Energy Jobline ZR
Technical Writer - Assay Development in Tucson
Energy Jobline ZR, Tucson, Arizona, United States, 85718
Job Details
Type : Contract, W2 only
Duration : 24+ months
Location : Tucson, AZ (Oro Valley)
Pay :
$27/hr
Please note that at this time we are unable to sponsor employment authorization (both new and transfer)
Job Description A leading global biotech company is seeking a Technical Writer - Assay Development to translate complex scientific information into clear, accurate documentation, attend meetings, and update the supervisor. You will be involved in the creation, review, revision and approval of documentation and labeling.
Skills, Experience & Education
3-5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry
Knowledge of current US and International regulations as they pertain to documentation (e.g., FDA, ISO, IVDD and 21 CFR 11), and control of electronic records
Demonstrable record of working on project teams while working on multiple projects
Experience with international regulatory requirements
Bachelor's degree in a scientific discipline or other related technical field
Equal Opportunity Employer We are an Equal Opportunity Employer and welcome talent across all aspects of background, , , and in an inclusive and non-discriminatory way. Applicants receive consideration without bias and based solely on the relevant qualifications, talents, skills, experiences, and business needs
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Duration : 24+ months
Location : Tucson, AZ (Oro Valley)
Pay :
$27/hr
Please note that at this time we are unable to sponsor employment authorization (both new and transfer)
Job Description A leading global biotech company is seeking a Technical Writer - Assay Development to translate complex scientific information into clear, accurate documentation, attend meetings, and update the supervisor. You will be involved in the creation, review, revision and approval of documentation and labeling.
Skills, Experience & Education
3-5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry
Knowledge of current US and International regulations as they pertain to documentation (e.g., FDA, ISO, IVDD and 21 CFR 11), and control of electronic records
Demonstrable record of working on project teams while working on multiple projects
Experience with international regulatory requirements
Bachelor's degree in a scientific discipline or other related technical field
Equal Opportunity Employer We are an Equal Opportunity Employer and welcome talent across all aspects of background, , , and in an inclusive and non-discriminatory way. Applicants receive consideration without bias and based solely on the relevant qualifications, talents, skills, experiences, and business needs
#J-18808-Ljbffr