fortil
fortil
fortil इंजीनियर-उद्यमियों द्वारा स्थापित और संचालित एक यूरोपीय इंजीनियरिंग एवं प्रौद्योगिकी परामर्श समूह है। कंपनी एयरोस्पेस, निर्माण और BIM, दूरसंचार, स्वास्थ्य सेवा तथा लॉजिस्टिक्स सहित विभिन्न क्षेत्रों में औद्योगिक और कॉर्पोरेट ग्राहकों को इंजीनियरिंग, डिज़ाइन और तकनीकी परामर्श सेवाएँ प्रदान करती है। 2,500 से अधिक कर्मचारियों वाली इसकी बहुविषयक टीम एक दर्जन से अधिक देशों में कार्य करती है और व्यवसायों को विशेषज्ञ इंजीनियरिंग विशेषज्ञता तथा भर्ती सहायता उपलब्ध कराती है। fortil की कर्मचारी-स्वामित्व वाली पूंजी संरचना इंजीनियरिंग-आधारित सहयोग और दीर्घकालिक तकनीकी सेवा पर इसके ध्यान को दर्शाती है।

QC Analyst – Biochemistry and Method Validation

Join fortil as a QC Analyst supporting biochemical testing and analytical method validation for regulated pharmaceutical projects. You will work with quality and analytical development teams in a collaborative environment.

विवरण

  • Conduct laboratory analyses and quality-control testing.
  • Apply analytical techniques including ELISA, Immunoblot / Western Blot, and qRT-PCR / qPCR.
  • Help implement and qualify new analytical methods on coagulation equipment.
  • Assist with preparing and executing analytical method protocols.
  • Analyze, verify, and review laboratory results.
  • Support investigations into atypical results, deviations, and nonconformities.
  • Maintain data traceability and compliant documentation in line with GMP requirements.
  • Work with QC, Quality Assurance, Analytical Development, and other project teams.
  • Contribute to analytical method transfer and lifecycle activities.

आवश्यकताएँ

  • Degree or equivalent training as a laboratory technician, biomedical analysis technician, biologist, biochemist, biotechnologist, or in a related field.
  • Some laboratory experience, preferably in pharmaceutical or biotechnology quality control or another strongly regulated setting.
  • Practical experience performing ELISA assays.
  • Experience using Immunoblot / Western Blot techniques.
  • Experience with qRT-PCR / qPCR methods.
  • Strong laboratory technique and documentation skills.
  • Familiarity with GMP / GxP requirements.
  • Ability to follow analytical protocols and interpret test results.
  • Detail-oriented, self-directed, and well organized.
  • Effective collaborator in multidisciplinary teams.
  • Fluent in French.
  • Professional working proficiency in English.
  • Experience with analytical method validation or transfer, coagulation assays, release or stability testing, analytical investigations, deviations and CAPA, or pharmaceutical QC is an advantage.

लाभ

  • Individual guidance to support your professional growth.
  • Work on innovative, high-value industrial projects.
  • Entrepreneurial culture with room to take initiative.
  • Opportunity to become a shareholder in the group.
  • Strong focus on innovation, corporate social responsibility, and employee development.
  • Policies designed to support parenthood and work-life balance.
  • Positions are open to applicants with disabilities, irrespective of gender, background, or sexual orientation.

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