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Supply Chain Planner

SOKOL GxP ServicesSummit, NJ

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Job Description

The Supply Chain Planner will manage material planning and purchasing activities to ensure on-time delivery and optimal inventory levels for clinical trial product manufacturing. This role coordinates with manufacturing, QA, QC, and cross-functional teams to align production schedules, resolve material shortages, and maintain supplier relationships. Responsibilities include developing replenishment strategies, managing supply forecasts, and driving process improvements within cGMP operations.

Requirements

Education:

Associate's degree required but prefer Bachelor's degree in Supply Chain, Engineering, Life Sciences, Information Systems, Business Management or related fields.

Qualifications & Experience:

• 3+ years of related experience in materials management and/or supply chain within cGMP operations. Cell therapy experience preferred.

• Experience in material planning and/or finite scheduling in a medium to high volume environment.

• Flexible and comfortable working with ambiguity. Strong understanding of current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) and other regulatory requirements (EMA, TGA).

• Strong organizational, analytical, and time management skills. 

• Ability to work well in a team environment with a positive attitude and a willingness to assist other areas of the organization.

• Excellent verbal and written communication skills as well as strong focus and attention to detail.

• Independence and self-starting mentality with an ability to handle multiple tasks at once in a fast-paced environment.

• APICS certification is a plus.

• Proficiency in ERP and MRP systems (I.e., Oracle, SAP, QAD, IBP).

Benefits

Competitive hourly rate: | $27.01 – $34.3/hour (W-2 only, no C2C)

12-month contract with possible extension 

Health benefits, holiday pay, and 401(k) program 

Paid time off (UTO) and professional development support 

Employee referral bonus program 

Opportunity to contribute to high-impact projects with a leading biopharma company

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Submit 10x as many applications with less effort than one manual application.

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