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Pharmaceutical Writing Jobs in Indiana (NOW HIRING)

Appeals Pharmacist (Remote)

Fort Wayne, IN ยท On-site

$52.25 - $63.75/hr

Remote Appeals Pharmacist - Fair Medication Access | Work From Home | Strong Clinical Writing Focus Combine clinical expertise with advocacy in a fully remote Appeals Pharmacist role. Review ...

New

Pharmacist

Bloomington, IN ยท On-site

$50.75 - $61/hr

... pharmaceutical care to customers Ensure pharmacies comply with all local, state and federal laws ... oral/written communication skills Knowledge of basic math (counting, addition, and subtraction ...

Pharmacist - PRN

Carmel, IN ยท On-site

$57.75 - $69.50/hr

Pharmacist Position Must be able to work some day shifts during the week as a requirement. Position ... Excellent verbal and written communication skills. * Strong organizational, time management and ...

Showing results 21-40

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.

How do you become a pharmaceutical writer?

To become a pharmaceutical writer, individuals typically need a strong background in life sciences, such as a degree in pharmacy, biology, or related fields. Gaining experience in medical or scientific writing, understanding regulatory guidelines, and developing skills in clear, accurate communication are essential; certifications like the American Medical Writers Association (AMWA) can also enhance credibility.

Is there a demand for pharmaceutical writers?

Pharmaceutical writing is a growing field due to the increasing need for clear, compliant scientific communication in the healthcare industry. Demand is strong for professionals skilled in medical and scientific writing, often requiring knowledge of regulatory guidelines and familiarity with tools like reference management software. Opportunities are available in pharmaceutical companies, contract research organizations, and medical communication agencies.

What are the key skills and qualifications needed to thrive in pharmaceutical writing, 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.

What is pharmaceutical writing?

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 can I get into pharmaceutical writing with no experience?

Pharmaceutical writing is a specialized field that typically requires a background in science or healthcare. To enter the field with no experience, consider gaining relevant knowledge through online courses, certifications in medical or scientific writing, and building a portfolio of sample documents; internships or entry-level positions can also provide practical experience and industry exposure.
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 August 2026, with employment types broken down into 1% Internship, 1% As Needed, 77% Full Time, 18% Part Time, 1% Temporary, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Deviation Writer

Stark Pharma Solutions Inc

Bloomington, IN โ€ข On-site

Contractor

Re-posted 28 days ago


Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

You can also follow Stark Pharma Solutions on LinkedIn for the latest job updates:

https://www.linkedin.com/company/99455976/

Role: Deviation Writer

Location: Indiana (Onsite)

Duration: 6-Month Contract

Position Overview:

We are seeking an experienced Deviation Writer to support Manufacturing Engineering and Quality Operations within a GMP-regulated pharmaceutical or biotechnology environment. This role will be responsible for authoring high-quality deviation investigations, performing root cause analysis, and collaborating with cross-functional teams to ensure timely and compliant resolution of quality events.

The ideal candidate will have strong technical writing skills, experience in deviation management, and the ability to translate complex manufacturing and engineering issues into clear, data-driven investigations.

Key Responsibilities

  • Author, review, and manage deviation investigations within a GMP-regulated environment.
  • Collaborate with Manufacturing, Production Engineering, MS&T, Supply Chain, Quality, and other stakeholders to gather facts and technical information.
  • Conduct and document root cause investigations using structured problem-solving methodologies.
  • Develop robust corrective and preventive action (CAPA) plans based on investigation outcomes.
  • Analyze manufacturing and quality data to support investigation conclusions.
  • Ensure investigations are completed accurately, thoroughly, and within required timelines.
  • Support continuous improvement initiatives related to quality systems and manufacturing processes.
  • Maintain compliance with GMP regulations, internal procedures, and quality standards.
  • Simplify complex technical events into clear, concise, and audit-ready documentation.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Chemistry, Biotechnology, or a related technical discipline.
  • Minimum 3 years of experience in technical writing within a regulated GMP environment.
  • Experience authoring deviation investigations in pharmaceutical, biopharmaceutical, or biotechnology manufacturing.

Strong knowledge of:

  • Root Cause Analysis
  • CAPA Development
  • Deviation Management
  • GMP Regulations
  • Experience using investigation tools such as:
  • Fishbone Analysis
  • 5 Whys
  • Failure Analysis Techniques
  • Familiarity with Electronic Quality Management Systems (eQMS).
  • Strong Microsoft Word and Excel skills.
  • Excellent communication, documentation, and cross-functional collaboration abilities.