Process Coordinator - Pharmaceutical Manufacturing

Process Coordinator – Pharmaceutical Manufacturing

Contract: 3–6 Months

Pay Rate: $32/hour

Schedule: 2-2-3 Day Shift (A or B Shift)

We are seeking a Process Coordinator to support pharmaceutical manufacturing operations in a cGMP-regulated environment. This role is responsible for coordinating manufacturing documentation, supporting investigations, maintaining production metrics, and ensuring accurate execution of SAP and Veeva transactions. The ideal candidate will have strong technical writing skills, experience with manufacturing documentation, and the ability to collaborate across departments to support commercial production activities.

Key Responsibilities

• Execute and manage SAP transactions required to support manufacturing process orders and production activities.
• Author and support investigations, line assessments, deviation documentation, CAPAs, and corrective actions.
• Create, revise, review, and maintain SOPs, work instructions, and Master Batch Records (MBRs) in compliance with cGMP standards.
• Review completed production records, logbooks, and batch documentation for accuracy, completeness, and compliance.
• Support tracking and reporting of production metrics and OEE performance data.
• Provide guidance to manufacturing teams on SOPs, batch records, and operational procedures.
• Coordinate cross-functionally with Quality, Manufacturing, and other departments to resolve issues and support operational goals.
• Participate in team meetings to communicate progress, initiatives, and manufacturing updates.
• Maintain compliance with cGMP requirements, safety procedures, PPE standards, and sterile gowning practices.
• Complete all assigned training and duty-based qualification packets.
  
  

Qualifications

• Experience in pharmaceutical or regulated manufacturing environments preferred.
• Familiarity with SAP, Veeva, and GMP documentation practices.
• Strong attention to detail and technical writing skills.
• Ability to manage multiple priorities in a fast-paced manufacturing setting.
• Experience with deviations, CAPAs, and batch record review is highly desirable.
  
  

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.

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.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.

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