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Intern Qa Ra Jobs in Minnesota (NOW HIRING)

Strategy Alignment through Site Hoshin Plans, Quality Plans, Validation master plans, associated quality improvement imperatives, and regular updates to QA RA weekly and monthly metrics, supporting ...

... QA Intern to join our team. This position is a full-time Fixed term - (6 months) role. In this role, you will be the backbone of our document management system, helping us maintain an efficient ...

Work closely with cross-function team, including design reviews with QA, RA, test engineers, hardware engineers to ensure the software design meets the product requirements, including safety ...

Work closely with cross-function team, including design reviews with QA, RA, test engineers, hardware engineers to ensure the software design meets the product requirements, including safety ...

Work closely with cross-function team, including design reviews with QA, RA, test engineers, hardware engineers to ensure the software design meets the product requirements, including safety ...

Pharmacy Intern

Minneapolis, MN · On-site

$20.50 - $24.25/hr

Quality Assurance * Customer Service * Inventory Management * Workflow Management excluding final prescription verification Primary Roles and Responsibility: A key component of the pharmacy intern ...

Pharmacy Intern

Apple Valley, MN · On-site

$20.50 - $24.25/hr

Quality Assurance * Customer Service * Inventory Management * Workflow Management excluding final prescription verification Primary Roles and Responsibility: A key component of the pharmacy intern ...

Pharmacy Intern

Woodbury, MN · On-site

$20.50 - $42/hr

Quality Assurance * Customer Service * Inventory Management * Workflow Management excluding final prescription verification Primary Roles and Responsibility: A key component of the pharmacy intern ...

Pharmacy Intern

Farmington, MN · On-site

$20.50 - $24.25/hr

Quality Assurance * Customer Service * Inventory Management * Workflow Management excluding final prescription verification Primary Roles and Responsibility: A key component of the pharmacy intern ...

Resident Assistant

Gaylord, MN · On-site

$18.36 - $23.46/hr

The Resident Assistant (RA) is responsible for providing tenants with the highest quality of direct ... Assurance and Performance Improvement (QAPI) program. According to the Service Plan for the tenant ...

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Showing results 1-20

Intern Qa Ra information

What does an intern QA RA do?

An Intern in QA (Quality Assurance) and RA (Regulatory Affairs) supports the quality and compliance processes within a company, often in the pharmaceutical, medical device, or biotech industries. Their responsibilities typically include assisting with document control, reviewing quality records, supporting audits, and helping ensure products meet regulatory standards. They work closely with QA and RA teams to learn about regulatory requirements and quality systems, gaining hands-on experience that prepares them for a career in compliance and quality management.

What are the key skills and qualifications needed to thrive as an intern QA RA?

To thrive as an Intern in QA/RA, you generally need a background in life sciences, engineering, or a related field and a basic understanding of industry regulations and quality standards. Familiarity with tools such as Microsoft Office, document control systems, and regulatory databases is often required. Strong attention to detail, organizational skills, and effective communication are standout soft skills in this role. These skills and qualifications are crucial for ensuring compliance, maintaining product quality, and supporting regulatory submissions in highly regulated industries.

What are the typical responsibilities of an intern QA RA?

As an Intern in QA/RA, you can expect to be involved in tasks such as reviewing documentation for compliance, assisting with internal audits, supporting the preparation of regulatory submissions, and helping maintain quality management systems. You will often work closely with experienced QA/RA professionals, learning to interpret regulatory guidelines and ensuring products meet industry standards. This role offers a hands-on introduction to both quality assurance and regulatory processes, which is valuable for understanding how organizations ensure product safety and compliance. Collaboration with different departments, such as R&D and manufacturing, is common, helping you develop a broad industry perspective.

What is the difference between Intern Qa Ra vs Intern Data Analyst?

AspectIntern Qa RaIntern Data Analyst
Required CredentialsBasic knowledge of QA and RA principles, often pursuing related degreesStrong analytical skills, basic understanding of data analysis tools, often pursuing related degrees
Work EnvironmentQuality assurance and regulatory compliance teams, often in healthcare or manufacturingData-focused teams in various industries like finance, marketing, or tech
Employer & Industry UsagePharmaceuticals, medical devices, manufacturingTech companies, finance firms, marketing agencies
Common Search & Comparison IntentUnderstanding entry-level QA/RA rolesExploring data analysis internship opportunities

Intern Qa Ra roles focus on quality assurance and regulatory affairs, ensuring products meet standards. Intern Data Analyst positions emphasize analyzing data to support business decisions. While both are entry-level, they serve different industry functions and require distinct skill sets.

Global Project Manager: Quality Systems AI Implementation

Boston Scientific

Arden Hills, MN • On-site

$122K/yr

Full-time

Posted 9 days ago


Boston Scientific rating

8.5

Company rating: 8.5 out of 10

Based on 120 frontline employees who took The Breakroom Quiz

32nd of 545 rated manufacturers


Job description

Additional Location(s): N/A; US-MN-Arden Hills
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions.
About the role:
Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.
Boston Scientific is seeking an experienced Project Manager to lead the successful deployment of generative AI-enabled automations and digital solutions across Global Quality Assurance (QA) and Regulatory Affairs (RA). This role will oversee global AI software system implementations spanning multiple quality system and regulatory subprocesses, supporting the organization's digital transformation and efficiency goals.
The Project Manager will work closely with business analysts, AI developers, data scientists, Quality Systems teams, AI governance leads and global QA/RA stakeholders to evaluate, design, build, validate and implement AI-enabled solutions. This individual will drive execution across multiple parallel workstreams, ensure alignment with software validation and lifecycle requirements, and deliver solutions that meet business, regulatory and quality system expectations.
Work model, sponsorship, relocation:
At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our Marlborough, Massachusetts, or Arden Hills, Minnesota, office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.
Your responsibilities will include:
  • Manage all phases of the project lifecycle, including initiating, planning, executing, controlling and closing processes.
  • Develop and implement comprehensive project plans and foster team ownership and accountability for deliverables.
  • Estimate project effort and resource needs using standardized tools and techniques in collaboration with relevant stakeholders.
  • Prepare detailed schedules, budgets and timelines using project management tools such as Microsoft Project.
  • Direct project execution through task assignment, timeline tracking, risk identification and contingency planning.
  • Coordinate cross-functional alignment with Quality, Regulatory, Data Science, IT, Legal and global site teams to support the successful delivery and adoption of AI-enabled solutions.
  • Identify and manage project dependencies and critical path elements while maintaining high project quality using methodologies such as GSM.
  • Communicate project status regularly through standard reports and executive-level updates.

Qualifications:
Required qualifications:
  • Bachelor's degree from an accredited institution.
  • Minimum of 5 years' experience coordinating and/or leading software validation projects or IT- or technology-related projects in a regulated environment.
  • Professional experience in the pharmaceutical and/or medical device industry.
  • Demonstrated knowledge of change management methodologies and their application in project environments.
  • Proven experience collaborating with multiple internal stakeholder groups, including site, division and regional Quality and Regulatory teams.
  • Ability to work effectively with individuals at all organizational levels and with external vendors or consultants.
  • Ability to meet project deliverables and performance expectations in fast-paced or evolving environments.
  • Ability to work independently and assume responsibility for assigned project outcomes.

Preferred qualifications:
  • Bachelor of Science degree in engineering or information technology.
  • Project Management Professional (PMP) certification.
  • Understanding of software validation and computer system validation (CSV) principles.

Requisition ID: 633163
Minimum Salary: $106800
Maximum Salary: $202900
The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.
Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.
Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination.

What Boston Scientific employees say

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About Boston Scientific

Sourced by ZipRecruiter

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.

Industry

Medical equipment and supplies manufacturing, manufacturing and construction

Company size

10,000+ Employees

Headquarters location

Marlborough, MA, US

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