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Labeling In Pharma Jobs in California (NOW HIRING)

ASK Consulting

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Senior Medical Content Writer (278811)

South San Francisco, CA · On-site

$68/hr

We are looking for a Senior Medical Content Writer who can do the hardest kind of writing in pharma ... Ensure fair balance, accurate ISI integration, and on-label alignment in all promotional content.

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Hippocratic AI

Director, Regulatory

Menlo Park, CA · On-site

$176K - $233K/yr

We are contracted with 5 of the top 20 pharma globally and are in a hyper growth phase for our Life ... Establish labelling operations frameworks for l delivery, ensuring responses are accurate, evidence ...

LGM Pharma, LLC

SUPERVISOR, QUALITY ASSURANCE

Irvine, CA · On-site

$90K - $105K/yr

... in supervision of various quality programs such as but limited to labeling, GMP training ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

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Labeling In Pharma information

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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What job categories do people searching Labeling In Pharma jobs in California look for? The top searched job categories for Labeling In Pharma jobs in California are:
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Labeling In Pharma jobs near you
Senior Medical Content Writer (278811)

Senior Medical Content Writer (278811)

ASK Consulting

South San Francisco, CA • On-site

$68/hr

Contractor

Posted 2 days ago

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Job description

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment".


Job Title: Senior Medical Content Writer

Location: South San Francisco, CA

Duration: 03 Months Contract

Pay Rate: $68/hr

 

Notes:

  • Working Model (hybrid, remote, fully onsite): Hybrid (Tue-Wed-Thu in office)
  • Working days: Monday through Friday
  • Working hours (e.g. 8 AM to 4 PM PT, 9 AM to 5 PM, etc.): 8am to 4pm
  • Interview Format (e.g. one round, two rounds, and length of interviews [30, 45, 60, 90 minutes]): Two interviews, 45 minutes each.

About the Role:

  • We are looking for a Senior Medical Content Writer who can do the hardest kind of writing in pharma: claims. You will develop, substantiate, and annotate promotional and educational claims, and write the medical content that carries them & mdash; accurately, clearly, and in a way that survives MLR review without losing its edge.
    You will work embedded in an in-house creative studio, alongside creative directors and designers, which means your writing needs to work as creative material, not just as reference text.

What You'll Do:

  • Draft, refine, and substantiate promotional and non-promotional claims grounded in clinical data, prescribing information, and peer-reviewed literature.
  • Build annotated references and claim substantiation packages ready for MLR submission.
  • Write medical content across formats: HCP materials, patient education, disease-state content, congress panels, digital assets, video scripts, and sales materials.
  • Ensure fair balance, accurate ISI integration, and on-label alignment in all promotional content.
  • Partner with medical affairs and regulatory reviewers to resolve claim language efficiently; anticipate objections and offer compliant alternatives proactively.
  • Collaborate with creative directors and designers so that copy and visual concepts develop together rather than sequentially.
  • Maintain claim libraries and reference databases to accelerate reuse across the portfolio.

What You Bring:

  • 5 - 8 years of medical writing experience in pharma, biotech, or a medical communications agency, with direct experience writing and substantiating claims.
  • Deep familiarity with the MLR review process and what makes claims approvable: substantiation standards, referencing conventions, and common reviewer objections.
  • Strong command of AMA style and the ability to read and accurately interpret clinical trial data, publications, and prescribing information.
  • Understanding of FDA/OPDP promotional regulations, fair balance requirements, and ISI standards.
  • Range as a writer: able to move between rigorous scientific accuracy and accessible, engaging language for different audiences (HCP, patient, internal).
  • Meticulous attention to detail in referencing, annotation, and version control.

Nice to Have:

  • Advanced degree in life sciences (PharmD, PhD, MS) or equivalent scientific depth.
  • Experience with Veeva Vault Promo Mats annotation workflows.
  • Oncology, immunology, or biologics therapeutic area experience.
  • Experience working inside an in-house studio or embedded content team.


About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities

ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.