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Production Planner

Cipla
Central, NY Full Time
POSTED ON 4/4/2025
AVAILABLE BEFORE 5/1/2025

About Cipla

Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.

InvaGen Pharmaceuticals, Inc.

InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States.

Equal Opportunity Employer

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter.

About the Salary / Pay Range : The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

Job Title

Production Planner

Organization Name

InvaGen Pharmaceuticals, Inc.

Location

Central Islip, NY location

Employment Type

Full Time

Salary Range

Base / salary)

72,000 to $83,200

Benefits

  • Competitive salary
  • Health, dental, and vision insurance
  • Opportunities for professional growth and development
  • Paid time off and company holidays

Work Hours / Shift / Remote

8 : 30 am - 5pm Mon- Fri

Responsibilities / Accountabilities

  • Production Planning & Scheduling :
  • Develop and maintain production schedules based on demand forecasts, customer orders, and available resources.

  • Coordinate production timelines to ensure timely delivery of products while minimizing stockouts and overproduction.
  • Monitor inventory levels of raw materials, components, and finished goods to ensure sufficient supply for production.
  • Adjust schedules and production plans to accommodate changes in customer demand, machine breakdowns, or supply chain disruptions.
  • Collaboration & Coordination :
  • Work closely with procurement, warehouse, and production teams to align schedules, inventory management, and delivery timelines.

  • Ensure coordination between production lines, equipment availability, and staffing to meet production targets.
  • Provide regular updates on production status to senior management and other stakeholders.
  • Regulatory Compliance :
  • Ensure that all production schedules comply with regulatory requirements (e.g., cGMP, FDA, EU regulations).

  • Ensure production processes are aligned with quality assurance and quality control standards.
  • Maintain proper documentation for audits and inspections, including production records and batch reports.
  • Problem-Solving & Optimization :
  • Identify and resolve production issues, including delays, inefficiencies, and quality concerns, in a timely and cost-effective manner.

  • Recommend process improvements to enhance production efficiency, minimize downtime, and reduce waste.
  • Analyze production data to identify trends, capacity constraints, and areas for improvement.
  • Forecasting & Reporting :
  • Analyze historical production data to develop accurate forecasts for future production needs.

  • Prepare regular reports on production status, inventory levels, and operational performance for management review.
  • Monitor Key Performance Indicators (KPIs) such as production efficiency, downtime, and on-time delivery.
  • Education Qualifications

  • Bachelor's degree in supply chain management, Manufacturing, Industrial Engineering, Pharmaceutical Sciences, or a related field.
  • Certification in production planning (e.g., APICS CPIM) is a plus.
  • Experience

  • Proven experience as a Production Planner, Manufacturing Planner, or similar role in the pharmaceutical or regulated industry.
  • Strong understanding of pharmaceutical production processes, cGMP, and quality control standards.
  • Experience working with ERP systems (e.g., SAP, Oracle) and advanced Excel skills for scheduling, data analysis, and reporting.
  • Skills / Competencies

  • Strong organizational, time management, and multitasking skills.
  • Excellent problem-solving abilities and attention to detail.
  • Strong communication and interpersonal skills to collaborate with cross-functional teams.
  • Ability to work under pressure and adapt to changing priorities.
  • Knowledge of lean manufacturing principles and continuous improvement methodologies.
  • Familiarity with regulatory standards (FDA, EMA, ICH guidelines) and quality management systems.
  • Experience in the pharmaceutical or life sciences industry
  • Salary : $72,000 - $83,200

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