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Position Summary:

The Sr. Document Control Specialist implements and maintains the Engineering Change Notice System. These changes will include product improvements, repairs, and new product development. Coordinates the interaction between engineering, manufacturing and marketing to en-sure appropriate changes are documented. Provides documentation such as good manufacturing practices (GMP) and good laboratory practices (GLP) procedure manuals and change authorization in accordance with company policies and government regulations. It will also include maintaining/ar-chiving paper and electronic documents such as Paper/electronic documents , training, internal and external auditing documents, filing and maintaining other quality documents as required.

Key Responsibilities:

Responsible for issuing part numbers and ECN's and processing documents into the QMS software (i.e., Master Control, Syteline, etc.)\nResponsible for communicating with customer for obtaining ECN approval.\nResponsible for compiling and maintaining control records such as release drawings, project documents, quality system documents and manufacturing documents.\nResponsible for making electronic changes to documents, release documents, and notifies affected departments.\nResponsible for maintaining related Document Control files.\nResponsible for ensuring documents are filed correctly and maintained per established procedures.\nPerform database searches, minor data analysis, and reporting to assist Quality Assurance team.\nMaintain logs and update CAPA, NCMR, Complaint and other Quality Systems files.\nPrepare reports and memorandums.\nEnsure Proper upkeep of quality records and documents.\nCoordinates Training program, which includes facilitating the training and input results into the training QMS system.\nResponsible for all shipping documentation entry and storage.\nIdentify and facilitate continuous improvement efforts to enhance the Document Control System apart of the Quality Management System.\nResponsible for archival of quality system documents/files off-site at storage facility, and retrieval of files when needed.\nArchive /perform data to be used for internal quality metrics.\nEnter all shipping information into database after shipping is complete.\nComplies with company, quality, and safety standards, policies, and procedures.

Must Have:

High School diploma or GED.\n5 years of Document Control experience in the Medical Device Industry required.\nPrior experience with PLM software system, such as Master Control is preferred.\nStrong knowledge in implementing, processing, and maintaining Cirtec and Customers documentation in ERP and PLM Software System.\nExtremely detail-oriented work habits.\nFlexible and motivated attitude.\nProficient with MS Word, Excel.\nMust be able to read, write and speak fluent English.\nKnowledge of document control procedures with data storage, maintenance, revision, and archival background.\nFamiliarity with FDA Quality System Regulation (QSR) and

ISO 13485.

Good to have: Medical Device Manufacturing experience preferred.

Salary Range:

$60,000-80,000 Per year Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process. We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec's goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Our benefits include Training and career development, Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs, Paid Time Off and 401(k) retirement savings with a company match.","type","jobPosting","source","LC","accountId","37946216","organizationName","Cirtec Medical","applicationUrl","https://cirteccareers.ttcportals.com/jobs/18255567-sr-document-control-specialist","Brooklyn Park, MN","isRemote","location",{"_277":278,"_279":280},"createdAt","2026-09-11T18:12:47.434656550Z","updatedAt","2026-09-20T12:27:45.046Z","publishedAt","2026-09-09T00:00:00Z","expiresAt","2026-10-22T00:00Z","status","active","isExpired","isDiscoverable",true,"isSearchable","isSpotlight","isDraft","careerSkills",[184,185,186,187,188,189,190,191,192,193,194,195,196,197,198,199,200,201,202,203,204,205,206,207,208,209,210,211,212,213],"requiredEducation","high_school","benefitCategories",[181,182,183],"amount",70000,"isEmailRequired","isPhoneRequired","formattedDescription","

Sr. Document Control Specialist Cirtec Medical $60,000.00 - $80,000.00 / yr paid time off, 401(k) United States, Minnesota, Brooklyn Park Sep 09, 2026 Description About us: For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems. Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team!

Position Summary:

Key Responsibilities:

Responsible for issuing part numbers and ECN's and processing documents into the QMS software (i.e., Master Control, Syteline, etc.)

Responsible for communicating with customer for obtaining ECN approval.

Responsible for compiling and maintaining control records such as release drawings, project documents, quality system documents and manufacturing documents.

Responsible for making electronic changes to documents, release documents, and notifies affected departments.

Responsible for maintaining related Document Control files.

Responsible for ensuring documents are filed correctly and maintained per established procedures.

Perform database searches, minor data analysis, and reporting to assist Quality Assurance team.

Maintain logs and update CAPA, NCMR, Complaint and other Quality Systems files.

Prepare reports and memorandums.

Ensure Proper upkeep of quality records and documents.

Coordinates Training program, which includes facilitating the training and input results into the training QMS system.

Responsible for all shipping documentation entry and storage.

Identify and facilitate continuous improvement efforts to enhance the Document Control System apart of the Quality Management System.

Responsible for archival of quality system documents/files off-site at storage facility, and retrieval of files when needed.

Archive /perform data to be used for internal quality metrics.

Enter all shipping information into database after shipping is complete.

Complies with company, quality, and safety standards, policies, and procedures.

Must Have:

High School diploma or GED.

5 years of Document Control experience in the Medical Device Industry required.

Prior experience with PLM software system, such as Master Control is preferred.

Strong knowledge in implementing, processing, and maintaining Cirtec and Customers documentation in ERP and PLM Software System.

Extremely detail-oriented work habits.

Flexible and motivated attitude.

Proficient with MS Word, Excel.

Must be able to read, write and speak fluent English.

Knowledge of document control procedures with data storage, maintenance, revision, and archival background.

Familiarity with FDA Quality System Regulation (QSR) and

ISO 13485.

Good to have: Medical Device Manufacturing experience preferred.

Salary Range:

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Find & Apply For Document Control / Management Specialist Jobs in Brooklyn Park, Minnesota

Sr. Document Control Specialist