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PSG Global Solutions Careers

Quality Assurance Associate

PSG Global Solutions Careers, East Hanover, New Jersey, us, 07936


Apply now and our proprietary system will quickly have you in front of a live recruiter.The OpportunityDescriptionWe're looking for a

Quality Assurance Associate , working in

Pharmaceuticals and Medical Products

industry in

1 Health Plaza, #Bldg 200, East Hanover, New Jersey, 07936, United States .

Interaction with both Quality organization as well as other supporting functions such franchises and Drug Safety.Responsibilities include project management, metrics, implementation of selected quality systems, and training programs.Develop and manage project plans and deliverable requirements as assigned.Act as the main point of contact between Quality function and other selected units and facilitate interactions and follow ups.Provide support including projects, processes, metrics.Facilitate and support the roll-out of training programs.Conduct gap assessments and perform baseline assessment, on specific Drug Safety Deliverables and manage implementation/coordination of remediation actions with 3rd party vendors.

Our Client

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

Bachelors degree in Biology, Chemistry, Microbiology, or related science or equivalent combination of education and experienceQuality Assurance/Quality Control professionalMinimum 7 years related pharmaceutical industryQA/compliance experience with a scientific background and solid understanding and knowledge of GMPs and Regulatory GuidelinesQuality System Administration experience preferredMust be proficient with all quality standards and compliance requirementsProficiency in project management skills

What Do You Think?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?