United BioSource Corporation.

QA Representative

Morgantown, US
18 Jul 2019
17 Aug 2019
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Job Title: Quality Control Specialist

Brief Description:

Responsible for completing quality control checks on assigned programs and assisting in the implementation, maintenance and documentation of quality control practices, procedures and programs.


• High School Graduate; college degree preferred

• Knowledge of Post Marketing Drug Surveillance programs

• Quality Control related experience in call centers, health care or pharmaceutical care

• Working knowledge of Microsoft Word, Excel, PowerPoint and other Office tools as


• Well-organized

• Strong attention to detail

• Good written/verbal skills

• Good interpersonal skills

• Good time management skills

Supervisory Responsibilities:


Specific Job Duties:

• Perform quality control checks on assigned programs, identify corrective and preventive actions, and perform follow-up activities.

• Review associates' documentation for accuracy.

• Print and review daily reports for assigned programs.

• Assist operational staff in developing and implementing operational quality control processes utilizing appropriate tools (checklists, double-data entry, etc).

• Monitor the effectiveness of the implemented quality control procedures and report summarized results of all quality control processes to the Director, Program Management & Quality Control and Senior Manager, Quality Assurance.

• Promote quality awareness.

• Other duties as assigned by the Director, Program Management & Quality Control and as determined by UBC SOPs.


United BioSource Corporation (UBC) is a leading provider of pharmaceutical support services, partnering with life science companies to make medicine and medical products safer and more accessible. Our services support the full lifecycle of medicine and medical products, including development, commercialization, and long-term value and safety.

While UBC offers employment within Patient Support, Nursing, Pharmacy and Corporate, two main focus areas for the company are Clinical Development & Research and Safety & Risk Management. Members of the Clinical Development and Research teams help evaluate study protocol, target study population, recruit physicians and patients, and collect, clean, validate and report data. As a result, sponsors are able to submit findings to regulatory authorities or make a no-go decision in a timely and clear-cut manner. Additionally, our Safety and Risk Management teams develop, deliver, and report evidence to reinforce safe and appropriate product use.

Through our Patient Access services, we help patients begin therapy quickly and remain on therapy, building strong relationships with patients to ensure optimal care.
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