Quality Document Supervisor

3 weeks ago

Franklin, United States Lubrizol Corporation Full time

**Job Title**:Quality Document Supervisor

**Job Location**:Franklin, Wisconsin

**Job Type**: Full-Time

**Type of Role**: On-site

**About Lubrizol**

**Join Our Thriving Team at Lubrizol as Quality Document Supervisor**

Unleash Your Potential. At Lubrizol we're transforming the Medical Device industry. We're looking for exceptional talent to join us on this journey. If you are ready to join an international company with talent around the world, and want to make a real impact, we want you on our team.

**What You'll Do**:
As a Quality Document Supervisor, you'll be at the forefront of our innovation by managing the document control (initiation, change, approval, implementation, distribution, retention, and retrieval), product release, Process Change Orders (initiation, change, approval, and implementation), and customer complaints. The Quality Document Supervisor will lead Document Control Administrators.

**What We're Looking For**:

- Directs the activities of site Document Control personnel.
- Participating in internal and external audits and perform internal audits as assigned.
- Responsible for managing Process Change Orders (PCOs).
- Responsible for managing Quality Systems Documentation and records.
- Manages current and archived (internal and external) documents (electronic, hard copy, etc.) per Vesta’s record retention policies and procedures.
- Reviews final production documentation (paper and electronic DHRs ‐ routers, shippers, labels, etc.) as part of final product acceptance and release process.
- Responsible for Barcode Labels management.
- Responsible for Customer Complaints and ensures the complaints are addressed and closed out to meet internal and regulations requirements. Includes initiation, investigation support, validation, response to customers and providing defined metrics to management.
- Other duties as assigned.

**Skills That Make a Difference**:

- Successful completion of four‐years of high school diploma. Completion of two years of college with an Associate degree (preferred).
- General understanding of ISO 13485:2016.
- General understanding of FDA 21 CFR Part 820. Six Sigma Green Belt (preferred).
- 5+ years experience in an FDA regulated business function‐Quality function is highly desired.
- Quality function experience in medical device, pharmaceutical, cosmetic, or food/beverage industry preferred.
- Experience with common data systems (Microsoft products, QCBD and ERP).
- 3 yeas of prior supervisory experience (preferred).

**Perks and Rewards That Inspire**:

- Competitive salary with performance-based bonus plans
- 401K Match plus Age Weighted Defined Contribution
- Competitive medical, dental & vision offerings
- Health Savings Account
- Paid Holidays, Vacation, Parental Leave
- Flexible work environment

**Nearest Major Market**:Milwaukee
**Job Segment**:Pharmaceutical, Six Sigma, Document Control, Chemical Research, Pharmaceutical Sales, Management, Science, Administrative, Engineering, Sales

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