2

Remote Biotech Technical Writer Jobs in Raleigh, NC

Senior Engineer, Process Validation

Raleigh, NC ยท On-site +1

$100K - $130K/yr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... Proficiency in technical writing with deviation investigations, root cause analysis, and risk ...

Senior Engineer, Process Validation

Raleigh, NC ยท On-site +1

$100K - $130K/yr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... Proficiency in technical writing with deviation investigations, root cause analysis, and risk ...

Strong written, verbal, and interpersonal communication skills in remote/hybrid environments * Excellent problem-solving, analytical, and mathematical reasoning abilities * Strong technical ...

Specialist IS Architect

Holly Springs, NC ยท On-site +1

$144K - $178K/yr

Write Software Development Life Cycle documentation including to build and maintain technical ... Flexible work models, including remote and hybrid work arrangements, where possible Apply now and ...

Technical Account Manager - Openshift

Raleigh, NC ยท On-site +1

$96K - $154K/yr

Outstanding verbal and written communication skills; ability to convey complex information to ... For positions with Remote-US locations, the actual salary range for the position may differ based ...

IT Project Manager - Remote

Raleigh, NC ยท On-site +1

$120K - $160K/yr

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... The IT Project Manager is responsible for delivering key technical business initiatives and will ...

... remote company. * Highly organized. We track everything in tickets and dashboards. * Ability to context-switch in a fast-paced, changing environment * Excellent business written and verbal technical ...

Discovery Diagnostic Sales Specialist

Raleigh, NC ยท On-site +1

$105K - $130K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Excellent communication skills (verbal and written) to present technical presentations and training.

Showing results 21-40

Remote Biotech Technical Writer information

See Raleigh, NC salary details

$13

$37

$64

How much do remote biotech technical writer jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for remote biotech technical writer in Raleigh, NC is $37.86, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $45.82 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a remote biotech technical writer?

To thrive as a Remote Biotech Technical Writer, you need a strong background in life sciences or biotechnology, excellent writing skills, and often a relevant degree or industry experience. Familiarity with scientific literature databases, document management systems, and regulatory writing standards such as ICH or FDA guidelines is typically required. Outstanding attention to detail, self-motivation, and the ability to communicate complex information clearly are vital soft skills. These abilities ensure the accurate, compliant, and accessible documentation that supports research, regulatory submissions, and internal communications in biotech organizations.

How does a remote biotech technical writer typically collaborate with scientists and subject matter experts while working off-site?

Remote Biotech Technical Writers often rely on virtual collaboration tools such as video conferencing, shared document platforms, and project management software to work closely with scientists and subject matter experts. Regular online meetings and clear communication channels are essential for clarifying complex scientific concepts, ensuring accuracy, and aligning on project goals. Writers may also participate in virtual lab tours or demonstrations to gain a deeper understanding of processes. Proactive communication and flexibility are key to overcoming time zone differences and ensuring high-quality deliverables.

What is the difference between Remote Biotech Technical Writer vs Remote Scientific Content Specialist?

AspectRemote Biotech Technical WriterRemote Scientific Content Specialist
CredentialsBiotech or life sciences degree, writing certificationsScience degree, content creation experience
Work EnvironmentRemote, biotech or pharma companiesRemote, research institutions or biotech firms
Employer UsageUsed in biotech, pharma, medical device industriesUsed in research, biotech, and educational sectors
Search & Comparison IntentUnderstanding technical writing roles in biotechComparing scientific content creation roles

The Remote Biotech Technical Writer focuses on creating clear, accurate documentation for biotech products, protocols, and regulatory submissions. The Remote Scientific Content Specialist, however, emphasizes developing scientific articles, educational materials, and marketing content. While both roles require a science background and strong writing skills, the technical writer is more regulatory and documentation-oriented, whereas the content specialist leans toward science communication and outreach.

What is a remote biotech technical writer?

A Remote Biotech Technical Writer is a professional who creates clear and accurate documentation related to biotechnology, such as research reports, regulatory submissions, standard operating procedures, and user manuals, while working from a location outside of a traditional office. They translate complex scientific information into understandable content for various audiences, including researchers, regulatory bodies, and the public. Remote Biotech Technical Writers often collaborate with scientists and regulatory experts using digital communication tools, allowing flexibility in their work environment. This role requires strong writing skills, attention to detail, and a solid understanding of biotech concepts and terminology.
What cities near Raleigh, NC are hiring for Remote Biotech Technical Writer jobs? Cities near Raleigh, NC with the most Remote Biotech Technical Writer job openings:

MSAT Technical Lead - Drug Substance (Sr Manager)

Sobi

Morrisville, NC โ€ข On-site, Remote

$106K - $146K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 16 days ago


Job description

Company Description
At Sobi, we believe diversity drives innovation and inclusion creates stronger teams. We are committed to building a workplace where everyone feels valued and empowered to contribute.
If this role excites you but you're unsure if you meet every requirement, we encourage you to apply. Your unique perspective and experiences could be exactly what we need. We look forward to hearing from you!

At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.
Our mission and culture at Sobi North America get us excited to come to work every day, but here are a few more reasons to join our team:
  • Competitive compensation for your work
  • Generous time off policy
  • Opportunity to broaden your horizons by attending popular conferences
  • Emphasis on work/life balance
  • Collaborative and team-oriented environment
  • Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments

Job Description
Location Requirement:
This position may be based near Raleigh, NC or Boston, MA. The role requires periodic travel between both locations to support cross-site collaboration and business needs.
Science and Technology (SAT) is part of the Global CMC, Science & Technology Department (GCSAT). GCSAT is responsible for the optimization and life-cycle management of Sobi's clinical and commercial manufacturing and analytical processes across internal and external networks. SAT ensures compliant, reliable, cost-effective, and sustainable manufacturing and testing of our products now and in the future. The SAT team holds the senior scientific and technical knowledge for the manufacturing and analytical testing of Sobi's clinical and commercial products and is responsible for maintaining the internal and external manufacturing/analytical processes at a validated stage.
Responsibilities:
  • Subject matter expert (SME) for Small Molecules Drug Substance Manufacturing.
  • Process owner of Small Molecules process validation for Sobi products.
  • Lead and execute MSAT projects such as manufacturing process and cost improvement as part of LCM.
  • Participate in internal activities related to (external) manufacturing, such as process changes, major/critical deviations, risk assessments, and CAPAs.
  • Issue, review, and approve applicable internal and external SOP's and manufacturing instructions.
  • Review and supervise the setup, execution, and documentation of technical studies, qualifications, and validations.
  • Write and review applicable sections of the APR/PQR.
  • Write and review applicable sections in registration files, variations, and market expansion.
  • Support in sourcing evaluation of new Small Molecules contract manufacturers and participation in developing supply and quality agreements.
  • Lead the technical part of a product transfer, scale-up activities, validations, and oversee manufacturing of Small Molecules processes at external manufacturers for Sobi projects in the clinical and commercial phase.
  • Be aware of external biopharmaceutical manufacturing technology advancements, understand and introduce new technologies, and how they may be applicable to process innovation, cost, or yield improvement

Qualifications
Requirements:
  • University degree in Chemistry, Biology, Biotechnology, Pharmacy, or similar
  • 6+ years of experience in the development and manufacturing of small-molecule drug substances for clinical and commercial use
  • 3+ years of experience in a commercial setting, leading the technical pieces of product transfer, scale-up, and validation
  • Experience reviewing applicable sections of the APR/PQR
  • Scientific and technical background in CMC development and manufacturing of drug substances, small molecules
  • Experience with regulatory guidelines, regulatory authorities communication, and file documentation
  • Experience overseeing external vendors such as CMOs, CDMOs, etc.
  • Demonstrable experience working in a cross-functional team with the ability to multitask, prioritize, and be an effective decision-maker

Personal Attributes
  • Fulfillment of all of Sobi's values
  • Ability to act independently and take initiative
  • Good communication skills, oral/written, and listening
  • Strong team player

Additional Information
Compensation and Total Rewards at Sobi
At Sobi, we are dedicated to providing our employees with a comprehensive and industry-competitive total rewards package. Our compensation philosophy is designed to recognize and reward talent, ensuring that your contributions are valued and reflected in your overall rewards.
Your total compensation at Sobi goes beyond just your base salary and annual bonus. It also includes a robust suite of benefits, such as:
  • A competitive 401(k) match to support your financial future.
  • Tuition and wellness reimbursements to invest in your personal and professional growth.
  • A comprehensive medical, dental, and vision package to prioritize your health and well-being.
  • Additional recognition awards to celebrate your achievements.

The base salary range for this role is $140,000 - $165,000. Each individual offer will be determined based on several factors, including your experience, qualifications, and location. Additionally, this role is eligible for both short-term and long-term bonuses, as outlined in the plan details.
All Sobi employees need to demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership and Partnership. Are you ready to be on the Sobi team? Come join a culture that empowers every person to be the person that makes a difference for rare disease.
Why Join Us?
We are a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we're ready to take on the world's diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others' lives because that's exactly what we do here. If you're seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you.
We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff.
Sobi Culture
At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases, and have used this knowledge to shape our business to find new ways of helping them.
As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can't change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth.
An Equal Opportunity Employer
Sobi is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Sobi are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity, protected veterans and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status or protected groups by the laws or regulations in the locations where we operate.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request reasonable accommodations by sending an email to irina.conc@sobi.com
Know Your Rights