Quality Assurance Associate II- cGMP compliance

EMAIL your resume in a simple MS WORD document to lois.martin@adeccona.com In the subject line of your email, please REFERENCE JOB# LM-G78196

NO THIRD PARTIES OR H1B VISA OR CORP TO CORP APPLICANTS
no relocation costs for interview or start... Bay Area Residents please
NOTE: Only Qualified Candidates will be contacted

We have an exciting Temporary position for a QA ASSOCIATE II with a background in Quality Engineering, cGMP compliance for one of our largest Bay Area clients.

DUTIES AND RESPONSIBILITIES

DUTIES
-- Soliciting/organize information from multiple groups, maintain current contact lists, ensure timely receipt from participants, and facilitate resolution of identified issues.
-- Compile, proofread, and review submitted data summaries to assure content accuracy, appropriate analysis, and valid conclusions.
-- Monitor draft review status, assemble feedback, and route reports for approval.
-- Develop and maintain timelines and proactively monitor deliverables. --- Provide timely status updates, generate quarterly meeting schedule, and author/issue meeting minutes.
-- Work with all levels of employee at multiple sites as required.
-- Perform other duties, including generating additional reports or supporting data and analysis.

SKILLS
-- 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.

EDUCATION
B.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.





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