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The primary purpose of the position is inspecting materials and products and following documented ISO processes and procedures for meeting customer specific requirements. To comply with all necessary regulatory quality system and business requirements as based on ISO 13485 and FDA requirements for medical device and Food manufacturing. Reporting to the site Quality Supervisor the person will need to work closely with the Account Teams Quality Engineers Materials Department and any other groups as necessary.
All job responsibilities are to be performed in accordance with the companys Mission/Values Statement and its Code of Business Conduct and Ethics.
The position serves as a resource helping to ensure that the medical device and other regulated operations function within regulatory and relevant standards requirements. This position also ensures all customer requirements are met and that the final product meets all customer requirements.
Responsibilities:
Duties which may be performed as need arises include:
Qualifications :
Additional Information :
Disclosure Statement:
The pay range for this role at the noted location is $15.76 to 19.06 per hour. The actual rate of pay offered may vary based upon but not limited to: education skills experience proficiency performance shift and location. In addition to base salary depending on the role the total compensation package may also include overtime shift differential callin and standby pay. RRD offers benefits including medical dental and vision coverage paid time off disability insurance 401(k) with match life insurance and other voluntary supplemental insurance coverages plus tuition assistance maternity leave adoption assistance and employer/partner discounts.
RRD is an Equal Opportunity Employer including disability/veterans
Remote Work :
No
Employment Type :
Fulltime
Full-time