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Quality Manager

Job

(Suppressed)

Waco, TX (In Person)

$103,000 Salary, Full-Time

Posted 4 weeks ago (Updated 2 weeks ago) • Actively hiring

Expires 6/3/2026

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Job Description

Salary Confidential Position range in McLennan County $72k - $134k Per Year Quality Manager (Suppressed)
Occupation:
Quality Control Systems Managers
Location:
Waco, TX - 76705
Job Type:
Regular, Full Time (30 Hours or More), Permanent Employment, Day Shift
Posted:
04/21/2026 Positions available: 1
Source:
WorkInTexas
Web Site:
WorkInTexas Onsite /
Remote:
Work onsite all of the time
Updated:
04/24/2026
Expires:
05/21/2026 Job #: 17004870 Job Requirements and Properties Help for Job Requirements and Properties. Work Onsite Full Time Education 2 Years at College or a Technical or Vocational School Experience 36 Month(s) Typing Speed 40 + wpm Language English, Well Schedule Full Time Job Type Regular Duration Permanent Employment Hours 40 Hours Per Week Shift Day Shift Public Transit Available Benefits Help for . Overview Quality Coordinator has primary responsibility for record-keeping and document management for regulated businesses, including Medical Device, Pharmaceutical, Life Sciences and Microelectronics. The Quality and Document Coordinator will interface with all levels of sales and operations, both within the US and Thailand. Assist in maintaining document control for ISO13585, cGMP quality system. Job Responsibilities Coordinate specifications approvals with sales and customers Organize distribution and process procedures to maintain compliance to
ISO 90001, ISO
13485, and cGMP Provide Certificates of Compliance for custom products, and technical documents such as technical data sheets as requested by Sales Team and customers Interact with regulatory agencies such as ISO certifying body, internal and external Regulatory professionals. Review, report and assist in maintaining the companys
ISO, 13485
regulatory compliance status. Maintain MRB (Material Review Board) area. Actively work to correct product issues and release products. Identify and resolve discrepancies in documentation and labeling Create and control new documentation as needed for
ISO 13485.
Prepare internal documentation for submittal to customers, inspectors and auditors from regulatory agencies, and certifying agency auditors. Other projects as assigned involving QA. Knowledge, Skills, and Abilities Required High level of organization skills is required Ability to work independently in a fast paced, high-pressure environment is required Advanced knowledge of Microsoft Excel, Word, and Outlook Advanced communication and problem-solving skills Qualifications 4-year college degree in science 5+ years working experience in regulatory and/or product development/product manufacturing. Familiarity with ISO 13485 and ISO 9001.

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