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HomeCompaniesHrrecruitingservice1QA MANAGER- Healthcare

QA MANAGER- Healthcare

Hrrecruitingservice1 · Boston, MA, United States · Active · SmartRecruiters

Job facts

FieldValue
CompanyHrrecruitingservice1
TitleQA MANAGER- Healthcare
Normalized title-
Department / teamHealth Care Provider
LocationBoston, MA, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerSmartRecruiters
Posted / first seen2014-10-30 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-23

Related slices

PageWhat it containsOpen
Company jobsActive postings from Hrrecruitingservice1.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SmartRecruiters.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Boston.Open
Department jobsActive postings in Health Care Provider.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

CompanyHrrecruitingservice1
Source0c9f9758-d6f9-4d17-8ec4-5f71653b6f3e
ATS providerSmartRecruiters

Description

Small company, the Quality team is made up of the manager and one associate, we need someone very good with rolling up their sleeves. The successful candidate will be responsible for maintaining the quality systems strategy and providing coordination and direction of existing quality programs to ensure production of products, services, and processes are consistent with established standards. Essential Duties: • Developing and overseeing execution of companies audit plans/strategies. • Process and evaluate audit findings to monitor overall compliance and to identify quality related trends/issues, areas of business and/or regulatory risk, and training needs • Provide consultation on regulatory compliance issues • Ensure performance and quality of products and services conform to established company and regulatory standards. • Host external regulatory agency and notified body assessments and inspections (example: FDA, ISO). Review and participate in issues and/or decisions related to assessments. • Serve as the site management representative, providing updates to the company and the VP of Bioservices regarding status of the quality system, compliance status and performance relating to quality. • Maintain the biological and chemical waste management programs to ensure compliance to Local, State and DOT regulations. • Act as a customer interface during on-site audits, conference calls and other standard means of communication. MUST HAVES: • BS in Physical, Biological Sciences, or technical/scientific discipline required • Experience with ISO 9001/13485 • Experience with validation • Experience guiding or managing the CAPA and NCR process • Experience in a pharmaceutical or life sciences organization • Experience leading FDA/ISO audits • Experience in GMP environment • CLIA experience helpful • 5-8 years (8 years maximum) experience as a Quality Professional in a regulated medical device, in vitro diagnostics, or life science industry. • 5 years previous supervisory experience, preferably in Quality Systems or Quality Assurance. • American Society for Quality certification desirable. • In-depth knowledge and application of regulations, guidelines and industry practices and the ability to interpret the regulations/guidelines • Ability to effectively present information to management, regulatory agencies and other departments. • Experience interpreting and complying with cGMP, CLIA, IVDD or MDD, working • Excellent interpersonal, communication, analytical, managerial, and organizational skills. • Strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines. All your information will be kept confidential according to EEO guidelines.

Full job record

Job ID6c754bb38aa643338955db1c5f66f5f9911aec82
Org IDcca08593-c415-4093-afa5-2700f37373c0
Source ID0c9f9758-d6f9-4d17-8ec4-5f71653b6f3e
Board ID0c9f9758-d6f9-4d17-8ec4-5f71653b6f3e
Providersmartrecruiters
Provider Job Key79816755
TitleQA MANAGER- Healthcare
Normalized Title
Statusactive
Activeyes
Location TextBoston, MA, United States
DepartmentHealth Care Provider
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionMA
CityBoston
Salary RawSmall company, the Quality team is made up of the manager and one associate, we need someone very good with rolling up their sleeves. The successful candidate will be responsible for maintaining the quality systems strategy and providing coordination and direction of existing quality programs to ensure production of products, services, and processes are consistent with established standards. Essential Duties: • Developing and overseeing execution of companies audit plans/strategies. • Process and evaluate audit findings to monitor overall compliance and to identify quality related trends/issues, areas of business and/or regulatory risk, and training needs • Provide consultation on regulatory compliance issues • Ensure performance and quality of products and services conform to established company and regulatory standards. • Host external regulatory agency and notified body assessments and inspections (example: FDA, ISO). Review and participate in issues and/or decisions related to assessments. • Serve as the site management representative, providing updates to the company and the VP of Bioservices regarding status of the quality system, compliance status and performance relating to quality. • Maintain the biological and chemical waste management programs to ensure compliance to Local, State and DOT regulations. • Act as a customer interface during on-site audits, conference calls and other standard means of communication. MUST HAVES: • BS in Physical, Biological Sciences, or technical/scientific discipline required • Experience with ISO 9001/13485 • Experience with validation • Experience guiding or managing the CAPA and NCR process • Experience in a pharmaceutical or life sciences organization • Experience leading FDA/ISO audits • Experience in GMP environment • CLIA experience helpful • 5-8 years (8 years maximum) experience as a Quality Professional in a regulated medical device, in vitro diagnostics, or life science industry. • 5 years previous supervisory experience, preferably in Quality Systems or Quality Assurance. • American Society for Quality certification desirable. • In-depth knowledge and application of regulations, guidelines and industry practices and the ability to interpret the regulations/guidelines • Ability to effectively present information to management, regulatory agencies and other departments. • Experience interpreting and complying with cGMP, CLIA, IVDD or MDD, working • Excellent interpersonal, communication, analytical, managerial, and organizational skills. • Strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines. All your information will be kept confidential according to EEO guidelines.
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://jobs.smartrecruiters.com/HRRecruitingService1/79816755-qa-manager-healthcare-
Apply URLhttps://jobs.smartrecruiters.com/HRRecruitingService1/79816755-qa-manager-healthcare-?oga=true
First Seen At2026-05-31 17:34:12Z
Last Seen At2026-06-23 10:47:17Z
Last Checked At2026-06-23 10:47:17Z
Last Changed At2026-05-31 17:34:12Z
Inactive At
Source Posted At2014-10-30 02:57:36Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=hrrecruitingservice1/date=2026-06-23/2026-06-23T10-47-15-238Z-bf6c9c8085b19da807b97f6a3d2e31538d93282d162d5e3396bd13acb5f07283.json
Event Fields
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Parsed Structured
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Extensions
{}
Native Structured
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