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project manager ii (non-it).

• north chicago , illinois

• posted 8 days ago

job details

summary

• $55 - $59.05 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference48331

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: North Chicago, Illinois

job type: Contract

salary: $55.00 - 59.05 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

• Primarily responsible for the oversight, execution, deployment and continuous improvement of R&D Quality System to ensure appropriate GxP alignment and compliance to evolving regulations.

• Conduct risk assessments, including the identification of hazards, estimation of risks, and evaluation of risk mitigation strategies.

• Work closely with the Quality Risk Management Quality System Owner and support other related Quality System processes as needed.

• Collaborate with cross-functional teams to develop and implement risk mitigation plans.

• Stay up-to-date with industry trends, regulatory changes, and emerging risks, and proactively recommend improvements to the R&D Quality Risk Management Program.

• Maintain deep understanding of the Quality Risk Management process, including linkages and interactions of all impacted functional areas.

qualifications:

• Bachelors' degree required in a scientific or technical field (Chemistry, Pharmacy, Biology, Microbiology or Engineering) required.

• Minimum of 6+ years of risk management industry experience in a regulated environment.

• Effective communication skills, with an ability to work and influence cross-functionally.

• Thorough understanding of polices, regulations, standards, and best practices of risk management. The scope of responsibilities is broad and requires the ability to communicate, understand and direct individuals in highly specialized risk management background.

• Excellent organizational skills, attention to detail, and strong analytical skills.

Preferred experience:

• Experience in two or more of the following areas: Quality Assurance, Compliance, Regulatory, Clinical Operation, Pharmacovigilance, Manufacturing, or Combination products or Medical devices.

• Experience using risk management software.

skills: GLP (Good Laboratory Practice), GCP (Good Clinical Practice), RMP (Risk Management Plan), 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).

Applications accepted on ongoing basis until filled.