Web Software Developer, Sr. designs and develops software solutions for websites and mobile applications that engage users and meet business requirements. Supports web administrators and designers through the full development lifecycle and contributes to the development of new site features. Being a Web Software Developer, Sr. develops, implements, and debugs software code. Designs and develops the web infrastructure including back-end database development and the construction of SQL queries via CGI scripting. Additionally, Web Software Developer, Sr. requires knowledge of web technologies and tools such as CSS, JavaScript, HTML, PERL, PHP, Active Server Pages, SQL, and C++. Typically requires a bachelor's degree in area of specialty. Typically reports to a project leader or manager. The Web Software Developer, Sr. work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Web Software Developer, Sr. typically requires 4 -7 years of related experience. (Copyright 2024 Salary.com)
Onsite with Hybrid option after training
The QA Documentation Control Specialist II is responsible for the maintenance of the cGMP controlled documentation system and for providing the various departments the documentation that is necessary to perform cGxP activities.
Other responsibilities include auditing existing documentation, reporting document trends to management, and managing electronic document systems.
Process requests for document changes utilizing the EDMS
Process document Special Handling requests
Provide department metrics to management
Participate in documentation audits
Process logbook requests and perform routine audits
Process laboratory notebook requests
Responsible for maintaining Archive Room : filing, assisting customers
Identifies improvements with group-level impact
Manages assigned work and takes on additional responsibilities
Involved with other projects as required
Preferred experience in auditing documentation
Proficiency in MS Word & MS Excel. Livelink and MS Access a plus
Legible penmanshipOrganizational skills to coordinate multi-discipline projects
Experience in participation in regulatory inspections a plus
Understanding and familiarity with FDA and European regulatory requirements, guidelines
Last updated : 2024-04-24
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