Quality Assurance Associate

• Quality Assurance Associate:
• Title: Quality Assurance Associate
• Location: Bend, OR
• Industry: Life Science/Pharmaceutical
• Salary: Based on Experience
• Employment Type: Direct Hire

Job Overview:

As a Quality Assurance Associate, you will be responsible for performing the day-to-day tasks of the QA Department in a GMP facility manufacturing pharmaceutical products. Tasks include production record review, analytical data review, internal Quality Assurance document review, and support of the production floor. Additional responsibilities include assisting in the maintenance of the electronic Quality Management System, conducting risk analyses and investigations, and participating in audits and inspections. Preference will be given to candidates within the pharmaceutical industry, while those with Quality oversight experience encouraged to apply.

Responsibilities:

• Supports the implementation and continuous improvement of the company s Quality systems
• Document authorship, review, and approval of SOPs, production, and quality control records including batch records, certificates of analysis, method validations, and equipment qualifications
• Oversight of investigation and CAPA program management
• Supports internal audits, client audits and regulatory inspections, as needed
• Other related duties as assigned

Qualifications:

• Minimum of a Bachelor's Degree, preferably in a scientific discipline
• 2+ years previous manufacturing, quality control, or quality assurance experience
• Knowledge of GMP and FDA regulations for clinical trial materials preferred
• Excellent verbal and written communication skills
• Excellent time management skills with a proven ability to meet deadlines
• Excellent organizational skills and attention to detail
• Demonstrated ability to collaborate and work in cross-functional teams
• Ability to function well in a high-paced and at times stressful environment
• Scientific curiosity and willingness to learn
• Demonstrated experience in characterization and analytical techniques relevant to the pharmaceutical industry
• Demonstrated experience with advanced laboratory and data analysis skills preferred
• Strong analytical and problem-solving skills
• Ability to prioritize tasks and to delegate them when appropriate
• Working knowledge of Veeva and/or SAP preferred
• Prolonged periods of sitting at a desk and working on a computer
• Must be able to lift up to 15 pounds

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to match professionals rapidly and precisely to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

EOE/ADA

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