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Safety Data Sheet Writer Jobs (NOW HIRING)

CYNET SYSTEMS

Safety Data Analyst

Boston, MA · On-site

$36 - $41/hr

Strong verbal and written communication skills across a team, collaborate with team members in ... Compile data, analyze, and report monthly on trends for progress towards annual safety key ...

Omni Inclusive

SDS Writer

New Brunswick, NJ · On-site

Author Safety Data Sheets using client software in SAP. * Complete and revise SDS requests within established timelines. * Regular communication with toxicologists, scientists and chemists for ...

Omni Inclusive

SDS Writer

New Brunswick, NJ · On-site

Author Safety Data Sheets using client software in SAP. * Complete and revise SDS requests within established timelines. * Regular communication with toxicologists, scientists and chemists for ...

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Safety Data Sheet Writer information

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How much do safety data sheet writer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for safety data sheet writer in the United States is $24.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $27.88 per hour, depending on experience, location, and employer.

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Infographic showing various Safety Data Sheet Writer job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $50,519 per year, or $24.3 per hour.

Associate Director, Safety Data Sciences

Florham Park, NJ • On-site

AbbVie
Scientific Research and Development Services • 10K+ employees
Learn more about AbbVieexternal

$141K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 25 days ago

Key responsibilities

  • Partner with cross functional stakeholders to support product safety profile and benefit risk throughout the product lifecycle.

  • Conduct standard surveillance activities by reviewing safety data from clinical trials, safety databases, and literature, and analyze data for signal assessment.

  • Prepare and review safety reports, summaries, and safety sections of regulatory documents, and communicate safety findings to inform risk minimization activities.

AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 103 frontline employees who took The Breakroom Quiz

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
This position can be based at any AbbVie hub location including: Lake County, IL, Irvine, CA, South San Francisco, CA, Florham Park, NJ.
This position partners with cross functional stakeholders in support of the product safety profile and benefit risk throughout product lifecycle through signal detection, signal evaluation, and preparation of written and verbal summaries of signal management activities and risks to patient safety to present to senior management and regulatory authorities globally.
Responsibilities
  • Responsible for standard surveillance activities for a product's life cycle (one or more assigned compounds and products) through review of safety data from clinical trials, safety databases, and the literature.
  • Collaborates with safety and clinical teams to develop strategies and approaches for signal assessments and regulatory requests by analyzing data from multiple sources.
    Independently analyzes data for signal assessment and leads preparation of materials of ad hoc regulatory safety requests using data from multiple sources.
  • Utilizes medical judgment to determine the impact of the safety issue on the product's benefit-risk profile.
    Communicates findings of surveillance activities and safety assessments to product teams and leadership to inform on necessary risk minimization activities, including label changes.
  • Collaborative preparation and maintenance of safety sections of Clinical Summary of Safety, Clinical Study Reports, Company Core Data Sheets and Risk Management Plan.
    Independently authors, strategizes and reviews global aggregate safety reports in accordance with regulatory requirements and standard operating procedures
  • Independently prepares summaries of key safety data for PST, SRB, senior management, Advisory and other similar meetings
    Partners to lead safety-related activities/initiatives internal to PPS.
  • Proficient in pharmacovigilance regulations, guidelines, and company standard operating procedures
    In depth understanding of compounds within assigned therapeutic areas, including safety profile and where applicable, labeling, literature, clinical and regulatory issues.
    Mentors and trains new safety scientists

Qualifications
  • Degree in a Health Sciences (e.g., Pharmacy, Epidemiology, Nursing);
    o Bachelors + 4 years clinical/pharma or safety work experience
    o Masters or doctorate + 2 years clinical/pharma or safety work experience (e.g. MPH, PharmD, PhD, or Masters in a Health Science)
  • Knowledge of the drug development process which includes conducting clinical trials, scientific strategy and operations management for the planning, execution and reporting of clinical development programs, regulatory requirements for submission, product launch and post marketing support.
    Demonstrates ability to connect regulatory obligations and safety science to support safety decision making.
  • Understanding of tools, standards and approaches used to efficiently evaluate drug safety is desirable.
    Serves as a resource to cross-functional colleagues by soliciting input and providing recommendations and conclusions. Demonstrates effectiveness in working in a multidisciplinary, matrix team situation.
    Demonstrates effectiveness in working in a multidisciplinary, matrix team situation
  • Effective oral and written communication skills with the ability to manage multiple projects simultaneously .
    Microsoft WORD and EXCEL skills and Basic Project Management skills.
    Able to work independently with minimal direct supervision.

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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