspector performs the following duties:

Essential Duties and Responsibilities:

• Reads and understands all Quality Management System procedures related to the position / function within the organization.
• Performs incoming, First Piece, in-process and final inspection per relevant specifications. Documents the results of these inspections on the appropriate Quality Plans.
• Prepares Nonconforming Material Reports (NCMR) and Customer Deviation Requests (CDR) as applicable for discrepant materials and components.
• Maintain accurate records within the Quality Assurance Database for inspection results and nonconforming material handling.
• Review and approve material and special process certifications.
• Prepares required documentation for finished product final release.
• Reviews and releases for distribution, sterile product from Customer Inventory.
• Review and verify Device History Records to ensure that all required documents are present, complete and accurate prior to scanning them into the Document Control System.
• Execute protocols and support Engineering on special projects such as Gage R&R and Component Qualification.
• Ensure that the Quality Assurance philosophy is disseminated to personnel in organization.
• Maintain a working knowledge of industry Quality Assurance standards

Supervisory Responsibilities

• This position has no direct supervisory responsibilities

Qualifications

• To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

Education and/or Experience

• High School diploma or equivalent and three to five years’ experience in a Manufacturing or Quality Assurance environment or equivalent combination of education and experience. Working knowledge of FDA 21CFR820 Quality System Regulations (QSR) and ISO 13485 Quality Management Systems.

Technical Skills

• Experience in the proper use of the following instruments and tools:
• Micrometers, calipers, thread gages and similar manual instruments,
• Surface-plate set-ups, Micro-Hites, drop indicators
• Coordinate Measuring Machines
• Non-contact instruments such as comparators and vision systems.

Language Skills

• Ability to read and interpret technical drawings and specifications.
• Ability to write reports and business correspondence.
• Ability to effectively present information and respond to questions from managers, employees and suppliers.

Mathematical Skills

• Ability to work with basic mathematical concepts

Reasoning Ability

• Ability to solve practical problems using a common sense approach.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Attention to detail.

Physical Ability

• 20/20 corrected vision and / or ability to distinguish colors, see fine imperfection and flawsComputer Skills
• Individual should have a good working knowledge of the elements within Microsoft Office and Adobe Acrobat.

Job Type: Full-time

Pay: $23.00 - $27.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Flexible spending account
• Health insurance
• Life insurance
• Paid time off
• Referral program
• Vision insurance

Ability to Commute:

• West Bridgewater, MA 02379 (Required)

Work Location: In person

Salary : $23 - $27