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Mastercontrol Qms Jobs in Arizona (NOW HIRING)

Mastercontrol Qms information

What is the difference between Mastercontrol Qms vs Quality Assurance Specialist?

AspectMastercontrol QmsQuality Assurance Specialist
CertificationsISO 9001, internal audits, compliance trainingISO 9001, Six Sigma, GMP certifications
Work EnvironmentQuality management systems, document control, compliance teamsLaboratories, manufacturing, production facilities
Employer & IndustryRegulated industries like healthcare, pharma, medical devicesManufacturing, pharmaceuticals, biotech

Mastercontrol Qms professionals focus on managing quality management systems, documentation, and compliance processes. Quality Assurance Specialists perform testing, inspections, and ensure product quality. While both roles support quality objectives, Mastercontrol Qms roles are more system and process-oriented, whereas Quality Assurance Specialists are more hands-on with product testing and validation.

What are common challenges when working with MasterControl Qms, and how can they be addressed?

Professionals working with MasterControl QMS often encounter challenges such as managing system configurations to fit evolving compliance requirements, training end-users effectively, and ensuring smooth integration with existing business processes. Successfully addressing these challenges involves staying updated on regulatory changes, investing time in thorough user training, and collaborating closely with IT and quality assurance teams. Regular communication and proactive troubleshooting are key to maximizing the system's efficiency and maintaining compliance.

What is MasterControl Qms?

MasterControl QMS (Quality Management System) is a cloud-based software platform designed to help organizations automate and manage their quality processes. It streamlines document control, training management, audit management, CAPA (Corrective and Preventive Actions), and other quality-related activities. The system is widely used in regulated industries such as life sciences, pharmaceuticals, and manufacturing to ensure compliance with standards like FDA, ISO, and others. MasterControl QMS helps companies improve efficiency, reduce errors, and maintain regulatory compliance through centralized and automated quality management.

What skills and qualifications are needed to work with MasterControl Qms?

To excel as a MasterControl QMS Specialist, you need a solid understanding of quality management principles, document control processes, and regulations such as FDA or ISO standards, typically supported by experience in quality assurance or a related field. Proficiency with the MasterControl Quality Management System software, electronic document management tools, and possibly certifications like Six Sigma or ASQ are highly valued. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure quality processes are maintained and improved. These skills are vital for maintaining compliance, streamlining workflows, and supporting continuous improvement in regulated industries.
What are popular job titles related to Mastercontrol Qms jobs in Arizona? For Mastercontrol Qms jobs in Arizona, the most frequently searched job titles are:
Infographic showing various Mastercontrol Qms job openings in Arizona as of August 2026, with employment types broken down into 92% Full Time, 1% Part Time, 6% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Quality Document Control Specialist

Becton, Dickinson and Company

Tempe, AZ • On-site

Full-time

Medical, Dental, Retirement

Posted yesterday

New


BD rating

7.3

Company rating: 7.3 out of 10

Based on 140 frontline employees who took The Breakroom Quiz

305th of 487 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Contract Opportunity - Assignment Ends December 28, 2028

This is a Fixed-Term Contract position with an anticipated end date of December 28, 2028.

Responsibilities

  • Manage the day-to-day administration of change requests, including:

  • Creating change requests and supporting documentation within the Electronic Document Management System (EDMS)

  • Reviewing and verifying change request documentation for accuracy and completeness

  • Creating, editing, and maintaining controlled documents

  • Managing the full lifecycle of change requests from initiation through closure

  • Tracking and reporting the status of change requests, workload, and key metrics to supervisors and project teams

  • Utilizing various software applications to support daily work activities.

  • Collaborating with project teams and document owners to drive changes to completion

  • Maintain a strong compliance-focused approach to regulatory requirements and quality standards

  • Participate in team and project meetings

  • Identify and recommend process improvements to enhance the effectiveness and efficiency of change management activities

  • Support departmental projects and related quality system processes

  • Perform other duties and special projects as assigned, including:

  • Assisting with investigations

  • Supporting regulatory audits and inspections

Education & Experience

  • High School Diploma or GED required

  • Associate's or Bachelor's degree preferred

  • Minimum of 1 year of experience in a documentation-related role, preferably within an FDA-regulated or similarly regulated environment

  • 1 to 3 years of relevant professional experience

Required Qualifications

  • Strong written, verbal, and reading proficiency in English

  • Exceptional attention to detail and accuracy

  • Proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint

  • Strong organizational and administrative skills with the ability to prioritize competing responsibilities

  • Ability to manage multiple tasks simultaneously in a fast-paced environment

  • Ability to work independently and collaboratively within cross-functional teams

  • Flexibility to adjust work schedules and work overtime when needed

  • Professional demeanor with a positive, team-oriented attitude.

Preferred Qualifications

  • Basic understanding of quality and regulatory requirements

  • Familiarity with Quality Management System (QMS) documentation and records

  • Experience in quality systems, manufacturing, laboratory operations, or product development environments

  • Experience using Electronic Document Management Systems (EDMS) such as MasterControl, Teamcenter, PEGA, or similar platforms.

This position is a Fixed-Term (limited-term) assignment designed to support a specific business need. Associates in this role are eligible for BD benefits, including medical, dental, health, and 401(k), subject to the eligibility requirements of BD Total Rewards policies. Employment is intended for a defined period and is expected to conclude upon completion of the assignment or fulfillment of the associated business objective, with an anticipated end date of December 28, 2028.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

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Primary Work LocationUSA AZ - Tempe HeadquartersAdditional LocationsWork Shift

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About BD

Sourced by ZipRecruiter

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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