Manufacturing Documentation Coordinator
Elanco
6 months ago
On-site
Elwood, KS
Operations
Your Role: Manufacturing Documentation Coordinator
Responsibilities:
- Review manufacturing documentation for accuracy and completeness
- Coordinate updates to documentation as needed by floor operation staff
- Investigate and improve process inefficiencies to ensure timely fulfillment of documentation
- Steward batch documentation lifecycle through operations, including chain-of-custody
- Support process teams through floor scheduling and documentation review
- Uphold strong safety and quality culture
- Support manufacturing through operational mentorship and technical coaching
What You Need to Succeed (minimum qualifications):
- Education: High school Diploma or greater
- Experience: 3 years of experience within GMP manufacturing
- Skills: Strong GMP documentation expertise; ability to review, improve, and ensure accuracy of batch records; effective cross-functional collaboration to resolve documentation issues
What will give you a competitive edge (preferred qualifications):
- Proven technical writing capability
- 3+ years experience within animal health pharmaceutical manufacturing
- SAP experience
- Familiarity with Veeva
- Cross-functional team work
- Strong coaching/mentorship skills
- Cradle to grave understanding of biologic manufacturing operations
Additional Information:
- Travel: occasional
- Location: Elwood, KS
- Standard business hours; occasional off-hour support needs may be required
Benefits and Perks (highlights):
- Multiple relocation packages
- 8-week parental leave
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Responsibilities:
- Review manufacturing documentation for accuracy and completeness
- Coordinate updates to documentation as needed by floor operation staff
- Investigate and improve process inefficiencies to ensure timely fulfillment of documentation
- Steward batch documentation lifecycle through operations, including chain-of-custody
- Support process teams through floor scheduling and documentation review
- Uphold strong safety and quality culture
- Support manufacturing through operational mentorship and technical coaching
What You Need to Succeed (minimum qualifications):
- Education: High school Diploma or greater
- Experience: 3 years of experience within GMP manufacturing
- Skills: Strong GMP documentation expertise; ability to review, improve, and ensure accuracy of batch records; effective cross-functional collaboration to resolve documentation issues
What will give you a competitive edge (preferred qualifications):
- Proven technical writing capability
- 3+ years experience within animal health pharmaceutical manufacturing
- SAP experience
- Familiarity with Veeva
- Cross-functional team work
- Strong coaching/mentorship skills
- Cradle to grave understanding of biologic manufacturing operations
Additional Information:
- Travel: occasional
- Location: Elwood, KS
- Standard business hours; occasional off-hour support needs may be required
Benefits and Perks (highlights):
- Multiple relocation packages
- 8-week parental leave
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching