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 ...
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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 ...
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Richardson, TX · On-site
$25 - $30/hr
Technical Writer Internship Immediate Opening Applied Concepts, Inc. - Richardson, TX Technical Writer Intern - Job Overview: The Technical Writer Intern is responsible for creating clear, accurate ...
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Richardson, TX · On-site
$25 - $30/hr
Technical Writer Internship Immediate Opening Applied Concepts, Inc. - Richardson, TX Technical Writer Intern - Job Overview: The Technical Writer Intern is responsible for creating clear, accurate ...
High Point, NC · On-site
$20 - $27/hr
... biotech, or biologics environment. - 1+ year direct experience authoring and leading QC laboratory investigations. - Advanced technical writing and documentation skills. - Strong knowledge of FDA ...
High Point, NC · On-site
$20 - $27/hr
... biotech, or biologics environment. - 1+ year direct experience authoring and leading QC laboratory investigations. - Advanced technical writing and documentation skills. - Strong knowledge of FDA ...
Prior internship, academic, or professional experience in technical writing, communications, journalism, or documentation support preferred
Prior internship, academic, or professional experience in technical writing, communications, journalism, or documentation support preferred
Prior experience in biotechnology area/ cell therapy area preferred good oral and written ... With Regards, Shiva Kapoor Technical Recruiter Direct: 732-429-1929
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 ...
Fort George G Meade, MD · On-site
Prior internship, academic, or professional experience in technical writing, communications, journalism, or documentation support preferred Requirements * Bachelor's Degree from an accredited college ...
Fort George G Meade, MD · On-site
Prior internship, academic, or professional experience in technical writing, communications, journalism, or documentation support preferred Requirements * Bachelor's Degree from an accredited college ...
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 ...
... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ... Authoring of technical protocols, reports, memorandum, records, and related correspondence Retrieve ...
... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ... Authoring of technical protocols, reports, memorandum, records, and related correspondence Retrieve ...
The Technical Document Writer will be responsible for producing high-quality cGMP documentation ... Prior experience working in a biotech/pharmaceutical company. Exceptional written/verbal ...
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;
Serve as mentor to interns. Technical Writer Mandatory Skills * Strong interpersonal communication skills in both developing collaborative relationships with SME and work with a wide range of people ...
Serve as mentor to interns. Technical Writer Mandatory Skills * Strong interpersonal communication skills in both developing collaborative relationships with SME and work with a wide range of people ...
Kenosha, WI · On-site
$60 - $75/hr
... biotech, or medical device manufacturing • Demonstrated experience authoring Deviation reports, CAPA records, and Change Control packages • Proficiency with electronic quality management systems ...
Kenosha, WI · On-site
$60 - $75/hr
... biotech, or medical device manufacturing • Demonstrated experience authoring Deviation reports, CAPA records, and Change Control packages • Proficiency with electronic quality management systems ...
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 ...
Technical Writer The Technical Writer leads and authors thorough investigations of deviations ... Experience working in a pharmaceutical, biotechnology, or other regulated manufacturing environment.
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Technical Writer The Technical Writer leads and authors thorough investigations of deviations ... Experience working in a pharmaceutical, biotechnology, or other regulated manufacturing environment.
Apply Early
$68K - $96K/yr
Biotechnology, medical device, or healthcare industry experience * Expertise in technical ... Good written and verbal communication skills in English, with strong interpersonal skills. * Good ...
New
$68K - $96K/yr
Biotechnology, medical device, or healthcare industry experience * Expertise in technical ... Good written and verbal communication skills in English, with strong interpersonal skills. * Good ...
New
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.
High Point, NC · On-site
$20/hr
Minimum 2 years of experience in a GMP-regulated pharmaceutical, biotechnology, or biologics ... Strong scientific writing and technical documentation skills. Preferred Qualifications Experience ...
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High Point, NC · On-site
$20/hr
Minimum 2 years of experience in a GMP-regulated pharmaceutical, biotechnology, or biologics ... Strong scientific writing and technical documentation skills. Preferred Qualifications Experience ...
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Process Documentation Engineer / Technical Writer This onsite Process Documentation Engineer role ... These solutions support industries such as pharmaceuticals and biotechnology, chemical ...
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Process Documentation Engineer / Technical Writer This onsite Process Documentation Engineer role ... These solutions support industries such as pharmaceuticals and biotechnology, chemical ...
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$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
Contractor
Posted 24 days ago
Be an early applicant
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:
