QC Document Control Specialist
Day Zero Diagnostics
Hazelwood, MO, USA
USD 22.5-34 / hour
Posted on Mar 25, 2026
Description
Position Summary
This role acts as a document specialist and administrative support for the Final QC and Quality Assurance departments. Responsible for following Good Documentation Practices. Ensures that quality documentation meets applicable customer, regulatory, and Company requirements. Ability to understand manufacturing specifications, requirements, procedures and departmental processes. Performs all duties using safety conscious and cGMP practices.
Primary Duties
This role requires High School Diploma, GED or equivalent and 5+ years experience of document review in a Quality /GMP environment (medical device preferred), including strong computer skills such as Microsoft Office Package (Excel, Word, etc.).Experience in cGMP document management systems and/or change management systems is preferred. Experience with Trackwise Digital and SAP is a plus
Knowledge, Skills, And Abilities
Ability to remain in stationary position, often standing, for prolonged periods.
Ability to wear PPE correctly most of the day.
Ability to adjust or move objects up to 50 pounds in all directions.
The estimated salary range for this role is between $22.50-$34.00. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux’s bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate’s experience and will be presented in writing at the time of the offer.
In addition, bioMérieux offers a competitive Total Rewards package that may include:
BioMérieux 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 BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).
Position Summary
This role acts as a document specialist and administrative support for the Final QC and Quality Assurance departments. Responsible for following Good Documentation Practices. Ensures that quality documentation meets applicable customer, regulatory, and Company requirements. Ability to understand manufacturing specifications, requirements, procedures and departmental processes. Performs all duties using safety conscious and cGMP practices.
Primary Duties
- Collaborate with cross-functional departments to ensure timely implementation of change controls
- Responsible for facilitating procedure updates with process owners.
- Route documents for review, approval and assure completion of the approval process.
- Reviews and distributes documents and correspondence.
- Performs data entry and prepares a variety of documents, related to quality system records
- Organizes meetings and/or appointments.
- Reasonable, reliable attendance and punctuality is an essential job function required for this position.
- Supports QC and other projects as requested by management.
- Perform all work in compliance with company quality procedures and standards.
- Perform other duties as assigned.
This role requires High School Diploma, GED or equivalent and 5+ years experience of document review in a Quality /GMP environment (medical device preferred), including strong computer skills such as Microsoft Office Package (Excel, Word, etc.).Experience in cGMP document management systems and/or change management systems is preferred. Experience with Trackwise Digital and SAP is a plus
Knowledge, Skills, And Abilities
- Consistently upholds and reflects the core ethical principles and values that bioMérieux promotes.
- Written Communications - including the ability to communicate technical data in written form
- Troubleshooting issues to identify and resolve problems efficiently
- Priority setting that align with business objectives
- Informing others by sharing clear, timely information to ensure alignment.
- Build and maintain positive, productive interactions with colleagues
- Must be able to demonstrate flexibility in responding to unexpected demands
- Skilled in MS Office tools to include but not limited to Outlook, Teams, Word, and Excel, applies skills independently in most situations; handles moderately complex tasks with occasional guidance
Ability to remain in stationary position, often standing, for prolonged periods.
Ability to wear PPE correctly most of the day.
Ability to adjust or move objects up to 50 pounds in all directions.
The estimated salary range for this role is between $22.50-$34.00. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux’s bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate’s experience and will be presented in writing at the time of the offer.
In addition, bioMérieux offers a competitive Total Rewards package that may include:
- A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options
- Company-Provided Life and Accidental Death Insurance
- Short and Long-Term Disability Insurance
- Retirement Plan including a generous non-discretionary employer contribution and employer match.
- Adoption Assistance
- Wellness Programs
- Employee Assistance Program
- Commuter Benefits
- Various voluntary benefit offerings
- Discount programs
- Parental leaves
BioMérieux 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 BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).