PSC Biotech Ltd
Location
Hyderabad | India
Job description
About PSC Biotech
Who we are
PSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona California USA with Global operations in Ireland India Singapore Australia and the US serving 350 clients in more than 23 countries worldwide. We provide cloudbased software solutions for Quality Management and Regulatory Inspections pharmaceuticals contract manufacturing professionals and metrology services to our clients.
Take your Career to a new Level
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of likeminded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diversecultural work setting.
Technical writer Entry level (College Grad with experience in Scientific writing)
Job Description:
Creates and ensures that the various types of PSC Software s templatedriven documentation deliverables are accurate readable well organized and geared toward the intended user of the documentation
Assists software engineers in gathering organizing and formatting information for inclusion in validation plans specifications and validation reports
Creates and submits new documents or document revisions into the document control system and tracks them to approval
Incorporates feedback from document reviewers to improve the final result.
Applies skills and develops documentation including customer facing literature operating procedures and process flow charts
Assists functions in gathering information for organizing formatting and writing domestic and international documents
Participates as an active team member in cross functional teams
Requirements
Bachelors degree in English Computer Science STEM or equivalent
2 years of technical writing experience in software or life sciences
Expertise in word processing software (e.g. Microsoft Word)
Familiarity with electronic document management systems (EDMS) (e.g. Microsoft SharePoint)
Preferred
Expertise in process flow chart tools (e.g. Microsoft Visio)
Expertise in presentation tools (e.g. Microsoft PowerPoint)
Familiarity with electronic quality management systems (eQMS) (e.g. Veeva Vault Sparta Systems TrackWise MasterControl)
Experience in continuous improvement projects documentation best practices and improvements
Shift
Fully REMOTE Work From Home
Working hours (normal): Monday to Friday 8 hours per day 40 hours per week
Working hours (onboarding/training): Monday to Friday 3pm 12 AM India time till Midnight India Time
#LISK1
Requirements Bachelor s degree business or a technical field, or equivalent. At least (1-2) years of industry experience in either procedure writing, technical writing, or engineering. Experience in the medical device industry preferable. Experience in continuous improvement projects- documentation best practices and improvements. Familiarity with enterprise resource planning systems (ERP) and electronic document management systems (EDMS) (e. g. MFGPro, JDE, and MasterControl).Job tags
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