Siegfried Holding AG Irvine , CA 92606
Posted 2 months ago
General Information
Country United States
City Irvine, California
Functional Area Operations
Job Group Supply Chain
Employment Type Permanent Contract
Working time Full-time
At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer.
Your role
The Production Planner/Scheduler will create and optimize manufacturing schedules to meet Irvine's revenue targets. The incumbent will balance customer demand and requirements with the site's manufacturing capacity providing production schedules in a dynamic, fast-paced environment. 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, Account Management, Engineering and Facilities, and Information Technology to achieve the client's timeline and department objectives.
Your profile
Responsibilities
Develops, finalizes, and communicates a weekly production schedule for the site that balances customer demand with efficient plant utilization.
Plans, prepares, and controls production schedules coordinating material requirements to ensure a controlled flow of approved materials meeting production requirements.
Advises management of the status of work in progress; material availability; and potential production problems to ensure that personnel; equipment; materials, and services are delivered as needed.
Schedules equipment; confirms material supply and demands; establishes ROP/ROQs based on forecasts and capacity.
Drive schedule that triggers work orders or purchase requests for the production or purchase of supporting facets of a master production schedule; CER load and inventory requirements.
Development and maintenance of scheduling KPIs (Production Schedule Performance, inventory turns, schedule adherence, etc.).
Maintains and reports key site metrics and KPI presentations to key stakeholders and Corporate leaders as required.
Required Education and Experience
Bachelor's degree with 3+ years' experience in production scheduling within a cGMP manufacturing environment.
Experience entering and retrieving data in ERP or MRP systems.
Strong understanding of pharmaceutical production scheduling concepts.
Bachelor's degree.
APICS and Lean Six Sigma certifications a plus.
SAP or Oracle ERP systems experience.
Working knowledge of Excel.
Salary Range: $65,000 - $80,000
Job Type: Full-time
Working at Siegfried
Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs.
Who we are
In the Midst of People's Lives
What we do in Irvine
Irvine is one of Siegfried's sterile drug product manufacturing sites, providing contract development and manufacturing services (CDMO) specializing in difficult to manufacture pharmaceuticals, ophthalmics, and drug delivery devices.
Main activities
Provides cGMP sterile drug product fill finish of biologics, suspensions, emulsions, ointments, and gels
All fully cGMP and SHE compliant
Features
Semi-automated and automated visual inspection
Automated packaging with digital data visual verification
Stability study services
Drug delivery
Laboratory services
Clinical Products small lot capability (semi-automated filling, batch sizes up to 5 K units)
Clinical manufacturing (batch sizes less than 5 K units)
Strategic importance
CDMO for innovative and difficult-to-manufacture products from clinical to commercial NDA and ANDA products
Provides contract sterile drug product manufacturing and laboratory services to the pharmaceutical and biotechnology industries
Siegfried Holding AG