
Description
R&D Specialist
Kelly Outsourcing Consulting Group Kelly OCG, a managed solution provider and business unit of Kelly Services, Inc., is currently seeking a R&D Specialist for a long-term engagement at one of our Global consumer products clients in Skillman, NJ.
Location: Skillman, NJ (will relocate to Summit, NJ or Fort Washington, PA in H1 2026)
Schedule: Monday-Friday, 9A-5P
Compensation: $32-46/hr
Duration: 1yr, can go longer
Summary
The Specialist R&D Quality & Compliance (R&D Q&C) is responsible for the administration of integrated and comprehensive quality systems and controls that are appropriate, effective, efficient and continuously improving in order to ensure that R&D functions are operating in full compliance with sound scientific practice, Current Good Manufacturing Practices (CGMP), and within company policies and Standard Operating Procedures.
The Specialist is responsible for participating on documentation quality review/approval of R&D Sales Samples and R&D Product Quality Complaints (PQCs). In addition to these tasks, supporting documentation maintenance and archival, quality inspections of R&D products, and in internal assessments on R&D processes specific to GxP. The Specialist must be knowledgeable to provide guidance on applicable Regulations (FDA, ICH, EU, and others) pertaining to business partners.
Responsibilities:
- Participate in GMP documentation review and approval of sales samples including identifying opportunities to optimize release processes for agility and speed to customer sales teams.
- Participate in working with various functional groups, as needed, to conduct problem identification and resolution along with assisting in compiling documentation to review and approve assessments and/or investigations for R&D Product Quality Complaints (PQC).
- Support in the development and implementation of GMP and Quality & Compliance processes and procedures including supporting GMP documentation review and approval.
- Support on internal assessments of R&D GMP processes and areas and identify opportunities to streamline.
- Support in inspection readiness activities.
- Support quality inspection of supplies for R&D studies.
Qualifications
- A minimum degree of BS in Science/Engineering is required.
- Minimum of 3yrs of industry experience in these responsibilities.
- Experience in Healthcare or Pharma industry a plus.
- Understanding of Regulatory requirements in R&D development.
- Experience with Trackwise,Veeva, and MS Office required.
- Strong Communication and Interpersonal skills required.
What happens next
Once you apply, you'll proceed to the next steps if your skills and experience look like a good fit. But don't worry—even if this position doesn't work out, you're still in our network. That means all our recruiters will have access to your profile, expanding your opportunities even more.
Helping you discover what's next in your career is what we're all about, #P1
Send resumes to Jacqueline.Sayoc@KellyScientific.com
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
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