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Pharmaceutical Writing Jobs in Indiana (NOW HIRING)

Pharmaceutical Detail Rep

Fort Wayne, IN ยท On-site

$89K - $119K/yr

Strong verbal and written communication skills * Works and leads collaboratively and puts integrity first, without exception Apply today with your resume. Pharmaceutical Sales Rep positions are ...

Pharmaceutical Detail Rep

Carmel, IN ยท On-site

$89K - $119K/yr

Strong verbal and written communication skills * Works and leads collaboratively and puts integrity first, without exception Apply today with your resume. Pharmaceutical Sales Rep positions are ...

Write audit reports in accordance with client specifications Required Qualifications * 5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries * Has been ...

Write audit reports in accordance with client specifications Required Qualifications * 5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries * Has been ...

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Pharmaceutical Writing information

What types of documents do pharmaceutical writers typically create, and who do they work with most often?

Pharmaceutical writers are primarily responsible for producing documents such as clinical study protocols, investigator brochures, regulatory submission materials, scientific manuscripts, and patient information leaflets. They frequently collaborate with clinical researchers, regulatory affairs professionals, medical reviewers, statisticians, and subject matter experts to ensure accuracy and compliance with industry standards. Typically, pharmaceutical writers work in teams within pharmaceutical companies, contract research organizations, or as independent consultants, often balancing multiple projects and deadlines. This role offers a dynamic mix of independent writing and collaborative teamwork, making it essential for candidates to be adept at both communication and project management.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Writing position, and why are they important?

To thrive in Pharmaceutical Writing, you need a solid understanding of medical and scientific concepts, proficiency in research, and strong written communication skills, often supported by a relevant degree such as pharmacy, life sciences, or a related field. Familiarity with referencing tools like EndNote, document management systems, and adherence to regulatory guidelines (such as ICH, FDA, or EMA requirements), along with certifications like the American Medical Writers Association (AMWA), are valuable. Attention to detail, clarity, and the ability to explain complex topics to diverse audiences are standout soft skills. These competencies enable clear, accurate, and compliant documentation that supports drug development, regulatory approvals, and effective communication within the pharmaceutical industry.

Do medical writers get paid well?

Pharmaceutical writers, a common role within medical writing, typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start lower, while experienced writers with specialized knowledge or certifications can command higher pay, often supplemented by freelance opportunities or consulting work.

What do pharmaceutical writers do?

Pharmaceutical writers create scientific and regulatory documents such as clinical study reports, drug approval submissions, and product labels. They ensure accuracy, clarity, and compliance with industry regulations, often working with data from research and clinical trials using tools like document management software. Strong writing skills and knowledge of medical terminology are essential for this role.

What are the highest paid writing jobs?

In pharmaceutical writing, senior medical writers and regulatory affairs writers tend to have the highest salaries, often exceeding six figures annually. These roles typically require advanced degrees, industry experience, and proficiency with regulatory guidelines and scientific terminology.

What is a Pharmaceutical Writing job?

A Pharmaceutical Writing job involves creating clear, accurate, and regulatory-compliant documents related to drugs, medical devices, or healthcare. Writers in this field produce clinical study reports, regulatory submissions, drug safety summaries, and marketing materials. They must translate complex medical and scientific data into language suitable for regulatory agencies, healthcare professionals, or patients. Strong writing skills, scientific knowledge, and familiarity with regulatory guidelines are essential for success in this role.

How much does a Medical Writer make at Pfizer?

A Medical Writer at Pfizer typically earns between $70,000 and $110,000 annually, depending on experience, education, and location. The role often requires strong scientific writing skills and familiarity with regulatory guidelines.
What are the most commonly searched types of Pharmaceutical Writing jobs in Indiana? The most popular types of Pharmaceutical Writing jobs in Indiana are:
Infographic showing various Pharmaceutical Writing job openings in Indiana as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, and 3% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.
Deviation Writer/Technical Writer (Pharmaceutical)

Deviation Writer/Technical Writer (Pharmaceutical)

Intellectt INC

Fishers, IN โ€ข On-site

Contractor

Posted 15 days ago


Job description

Hello,
I hope youโ€™re doing well.
My name is Jayadev, and Iโ€™m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a Deviation Writer/Technical Writer (Pharmaceutical)
based in Fishers, Indianaย ย with one of our prestigious clients.
I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at ย jayadev.g@intellectt.com
ย 

Position: Deviation Writer
Location: Fishers, IN

Job Summary

Seeking an experienced Deviation Writer to support GMP manufacturing operations by investigating deviations, non-conformances, and quality events. The role involves root cause analysis, CAPA development, technical writing, and collaboration with cross-functional teams.

Key Responsibilities

  • Write and investigate GMP deviations, non-conformances, and quality events.
  • Gather facts, review data, and determine root causes.
  • Perform Root Cause Analysis using 5 Why and Fishbone methodologies.
  • Develop and document CAPAs (Corrective and Preventive Actions).
  • Review historical deviations and identify trends.
  • Prepare clear and detailed investigation reports.
  • Collaborate with Manufacturing, Quality, Engineering, MS&T, and Supply Chain teams.
Required Qualifications
  • Bachelor's degree in Science, Engineering, or related field.
  • 4+ years of technical writing experience in a GMP-regulated environment.
  • Strong knowledge of GMP, deviation investigations, CAPA, and quality systems.
  • Experience with eQMS/EDMS systems.
  • Proficiency in Microsoft Word and Excel.
Must-Have Skills
  • Deviation Investigation Writing
  • GMP Manufacturing Experience
  • Root Cause Analysis (5 Why, Fishbone)
  • CAPA Development
  • Technical Writing
  • Pharmaceutical/Biotech Industry Experience
  • Quality Systems (eQMS, EDMS)
  • Cross-Functional Collaboration
    Thanks Regards,
    JAYADEV
    Sourcing Specialist
    Phone ย (732)-997-6982 ย  Ext: 308
    Email jayadev.g@intellectt.com