Swiftwater, PA · On-site
Pharmaceutical / Biotech Manufacturing Position Overview We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical ...
New
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Swiftwater, PA · On-site
Pharmaceutical / Biotech Manufacturing Position Overview We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical ...
New
South San Francisco, CA · On-site
Prior experience in biotechnology area/ cell therapy area preferred good oral and written ... With Regards, Shiva Kapoor Technical Recruiter Direct: 732-429-1929
South San Francisco, CA · On-site
Prior experience in biotechnology area/ cell therapy area preferred good oral and written ... With Regards, Shiva Kapoor Technical Recruiter Direct: 732-429-1929
Experience: * Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. * Experience writing technical ...
Experience: * Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. * Experience writing technical ...
I want a senior level persons who can self Manage and motivate and some biology, life science, pharma, biotech or cro experience. Sr Technical Writer/Lead to assist with writing requirements, FS ...
I want a senior level persons who can self Manage and motivate and some biology, life science, pharma, biotech or cro experience. Sr Technical Writer/Lead to assist with writing requirements, FS ...
Barceloneta, PR · On-site
Position Overview We are seeking experienced Technical Writers / Manufacturing SOP Specialists to support a major initiative within a Biotech Drug Substance Manufacturing Operation in Barceloneta ...
Barceloneta, PR · On-site
Position Overview We are seeking experienced Technical Writers / Manufacturing SOP Specialists to support a major initiative within a Biotech Drug Substance Manufacturing Operation in Barceloneta ...
Andover, MA · On-site
... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ... Authoring of technical protocols, reports, memorandum, records, and related correspondence Retrieve ...
Andover, MA · On-site
... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ... Authoring of technical protocols, reports, memorandum, records, and related correspondence Retrieve ...
Support documentation activities related to fill/finish manufacturing processes Qualifications: * 5-8 years of Technical Writing experience within the pharmaceutical or biotech industry * Strong ...
Support documentation activities related to fill/finish manufacturing processes Qualifications: * 5-8 years of Technical Writing experience within the pharmaceutical or biotech industry * Strong ...
... or biotech environments (e.g., Veeva) preferred Proficiency in PowerPoint with the ability to ... technical writer is responsible for supporting on-time implementation of OneLIMS EM global system ...
... or biotech environments (e.g., Veeva) preferred Proficiency in PowerPoint with the ability to ... technical writer is responsible for supporting on-time implementation of OneLIMS EM global system ...
Marlborough, MA · On-site
The Technical Document Writer will be responsible for producing high-quality cGMP documentation ... Prior experience working in a biotech/pharmaceutical company. Exceptional written/verbal ...
Marlborough, MA · On-site
The Technical Document Writer will be responsible for producing high-quality cGMP documentation ... Prior experience working in a biotech/pharmaceutical company. Exceptional written/verbal ...
... biotechnology or pharmaceutical industry Direct experience in GXP-compliant quality systems is ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
... biotechnology or pharmaceutical industry Direct experience in GXP-compliant quality systems is ... Excellent communication skills including: technical writing, interpersonal and collaborative skills;
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Sunnyvale, CA · On-site
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Sunnyvale, CA · On-site
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Sunnyvale, CA · On-site
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
Sunnyvale, CA · On-site
Qualifications Required Skills and Experience * 5 to 8 years technical writing experience in a hardware, software, biotechnology, or medical environment, including documentation for a highly ...
San Dimas, CA · On-site
Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
San Dimas, CA · On-site
Demonstrates strong verbal, written, and interpersonal communication skills. Demonstrates ... Previous experience in Pharmaceutical or Biotechnology industry, preferably in Quality Control.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
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Minimum 2 years of experience in technical writing for Regulatory CMC documentation within the pharmaceutical or biotechnology industry. * Familiarity with eCTD structure for regulatory submissions.
Job ID: 21-12907 Skills: -Ability to write technical documents, and tenacious attention to detail ... in the biotech or pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad ...
Job ID: 21-12907 Skills: -Ability to write technical documents, and tenacious attention to detail ... in the biotech or pharmaceutical manufacturing industry is beneficial. -Proficiency in a broad ...
Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. Experience writing technical documentation, including ...
Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. Experience writing technical documentation, including ...
Experience: * Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. * Experience writing technical ...
Experience: * Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry. * Experience writing technical ...
$13.70 - $18.47
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$18.47 - $23.23
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$23.23 - $27.99
12% of jobs
$29.11 is the 25th percentile. Wages below this are outliers.
$27.99 - $32.76
16% of jobs
The median wage is $36.33 / hr.
$32.76 - $37.52
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$45.38 is the 75th percentile. Wages above this are outliers.
$42.29 - $47.05
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$13
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$66
Biotech Technical Writers often encounter the challenge of translating highly technical and complex scientific data into clear, concise documents for diverse audiences, including regulatory agencies and non-specialist stakeholders. They must stay up-to-date with evolving regulations and industry best practices, which can be demanding in a rapidly changing biotech landscape. Additionally, working closely with subject matter experts from research, development, and regulatory teams requires strong collaboration and communication skills to ensure accuracy and consistency. Overcoming these challenges not only sharpens your abilities but also makes you an invaluable asset within interdisciplinary biotech environments.
To thrive as a Biotech Technical Writer, you need a solid understanding of scientific concepts, excellent written communication skills, and often a degree in life sciences, biotechnology, or a related field. Familiarity with document management systems, scientific publishing software, and regulatory compliance guidelines such as Good Laboratory Practices (GLP) or FDA requirements is typically required. Strong attention to detail, adaptability, and the ability to collaborate with cross-functional teams are essential soft skills in this position. These competencies are crucial for effectively translating complex scientific content into clear, accurate documentation that supports research, product development, and regulatory submissions.
A Biotech Technical Writer creates clear, accurate, and concise documentation related to biotechnology, such as research reports, regulatory submissions, standard operating procedures (SOPs), and product manuals. They translate complex scientific concepts into understandable content for various audiences, including researchers, regulators, and the general public. This role requires strong writing skills, attention to detail, and knowledge of biotech terminology and industry regulations. Biotech Technical Writers often collaborate with scientists, engineers, and regulatory professionals to ensure documentation meets industry standards.
Contractor
Posted yesterday
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: Technical Writer
Location: Swiftwater, PA
Duration: 6-Month Contract
Industry: Pharmaceutical / Biotech Manufacturing
Position Overview
We are seeking a Technical Writer to support the implementation of a new digital platform by developing, updating, and converting technical and quality-related content into user-friendly training materials and documentation. This role will work closely with cross-functional teams to create compliant documentation, training content, and process materials within a GMP-regulated environment.
The ideal candidate will have experience in technical writing, quality systems documentation, and digital system deployments within pharmaceutical, biotechnology, laboratory, or manufacturing environments.
Key Responsibilities
Required Qualifications
Hands-on experience with quality systems and applications such as:
Proficiency with:
