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Labeling In Pharma Jobs (NOW HIRING)

Incyte Corporation

New Product Planning

Chadds Ford, PA · On-site

$125K - $165K/yr

... labeling strategy, and differentiation vs. standard of care; translate scientific and clinical data ... * 8-12+ years in pharma/biotech * Experience in one or more: New Product Planning; Clinical ...

Sumitomo Pharma

Senior Medical Director, PVRM

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the ... Contribute to preparation and update of Company Core Data Sheets (CCDS), Locally labels such as ...

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How much do labeling in pharma jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for labeling in pharma in the United States is $13.97, according to ZipRecruiter salary data. Most workers in this role earn between $12.50 and $15.38 per hour, depending on experience, location, and employer.

What is the difference between Labeling In Pharma vs Packaging Technician?

AspectLabeling In PharmaPackaging Technician
CredentialsHigh school diploma or equivalent; GMP training often requiredHigh school diploma or equivalent; GMP and safety training
Work EnvironmentCleanroom settings, pharmaceutical manufacturing facilitiesManufacturing lines, production areas
Industry UsageSpecifically in pharmaceutical labeling and complianceGeneral packaging across various industries, including pharma
Job FocusApplying labels accurately, ensuring regulatory complianceAssembling, packing, and preparing products for shipment

Labeling In Pharma involves precise application of labels in sterile, regulated environments, focusing on compliance. Packaging Technicians handle broader packaging tasks, often in less regulated settings. Both roles are essential in pharmaceutical manufacturing but differ in scope and specific responsibilities.

What is a labelling job?

A labeling job in pharma involves applying labels to medication bottles, boxes, or packaging to ensure proper identification, dosage, and safety information. It requires attention to detail, knowledge of regulatory standards, and often involves working in clean environments with specialized tools or machines.

What is the highest paying job in pharma?

In the pharmaceutical industry, senior roles such as Pharmaceutical Executive, Vice President of R&D, or Director of Regulatory Affairs tend to be the highest paying jobs. These positions require extensive experience, advanced degrees, and leadership skills, often offering salaries significantly higher than entry-level roles like labeling specialists.

What is a label job description?

A labeling in pharma job involves preparing and applying labels to pharmaceutical products, ensuring accuracy and compliance with regulatory standards. The role often requires attention to detail, knowledge of labeling regulations, and familiarity with tools like printers and label applicators. It may also involve quality checks and documentation to ensure proper product identification and safety.

What are common pharma job titles?

Common pharma job titles include Quality Control Analyst, Manufacturing Technician, Packaging Operator, Validation Specialist, and Regulatory Affairs Associate. These roles often require knowledge of Good Manufacturing Practices (GMP), attention to detail, and sometimes certifications such as cGMP training or laboratory skills.
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Labeling In Pharma jobs near you
Pharmacovigilance (PV) Audit Manager (P/T Consultant)

Pharmacovigilance (PV) Audit Manager (P/T Consultant)

Mitsubishi Tanabe Pharma America

Jersey City, NJ • On-site

Contractor

Posted 11 days ago

Key responsibilities

  • Supervise PV activities within MTDA under Senior Director QA.

  • Perform internal process audits of MTDA processes and prepare audit reports in a timely manner.

  • Provide QA input to MTDA working groups and systems development as appropriate.

Job description

Company Description
Entrepreneurial
Spirit, Rooted in Tradition. At Mitsubishi Tanabe Pharma Development America (MTDA), we can tout a storied reputation more than 300 years in the making. Our parent company, Mitsubishi Tanabe Pharma Corporation (MTPC), is a research-driven pharmaceutical company with global reach - and one of Japan's
oldest and most respected companies.
Relatively new to the U.S. market, the innovative compounds of the Mitsubishi Tanabe Pharma Group have already enjoyed commercial success under the brand labels of our U.S. partners. In this next phase of development, we plan to bring exciting new compounds to market under our own MT Pharma America label. We're currently building a new commercial organization and expanding our other functions to support this strategy.
A need has arisen for a dynamic individual to join our QA team as a part-time consultant to deliver assurance of quality throughout MTDA. The selected Consultant will assist the Senior Director of QA, MTDA in the ongoing delivery of an integrated, coordinated and robust PV QA program. Duties will touch upon all aspects related to the development and maintenance of an MTDA Quality system, including: SOPs, audits, inspection preparation, QA metrics, regulatory intelligence, process mapping, computer validation, etc. The consultant will also work
collaboratively with the Manager of QA, MTDA to provide day-to-day assurance of:
  1. Protection
    of Subjects
  2. Veracity
    of Data
  3. Legal
    Protection of Company

This fixed-term 12-month consulting assignment offers a flexible 4-day per month schedule.
Job Description
  • Supervise PV activities within MTDA under Senior Director QA.
  • Manage own workload to ensure appropriate coverage of projects and activities
  • Provide QA input to MTDA working groups and systems development as appropriate
  • Provide advice on QA, PV matters to MTDA staff
  • Liaise with Regulatory Affairs Department in maintaining as awareness of on-going regulatory changes
  • Participate in internal and external meetings as appropriate
  • Liaise with relevant parties to arrange the audits as required by audit plans
  • Perform Internal Process Audits of MTDA processes
  • Prepare in a timely manner [30 days] reports of audits performed
  • Distribute relevant audit reports in accordance with MTDA
    policy
  • Assist Senior Director of QA, MTDA in providing local US perspective in relation to global activities and systems arising from MTPC
  • To liaise with QA MTPC & MTPE as required on global programs
  • Assist Senior Director of QA, MTDA in hosting PV related audits and regulatory inspections of
    MTDA activities

Qualifications
  • Minimum of a Bachelor's degree in scientific discipline or related field
  • Minimum of 5 years of experience as 'stand-alone' auditor; i.e. performing audits alone.
  • Experience with at least 2 regulatory inspections; at least one of which was an FDA PV Inspection.
  • Related professional association membership (e.g., DIA, SQA, etc.)
  • Proficiency in common office software (Windows, MS Office Suite)
  • Ability to perform CSV audits is an advantage
  • Willingness to travel approximately 50% both domestically and internationally.

Additional Information
Our Value Proposition:
Enjoy the fast-moving, entrepreneurial spirit more typically found in a small biotech, complemented by the benefits of a global pharmaceutical/chemical conglomerate.

Apply