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Hovione

CDMO for complex drug APIs manufacturing

Associate Operator

Bioprocess & BiomanufacturingUpdated on Nov 13
Full-timeEast Windsor, NJ, USAIn-person

About the Job

Requirements

  • Full secondary school qualifications or equivalent are mandatory; a vocational qualification is highly desirable.
  • Experience working in a manufacturing or production environment is mandatory.
  • Formal knowledge of, or experience working with, process systems used in fine chemicals or pharmaceutical operations is mandatory.
  • Successful completion of all mandatory training as an Operator is mandatory.
  • A solid understanding of Hovione unit operations is mandatory.
  • Ability to comply with the tasks described in the technical competences matrix applicable to the functional area.
  • Numerical capability for simple arithmetic.
  • Competent written and verbal English is highly desirable.
  • Ability to work in shift patterns.
  • Computer literacy.
  • Knowledge, experience, and skills to conduct tasks in accordance with established rules and procedures.

Responsibilities

  • Execute production and HSE activities efficiently and professionally, adhering to applicable procedures and instructions from ascending colleagues.
  • Execute production and HSE processes with supervision.
  • Complete and maintain all documentation under direct responsibility correctly.
  • Promote safe operations and high-quality performance, alerting ascending colleagues to potential risks and suggesting production and HSE optimizations or improvements.
  • Develop and accumulate strong production and HSE knowledge.
  • Maintain professionalism in the workplace.
  • Ensure facility activities comply with applicable GMP, legal, HSE regulations, and standards in the country of operation, and comply with and enforce Hovione processes and good practice.
  • Operate assigned equipment safely and efficiently, as applicable to the allocated Production/HSE Area.
  • Maintain clean and organized facilities.
  • Attend and participate fully in assigned meetings and training.
  • Communicate openly with colleagues and report production, HSE, quality, or other issues to management according to required processes.
  • Suggest and participate in improvements in the assigned area.
  • Check and calibrate all equipment before use.
  • Ensure equipment is correctly identified and used, including labels, plates, and logbooks.
  • Prepare samples according to the allocated area.
  • Execute production and HSE tasks correctly in Hovione systems, including SAP, LIMS, and SchedulePro.
  • Use personal protective equipment and keep it in good condition.
  • Use computer programs correctly, including email, SAP, LIMS, SchedulePro, and XNET.
  • Collaborate in revising area documents, including IOPs, as requested.
  • Collaborate in internal and external audits or inspections as requested.
  • Participate as required in induction and training of new Operators and collaborate in integrating Operators transferred from other areas.
  • Follow annual performance review requirements, including completing the self-assessment.
  • Undertake additional tasks commensurate with the role as required.
  • Carry out assigned tasks and duties safely, following instructions and environmental, health, and safety rules, procedures, regulations, and codes of practice.

Desired Qualifications

  • A vocational qualification.
  • Competent written and verbal English.

About the Company

Hovione

CDMO for complex drug APIs manufacturing

Hovione is a contract development and manufacturing organization that creates and scales active pharmaceutical ingredients (APIs) for medicines. It handles complex chemistry and specializes in processes like particle engineering and spray drying to improve drug absorption. It differentiates itself through a long history of tackling difficult compounds, deep manufacturing expertise, and an FDA-inspected global footprint across Portugal, Ireland, China, and the US. Its goal is to help drug developers bring new medicines to market efficiently by providing high-quality, scalable manufacturing and expanding capacity, especially in the U.S.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Loures, Portugal
Founded
1959

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