2

Remote Pharmaceutical Labeling Jobs (NOW HIRING)

We also have extensive pharmaceutical expertise, offering innovative medicines that aim to prevent ... This will be a remote position. RESPONSIBILITIES: D2D Project Execution & Workflow Management

Verification Pharmacist - FuzeRx

Sharonville, OH · On-site +1

$53.50 - $64.25/hr

Operating in a remote capacity, the Verification Pharmacist supports remote verification functions ... labeling, and patient instructions. Required Experience & Qualifications: Minimum Qualifications:

In this role, you will assist pharmacists in providing pharmaceutical services while ensuring ... Prepare, compound, and label intravenous admixtures, chemotherapy medications, and parenteral ...

$62.89 - $92.44/hr

Pharmaceutical Care * Project Management * Quality Improvement * Problem Solving * Federal Pharmacy ... Ongoing need for employee to see and read information, labels, documents, monitors, identify ...

next page

Showing results 1-20

Remote Pharmaceutical Labeling information

See salary details

$14

$19

$25

How much do remote pharmaceutical labeling jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for remote pharmaceutical labeling in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What are the main challenges of working in remote pharmaceutical labeling, and how can I overcome them?

One of the primary challenges in remote pharmaceutical labeling is ensuring accuracy and compliance with regulatory standards without the benefit of in-person collaboration. Communication with cross-functional teams, such as regulatory affairs, quality assurance, and medical writers, is often conducted virtually, which requires strong organizational and interpersonal skills. To overcome these challenges, it's important to establish clear communication channels, stay updated on changing regulations, and use secure, collaborative technology platforms. Proactively seeking feedback and participating in virtual team meetings can also help maintain the quality and consistency of labeling documentation.

What is the difference between Remote Pharmaceutical Labeling vs Remote Pharmaceutical Packaging Specialist?

AspectRemote Pharmaceutical LabelingRemote Pharmaceutical Packaging Specialist
CredentialsKnowledge of labeling regulations, GMP complianceUnderstanding of packaging processes, GMP standards
Work EnvironmentPrimarily office-based, document review, compliance checksCombination of remote coordination and on-site packaging tasks
Industry UsageCommon in pharmaceutical companies for label approvalInvolved in packaging line operations and quality checks

Remote Pharmaceutical Labeling focuses on ensuring labels meet regulatory standards and reviewing labeling documentation remotely. In contrast, Remote Pharmaceutical Packaging Specialists handle packaging processes, often coordinating packaging activities remotely while ensuring quality and compliance. Both roles require GMP knowledge but differ in their core responsibilities within the pharmaceutical manufacturing process.

What is remote pharmaceutical labeling?

Remote pharmaceutical labeling refers to the process of reviewing, creating, updating, and ensuring the compliance of medication labels and packaging information from a remote location, rather than on-site at a pharmaceutical company. Professionals in this role ensure that drug labels meet regulatory requirements and provide accurate usage, dosage, and safety information. This job often involves collaboration with regulatory affairs, medical, and legal teams using digital tools and secure platforms. Remote pharmaceutical labeling specialists must stay up-to-date on changing regulations and guidelines in various markets. Their work is essential for patient safety and effective communication of drug information.

What are the key skills and qualifications needed to thrive as a Remote Pharmaceutical Labeling Specialist, and why are they important?

To excel as a Remote Pharmaceutical Labeling Specialist, you generally need a background in pharmacy, life sciences, or regulatory affairs, with detailed knowledge of global labeling regulations. Familiarity with regulatory submission systems, document management software, and tools like Adobe Acrobat or TrackWise is typically required. Strong attention to detail, excellent written communication, and the ability to collaborate virtually are essential soft skills for this role. These competencies ensure precise, compliant labeling that upholds patient safety and meets international regulatory standards.
More about Remote Pharmaceutical Labeling jobs
What cities are hiring for Remote Pharmaceutical Labeling jobs? Cities with the most Remote Pharmaceutical Labeling job openings:
What are the most commonly searched types of Pharmaceutical Labeling jobs? The most popular types of Pharmaceutical Labeling jobs are:
What states have the most Remote Pharmaceutical Labeling jobs? States with the most job openings for Remote Pharmaceutical Labeling jobs include:
Infographic showing various Remote Pharmaceutical Labeling job openings in the United States as of July 2026, with employment types broken down into 28% Full Time, 8% Part Time, and 64% Contract. Highlights an 36% Physical, and 64% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Associate Regulatory Affairs Labeling Associate

Civica Rx

Lehi, UT • On-site, Remote

Full-time

Posted 10 days ago


Job description

Job Description

Our Regulatory Affairs team brings essential generic quality medicines to U.S. patients by providing Regulatory leadership and establishing regulatory systems and processes that support Civica’s mission.

The Associate, Regulatory Affairs Labeling and Artwork (remote position):

· Supports all aspects of product labeling and artwork development, review, approval, implementation and maintenance for Civica’s private label distribution (PLD) products.

· Follow labeling and artwork procedures that comply with FDA, GMP, ISO and other applicable standards and regulations.

· Coordinates and prepares Office of Prescription Drug Promotion (OPDP) submissions as needed.

· Works within systems to maintain labeling and artwork.

· Owns or impact assesses change controls for PLD labeling impact.

Responsibilities Include:
· Coordinate labeling and artwork design by an external vendor

· Collaborate with the supply chain, contract manufacturers, packagers, and external vendors to ensure timely implementation of approved labeling changes.

· Maintain labeling and artwork records within applicable electronic systems and document repositories.

· Support preparation and submission of Office of Prescription Drug Promotion (OPDP) materials, as needed.

· Maintain FDA drug listings information and associated regulatory records.

· Participate in change control activities as a change owner, contributor, or impact assessor, as appropriate, to evaluate and implement labeling-related changes.

· Review labeling components and artwork for accuracy, consistency, completeness, and compliance with approved regulatory content.

· Ensure labeling information included in regulatory submissions is complete, accurate, and consistent.

· Support continuous improvement initiatives related to labeling processes, systems, and workflows.

· Perform any other tasks/duties as assigned by management.

What we look for:

We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue doing what is in the best interest for our patients.

Technical Skills;

Proven experience in critically reviewing documents for consistency and accuracy. Excellent proofreading/editing skills are required.

Strong organizational skills.

Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strives to continuously improve and build knowledge and skills.

Teamwork:

Balances team and individual responsibilities; Exhibits objectivity and openness to others' views; Gives and welcomes feedback; Contributes to building a positive team spirit; Inspires respect and trust.

Quality Management:

Looks for ways to improve and promote quality; Demonstrates accuracy and thoroughness.

Education Minimum Requirement :

Bachelor’s degree required, focus in Life Sciences preferred.

Required Experience and Skills :

At least one to two 2+ years of relevant experience within the pharmaceutical regulatory environment, with a concentration in pharmaceutical labeling and/or artwork development or promotional review.

Physical demands of the position include only those required for work in a typical office environment. Minimal travel (0-5%) may be necessary in the execution of the listed duties


Civica Rx logo

About Civica Rx

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

51 - 200 Employees

Headquarters location

Lehi, UT, US

Year founded

2018