My client, a very successful national pharmaceutical packaging company located in New Jersey is seeking a full-time permanent Documentation Manager to join their growing quality department.
The position will be responsible for the proper and timely handling and execution of Quality documentation.
The QDM is responsible for the control, security, accessibility, and timeliness of organizational documents that will be used by all stakeholders within and outside of the organization.
Criteria; Recent experience in a quality documentation rolein a production/manufacturing environment.
Knowledge of regulations, guidelines, and quality best practices.
Experience working with batch record documentation and quality systems.
Experience leading a team of direct reports within the quality department.
Bilingual in Spanish a plus but not mandatory Team player attitude, sold multi-tasker with the ability to effectively prioritize your time.
Ready to learn more about this opportunity?
Great This position offers the following; a competitive salary, great benefits and growth potential Instructions to Apply: If interested in learning more about this unique opportunity, please email your resume The subject line should read Quality Documentation Manager
– First and last name.
In the body of the email, please list why you would be a good fit for the role, along with your salary requirements.
No Zip Files, or Google file links accepted.
Applicants emailing directly to the email provided above will receive priority consideration over those applying via the platform.
Please note: Must have a vehicle to get to and from work on a daily basis.
This is NOT a remote position.
MUST be able to be onsite Monday-Friday/40 hours per week.
This position will NOT provide VISA sponsorship.
Must be either a U.S.
citizen or permanent Green Card holder.
There are no exceptions on this requirement.
Must have a minimum of one dose of the vaccine to be considered for a position with this client.
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