Value Stream Planner II at Revvity in San Diego, CA

BioLegend, Inc. (a revvity Company) develops world-class, cutting-edge antibodies and reagents for biomedical research, manufactured in our state-of-the-art facility in San Diego, CA. Our mission is to accelerate research and discovery by providing the highest quality products at an outstanding value, along with superior customer service and technical support. Our product expertise covers a diverse set of research areas including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology.

Job Summary

The Value Stream Planner II to coordinate and expedite production for GMP Diagnostics and GMP Bioprocessing according to demand and quality standards. This position will ensure our products are produced on time for distribution. Applicant should be well-versed in production procedures, well organized, results-driven with problem-solving skills and process development skills. Advanced communication and computer skills are vital for this role.

Essential Functions

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Create Production orders in the ERP system.
Production Order Follow-up for on time delivery of production requirements.
Prioritize and Expedite Production Orders.
Monitor Material Sell-by and Expiration Dating
Review and schedule product replenishments to meet the master production schedule and satisfy manufacturing production targets.
Proficiency with performing strategic inventory calculations to optimize production capacity and inventory levels.
Work independently to review and manage assigned lab(s) production schedule/plan including demand, capacity, and material availability.
Monitor inventory levels in ERP system to ensure that inventories are well stocked and products are updated.
Review ERP Reorder messages and/or MRP suggestions and take appropriate actions
Request material transfers when material is available
Communicate timely responses to company departments/divisions in relation to; emails, ETA requests, scheduling, work order information requests.
Recommend material for disposition(s) based on "Sell-by" dating and or "Expiration" dates.
Coordinate production schedule with production departments.
Release Work Orders based on demand, material availability and work center capacity.
Work Closely with Production, QC, Customer Service and Procurement groups to coordinate material and resource requirements to meet the production plan.
Review ERP Reorder Point messages and/or MRP suggestions and take appropriate actions.
Optimize material stocking levels and take appropriate actions to minimize excess stock or scrap risk.
Determine MRP system settings to support product inventory targets and strategies.
Propose alternate activities to resolve Backorders.
Analyze, update and maintain complex spreadsheets. Generate reports and metrics.
Create and maintain documentation (SOP's, Forms, Checklists) to ensure all processes are documented.
Ensures compliance with company and department policies, procedures, checklists.
Create & Track KPI metrics for planning and manufacturing analysis.
Performs other duties as assigned/required.
Manage special projects or responsibilities as may be required.

Minimum Qualifications - Education and Experience

BA or equivalent work experience in the areas of: Business Administration, Supply Chain, Life science, Operations or related field.
4 - 6 years Production Planning experience required.
2 years of experience in an ISO13485 environment and FDA regulated environment.

Preferred Qualifications - Education and Experience

Prior experience managing GMP Diagnostics Bioprocessing products.
Prior production planning experience utilizing ERP/MRP Systems. Prior experience with Microsoft Dynamics NAV is a plus.
Prior experience handling multiple product lines with high volume and high mix of SKU's.
Ability to multi-task, work at a fast pace and handle a high-volume workload.
Prior experience managing products with expiration dating.
Experience with leading continuous improvement projects and initiatives.
Familiar with ISO compliance and GMP regulatory requirements.
Prior experience in life science, biotechnology industry or process manufacturing industry. Understanding of Lean Six Sigma, JIT, Kanban, root cause analysis, cost-benefit analysis.

The base salary range for this full-time position is $80,000-$85,000/Year. This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.

Work Environment & Physical Demands Office

While performing the duties of this job, the employee regularly works in an office setting. Occasional exposure to a laboratory and warehouse environment.

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. The employee is frequently required to stand, talk and hear.