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Hovione

CDMO for complex drug APIs manufacturing

Associate Operator

Bioprocess & BiomanufacturingPosted on Nov 10
Full-timeEast Windsor, NJ, USA$22.50 - $34.62 /hrIn-person

About the Job

Requirements

  • A full secondary school qualification or equivalent is mandatory; a vocational qualification is highly desirable.
  • Experience working in a manufacturing or production environment is mandatory.
  • Formal knowledge 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 and a very strong understanding of GMP regulations are mandatory.
  • Ability to comply with tasks described in the technical competences matrix for the applicable 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 sufficient to conduct tasks in accordance with established rules and procedures.

Responsibilities

  • Organize and execute production activities efficiently and professionally, following applicable procedures and instructions from senior colleagues.
  • Execute production processes autonomously.
  • Complete and maintain all documentation under direct responsibility.
  • Promote safe operation and high-quality performance, report potential risks, and suggest production optimizations or improvements.
  • Develop and accumulate strong production knowledge.
  • Help induct and train new operators when requested, sharing expertise and practical knowledge.
  • Ensure facility activities comply with applicable GMP, legal, HSE regulations, standards, and company processes and good practices.
  • Operate production equipment safely and efficiently.
  • Maintain clean and organized facilities.
  • Attend and participate in assigned meetings and training.
  • Communicate with colleagues and report production, HSE, quality, or other issues to management; assess issues and proactively propose solutions.
  • Check and calibrate equipment before use, and ensure its correct identification and use, including labels, plates, and logbooks.
  • Prepare and supervise sample processes according to the assigned area.
  • Carry out production and HSE tasks correctly in company systems, including SAP, LIMS, and SchedulePro, and use computer programs including email, SAP, LIMS, SchedulePro, and XNET correctly.
  • Troubleshoot systems and take appropriate action.
  • Use and maintain personal protective equipment.
  • Collaborate in internal and external audits or inspections as requested.
  • Participate in investigations of abnormal or unexpected events.
  • Complete required annual performance review activities, including self-assessment.
  • Suggest and participate in improvements in the assigned area.
  • Collaborate in revisions of area documents, including IOPs, when requested.
  • Participate in induction, training, and support of new operators across Hovione, and help integrate operators transferred from other areas.
  • Undertake additional tasks commensurate with the role as required.
  • Carry out assigned tasks safely, follow instructions, and comply with environmental, health, and safety rules, procedures, regulations, and codes of practice.

Desired Qualifications

  • A vocational qualification.

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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