Top 29 Qa associate documentation i Jobs in Cumberland Ri

QA Associate Documentation I
Boston Scientific —Coventry, RI
- $47,200 - $89,700 a year
- Full-time
- Engineering
- Neurology
- In-person
Quality Assurance Associate I
CEDENT —Cumberland, RI
- Full-time
- Mid-level
- Communication skills
Sr. Manufacturing Associate I, Label & Packaging
Moderna, Inc. —Norwood, MA
- $74,000 - $118,400 a year
- Overtime
- Mid-level
- High school diploma or GED
- Continuous improvement
- Paid time off
- Adoption assistance
7d
Document Control Associate
Sebela Pharmaceuticals Inc. —Holbrook, MA
- $22 - $26 an hour
- Mid-level
- High school diploma or GED
- Organizational skills
Quick Apply
Systems Analyst
Fidelity TalentSource —Smithfield, RI
- $41.79 - $81.79 an hour
- Temporary
- Bachelor of Science
- Office
- SQL
Quality Assurance Technician
Cresco Labs —Fall River, MA
- $22 an hour
- Part-time
- Ability to lift 50 pounds
- 21 years or older
- Travel
- Health savings account
- AD&D insurance
Quick Apply
13d
Insurance Quality Control III
AAA Northeast —Providence, RI
- $24.75 - $27.40 an hour
- Full-time
- Remote
- Office
- High school diploma or GED
- Analysis skills
Quick Apply
Aerospace QA Technical Analyst
PPG —Avon, MA
- $70,000 - $80,000 a year
- Full-time
- Engineering
- Mid-level
- Continuous improvement
- Paid holidays
- Disability insurance
Quick Apply
Specialist, Quality Assurance
Moderna, Inc. —Norwood, MA
- $74,000 - $118,400 a year
- Weekends as needed
- Mid-level
- 3 years
- Continuous improvement
- Paid time off
- Adoption assistance
2d
Mental Health Worker Pedi PD
Brown University Health —Providence, RI
- Day shift
- 18 years or older
- CPR Certification
- Hospital
QA Operations Specialist
Cipla —Fall River, MA
- 8 hour shift
- English
- Mid-level
- 3 years
Associate Contract Manager, Project Controls (Hybrid Schedule)
Eversource Energy Service Company —Westwood, MA
- $71,860 - $79,840 a year
- Full-time
- Hybrid work
- Office
- Finance
- Driver's License
Associate Director, Sterility Assurance
Moderna, Inc. —Norwood, MA
- $142,500 - $256,500 a year
- Full-time
- Office
- Master's degree
- Bachelor's degree
- Health insurance
- Paid time off
Project Management Team Lead
Staples, Inc. —Framingham, MA
- $96,000 - $138,000 a year
- 3 years
- Supervising experience
- Product management
- Paid holidays
- Paid time off
Electrical Designer
Mott MacDonald —Westwood, MA
- $97,000 - $119,000 a year
- Full-time
- Mid-level
- Office
- 3 years
- Paid holidays
- Disability insurance
Oncology Nurse Navigator Per Diem
Dana-Farber Cancer Institute —Foxborough, MA
- $88,100 - $99,200 a year
- Per diem
- Nursing
- BLS Certification
- English
Paramedic EMT Paramedic
EPOCH HEALTHCARE LLC —Norwood, MA
- $30 - $42 an hour
- Full-time
- Background check
- Spanish
- CPR Certification
- 401(k)
- Paid time off
Quick Apply
Data Center CoE - Sr. Field Service Technician
ABB Inc. —Providence, RI
- $46 - $65 an hour
- Full-time
- Management
- 5 years
- Military
- Health savings account
- AD&D insurance
Quick Apply
9d
Data Center CoE Sr. Field Service Technician
ABB Inc. —Providence, RI
- $46 - $65 an hour
- Full-time
- Management
- 5 years
- Military
- Health savings account
- AD&D insurance
Quick Apply
11d

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QA Associate Documentation I

Boston Scientific -
Coventry, RI

Apply Now

Job Details

Full-time
$47,200 - $89,700 a year

Qualifications

Content creation for technical audiences
Regulatory compliance
Technical writing experience within manufacturing
Change management
Manufacturing facility experience
Compliance documentation
Production batch record review
Cross-functional collaboration
Quality control records management
Cross-functional communication

Full Job Description

Additional Location(s): N/A

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:
This role would attract someone who enjoys being at the center of quality documentation and compliance, ensuring every product meets strict internal and regulatory standards. It makes a strong impact by safeguarding product safety, maintaining accurate and audit-ready records, and supporting engineers and site teams to keep processes consistent and reliable. It also offers the opportunity to influence how documentation supports overall quality and operational excellence within the Coventry facility.

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.

Work model, sponsorship, relocation:
This position is an onsite role based in Coventry. 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:

Perform the review and approval of sterilization batch records to ensure all processing parameters are met according to Boston Scientific specifications.

Assist in maintaining Boston Scientific policies and procedures related to sterilization and batch approvals.
Coordinate the review and revision of documentation submitted through change requests in accordance with internal and regulatory policies and procedures.
Copy, distribute and maintain documents in accordance with company procedures.
Review final versions of documentation changes for potential issues and collaborate with staff to resolve discrepancies.
Store and maintain all quality records, policies and procedures required for compliance according to internal policies and procedures.
Support the Change Notice (CN) process through various stages, including CN creation, submission review, implementation and document issuance.
Manage the distribution of documents as required throughout the change management process.
Assist in gathering change metrics and preparing reports as required.
Represent the site and participate in Global Community of Practice groups and associated projects as required.
Process site nonconformance activities for the Documents and Records subprocess.
Interpret and implement corporate documentation requirements as they relate to local documentation processes.
Provide documentation and change management support as required.
Partner with engineers to determine work instruction accuracy and technical writing documentation requirements.

Qualifications:

Required qualifications:

Minimum of 2 years’ experience reviewing and approving batch records, managing documentation changes, and maintaining quality records in a regulated environment.

Minimum of 2 years’ experience supporting documentation control, change management and compliance activities within a manufacturing, quality or regulated industry environment.
Equivalent of 5 years of hands-on experience in documentation control, quality records management or regulated manufacturing processes in lieu of a degree. Approximately 4 years of directly related experience would replace the degree requirement.
Demonstrated experience working with documentation control systems, batch record review processes and change management workflows.
Demonstrated ability to adapt to frequent documentation updates, evolving procedures and changes in regulatory or internal requirements.
Proven knowledge of compliance requirements related to document control, quality records and regulated manufacturing environments.
Ability to manage multiple documentation workflows while maintaining accuracy and attention to detail.
Strong technical writing and document review experience supporting engineers and cross-functional teams.
Ability to work onsite in Coventry on a full-time basis.

Preferred qualifications:

Bachelor’s degree in Engineering, Quality or a related field preferred.

Experience working in a regulated medical device environment, particularly in documentation control, sterilization processes or quality systems.
Preferred experience with electronic document management systems, change control platforms, Windchill, PDF tools, Excel and batch record review systems to support immediate productivity.
Proven ability to adapt to frequent procedural updates, manage multiple documentation workflows and collaborate effectively with cross-functional teams.

Requisition ID: 629260

Minimum Salary: $ 47200

Maximum Salary: $ 89700

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.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

Apply Now

Refine Your Search

qa associate documentation i jobs in cumberland ri

QA Associate Documentation I

Quality Assurance Associate I

Sr. Manufacturing Associate I, Label & Packaging

Document Control Associate

Systems Analyst

Quality Assurance Technician

Insurance Quality Control III

Aerospace QA Technical Analyst

Specialist, Quality Assurance

Mental Health Worker Pedi PD

QA Operations Specialist

Associate Contract Manager, Project Controls (Hybrid Schedule)

Associate Director, Sterility Assurance

Project Management Team Lead

Electrical Designer

Oncology Nurse Navigator Per Diem

Paramedic EMT Paramedic

Data Center CoE - Sr. Field Service Technician

Data Center CoE Sr. Field Service Technician

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