Sr Doc Control Specialist

Position Summary:

The purpose of this position is to support implementation and sustainability of the Document Control and Change Management programs at the St. Louis site. Facilitate creation, modification, and approval of changes via the site Change Management program. Support the lifecycle of documentation within the Quality System. Operates as a support function that collaborates with all local functions within the bioMerieux Inc., St. Louis facility. Ensures that quality documentation meets applicable customer, regulatory, and Company requirements. Ability to understand manufacturing specifications, requirements, procedures and departmental processes. Maintain quality records including filing, preparing documents for scanning and shredding of documents per procedure. Provide input regarding the continuous improvement of each. Support internal customers to ensure proper GMP compliance in editing and revising Quality records.

Primary Duties:

1. Monitor the change process so that only approved and validated changes are incorporated in released product documentation.
2. Train new employees and internal customers on internal processes.
3. Collaborate with cross-functional departments to ensure timely implementation of change controls.
4. Responsible for facilitating procedure updates in a timely fashion with process owners.
5. Route documents for review, approval and assure completion of the approval process.
6. Own the site Periodic Review process ensuring site procedures are reviewed and updated in accordance with their periodic review requirements.
7. Reviews and distributes documents and correspondence.
8. Maintains accurate filing systems.
9. Performs data entry and prepares a variety of documents, related to quality system records.
10. Responsible for the archival and retrieval of records in accordance with established procedures.
11. Organize the transfer of documentation to and from the offsite storage facility, as needed.
12. Ability to walk within the company campus which includes 6 buildings to transfer documentation.
13. Organizes meetings and/or appointments.
14. Support internal and external audit activities.
15. Support quality projects with departments and the facility, as needed.

Qualifications-Knowledge, Experience & Skills:

1. Requires an Associates Degree and 2 years of quality/document review experience in a GMP environment (medical device preferred) OR in lieu of an Associates Degree, 4 years of quality/document review experience in a GMP environment (medical device preferred).
2. Requires strong computer skills including Microsoft Office Package (Excel, Word, etc.).
3. Strong written communication skills and attention to detail are required.
4. Must have sound knowledge of regulatory requirements such as ISO, FDA, etc.
5. Ability to proficiently use Microsoft Office Tools.
6. Ability to inspire, motivate, and build the confidence within the team to reach goals, consistently pushing self and others to achieve results.
7. Ability to influence peers, managers and internal customers of Document Control.
8. Must demonstrate team leadership skills.
9. Ability to work both independently and in a team environment.

Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMerieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at [emailprotected].

BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).