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Senior Manager, Software Device Quality
USA - 3316 Takeda Development Center Americas, Inc.
Lexington, MA
Strong cross-functional collaboration and project/program management experience
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Senior Project Manager / Site Lead
CACI, INC.-FEDERAL
Crane, IN
Job Title: Senior Project Manager / Site Lead
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A
Field Reimbursement Manager Des Moines IA
adecco
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- $54.33 USD / hour
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Added 1 min ago
SO
Operations Manager
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Manchester, TN
- $100,000 USD / year
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Added 2 mins ago
Structure Analyst 1
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The Product Structure Analyst I will report directly to the Manager of Production Services.
Added 3 mins ago
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- $40 to $55 USD / hour
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Associate Project Manager, Aulani/Facilities Asset Management ($97,000 - $130,000)
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…including Low-Income Housing Tax Credit (LIHTC), Section 8, project based vouchers and HUD program…
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Bertelsmann-Jobs

Quality Manager

Memphis, TN, United States

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Job details

Experience: 5+ years of experience in a quality role in a regulated environment (medical device, pharma, biotech, or logistics)
Posting language: English
Posted: Nov 13, 2026

Original job description

Company Description Arvato is an innovative and leading global 3PL service provider in supply chain management and e-commerce. With 20,000 team members at over 100 locations, we focus on the Consumer Products, Tech, Healthcare, Automotive and Publisher industries.

You will work in an environment built on collaboration, respect, commitment and curiosity, where you can grow, contribute your ideas, and make an impact. Be part of the team that delivers logistics excellence and shapes supply chains globally. Working at Arvato means: Together, we’re on it.

Job Description

The position of the QA Manager Healthcare includes all activities related to Quality Assurance of

pharmaceutical products and medical devices to ensure a proper implementation of the quality

policy, the quality assurance system, the compliance with GMP/GDP rules and all GxP

requirements in accordance with e.g. EN ISO 9001, EN ISO 13845 and other country specific

requirements. This role is also responsible for ensuring that all requirements for Quality Assurance are

understood and adhered to by the respective departments.

YOUR TASKS

Continuous improvement and compliance of the local quality management system (ISO 9001, ISO 13485 and other country specific requirements (e.g. GDP, GMP, FDA, etc.)
Flexible adaptation of the Quality Management System to all requirements (e.g. requirements of authorities, customer requirements)
Oversight of all quality technical related processes, e.g. maintenance, calibration, pest control
Supporting the strategic implementation of the Quality policy and Global Quality System
Reporting of quality KPIs and enforcement of the specified quality in cooperation with all departments involved, including Complaints / Deviations / CAPA / Change Management
Responsible for the execution of training, according to the respective requirements• Decision on the further use of products (blocking, release)
Guarantee of the written separation of responsibility with the customer and suppliers regarding all activities
Close collaboration with other departments, e.g. sales and account management, as well as the global quality team
Participation in project and process alignments, preparation and performance of management reviews
Completes assigned MasterControl Action Items within required timelines to ensure timely resolution and compliance with quality system expectations

YOUR PROFILE

Bachelor’s degree in a scientific, technical, or quality-related field; or equivalent work experience
5+ years of experience in a quality role in a regulated environment (medical device, pharma, biotech, or logistics)
Working knowledge of ISO 9001, ISO 13485, and FDA 21 CFR Part 820 requirements
Proficient in document control systems and training program coordination
Excellent attention to detail and organizational skills
Strong verbal and written communication abilities
Proficiency with Microsoft Office.
ISO Lead Auditor Certification preferred
Experience with MasterControl or similar eQMS platforms preferred

WE OFFER

Medical, Dental, Vision, Life Insurance, and Disability Pay
401(k) with company matching up to 6%
Paid Time Off, including paid holidays
Flexible Spending Accounts
Voluntary benefits such as legal and financial assistance, pet insurance, and more
Employee Assistance Program
Ongoing employee development opportunities including tuition reimbursement, scholarships, and training
Commuter benefits
Employee engagement activities

Additional Information All your information will be kept confidential according to EEO guidelines.

Disclosure requirements pertaining to the collection of your personal data:

Responsible for processing the information provided in your application is the company specified in the job advertisement, with its registered office as indicated. The company processes your data for the purpose of establishing an employment relationship on the basis of Art. 6 (1) b GDPR / Section 26 (1) sentence 1 BDSG. The retention period for your data is determined by the statutory time limits applicable in the respective country, beginning upon completion of the recruitment process. You can find these here. You can contact the company’s Data Protection Officer at the above-mentioned postal address. Further information on data protection and your rights can be found here. We strive to be an equitable and inclusive workplace for our employees and value their diverse perspectives, which contribute to the diversity of our company. Therefore, we welcome applications from people who enrich our company with their identity, background and personal experience. We want to keep the application process as simple as possible for you: focus on a meaningful resume; we do not require an elaborate cover letter. Please know that we can only accept your application through our online application portal. Learn more about our commitment to Equal Opportunity and Accommodation Information here. Recruiting-Platform powered by SmartRecruiters.

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Jobs in the United States