QA Associate

DESCRIPTIONJoin MedFocus, a leading provider of contract-consulting opportunities to the pharmaceutical market. Our nationwide recruiting services provide excellent career opportunities for Laboratory and Clinical Research Professionals at pharmaceutical and medical device companies. All consultants are eligible for medical benefits, dental, vision and 401k.

Currently, one of our clients in South San Francisco is looking for a QA Associate II to join their team immediately.

Candidate will be responsible for soliciting/organize information from multiple groups, maintaining current contact lists, ensuring timely receipt from participants, and facilitating resolution of identified issues. Compile, proof-read, and review submitted data summaries to assure content accuracy, appropriate analysis, and valid conclusions as well as monitor draft review status, assemble feedback, and route reports for approval. Develop and maintain timelines and proactively monitor deliverables while providing timely status updates, generating quarterly meeting schedule, and author/issue meeting minutes. Work with all levels of employee at multiple sites as required.

Knowledge of cGMPs, quality systems, and quality assurance concepts is highly desirable. Ability to work independently as well as with a team in achieving goals and objectives, handle multiple projects, demonstrate initiative, and drive assigned tasks/projects to meet deadlines. Demonstrate solid proof-reading and grammatical skills. Excellent communication (verbal and written); good problem-solving ability; attention to detail; ability to prioritize; interpersonal, documentation, and organizational skills are necessary. Ability to support/handle multiple priorities within a fast-paced environment in a positive and collaborative manner is necessary. Proficient experience with computer systems/software applications such as Microsoft Office (Word, Excel) and Adobe Acrobat is highly desirable.REQUIREMENTSB.S. in Life Sciences, Quality Engineering, or other relevant discipline with 2 years of applicable pharmaceutical or biotechnology experience in Quality systems and cGMP compliance. Knowledge of manufacturing processes and pharmaceutical operation procedures and practices is desired.