Production Scheduler

Bloomington, IN, United States

Job Description


Production Scheduler

This is a full-time, hourly position. The shift is Friday \xe2\x80\x93 Sunday alternating Thursdays, 6:00am to 6:30pm.

The Production Scheduler is responsible for the daily manufacturing schedule for all cGMP activities, coordinating personnel, equipment, and facilities to ensure production commitments are achieved. This role leverages a learned understanding of our biomanufacturing processes and equipment to help proactively identify executional risks and creatively resolve scheduling impediments. The Production Scheduler supports the tracking of key performance indictors (KPIs) and provides regular status updates of projects. This role will report to the Manufacturing Supervisor or above, Indirect Operations.

Catalent Biologics in Bloomington, Indiana is a state-of-the-art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services. This award-winning facility helps customers accelerate biologic drug development programs and bring better treatments to help patients live better, healthier lives.

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

The Role:

  • Employs and enhances the capacity model and finite scheduling tools to support the efficient and timely execution of all cGMP activities.
  • Provides forecasting feedback to the Master Schedulers/Planners regarding resource availability and schedule optimization.
  • Collaborates with Manufacturing personnel, and members of other departments to load new projects into the schedule.
  • Collaborates with Manufacturing Science & Technology, Manufacturing, Quality, and Supply Chain to ensure timely completion of manufacturing readiness activities (e.g., tech transfer, documentation, material availability).
  • Schedules, manages, and tracks solution preparation activities; Drives schedule adherence of unit operations in cGMP Biomanufacturing across multiple teams.
  • Makes finite scheduling adjustments when impediments arise or changes are needed.
  • Helps to Coordinates workload across shifts and teams to minimize overtime and support work/life balance initiatives. Identifies resource constraints and makes recommendations for resolution (e.g., cross-training, additional headcount, capital investment).
  • Coordinates with Facilities on facilities and equipment preventative maintenances, services, and cleaning; Supports continuous improvement initiatives to drive process efficiencies and optimizations.
  • Other duties as assigned
The Candidate:
  • High School Diploma/GED with 2-4 years relevant experience required OR
  • Bachelors Degree with 1+ years experience
  • GMP experience preferred
  • Expertise in manufacturing capacity modeling preferred
  • MS Project experience \xe2\x80\x93 highly preferred
Why you should join Catalent:
  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • 152 hours of paid time off annually + 8 paid holidays
  • Competitive salary with yearly bonus potential
  • Community engagement and green initiatives
  • Generous 401K match and Paid Time Off accrual
  • Medical, dental and vision benefits effective day one of employment
  • Tuition Reimbursement
About Catalent:
Catalent Pharma Solutions is the leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products. With over 80 years serving the industry, Catalent has proven expertise in bringing more customer products to market faster, enhancing product performance and ensuring reliable clinical and commercial product supply. Catalent is headquartered in Somerset, N.J. For more information, visit www.catalent.com.

To perform this job successfully, an individual must be able to perform each duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
This job description reflects the general duties of the job but is not a detailed description of all duties which may be inherent to this position.

Catalent may assign reasonably related additional duties to individual employees, consistent with company policy.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone\xe2\x80\x99s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

personal initiative. dynamic pace. meaningful work.

Visit to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond\xe2\x80\x94 it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice .

Catalent

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Job Detail

  • Job Id
    JD4332431
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Bloomington, IN, United States
  • Education
    Not mentioned