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HomeCompaniesCareers Praxispackaging Icims ComQuality Operations Manager

Quality Operations Manager

Careers Praxispackaging Icims Com · Grand Rapids, MI, US · Deleted · iCIMS

Job facts

FieldValue
CompanyCareers Praxispackaging Icims Com
TitleQuality Operations Manager
Normalized title-
Department / team-
LocationGrand Rapids, MI, United States
Work model-
Employment typeFull Time
Salary-
Statusdeleted
ATS provideriCIMS
Posted / first seen2026-05-06 / 2026-05-31
Changed / last seen2026-06-04 / 2026-06-02

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PageWhat it containsOpen
Company jobsActive postings from Careers Praxispackaging Icims Com.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through iCIMS.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Grand Rapids.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

CompanyCareers Praxispackaging Icims Com
Sourcedd95bc8b-a02c-4b85-b77c-10aa756d5df3
ATS provideriCIMS

Description

Overview Responsible for compliance with the requirements of 21CFR Parts 110/111 and 210/211. This position works closely with the Quality Managers and the Production Department to ensure Quality Assurance compliance with regulatory and customer requirements. This position works with all supervision and employees to ensure that cGMPs and Praxis SOPs, policies and work instructions are being followed. Responsibilities Ensures the content and executional effectiveness of the QA Programs. Responsible to ensure products meet qualityand efficiency standards set by the company. Develops quality assurance plans by conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions, and verification procedures; monitoring inventories. Validates quality processes by establishing product specifications and quality attributes; measuring production; documenting evidence; determining operational and performance qualification; writing and updating quality assurance procedures. Maintains and improves product quality by completing product, company, system, compliance, and surveillance audits; investigating customer complaints. Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. Direct and supervise Quality Assurance Team. Reviews and updates QMS SOPs, WIs, and Forms, as required, to match current practices. Maintains Major Equipment and Portable Equipment Log books. Maintains Non-TEP book (fills out when Non-TEP product is received). Collaborates with the Engineering Administrator and Director of Quality, to ensure compliant validation/qualification of all appropriate equipment and/or processes. Responsible for adherence to all Company policies and procedures. Works to improve the effectiveness of the quality management system through the use of the quality policy, quality objectives, audit results, analysis of data, corrective and preventive actions. Supervises a diverse workforce, @ 5-10 Quality Employees. Assists Human Resources with interviewing and managing performance. Ensures employees are trained according to their roles. Addresses complaints and problems, elevates to Leadership when needed. Ensures proper PPE’s and Safety procedures are followed. Instills a sense of quality through modeled quality behaviors and mindset. Flexibly works other shifts, shifts maybe 8, 10 or 12 hours as needed. Qualifications Bachelor’s degree, required or equivalent combination. 3-5 years Quality experience required. Supervision experience required. Experience in managing various levels of employees with different educational backgrounds, work style habits, and employment histories.

Full job record

Job ID26975e65d9a2f411d37f0fac86d4000bbb2dffce
Org ID1a3c4d6f-014b-4140-9625-9c0ec4c8da70
Source IDdd95bc8b-a02c-4b85-b77c-10aa756d5df3
Board IDdd95bc8b-a02c-4b85-b77c-10aa756d5df3
Providericims
Provider Job Key1274
TitleQuality Operations Manager
Normalized Title
Statusdeleted
Activeno
Location TextGrand Rapids, MI, US
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionMI
CityGrand Rapids
Salary RawOverview Responsible for compliance with the requirements of 21CFR Parts 110/111 and 210/211. This position works closely with the Quality Managers and the Production Department to ensure Quality Assurance compliance with regulatory and customer requirements. This position works with all supervision and employees to ensure that cGMPs and Praxis SOPs, policies and work instructions are being followed. Responsibilities Ensures the content and executional effectiveness of the QA Programs. Responsible to ensure products meet qualityand efficiency standards set by the company. Develops quality assurance plans by conducting hazard analyses; identifying critical control points and preventive measures; establishing critical limits, monitoring procedures, corrective actions, and verification procedures; monitoring inventories. Validates quality processes by establishing product specifications and quality attributes; measuring production; documenting evidence; determining operational and performance qualification; writing and updating quality assurance procedures. Maintains and improves product quality by completing product, company, system, compliance, and surveillance audits; investigating customer complaints. Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. Direct and supervise Quality Assurance Team. Reviews and updates QMS SOPs, WIs, and Forms, as required, to match current practices. Maintains Major Equipment and Portable Equipment Log books. Maintains Non-TEP book (fills out when Non-TEP product is received). Collaborates with the Engineering Administrator and Director of Quality, to ensure compliant validation/qualification of all appropriate equipment and/or processes. Responsible for adherence to all Company policies and procedures. Works to improve the effectiveness of the quality management system through the use of the quality policy, quality objectives, audit results, analysis of data, corrective and preventive actions. Supervises a diverse workforce, @ 5-10 Quality Employees. Assists Human Resources with interviewing and managing performance. Ensures employees are trained according to their roles. Addresses complaints and problems, elevates to Leadership when needed. Ensures proper PPE’s and Safety procedures are followed. Instills a sense of quality through modeled quality behaviors and mindset. Flexibly works other shifts, shifts maybe 8, 10 or 12 hours as needed. Qualifications Bachelor’s degree, required or equivalent combination. 3-5 years Quality experience required. Supervision experience required. Experience in managing various levels of employees with different educational backgrounds, work style habits, and employment histories.
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://careers-praxispackaging.icims.com/jobs/1274/quality-operations-manager/job
Apply URLhttps://careers-praxispackaging.icims.com/jobs/1274/quality-operations-manager/job
First Seen At2026-05-31 18:48:53Z
Last Seen At2026-06-02 14:05:08Z
Last Checked At2026-06-04 14:25:09Z
Last Changed At2026-06-04 14:25:09Z
Inactive At2026-06-04 14:25:09Z
Source Posted At2026-05-06 04:00:00Z
Source Updated At2026-05-06 19:30:17Z
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=icims/board=careers-praxispackaging.icims.com/date=2026-06-02/2026-06-02T14-05-07-155Z-56a4db3328b4571f497d64b315389c947b26ac76821d4dcf158e70df201f75c9.json
Event Fields
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Parsed Structured
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Extensions
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Native Structured
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