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Quality Engineer

Global Contract Development and Manufacturing Organization (CDMO)
Olive Branch, MS
  • Expired: over a month ago. Applications are no longer accepted.
Job Description

Masis Professional Group is seeking an experienced Quality Engineer to work for a local med device company in Olive Branch, MS.  This role is being offered as contract to hire, but there is potential for a direct hire opportunity. 

 

Salary potential starting at 60K/YR.

 

Quality Engineer RESPONSIBILITIES:

 

•        Responsible for providing Prevention, Appraisal, and Failure tasks associated with ongoing process operations including:

•        Contract/Purchase Order (PO) review

•        Drawing/specification review

•        Inspection requirements planning

•        Gage & inspection tool design

•        Metrology & calibration

•        Validation & verification

•        Inspection monitoring

•        Process surveillance

•        Internal audit

•        Data analysis

•        Corrective & preventive action investigation & reporting

•        Material review

•        Complaint investigation and improvement studies

 

•        Assist in the creation and maintenance of system procedures & work instructions as well as prepare Inspection Reports for use in operations

 

•        Works seamlessly with customers and calibrate with workmanship expectations

 

•        May also serve as Tissue Bank Director for regulatory purposes

 

•        Consistently above average when it comes to productivity/efficiencies, sets the pace for others

 

•        All other duties as assigned

 

Quality Engineer KNOWLEDGE & SKILLS:

 

•        Bachelor’s Degree with at least 2 years of Quality Engineering experience (associate degree with at least 5 years of experience may be considered).

 

•        Advanced inspection and mechanical aptitude

 

•        Excellent verbal and written English communication skills

 

•        High attention to detail and the ability to work in a team environment are essential

 

•        Understanding of GD&T

 

•        Knowledge and execution of issues related to FDA/GMP compliance

 

•        CAD/CAM, Solidworks/Unigraphics or similar experience

 

•        Ability to use standard measuring instruments, gauges, read and understand basic prints/drawings

 

•        Advanced Math skills in algebra, trigonometry, & basic statistics concepts

 

•        Capability to develop/design fixtures

 

•        Advanced ability to create Microsoft Excel, PowerPoint & Word documents with expert ability to incorporate functions & write macros. Microsoft Office certification a plus.

 

•        Excellent interpersonal and customer service skills

 

•        Easily able to recognize & communicate potential issues

 

•        Ability to follow and review department procedures for correctness and write/re-write procedures when necessary

 

•        Excellent interpersonal and customer service skills

 

•        Works well with internal customers from various levels of the organization

 

•        Capacity to train others, including “training the trainer”

 

•        Works independently and easily resolves minor daily issues/problems

 

•        ASQ CQE certification highly preferred

 

•        Six Sigma training a plus

 

Quality Engineer PHYSICAL REQUIREMENTS:

 

Standing, stooping, light lifting (25 lbs. or less), manual dexterity, ability to read fine print, 20/20 vision or corrected 20/20 vision

 

 

Company Description
Global Pharmaceutical CDMO specializing in solid oral, liquid and semi-solid dosage forms.

Global Contract Development and Manufacturing Organization (CDMO)

Address

Olive Branch, MS
USA

Industry

Manufacturing