TECH WRITER

 

arry out validation activities for manufacturing processes, which include equipment qualifications, process qualifications, software validations, process capability studies, and process improvements.
    
Engage with clients, scope requirements and support projects in the following areas
    Create and execute validation protocols
    Create and execute URS, IQ, OQ, PQ, TMV, Risk assessments
    Review data and generate reports
    Review and implement international test standard
Skills and Education     
    
Education: BS/MS degree in a health and life sciences related fields, preferably Pharmaceutical Science, Regulatory Science, Biology, Chemistry, microbiology, biochemistry.
Demonstrated problem-solving and troubleshooting skills
    Demonstrated good interpersonal and written communication skills
    Demonstrated results orientation, team skills, ability to multitask, ability to learn quickly and the ability to respond to urgent needs of the team and deliver expected results within expected deadlines
    Demonstrated ability to serve as a technical resource for assessing validation requirements and solving test related problems
    Demonstrated proficiency in standard office software, including Word, Excel, Project, and PowerPoint