Top 8 Labeling and technical documentation specialist Jobs in Covington, Ky

Labeling and Technical Documentation Specialist
Meridian Bioscience, Inc. —Cincinnati, OH
- Full-time
- Ability to walk for extended periods
- Computer literacy
- Mid-level
Central Processing Specialist I
St. Elizabeth Healthcare —Edgewood, KY
- 8 hour shift
- High school diploma or GED
- Organizational skills
- Typing
- Health insurance
- Tuition reimbursement
Stores Process Specialist
Atlas Air —Erlanger, KY
- $62,000 - $89,000 a year
- ERP systems
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Stores Process Specialist
Atlas Air —Erlanger, KY
- $62,000 - $89,000 a year
- ERP systems
- Mid-level
- 3 years
Food Labeling Compliance Specialist
Lyons Magnus LLC —Walton, KY
- Full-time
- Customer service
- Computer literacy
- Bachelor of Science
- Disability insurance
- Health insurance
Quick Apply
IT Support Specialist II
Steel & O'Brien Manufacturing —West Chester, OH
- $62,000 - $68,000 a year
- Full-time
- ERP systems
- Mid-level
- Office
Quick Apply
Cyber Security Specialist
The Armor Group, Inc. —Mason, OH
- Computer Science
- System design
- Office
Quick Apply
Lean Material Flow Specialist
TEDIA COMPANY LLC —Fairfield, OH
- Weekends as needed
- Mid-level
- High school diploma or GED
- Ability to lift 50 pounds
Quick Apply

More jobs to discover

Find similar jobs that you might be interested in.

Central Processing Specialist I
St. Elizabeth Healthcare —Edgewood, KY
Provide support to clients, draw locations and technical departments in a courteous and respectful manner to assure delivery of quality service.
Sales and Marketing Operations Specialist
Brands Insurance Agency, Inc —West Chester, OH
Professional Communication: Managing daily email and phone correspondence with clients, underwriters, and industry partners.
$18 - $22 an hour
Quick Apply

Show more similar jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

QA Calibration Specialist
Eliquent Life Sciences, Inc —Columbus, OH
Define spare/standard strategy (transfer standards, environmental references, field kits) and quarantine/lockout for failed instruments.
$90,000 - $110,000 a year
Quick Apply

I want to receive the latest job alert for labeling and technical documentation specialist in covington, ky

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

labeling and technical documentation specialist jobs near covington, ky

Document Specialist jobs in Cincinnati, OH

It Support Specialist jobs in Omaha, NE

It Support Specialist jobs in New Orleans, LA

Chat Support jobs in Tacoma, WA

It Support Specialist jobs in Edison, NJ

Contract Specialist jobs in Philadelphia, PA

It No Clearance Required jobs in Maryland

It Support Specialist jobs in Memphis, TN

Early Intervention Specialist jobs in Michigan

Document Specialist jobs in Gilbert, AZ

Document Specialist jobs in Fort Worth, TX

Document Specialist jobs in Cedar Rapids, IA

Visual Information Specialist jobs in Washington, DC

Document Specialist jobs in California

Document Specialist jobs in Kansas City, MO

Document Scanning jobs in Las Vegas, NV

Compliance Officer jobs in Grand Rapids, MI

Healthcare Compliance Analyst jobs in California

Compliance Officer jobs in Kansas City, MO

Chief Human Resources Officer jobs in Texas

Labeling and Technical Documentation Specialist

Meridian Bioscience, Inc. -
Cincinnati, OH

Apply Now

Job Details

Full-time

Qualifications

Computer literacy
Bachelor's degree

Full Job Description

About Meridian:

Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals that help drive our vision. Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting edge solutions to tough problems.

Job Summary:

Responsible for providing equal support for technical writing and product labeling coordination activities for FDA-regulated diagnostic products. This position coordinates the creation, revision, approval, and maintenance of product labeling while also developing, revising, and managing controlled quality and regulatory documentation. The role works collaboratively with Regulatory Affairs, Quality Assurance, Manufacturing, Marketing Communications, and external partners to ensure documentation and labeling are accurate, compliant, and completed according to project timelines. The position serves as a key contributor to document control, change management, and technical documentation processes within Meridian’s Quality Management System.

Key Duties:

Major Duties and Responsibilities

Labeling Coordination Responsibilities (Approximately 50%)

Coordinate the creation, revision, approval, and maintenance of product labeling, labeling specifications, translations, artwork files, and associated documentation.
Prepare labeling files, label approval packages, specifications, and print-ready materials using approved software and document management systems.
Serve as the primary liaison between Meridian and contract manufacturers regarding labeling activities, ensuring timelines, approvals, and deliverables are achieved.
Collaborate with Regulatory Affairs, Quality Assurance, Manufacturing, and Marketing Communications to implement compliant labeling changes.
Maintain labeling records and ensure documentation is current, accurate, and compliant with applicable regulatory requirements and internal procedures.

Technical Writing Responsibilities (Approximately 50%)

Develop, revise, format, and maintain controlled quality, regulatory, and operational documentation including procedures, work instructions, specifications, forms, product labeling, and Instructions for Use (IFUs).
Partner with subject matter experts to gather information and translate technical content into clear, concise, and compliant documentation.
Review documentation for accuracy, consistency, readability, formatting, and compliance with company standards and regulatory requirements.
Coordinate document revisions, change control activities, and approval workflows through the electronic document management system.
Support document control processes including version management, document archival, periodic reviews, and records maintenance.
Assist with continuous improvement initiatives related to documentation, labeling processes, and quality system compliance.
Other duties as assigned.

Other Duties/Physical Requirements

Physical
- Ability to walk up and down several flights of stairs throughout the workday in a multi-location facility.
Other
- Ability to work on a computer including repetitive use of a keyboard and mouse for long periods throughout the course of the workday.

Qualifications:

Minimum Education or Equivalent Experience Required/Preferred

Bachelor’s degree required. Technical Communication, Life Sciences, Business, or related degree preferred.
Minimum 2 years of experience in an FDA or ISO-regulated environment.
Experience with product labeling, document control, technical writing, or regulatory documentation preferred.

Competencies Required or preferred

Ability to read, understand and follow all company SOPs and Guidelines.
Computer proficiency (Word, Excel, Adobe, Bartender and Visio).
Excellent interpersonal, organizational, written and oral communication skills.
Must be well organized and able to meet strict deadlines and perform under pressure in a fast-paced environment.
Must be able to work independently as well as collaboratively in a team setting with peers and other departments in a cross functional setting.
Must be a self-starter, detail oriented and able to prioritize and balance both workload and timelines.
Strong written communication, proofreading, and document formatting skills.
Excellent attention to detail with the ability to identify inconsistencies, errors, and gaps in documentation.
Knowledge of change control, version management, and document control practices.
Familiarity with document management systems and electronic quality management systems preferred.
Understanding of regulatory documentation requirements within FDA-regulated and ISO-regulated environments preferred.
Excellent organizational skills with the ability to manage multiple projects and deadlines.
Ability to work independently and collaboratively in a cross-functional environment.

Required Travel

% None

*All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. (USA Only)*

Apply Now

Refine Your Search

labeling and technical documentation specialist jobs in covington, ky

Labeling and Technical Documentation Specialist

Central Processing Specialist I

Stores Process Specialist

Stores Process Specialist

Food Labeling Compliance Specialist

IT Support Specialist II

Cyber Security Specialist

Lean Material Flow Specialist

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for labeling and technical documentation specialist in covington, ky

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected