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Full Time Biotech Technical Writer Jobs in Indiana

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

... biotechnology companies. Our leading CDMO client is eager to hire an Aseptic Downstream Process ... This is a full-time role directly with the client - an outstanding opportunity to join an ...

City of Elkhart

Technical Director

Elkhart, IN · On-site

$57K/yr

... Full-Time CATEGORY Salary, Up to $57,400 FLSA Non-Exempt REPORTS TO Director of Operations DATE ... Ability to understand and follow oral and written instructions. * Ability to establish and maintain ...

The City of Elkhart

Technical Director

Elkhart, IN · On-site

$48K - $57K/yr

... Full-Time CATEGORY Salary, Up to $57,400 FLSA Non-Exempt REPORTS TO Director of Operations DATE ... Ability to understand and follow oral and written instructions. * Ability to establish and maintain ...

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All JobsBiotech Technical Writer JobsFull Time Biotech Technical Writer JobsFull Time Biotech Technical Writer Jobs in Indiana

Full Time Biotech Technical Writer information

What is the difference between Full Time Biotech Technical Writer vs Full Time Medical Writer?

AspectFull Time Biotech Technical WriterFull Time Medical Writer
CredentialsBachelor's degree in life sciences, writing experienceAdvanced degree (MD, PhD), medical/scientific background
Work EnvironmentBiotech companies, research labs, CROsPharmaceutical companies, medical communications firms
Industry UsageDevelops technical documentation for biotech productsCreates clinical, regulatory, and medical education content

Full Time Biotech Technical Writers focus on creating technical documents related to biotech products, often with a background in life sciences. Full Time Medical Writers typically have advanced medical or scientific degrees and produce clinical and regulatory content for the medical and pharmaceutical industries. While both roles require strong writing skills, their focus areas and required credentials differ significantly.

What are the most commonly searched types of Biotech Technical Writer jobs in Indiana? The most popular types of Biotech Technical Writer jobs in Indiana are:
What cities in Indiana are hiring for Full Time Biotech Technical Writer jobs? Cities in Indiana with the most Full Time Biotech Technical Writer job openings:
Full Time Biotech Technical Writer jobs near you
Infographic showing various Full Time Biotech Technical Writer job openings in Indiana as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution.

Sterility Assurance Validation Associate I (1st shift)

Simtra BioPharma Solutions

Bloomington, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Job description

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.
Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.
While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide.
Why join Team Simtra?Because we:
Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers.
Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways.
Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members.
Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health.
This role:
The Sterility Assurance Validation Associate I is responsible for the management and the execution of project and system qualifications, and validation confirmations including equipment and processes. The Validation Associate I ensures compliance that meets worldwide regulatory agency requirements, internal company standards/best practices and current industry practices. This position is 100% onsite at the Bloomington facility and reports to the Sr. Technical Services Validation Manager.
The responsibilities:
  • Document (protocols, SOPs, summary reports) new processes and update existing processes where vital that will be reviewed by clients, corporate and regulatory auditors
  • Conduct development studies on critical equipment
  • Owns and onboards new client projects, including the relevant validations on syringe lines
  • Serve as line owner, conducting gap assessments and determining validation approaches when onboarding new projects
  • Collaborates directly with client representatives
  • Owns non-conformance investigations (NCR)
  • Owns corrective and preventive actions (CAPA)
  • Owns change control management tasks (CCM)
  • Participates in client audits and provides rationale / justification for practices with aid from senior team member / management Responds to audit observations and owns deliverables
  • Subject matter expert for up to 3 processes, technologies or process equipment
  • Owns, plans interventions and leads syringe line media fills and has full ownership through closure of the summary
  • Owns & drives value improvement projects (VIP) to realize savings
  • Become trained and perform semi-annual HEPA filter certification testing (integrity testing, velocity testing, visible smoke testing)

Required qualifications:
  • BS degree in science related field with laboratory experience or High School diploma/GED with a minimum of 6 years related experience within a pharmaceutical, biotechnology or related industry including responsibilities comparable to this position (e.g., technical writing, audit experience, project lead, authoring and performing studies, etc.)
  • Microsoft Office Suite (Word, Excel, Outlook) intermediate proficiency
  • Ability to use enterprise software (JDE, BPLM, Pilgrim, Trackwise, Ellab Valsuite Pro, etc.)
  • Critical thinking and problem-solving skills
  • High initiative and ability to deal with ambiguity
  • Skills to interact professionally and collaboratively with the client representatives
  • Good writing skills - including technical writing
  • Strong oral and written communication - including communication with external clients

Physical / safety requirements:
  • Ability to meet Grade A and B gowning requirements.
  • Ability to lift 50 lbs.
  • Must be able to climb and work from ladders.
  • Duties will require some overtime work, including nights and weekends
  • Position requires standing for long hours, but may involve walking or sitting for periods of time

In return, you'll be eligible for[1]:
  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
    • Employee Ownership Plan
  • Additional Benefits
    • Short and Long-Term Disability Insurance
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

[1] Current benefit offerings are in effect through 12/31/26
Disclaimer
This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.
Equal Employment Opportunity
Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Data Privacy
To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/

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