Software Guidance & Assistance, Inc. (SGA, Inc.)
Technical Writer - Assay Development
Software Guidance & Assistance, Inc. (SGA, Inc.), Tucson, Arizona, United States, 85718
Technical Writer – Assay Development (Contract)
Software Guidance & Assistance, Inc. (SGA) is seeking a Technical Writer for a contract assignment with a premier pharmaceutical services client in Tucson, AZ.
Responsibilities
Act as the Technical Writer on project teams, attend meetings, and update the supervisor.
Involved in the creation, review, revision, and approval of documentation and labeling for the firm's Tissue Diagnostics products.
Required Skills
Bachelor's degree in a scientific discipline or other related technical field.
3‑5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry.
Knowledge of current U.S. and international regulations as they pertain to documentation (e.g., FDA, ISO, IVDD, 21 CFR 11) and control of electronic records.
Demonstrable record of working on project teams while handling multiple projects.
Preferred Skills
Experience with international regulatory requirements.
SGA is a technology and resource solutions provider that is a women‑owned business. Our mission is to solve big IT problems with a more personal, boutique approach. We match consultants to over 1,000 engagements each year. We value customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do, and find your passion at work. Find us at https://sgainc.com/.
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or other legally protected status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment.
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Responsibilities
Act as the Technical Writer on project teams, attend meetings, and update the supervisor.
Involved in the creation, review, revision, and approval of documentation and labeling for the firm's Tissue Diagnostics products.
Required Skills
Bachelor's degree in a scientific discipline or other related technical field.
3‑5 years of direct documentation experience in medical device, software, pharmaceutical, or biotechnology industry.
Knowledge of current U.S. and international regulations as they pertain to documentation (e.g., FDA, ISO, IVDD, 21 CFR 11) and control of electronic records.
Demonstrable record of working on project teams while handling multiple projects.
Preferred Skills
Experience with international regulatory requirements.
SGA is a technology and resource solutions provider that is a women‑owned business. Our mission is to solve big IT problems with a more personal, boutique approach. We match consultants to over 1,000 engagements each year. We value customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do, and find your passion at work. Find us at https://sgainc.com/.
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or other legally protected status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment.
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