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Catalent

Global contract drug formulation, manufacturing, packaging

Junior Packaging Development Analyst

Manufacturing EngineeringUpdated on Nov 12
Full-timeIndaiatuba - State of São Paulo, BrazilNo salary listedIn-person

About the Job

Requirements

  • A completed university-level degree in Pharmacy, Chemistry, or Engineering.
  • Preferred previous experience in DME or Quality Documentation, or in areas involving production-process activities interfacing with equipment, such as Maintenance and Engineering, Production, Technical Services, or Validation, in the pharmaceutical, food, or chemical industry.
  • User-level knowledge of Microsoft Office and advanced Excel and PowerPoint skills.
  • Intermediate English proficiency.
  • Ability to prepare standard operating procedures and deliver training, including in English.
  • Knowledge of production processes and industrial equipment, and of process qualification and validation requirements.
  • Preferred knowledge of Good Manufacturing Practices and ANVISA regulations.
  • Preferred knowledge of Minitab.

Responsibilities

  • Prepare protocols and study reports for investigations, process adaptations, or improvements in the production area; request material registration and invoice issuance; and follow up on quality-system actions related to the area.
  • Prepare functional requirements and develop and conduct Factory Acceptance Tests and Site Acceptance Tests for implementation of new equipment or areas; request the inclusion or removal of equipment and accessories in the production area.
  • Prepare, review, and conduct training on procedures for new equipment or production-process improvements; do the same for Master Batch Records, packaging-material specifications, and product engineering.
  • Monitor and analyze production processes to identify improvements; research and request service quotations and purchase requisitions for production-area implementations; request service quotations for instrument and equipment calibration; and schedule and monitor calibration work.
  • Participate in investigations and root-cause analysis, help develop corrective and preventive action plans, and provide technical support to the production area as needed.
  • Participate in implementation of new equipment and projects, and provide technical support for operation of new equipment in the production area.
  • Support implementation of New Product Introduction with technical monitoring in the production area; monitor and support production of pilot and transfer batches for new products or equipment; and identify opportunities to improve production processes.
  • Monitor and analyze production processes for improvement and implement identified solutions.
  • Comply with and promote Good Manufacturing Practices and share the concept with colleagues; consistently comply with and promote internal Environment, Health, and Safety standards.
  • Use the personal protective equipment required by procedures or production orders; participate in safety dialogue meetings, communicate risks, and take part in Environment, Health, and Safety actions.

Desired Qualifications

  • Previous experience in DME or Quality Documentation, or in production-process areas that interface with equipment in pharmaceutical, food, or chemical industries.
  • Knowledge of Good Manufacturing Practices and ANVISA regulations.
  • Knowledge of Minitab.

About the Company

Catalent

Global contract drug formulation, manufacturing, packaging

Catalent provides end-to-end contract development and manufacturing services for pharmaceutical, biotechnology, and consumer health products. Its offerings cover drug formulation, large-scale manufacturing, clinical supply, and packaging under long-term partnerships, coordinating through a connected supply chain to move products from development to market. It differentiates itself with a broad, integrated service platform and long-standing customer relationships that help clients accelerate development and ensure reliable supply. The company aims to help clients bring products to market efficiently while balancing quality, cost, and sustainability across the product lifecycle.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Franklin Township, NJ
Founded
1996

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