Document Control & SOP Specialist – Manufacturing

Marine; Sparta (TN); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical/Dental/Vision Insurance

Employee Assistance Program (EAP)

Disability insurance (STD/LTD)

401(k) with company match

PTO

Company holidays + floating holidays

Maternity/paternity leave

Tuition assistance

Membership reimbursement

Employee discounts

Job summary

Dometic in Sparta, TN seeks a dedicated Document Control Specialist to manage controlled documents, link engineering prints, and develop SOPs for production. You will work with Engineering, Quality, and Production to keep the 1Factory QMS current and ensure documents are accurate and accessible for manufacturing teams.

Responsibilities include creating and revising SOPs, supporting ISO requirements, and maintaining records. Strong technical writing and office software skills are essential.

Qualifications

• AS or BS degree in a technical discipline and 2-5 years in a related field.
• Technical writing and presentation skills.
• Ability to read drawings and interpret product specifications.
• Working knowledge of Manufacturing (QMS) Systems.
• High proficiency in Microsoft Office applications.

Responsibilities

• Develop SOPs for all new production releases.
• Revise SOPs and Work Instructions to the new standard.
• Support ISO management system requirements, SOPs, and document control.
• Update and maintain documents in 1Factory QMS.
• Obtain and catalog photos for SOPs and work instructions.
• Recordkeeping, organization and archiving of records.
• Assist with training and cross-functional SOP adoption.
• Review and organize product records and files.
• Assist with corrective actions and process improvements.

Education

AS or BS degree in a technical discipline

Tools

Microsoft Office (Excel, Word, PPT, Teams, Access)

QMS Systems

Job description

Dometic in Sparta, TN seeks a dedicated Document Control Specialist to manage controlled documents, link engineering prints, and develop SOPs for production. You will work with Engineering, Quality, and Production to keep the 1Factory QMS current and ensure documents are accurate and accessible for manufacturing teams.

Responsibilities include creating and revising SOPs, supporting ISO requirements, and maintaining records. Strong technical writing and office software skills are essential.