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Kelly Services Project Manager - GMP and auditing experience in Horsham, Pennsylvania

Seeking a Project Manager for a 3 month assignment in Horsham, PA

Pay Rate: $38-44/hr

Job Description: Maintain audit and inspection master schedule with regular updated information. Coordinate audit scheduling, prepare and confirm subject matter expert SME lists, plan audit logistics, etc. Manage pre-audit requests for information and respond to incoming queries during inspections and audits and ensure timely and accurate responses. Triage and manage incoming inspection and audit requests concerning GMO and OCMS processes to subject matter experts SMEs. Initiate and distribute communications to stakeholder groups before, during and after audit/inspection as required. Coordinate back-room audit and inspection activities. Provide tactical response support during audits and inspections as a global single point-of-contact for GMO and OCMS SMEs. Maintain contact lists, organization charts, overview presentations, and information related to past HA inspection findings. Monitor and respond to GMO Inspection Readiness CSA PV Inspection Audit Support department mailbox. Prepare and communicate audit/inspection related metrics and reports on periodic basis. System support and content management. Perform other duties as necessary

Qualifications:Bachelors degree required, a discipline in technical or science field preferred; Minimum of 4 years relevant experience is required; Demonstrated experience in participation, management or conduct of audits/inspections required; Experience working in pharmaceutical or other related regulated industry is required; Project Management skills and experience with organizing actions and managing team activities is required; Highly organized; Ability to independently plan, organize, coordinate, manage and execute assigned tasks; Can utilize appropriate initiative and autonomy in achieving objectives; Strong proficiency in Microsoft Excel and Sharepoint is required; Knowledge of PV regulatory requirements and experience with safety processing, clinical study safety reporting, pharmacovigilance and medical information preferred; Must be able to read, write and speak English; Requires problem solving skills to interpret data information, analyze and make recommendations; At least 1 year core project management experience; Pharma experience; Stable work history

Why Kelly ® ?

With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 9,000 scientific professionals last year.

You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today.

AboutKelly Services ®

As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connect with us on Facebook , LinkedIn and Twitter .

Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.