Product Surveillance Quality Associate II; temp

Position: Product Surveillance Quality Associate II (temp)
** Kelly Science & Clinical*
* ** Product Surveillance Quality Associate II (Contract)*
* *
* Location:

** Bloomington, IN (Hybrid - approximately 1 day onsite per week after training)

*
* Schedule:

** Full-Time, Monday-Friday

** Shift:
** Flexible start times (typically 7:00 AM-4:00 PM or 8:00 AM-5:00 PM)

** Pay Rate:**  $44.00-$45.70/hour

** Contract Type:
** Contract through December 2026

** Position Overview*
* Kelly Science & Clinical is seeking a Product Surveillance Quality Associate II to support complaint investigations and quality surveillance activities within a regulated pharmaceutical manufacturing environment. This position is a temporary assignment through December 2026 covering a team member's leave of absence.

The successful candidate will investigate customer-reported product complaints, perform root cause analysis, author technical reports, and collaborate with quality, manufacturing, and technical teams to ensure timely and compliant complaint resolution.

** Responsibilities*
* + Investigate and manage customer product complaints from initiation through closure

+ Communicate with customers to obtain information and provide updates

+ Review batch records, SOPs, and manufacturing documentation

+ Perform root cause analysis and support CAPA activities

+ Evaluate complaint samples and investigation data

+ Collaborate with SMEs and manufacturing personnel to determine corrective actions

+ Author technical investigation reports and complaint closures

+ Maintain documentation within electronic quality systems

** Qualifications*
* *
* Required:

*
* + Bachelor's degree in Chemistry, Biology, Engineering, or related scientific discipline

+ Minimum 2 years of experience in pharmaceutical, biotech, medical device, or regulated manufacturing environments

+

Experience with complaint investigations, deviations, CAPAs, or quality systems

+ Strong technical writing and documentation skills

+ Excellent communication and problem-solving abilities

** Preferred:*
* + FDA-regulated industry experience

+ Root cause analysis experience

+

Experience with Veeva, Track Wise, or similar quality systems

** Technical Skills*
* + Complaint Investigations

+ Root Cause Analysis (RCA)

+ CAPA Management

+ Technical Writing

+ Batch Record Review

+ GMP/cGMP Compliance

+ Quality Systems (Veeva preferred)

+ Microsoft Office Suite

** Work Environment*
* + Hybrid schedule following training

+ Increased onsite presence during onboarding

** P1*
* 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.  ()  for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly ®  Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

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