Sr. Production Planning Specialist

Alliance Medical Products, Inc.; Irvine (CA); On-site; USD 110,000 - 125,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life Voluntary Accident

Hospital

Pet 401K

Generous Time Off Structure including

Holidays

Sick & Personal

Job summary

Siegfried is seeking a Material Planner in Irvine, CA to evaluate material demand and support manufacturing schedules. You will collaborate with Operations, QA, Customer Service, and IT to align with the site’s financial targets and customer service levels.

Role requires strong communication, data analysis, and ERP/MRP experience in a regulated manufacturing setting. Excel proficiency and SAP/Oracle knowledge are valued.

Qualifications

• Bachelor's degree with 5+ years in production scheduling in regulated manufacturing (cGMP, FDA, ISO).
• Experience inputting and retrieving data in ERP or MRP systems; SAP or Oracle preferred.
• Strong understanding of material requirements concepts.
• APICS and Lean Six Sigma certifications a plus.
• Proficiency in Excel and data analysis for planning.

Responsibilities

• Develops, finalizes, and communicates the material requirements plan to meet customer demand on time.
• Plans, prepares, and controls material availability to support production needs.
• Create Process Orders in ERP to support the materials plan.
• Ensures on-time deliveries by coordinating with brokers and freight forwarders.
• Monitors supplier performance and reports KPIs.

Skills

Self-starter

Organized

Data analysis

Problem solving

Business acumen

Communication skills

Time management

Education

Bachelor's degree (MRP)

ERP/MRP experience

APICS/Lean Six Sigma

Excel proficiency

SAP/Oracle experience

MRP concepts

Job description

\"Expect to grow\", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions offering long-term opportunities to grow and make an impact.

Your Role:

The Material Planner will evalaute materials demand to support the manufacturing schedules to meet revenue targets. The incumbent will evalaute materials requirements to support the site's financial targets. This position requires excellent communication and analytical skills and works closely with all departments to meet business goals and best-in-class customer service levels. The incumbent will work closely with Manufacturing Operations, Supply Chain, Quality Assurance, Customer Service, Engineering and Facilities, and Information Technology to achieve the client'’s timeline and department objectives.

• Develops, finalizes, and communicates the material requirements plan for the site that meets customer demand on timely availability.
• Plans, prepares, and controls material availability to ensure a flow of approved materials meeting production requirements considering storage conditions and capacity.
• Create Process Orders in our ERP System to support the materials plan.
• Ensures on time deliveries by follow up and working with brokers and freight forwarders as needed.
• Advises management of material events that can potential disrupt the production plans.
• Schedules timely delivery of materials; evaluates material supply and demand; establishes ROP/ROQs based on forecasts and storage capacity.
• Coordinates interdepartmental activities with quality assurance, manufacturing, facilities and supply chain management.
• Schedules and expedites the approval of materials to support the production schedule and other Project activities.
• Follow established departmental policies, procedures, and objectives. Supports continuous quality improvement objectives, and safety regulations.
• Development and maintenance of SCM KPIs (inventory turns, schedule adherence, obsolete inventory, etc.).
• Maintains and reports key site metrics and KPI presentations to key stakeholders and corporate leaders as required.
• Measure supplier delivery performance and address opportunities.
• Responsible for supporting the training of other teammates as needed.
• Responsible for Change Control management activities related to Supply Chain such as: new source of supplies, change in specifications, vendor change, others.
• Support the creation and maintenance of Master data and BOM's.
• In addition, the jobholder is obliged to carry out other tasks as may be instructed by his/her superior - individual tasks which by their nature belong to his activities or result from operational requirements.
• Inform their superior about any extraordinary events.

Required Knowledge, Skills, and Abilities

• Self-starter, organized and detail-oriented.
• Strong problem solving, data analysis and computer systems skills.
• Good business acumen.
• Good communication skills, both verbal and written.
• Multi-tasking and excellent time management skills.

Required Education and Experience

• Bachelor's degree with 5+ years' experience in production scheduling, demand or MRP within a regulated manufacturing environment (cGMP, FDA, ISO).
• Experience inputting and retrieving data in ERP or MRP systems. SAP or Oracle preferred.
• Strong understanding of material requirement concepts.
• APICS and Lean Six Sigma certifications a plus.
• Experience working in a dynamic high-paced environment.
• Excel experienced. - Be prepared to demonstrate proficiency in Excel during the interview process.

Target Salary Range: $110,000 - $125,000 annually

Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications, and other job-related reasons.

Your Benefits:

• Medical
• Dental
• Vision
• Life Voluntary Accident
• Hospital
• Pet 401K
• Generous Time Off Structure including PTO
• Holidays
• Sick & Personal

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.