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
Quick apply
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
Springfield, NJ · On-site
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 ...
Springfield, NJ · On-site
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.
Quick apply
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 ...
Aberdeen Proving Ground, MD · On-site
$51K - $82K/yr
Perform high quality technical writing, editing, and formatting of deliverables/documents, to ... Occasional overnight travel #PLABS26 Qualifications * Active Secret clearance and ability to obtain ...
Aberdeen Proving Ground, MD · On-site
$51K - $82K/yr
Perform high quality technical writing, editing, and formatting of deliverables/documents, to ... Occasional overnight travel #PLABS26 Qualifications * Active Secret clearance and ability to obtain ...
Aberdeen Proving Ground, MD · On-site
$51K - $82K/yr
Perform high quality technical writing, editing, and formatting of deliverables/documents, to ... Occasional overnight travel #PLABS26 Qualifications * Active Secret clearance and ability to obtain ...
Aberdeen Proving Ground, MD · On-site
$51K - $82K/yr
Perform high quality technical writing, editing, and formatting of deliverables/documents, to ... Occasional overnight travel #PLABS26 Qualifications * Active Secret clearance and ability to obtain ...
$13.70 - $18.47
2% of jobs
$18.47 - $23.23
7% of jobs
$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
17% of jobs
$37.52 - $42.29
14% of jobs
$45.38 is the 75th percentile. Wages above this are outliers.
$42.29 - $47.05
11% of jobs
$47.05 - $51.81
10% of jobs
$51.81 - $56.58
5% of jobs
$56.58 - $61.34
3% of jobs
$61.34 - $66.11
3% of jobs
$13
$38
$66
| Aspect | Overnight Biotech Technical Writer | Biotech Scientific Writer |
|---|---|---|
| Credentials | Bachelor's degree in life sciences or related field; technical writing experience | Master's or PhD in life sciences; scientific research background |
| Work Environment | Fast-paced biotech companies, often overnight shifts for global teams | Research labs, academic institutions, or biotech firms, typically daytime hours |
| Employer & Industry Usage | Common in biotech firms requiring 24/7 documentation support | Used in research-focused roles, less common in overnight settings |
Overnight Biotech Technical Writers focus on creating clear documentation for biotech products during overnight shifts, often requiring quick turnaround and technical expertise. Biotech Scientific Writers generally work on research papers and scientific content during regular hours, with a stronger emphasis on research background. The roles overlap in industry but differ mainly in work hours and specific focus areas.
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:
