As the world's 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: Pennington, New Jersey
job type: Contract
salary: $41.03 - 48.27 per hour
work hours: 9 to 5
education: Associate
responsibilities:
General Description:
- Understand GxP training and LMS software to troubleshoot problems and provide compliant and practical solutions to meet user needs.
- Build and maintain items in the LMS such as training items, curricula, user groups, quizzes, smart forms and assignments.
- Build reports, queries and data extracts as requested.
- Cross-functional collaboration to ensure the GMP compliance of day-to-day operations.
- Manage new employees' related GMP training.
- Provide support for personnel training records and archiving.
- Ensure site training compliance expectations are communicated.
- Create training job aids with critical information for training and on-boarding.
- Provide KPIs to management for tracking of essential training requirements.
- Assist in the site training and documentation operations with the close collaboration with global teams.
- Maintain accurate records and documentation, a necessary.
- Ensure compliance with regulatory requirements, industry standards, and company policies in all training activities.
- Undertake any other duties, either for this department or any other department within the business, which may be requested by the Line Manager, for which training and/or an explanation has been provided and understood.
qualifications:
- Strong PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint), Visio, Smartsheet, Veeva, LMS training software.
- Experience managing enterprise applications and/or systems management.
- Experience with ComplianceWire or similar LMS
- Experience with Document Management Systems (preferably Veeva QualityDocs) and Human Resource Information Systems (preferably Workday)
- Customer focused
- Ability to collaborate with global teams and learners from diverse backgrounds
- Excellent leadership and communication skills
- Excellent analytical and troubleshooting skills
- Understanding of GAMP and or 21 CFR Part 11
- PHARMACEUTICAL MANUFACTURING
- CGMP
- DETAIL ORIENTED
- DOCUMENT MANAGEMENT SYSTEMS
- LEARNING MANAGEMENT SOFTWARE
- Minimum Associates Degree
skills: MS-EXCEL, 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.
