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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!
location: Lake Zurich, Illinois
job type: Contract
salary: $30.00 - 36.21 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Manage product data on both internal Regulatory Affairs and external FDA data tracking/collection databases to ensure the company's products, processes and physical sites continue to operate in a legal and ethical manner.
- Maintain current knowledge of federal and international regulations/standards/guidance documents, and internal policies and procedures to ensure compliance within Regulatory Affairs.
- Prepare, verify, and/or maintain technical files pertaining to submissions or other FDA-required activities throughout the product lifecycle. Understand and support the regulatory implications of the product profile
- Other duties as assigned by management
qualifications:
- Minimum of Bachelor's Degree, preferably in a scientific discipline
- 1-3 years experience in pharmaceutical Regulatory Affairs (experience in Quality Assurance will be considered in lieu of Regulatory Affairs experience)
- Strong problem solving and critical thinking skills
- Excellent written, verbal, and non-verbal communication skills
- Excellent attention to the details
- Solid organizational skills with capability to support multiple simultaneous projects
- Strong technical (system) and computer skills with proficiency in Microsoft applications (e.g., Word, Excel, PowerPoint, etc.)
- Strong knowledge of applicable regulations, standards and guidelines
skills: FDA, Quality Assurance, GCP (Good Clinical Practice), Regulatory Briefing Documents
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.
