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Labeling In Pharma Jobs (NOW HIRING)

Packaging Operator

New Brunswick, NJ ยท On-site

$16.75/hr

Inspect finished products to ensure correct labeling, weight, and packaging quality * Load ... Maintain clean and organized work areas in compliance with safety and hygiene standards * Complete ...

Packaging Operator

New Brunswick, NJ ยท On-site

$16.75/hr

Inspect finished products to ensure correct labeling, weight, and packaging quality * Load ... Maintain clean and organized work areas in compliance with safety and hygiene standards * Complete ...

... labeling processes * Develop and implement policies and procedures to maintain compliance with ... At Azend Pharma , we bring together a team of experienced pharmacy consultants with over 50 years ...

Pharmacist in Charge

Bronx, NY ยท On-site

$60 - $65/day

... labeling processes * Develop and implement policies and procedures to maintain compliance with ... At Azend Pharma , we bring together a team of experienced pharmacy consultants with over 50 years ...

New Product Planning

Chadds Ford, PA ยท 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 ...

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Labeling In Pharma information

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How much do labeling in pharma jobs pay per hour?

As of Jul 21, 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 the highest paying job in pharmaceuticals?

In pharmaceutical labeling and related fields, senior regulatory affairs managers and pharmaceutical executives typically earn the highest salaries, often exceeding six figures. These roles require extensive industry experience, advanced certifications, and leadership skills, and they oversee compliance, strategy, and regulatory submissions within the industry.

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 machinery.

Which job is highest paid in pharmacy?

In pharmacy, roles such as Pharmaceutical Executive, Pharmacist Manager, or Director of Pharmacy typically have the highest salaries. These positions often require advanced degrees, extensive experience, and leadership skills, and they can earn significantly more than entry-level or technical roles like labeling specialists.

Who are the big 4 in pharma?

The 'Big 4' in the pharmaceutical industry typically refers to Pfizer, Novartis, Roche, and Merck & Co., which are among the largest global pharmaceutical companies. These companies often have extensive labeling departments responsible for regulatory compliance, documentation, and ensuring product safety, making them key employers for labeling professionals in pharma.
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Infographic showing various Labeling In Pharma job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, and 5% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $29,053 per year, or $14 per hour.

Associate Medical Director, Endocrine Medical Sciences - Job ID: 1965

Ascendis Pharma

Princeton, NJ โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 days ago


Job description

Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.

Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues.

Guided by our core values of Patients, Science, and Passion, we use our TransConยฎ drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.

Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills.

Do you want to be part of building a fully integrated biopharmaceutical company together with a team of highly skilled colleagues who are enthusiastic about developing best-in-class therapeutics that address significant unmet medical needs? Then Ascendis Pharma is committed to support your personal development on our journey towards becoming a leading company in rare diseases.

Ascendis Pharma is looking to hire an experienced pharmaceutical clinician to join our Endocrine Medical Sciences team. This is an exciting opportunity to join a rapidly growing, innovative company!

Position Summary

As a member of the Endocrine Medical Sciences team for the US business, the Associate Medical Director supports the US Medical Director for deliverables and activities associated with management and implementation of phase 4 studies and registries; pre-launch-, launch-, and post- launch activities; as well as medical review of promotional materials for marketed product(s). You are a scientific contributor with expertise in endocrine and rare disorders. Responsible for either the growth-related disorders and/or hypoparathyroidism for highly visibility Ascendis TransCon Program(s), a specific focus/expertise in these areas is a major advantage. The candidate is expected to support the US Medical Director in key strategic, cross-as well functional projects as part of the US Medical Affairs Team. They will be accountable and help the US Medical Director in the development and implementation of the product medical and medical launch strategy as well as working intricately within the other medical affairs and cross -functional teams.

The candidate is expected to provide medical expertise and collaborate with a cross-functional team in the development and review of Labeling, advertising, and promotional materials. You are responsible for ensuring all promotional material for our products are medically and scientifically accurate, balanced, and aligned with brand strategy and approved indications. The ideal candidate will have significant experience in promotional reviews of materials.

The candidate may function as mentor to colleagues, support education and training of the MSL team and therapeutically focused commercial personnel (within the boundaries of company compliance SOPโ€™s and US regulations). The Associate Medical Director is expected to develop and deliver impactful presentations and support the US Medical Director in the review and authoring of publications and collaborating/influencing publication strategy, medical information, and medical communications. Effectively conveying and communicating sound and fair balanced medical information. Represents Ascendis Medical Affairs at internal and external meetings of all levels, scientific conventions, and corporate liaison boards.

The position reports to the US Medical Director. The candidate must have availability to work in the Princeton, NJ on a weekly basis.

Key Responsibilities

  • Serve as the medical/scientific reviewer of promotional assets for assigned product(s), and collaborate with Commercial, Legal, and Regulatory for development and review of Labeling, advertising, and promotional materials.
    • Ensure the materials are medically accurate, including that claims are appropriately supported by evidence, references are correctly cited, and the overall impression is fair and not misleading.
    • Verify that statements in the promotional materials are consistent with the approved indication/label.
    • Cross-check everything against the underlying clinical data, literature, abstracts/manuscripts and ensure that summary data are accurate and in context.
    • Provide ongoing therapeutic area, product and competitive intelligence knowledge to the team to maintain up-to-date scientific accuracy.
  • Build and manage relationships and strategic partnerships, and interact regularly with Key Opinion Leaders/Influencers, clinical investigators, healthcare customers, strategic alliance partners, vendors, professional societies and organizations, and patient advocacy groups.
  • Work with internal stakeholders including Commercial, Legal, Regulatory, Clinical Development, Clinical Operations, Compliance, Pharmacovigilance, Biometrics, Global Communications, and other functional group contributors to support the US Medical Director in successful management of Medical Affairs projects.
  • Support the US Medical Director in the design and implement medical strategies and tactical plans while providing thought leadership for medical publication planning, medical education, and medical information system development.
  • Serve as a scientific expert for Medical Affairs projects within the designated TransCon Program(s).
  • Support the US Medical Director in the development of strategic imperatives and tactical medical plans to enhance healthcare practitioner education to improve patient outcome.
  • Support the Medical Affairs team and the US Medical Director in design and conducting post-marketing studies and medical materials review.
  • Support the development, management, and execution of US Medical Advisory Boards.
  • Develop and deliver presentations on MA projects to both internal and external audiences within legal, compliance and regulatory guidelines.
  • Represent Ascendis Medical Affairs internally and externally.
  • Stay abreast of up-to-date knowledge on all clinical data relevant to TransCon programs, competitive landscape, new therapies, clinical trends, and newly issued regulatory rules and FDA guidance to promptly identify any potential impact on existing medical programs or strategies, competitive environment, or changes to product programs.

Requirements

  • MD/DO degree with at least 8 years of total work experience, including a minimum of 3 yearsโ€™ industry experience in medical affairs in a relevant therapeutic area and at least 3 years of medical promotional review experience.
  • Relevant clinical experience preferred.
  • Substantial knowledge/experience with rare endocrine disorder or (non-Oncology related) rare diseases (preferred)
  • Strong record of scientific and clinical inquiry
  • Demonstrated leadership and team building skills as well as the ability to perform effectively in a dynamic environment.
  • Flexibility to adapt culturally
  • Demonstrated strategic and critical thinking.
  • Excellent communication skills (oral and written) and proven organizational skills.
  • The ability to lead directly and indirectly by influence, including strong problem solving, conflict resolution, and analysis.

The estimated salary range for this position is $240-255k. Actual salary determination is dependent on a variety of factors some of which include: experience, qualifications, and geographic location. This position may be eligible for a discretionary annual bonus or an incentive compensation plan (eligibility varies based on role and position level), discretionary stock-based long-term incentives, paid time off, and a comprehensive benefits package.

Benefits

  • 401(k) plan with company match
  • Medical, dental, and vision plans
  • Company-offered Life and Accidental Death & Dismemberment (AD&D) insurance
  • Company-provided short and long-term disability benefits
  • Unique offerings of Pet Insurance and Legal Insurance
  • Employee Assistance Program
  • Employee Discounts
  • Professional Development
  • Health Saving Account (HSA)
  • Flexible Spending Accounts
  • Various incentive compensation plans
  • Accident, Critical Illness, and Hospital Indemnity Insurance
  • Mental Health resources
  • Paid leave benefits for new parents

Ascendis Pharma is proud to be an equal opportunity employer. We are committed to creating an inclusive environment for all employees.

A note to recruiters:

We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed. If this occurs your ownership of these candidates will not be acknowledged.