quality assurance iii.

• waukegan , illinois

• posted 10 days ago

job details

summary

• $35 - $46.32 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference49031

job details

job summary:

As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you!

location: Waukegan, Illinois

job type: Contract

salary: $35.00 - 46.32 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

• Lead meetings to facilitate and/or support the DSPP Project.

• Actively collaborate with a cross-functional team to complete project milestones and DSPPs per established timeline.

• Assist the functional areas on completing the DSPP risk factors and input in the DSPP.

• QA review of DSPP content in compliance with established governing documents.

• Oversee, monitor and track key deliverables associated with DSPP Implementation Project Metrics and related initiatives.

• Support other DSPP Project deliverables or initiatives as requested.

qualifications:

• Bachelor's degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering, or other technical/scientific area.

• Minimum of 5 years of experience in Quality Assurance and/or Quality System oversight. Risk Management, supply chain, compliance and drug shortages experience preferred.

• Lead meetings with technical professionals and experience in leading cross-functional teams with a results-orientated approach.

• Preferred: Knowledge of regulatory documents such as ICH, US / EU and other key GMP regulations.

• Skills: Result-oriented, strong oral and written communication skills, excellent interpersonal skills, initiative, attention to details, time management in a fast-paced environment, teamwork, problem solving and project management.

• Computer system skills including Microsoft Office; proficient in Power Point and Excel.

skills: SOP, Quality Assurance, MS-EXCEL, MS-Powerpoint, ICH Regulations, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.