Quality Control Technical Expert
Hovione
Loures
há 5 horas

Hovione

Hovione is a 60 yearsPortuguese multinational company. From the beginning, we have set ourselvesabove and apart through our innovative technological and productivecapabilities, reaching a top spot in the world market as an integrated contractdevelopment and manufacturing organization (CDMO) offering from drug substanceto drug product intermediate to drug product.

Hovione recognizes that people are the main asset for the company’scontinued success, reaching over 1700 team members, from 20 different nationalitieslocated in Portugal, US, Macao, Ireland, Hong Kong, Japan, India andSwitzerland, including several production sites.

In 2019, we were recognized asthe third most attractive company to work for in Portugal.

Working at Hovione means reaching for innovation and excellence in everythingwe do : for our clients, our partners and, above all, our patients.

We are looking to reinforce our Quality Control Group with a TechnicalExpert, who enjoys challenges and scientific work.

As a Quality Control Technical Expert you will be responsible for :

  • Ensure the information flow between the laboratory and the several internal and external customers;
  • Represent the laboratory on meetings with clients, external and internal audits and for the Product / Project teams;
  • Prepare, review or approve analytical test methods to be executed by Analytical areas;
  • Prepare and review the protocols for work to be excuted in QC Labs;
  • Prepare and review reports related with work carried out within the QC Laboratory;
  • Define analytical strategies to allow the resolution of analyticalproblems detected;
  • Verifyand approve the analyses performed within the Quality Control Production Group whenever necessary;
  • Supporttechnically the analysts when conducting investigations or troubleshooting inthe analytical lab;
  • Assureand promote compliance on Health, Safety and Environment in the QualityControl Production team.
  • We are looking to recruit :

  • University, or equivalent, degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or in similar Chemistry / Biochemistry / Health Sciences fields;
  • GMP knowledge;
  • Minimum of 3 years of experience in related work;
  • Specific training in Analytical area, including Wet Chemistry and Chromatography;
  • Analytical, organizational and communication ability;
  • Critical and Creative;
  • Capacity or organization, discipline and methodologies;
  • Good interpersonal relationship;
  • Communication skills;
  • Fluent in English.
  • We offer :

  • Full time opportunity;
  • Remuneration and social benefits adjusted to the job function and matching the experience;
  • Excellent work environment, with a strong focus on quality.
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