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Quality Manager

B3b9327b 9bd0 4bbe A74b 6a6ad8e50a41 19000101 000001 · Hernando, MS, US, Hernando, MS · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyB3b9327b 9bd0 4bbe A74b 6a6ad8e50a41 19000101 000001
TitleQuality Manager
Normalized title-
Department / team-
LocationHernando, MS, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-05-13 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from B3b9327b 9bd0 4bbe A74b 6a6ad8e50a41 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Hernando.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyB3b9327b 9bd0 4bbe A74b 6a6ad8e50a41 19000101 000001
Source651accaa-5801-4e32-b6f3-1741f9a6024c
ATS providerADP Workforce Now Recruiting

Description

Job Summary: The Quality Manager is responsible for the oversight of quality functions in compliance with the FDA Quality System Regulations (QSR's), ISO 9001, ISO 14001, ISO 45001, IATF 16949 standards, and company policies and procedures. The Quality Manager has strong communication skills at all levels and manages the quality engineering and quality inspection groups in all functional activities. Role and Responsibilities: The individual must be capable of working independently and in a team setting. Major responsibilities include: Manage resources within the quality engineering and inspection functions providing guidance with day-to-day operational aspects and managing time and attendance through ADP. Provide leadership and support to quality engineering for planning, executing, and finalizing projects, defining objectives, and assuring deliverables are accurate and completed according to strict deadlines and within budget. Provides leadership and support to quality control functions providing guidance with prioritizing receiving, pre-outsource, pre-inventory, in-process, and final inspections assuring quality and delivery to our customers to meet on time delivery. Assign responsibilities and effectively communicate project expectations to team members and stakeholders in a timely and clear fashion. Communicate management by objectives (MbO) and hold initial, mid-year, and final yearly reviews with direct reports and complete personal MbO's with evidence of completion. Prevention and mitigation of financial risks caused by non-conformities Effective and efficient BMS with competent BPE including regulated interfaces between all departments. Support Quality and Regulatory functions by assisting with establishing and following policies, procedures, and accountability measures that ensure regulatory compliance and continuous quality performance improvement. Lead the efforts for customer communication, receiving and understanding requirements and assuring compliance to customer expectations. Maintenance, monitoring, improvement and further development of the certified management systems. Partner with Operations and Engineering to assure alignment of goals, objectives and strategies. Mentor team members in all quality disciplines to improve and strengthen the quality team. Identify quality engineering and inspection metrics; analyze and report trends to management. Assist in CAPA and continuous improvement activities. Promotion of continuous quality awareness in alignment with the company objectives and the SFS group Quality Policy (F-00028). Management of the BMS (P-00031) ensuring high degree of BMS maturity. Process owner and consultant specialist of assigned BMS documents. Aid with internal and customer audits, and regulatory agency inspections as applicable.\ Ensure completeness and adequacy of Tegra Medical documentation and records. Support and conduct Mid-term planning, and annual budget. Define QIP and KPI goals. Further or additional duties according to the need of the respective site. Qualifications Quality management experience in the medical device industry, a plus. High understanding of the FDA Quality System Regulation. Ability to analyze operation and provide cost effective suggestions and targets to lower inspection costs. High technical aptitude. Good interpersonal and leadership skills. Growth mindset, attention to detail and excellent work ethic. Experience with Microsoft Project, Microsoft Office, Job Boss, Solid Works and other relevant software systems. Positive attitude, team player. Excellent written and verbal communication skills. Education Requirements: Bachelor's Degree with a minimum of 5 years of experience in the medical device industry or 8+ years of experience in an engineering and/or quality discipline role. Physical Requirements: Frequently performing repetitive work. Occasional lifting (max. 40 lbs.) Occasional carrying (max. 40 lbs.) Subject to physical hazards from moving equipment and machine parts Constant safety glasses Constant full PPE Frequent standing Occasionally sitting, walking, pushing, pulling, reaching. 1st Shift-M-F 7:00am - 4:00pm

Full job record

Job IDa3b677515572b5ab2d0a3e37bfa6ddd29c0bca81
Org ID2d394211-a5da-40a4-8349-6fae3cbaf1f7
Source ID651accaa-5801-4e32-b6f3-1741f9a6024c
Board ID651accaa-5801-4e32-b6f3-1741f9a6024c
Provideradp_workforcenow
Provider Job Key584005
TitleQuality Manager
Normalized Title—
Statusactive
Activeyes
Location TextHernando, MS, US, Hernando, MS
Department—
Team—
Employment Typefull_time
Workplace Type—
Remote Policy—
CountryUnited States
RegionMS
CityHernando
Salary Raw—
Salary Min—
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Source URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=b3b9327b-9bd0-4bbe-a74b-6a6ad8e50a41&ccId=19000101_000001&lang=en_US&type=JS&jobId=584005&jwId=9201211063420_1
Apply URLhttps://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=b3b9327b-9bd0-4bbe-a74b-6a6ad8e50a41&ccId=19000101_000001&lang=en_US&type=JS&jobId=584005&jwId=9201211063420_1
First Seen At2026-05-31 18:33:20Z
Last Seen At2026-06-06 12:23:10Z
Last Checked At2026-06-06 12:23:10Z
Last Changed At2026-06-06 12:23:10Z
Inactive At—
Source Posted At2026-05-13 20:34:00Z
Source Updated At—
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=b3b9327b-9bd0-4bbe-a74b-6a6ad8e50a41|19000101_000001/date=2026-06-06/2026-06-06T12-23-09-039Z-a15c36f0fd7186e9d393a5a5b2abd8027c5629dbf0953c63b909688d2c10c6de.json
Event Fields
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Extensions
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style=\"font-size:15px;\">Prevention and mitigation of financial risks caused by non-conformities</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Effective and efficient BMS with competent BPE including regulated interfaces between all departments.&nbsp;</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Support Quality and Regulatory functions by assisting with establishing and following policies, procedures, and accountability measures that ensure regulatory compliance and continuous quality performance improvement.</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Lead the efforts for customer communication, receiving and understanding requirements and assuring compliance to customer expectations.</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Maintenance, monitoring, improvement and further development of the certified management systems.</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Partner with Operations and Engineering to assure alignment of goals, objectives and strategies.</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Mentor team members in all quality disciplines to improve and strengthen the quality team.</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Identify quality engineering and inspection metrics; analyze and report trends to management.</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Assist in CAPA and continuous improvement activities.</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Promotion of continuous quality awareness in alignment with the company objectives and the SFS group Quality Policy (F-00028).</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Management of the BMS (P-00031) ensuring high degree of BMS maturity.&nbsp;</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Process owner and consultant specialist of assigned BMS documents.&nbsp;</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Aid with internal and customer audits, and regulatory agency inspections as applicable.\\</span></li><li style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; font-size: 16px; font-family: initial; line-height: 1.15;\"><span style=\"font-size:15px;\">Ensure completeness and adequacy of Tegra Medical documentation and records.</span></li><li><span style=\"font-size:15px;\">Support and conduct Mid-term planning, and annual budget.&nbsp;</span></li><li><span style=\"font-size:15px;\">Define QIP and KPI goals.&nbsp;</span></li><li><span style=\"font-size:15px;\">Further or additional duties according to the need of the respective site.</span></li></ul></div><p style='margin:0in;font-size:15px;font-family:\"Times New Roman\",serif;color:black;text-align:justify;'><span style=\"font-size:15px;\">&nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Times New Roman\",serif;color:black;text-align:justify;'><strong><span style=\"font-size:15px;\">Qualifications</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 21.5px;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Quality management experience in the medical device industry, a plus.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">High understanding of the FDA Quality System Regulation.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Ability to analyze operation and provide cost effective suggestions and targets to lower inspection costs.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">High technical aptitude.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Good interpersonal and leadership skills.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Growth mindset, attention to detail and excellent work ethic.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Experience with Microsoft Project, Microsoft Office, Job Boss, Solid Works and other relevant software systems.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Positive attitude, team player.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Excellent written and verbal communication skills.</span></li></ul></div><p style='margin:0in;font-size:15px;font-family:\"Times New Roman\",serif;color:black;margin-left:-4.5pt;text-align:justify;'><strong><span style=\"font-size:15px;\">&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;margin-right:4.3pt;'><strong><span style=\"font-size:15px;font-family:Times;\">Education Requirements:</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><span style=\"font-size:15px;\">Bachelor&#39;s Degree with a minimum of 5 years of experience in the medical device industry or 8+ years of experience in an engineering and/or quality discipline role.</span></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong><span style=\"font-size:15px;font-family:Times;\">&nbsp;</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong><span style=\"font-size:15px;font-family:Times;\">Physical Requirements:</span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 21.5px;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Frequently performing repetitive work.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Occasional lifting (max. 40 lbs.)</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Occasional carrying (max. 40 lbs.)</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Subject to physical hazards from moving equipment and machine parts</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Constant safety glasses</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Constant full PPE</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Frequent standing</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Occasionally sitting, walking, pushing, pulling, reaching.</span></li></ul></div><p><br></p></div></div></div>\n<br/>1st Shift-M-F 7:00am - 4:00pm",
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    "content_type": "application/json;charset=UTF-8",
    "response_bytes": 16585
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/a3b677515572b5ab2d0a3e37bfa6ddd29c0bca81?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/2d394211-a5da-40a4-8349-6fae3cbaf1f7JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/651accaa-5801-4e32-b6f3-1741f9a6024cJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/a3b677515572b5ab2d0a3e37bfa6ddd29c0bca81/eventsJSON

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