- Monitor commercial business activities.
- Validation, analysis and follow-up of data provided by source systems.
Report observations, remediation and anomalies to oversight team and certifiers. - Maintain Dashboard, including business rules, documentation, and follow-up activities.
- Work on ad-hoc projects as business needs arise.
- Advanced user of Microsoft suite of tools, including Microsoft Excel, Access and PowerPoint.
- Experience with one or more of the following areas: quality, risk management, compliance, auditing/monitoring, pharmaceutical process improvement..
- Strong written and verbal communication skills.
- Sound business acumen, keen analytical and problem-solving skills.
- Ability to present complex information.
- Education: College degree and 3-6 years experience.
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Validation Specialist III - Bridgewater, United States - PSG Global Solutions Careers
Description
Apply now and our proprietary system will quickly have you in front of a live recruiter.
The Opportunity
Description
We're looking for a Validation Specialist III, working in Pharmaceuticals and Medical Products industry in 55 Corporate Drive, Bridgewater, New Jersey, 08807, United States.
Responsibilities:
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Skills/Qualifications:
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
