QA Associate

*Overview:* TekWissen Group is a workforce management provider throughout the USA and many other countries in the world.
The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs.
The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.
*Description:* * Provides clerical and administrative support related to documentation processes and systems.
* Creates logbooks and other control issued documents.
* Assists in maintaining the document archival room.
* Responsible for filing and maintenance of controlled documents and records.
* Ensures files are accurate and easily retrievable.
* Scans, verifies and archives documentation and records.
* Performs general word processing tasks and support ensuring accuracy.
* Ensure the correct and timely input of database entries.
* Data input accuracy is critical.
Participates in training on issues affecting own area of work.
* Notifies manager of compliance questions and issues.
* Provides additional support and assistance on tasks and projects as directed by management.
*Skills Critical to this Job:* * Attention to detail * Ability to multitask * Organizational skills * Typing and computer skills * Verbal and written communication *Educational Requirements:* * High school diploma or equivalent required.
* Bachelors degree in a related field is preferred.
*TekWissen® Group is an equal opportunity employer supporting workforce diversity.
* Job Types: Full-time, Contract Pay: $25.
00 - $27.
00 per hour Work setting: * In-person Experience: * documentation: 1 year (Preferred) * Biotech or Pharmaceutical industry: 1 year (Preferred) * GMP & GDP: 1 year (Preferred) Work Location: In person