SQA Solution
About the job Technical Writer - Assay Development
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)
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 (preferred) Bachelor's degree in a scientific discipline or other related technical field
We are an Equal Opportunity Employer and welcome talent across all aspects of background, orientation, origin, and identity 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
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)
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 (preferred) Bachelor's degree in a scientific discipline or other related technical field
We are an Equal Opportunity Employer and welcome talent across all aspects of background, orientation, origin, and identity 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