Job Title:
Associate II - Documentation
Experience:
Less than 1 Year
Location:
St. Joseph, MO 64506
Status:
Full Time, Employee
Job Category:
Manufacturing/Production/Operations
Career Level:
Entry Level



U.S. Awards and Recognition

Boehringer Ingelheim is committed to excellence in everything we do. Our goal is to produce optimal results for our customers, shareholders, and the communities in which we operate. Below are some examples of our recent acknowledgements.


Diversity Counsil Honors Award
#1 Diversity Council Honors Award

Philip Crosby Total Quality Excellence
2009 Best Places to Work
Corporate Equality Index

Philip Crosby Total Quality Excellence
2008: Governor's Environmental Excellence Award; Silver awarded by the Commonwealth of Virginia
(Petersburg, VA)

2008 Best Places to Work Corporate Equality Index
2008 Best Places to Work
Corporate Equality Index

Science 2007 Top Employer Award
#1 in Science Magazine for Top Employers
(Ridgefield, CT)

TargetRX Award
#1 in Reaching Primary Care Physicians
(U.S. Sales Force)

McKesson Award
2007 Pharmaceutical Supplier of the Year
(Ridgefield, CT)

Danbury Friendly Family Award
The Greater Danbury Family Friendly Award
(Ridgefield, CT)

Manny Award
2007 Manny Award Winner for Best Manufacturing Workplace
(Cleveland, OH)

Amerisource Bergen
2006 Vendor of the Year Award
(Ridgefield, CT)
Our Culture

At Boehringer Ingelheim, we deliver Value through Innovation by living our fundamental principles of Lead & Learn. We have high expectations for our employees. We require employees at all levels of the organization to take initiative, stay connected, grow together, and achieve outstanding results. To enable high performance, we provide opportunities for personal growth, a collaborative and inclusive work environment, and exceptional employee benefits. We reward high achievement with recognition, opportunities and competitive pay. We hold ourselves to the highest standard of excellence and count on each other to go the extra mile in everything we do.

Associate II - Documentation


QUALIFICATIONS:

  • High School degree and 2 years related experience

  • Proficient computer skills with specific experience with word processing, spreadshets, and database management

  • Must be detailed oriented and able to perform with minimal direct supervision

  • General understanding of biological production processes

  • Ability to handle several projects in quick-paced environment while maintaining traceability of work performed and communication to other departments

  • Ability to draft portions of technical documents and strong proofreading skills and excellent communication and written skill sets

DUTIES & RESPONSIBILITIES:

  • Prepare, route and track packets for Standard Operati ng Procedures and controlled forms

  • Assemble folders with required batch records and support documents for each lot produced.  Assemble folders for all cleaning doumentation, autoclave runs, filter testing, bioreactor and tank logs

  • Prepare shop packets as needed and enter data into MAPICS after completion of process.  Assist in ordering required materials to production to support shop packets as needed

  • Assist with tracking and preparing supporting documentation for Unususal occurances and CAPA items

  • Monitors documentation for working cells and viruses forms for errors and applies  improvements in those forms to reduce errors

  • Maintain database for harvest results

  • Compile and transfer completed records, logs and seed records to Doc Center for storage and archiving

  • Assembles and monitors procgress of  test reports for timely release of antigens

  • Assist in the retrieval and archiving of cell culture  and seed records for QA  review

  • Assist in the completion and tracking of UO's and CAPA's