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Remote Pharmaceutical Labeling Jobs (NOW HIRING)

IntePros

Remote Customer Care Sales Coordinator

$18.50 - $24/hr

IntePros is seeking a Customer Care Sales Coordinator to join our global pharmaceutical services ... Generate and distribute return shipping labels for approved product returns. * Coordinate with ...

Jobot

Senior FDA Attorney

Pine Brook, NJ · On-site +1

$250K - $400K/yr

A fully remote arrangement may also be considered for an attorney located in another state. Why ... labeling, inspection, and compliance obligations. Counsel bulk active pharmaceutical ingredient ...

Ipsen

$163K - $216K/yr

... Labeling Operations and Business Ethics for the purpose of providing regulatory advice and guidance ... Minimum of 8 years' experience in the pharmaceutical industry and a minimum of 6 years in ...

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Remote Pharmaceutical Labeling information

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How much do remote pharmaceutical labeling jobs pay per hour?

As of Sep 12, 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 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?

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.

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.

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The most popular types of Pharmaceutical Labeling jobs are:

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Remote Pharmaceutical Labeling jobs near you
Infographic showing various Remote Pharmaceutical Labeling job openings in the United States as of September 2026, with employment types broken down into 82% Full Time, and 18% Contract. Highlights an 9% Hybrid, and 91% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Associate Director, Quality Operations

Cambridge, MA • On-site, Remote

Amylyx Pharmaceuticals
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Amylyx Pharmaceuticalsexternal

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

The Opportunity

This position is responsible for providing CMC quality oversight of drug substance, drug product, and finished drug product manufacturing, testing, packaging, labeling and distribution for non-commercial products that are in various development stages.

As the GMP quality expert, this role is accountable for ensuring all company, regional, and global GMP and GDP standards and regulations are met, and that the GMP Quality department performs to a standard that ensures the quality of products and materials produced by Amylyx contracted partners. 

We anticipate hiring the Associate Director, Quality Operations in September 2026.

Responsibilities

  • Provide quality oversight of production, labeling and testing activities, including warehousing and distribution of clinical trial materials.
    • Provide QA review and approval on quality technical agreements, master production records, product specifications (in-process, release, and stability), analytical method qualification/validation documents, method transfer documents, and stability plans.
    • Review executed Batch Production and QC Control Records to ensure all approved procedures were followed and all specifications are met.
    • Prepare and /or approve batch disposition packages.
    • Provide QA review and approval on quality system records, including but not limited to deviations, OOS, change controls, CAPAs, and product quality complaints.
    • Lead or participate in regular meetings internally and externally as CMC Quality SME to ensure Amylyx's quality expectations are met in the areas of Good Manufacturing Practice, Good Distribution Practice, and Good Documentation Practice.
  • Provide QA review on INDs. Assure that source data and information used in regulatory submissions and validation activities is maintained and traceable.
  • Write, review and/or approve SOPs as QA SME for manufacturing, testing, labeling, packaging, and transportation of early-stage products.
  • Support FDA, EMA or other regulatory agency inspections.

Required Qualifications

  • Bachelors degree
  • 8+ years of experience within the Pharmaceutical or Biotechnology industry in a quality role.
  • Experience with authoring and reviewing IND CMC sections and addressing Regulatory Filing requirements in FDA cGMP regulations, Eudralex and ICH Guidance, as well as other Biopharma industry guidance and regulations.
  • Ability to work with all levels of the organization and external contract service providers to ensure compliance with current regulations.
  • Travel may be required up to 10%, which may include on-site review of third-party operations.

Preferred Requirements

  • QC/AD experience 
  • Small molecule and peptides experience

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.

Apply