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Remote Pharmaceutical Writing Jobs in Indiana (NOW HIRING)

SQA Services

Quality Auditor - Pharmaceutical

Carmel, IN · Remote

$1.3K/day

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...

SQA Services

Quality Auditor - Pharmaceutical

Warren, IN · Remote

$1.3K/day

... remote surveillance, corrective actions, remediation, inspections, and engineering solutions to ... Write audit reports in accordance with client specifications Required Qualifications * 5+ years of ...

Veristat

Benefits vary by location and may include: o Remote working o Flexible time off o Paid holidays o ... years of medical writing experience in a contract research organization or pharmaceutical ...

Veristat

Remote working * Flexible time off * Paid holidays * Medical insurance * Tuition reimbursement ... years of medical writing experience in a contract research organization or pharmaceutical ...

True Rx Management Services.

Dietitian

Washington, IN · Remote

Excellent verbal and written communication skills. * Tech-Savvy: Proficiency in MS Word, Excel, and ... Flex Time, Hybrid/Fully Remote Work, Paid Time Off, and 8 Paid Holidays for a well-rounded ...

Viatris

$100K - $150K/yr

... pharmaceutical sales experience. * Proficiency in speaking, comprehending, reading and writing ... Remote

Viatris

$100K - $150K/yr

... pharmaceutical sales experience. * Proficiency in speaking, comprehending, reading and writing ... Remote

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Remote Pharmaceutical Writing information

What is remote pharmaceutical writing?

Remote pharmaceutical writing involves creating, editing, and reviewing scientific documents related to pharmaceuticals, such as clinical trial reports, regulatory submissions, and medical publications, while working from a location outside of a traditional office. These writers use their expertise in science and medicine to communicate complex information clearly and accurately for regulatory authorities, healthcare professionals, and the public. Remote roles offer flexibility and often require strong research, writing, and project management skills, in addition to familiarity with industry guidelines and standards.

What are some common challenges faced by remote pharmaceutical writers, and how can they be managed?

Remote pharmaceutical writers often encounter challenges such as collaborating across time zones, managing strict regulatory deadlines, and ensuring clear communication with cross-functional teams like medical, regulatory, and marketing. To address these issues, it's helpful to establish regular virtual check-ins, use collaborative project management tools, and maintain thorough documentation of project progress. Being proactive about clarifying expectations and seeking feedback also helps ensure accuracy and alignment with client or team objectives.

What are the key skills and qualifications needed to thrive as a Remote Pharmaceutical Writer, and why are they important?

To thrive as a Remote Pharmaceutical Writer, you typically need a strong background in life sciences or pharmacy, excellent writing skills, and familiarity with regulatory and medical terminology. Proficiency in using document management systems, referencing software, and adhering to formats like ICH guidelines or AMA style is common. Attention to detail, time management, and effective communication are vital soft skills for working independently and collaborating remotely with cross-functional teams. These skills ensure the creation of accurate, compliant, and clear scientific documents essential for regulatory submissions and medical communications.
What are popular job titles related to Remote Pharmaceutical Writing jobs in Indiana? For Remote Pharmaceutical Writing jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Remote Pharmaceutical Writing jobs in Indiana look for? The top searched job categories for Remote Pharmaceutical Writing jobs in Indiana are:
What cities in Indiana are hiring for Remote Pharmaceutical Writing jobs? Cities in Indiana with the most Remote Pharmaceutical Writing job openings:
Remote Pharmaceutical Writing jobs near you
Infographic showing various Remote Pharmaceutical Writing job openings in Indiana as of July 2026, with employment types broken down into 5% Internship, 85% Full Time, and 10% Contract. Highlights an 100% Remote job distribution.
Quality Auditor - Pharmaceutical

Quality Auditor - Pharmaceutical

SQA Services

Indianapolis, IN • Remote

$1.3K/day

Other

Posted 4 days ago

Job description

For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across all industries. We deliver these services by deploying a network of highly skilled associates based throughout the United States and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our competitors.
 
We're hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform supplier quality  audits at various suppliers in the Midwest. These audits are generally 1-2 days long. You are given the flexibility to accept or reject these assignments according to your own availability. 
Key Responsibilities
  • Perform supplier audits at various sites within your region of residence
  • Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries
  • Coordinate, prepare, execute, and deliver supplier audits based on your own and the client schedule
  • Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc...
  • Respond to the Content team in a timely manner regarding edits/questions to your audit report
  • 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 the lead auditor in at least 10 audits
  • Direct audit experience to 21 CFR part 210/211, EU Vol 4, and Canada GMP
  • Strong communication and writing skills
  • Proven ability to deescalate workplace conflicts effectively
  • Ability to adapt to new technology and software.
  • Willingness to travel regionally
Preferred Qualifications
  • Direct audit experience to ISO 17025, ISO 15378, IPEC GDP, ICH Q7, ISO 13485, 21 CFR 100, and/or 21 CFR 507
  • ISO certifications are a plus but not mandatory
$1,300 - $1,300 a day
Pay Rate: 
 
$1300 for a 1-day audit. Includes: Time spent preparing for the audit, traveling, performing the audit, writing the report, and responding to questions from our Content team of editors and the client until the report is finalized. Does not include: Following up on CAPA for any findings or reimbursement for travel expenses - expenses are reimbursed at cost with receipts per SQA travel policy. Note that SQA helps with the preparation of the audit and proofreads all audit reports.
 
Note: SQA is an Equal Opportunity Employer. Employment is based on merit and qualifications, and is not influenced by race, color, religion, gender, national origin, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.
 
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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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