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Empleo en Igc pharma sas

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- Hibrido

  • Data engineer

    COP

  • industry IGC PHARMA SAS

  • $6 a $8 millones Bogotá country Publicado 30 Abr 2025
  • Independence Teamwork Proactivity

  • Data engineer

    COP
  • $6 a $8 millones
  • Job description: 
    The Company works in the Alzheimer’s space. We are building AI models that seek to uncover clues on early detection and to predict the course of the disease based on patient signatures.  
    We are seeking individuals that can work with the AI Engineers to harmonize very large databases that can be used in AI models. The Data Engineer will work closely with the AI team and harmonize longitudinal study databases, ensuring that the database is free of errors and consistent with other databases that are used in the AI models.  

    Responsibilities: 
    -Extract variables of interest from multiple databases. 
    -Harmonize variables across databases. 
    -Ensure correctness of data ranges based on data dictionaries. 
    -Process and encode databases for AI algorithms. 

    Requirements:  
    -2 – 4 years of experience.
    -Knowledge in data handling using Python and common libraries in the data science industry.  
    -Fluency in pandas is required, along with knowledge of other libraries and/or techniques for exploratory analysis and data profiling.  
    -Statistical foundation to understand and report on the variables within a dataset.  
    -Skilled at generating visualizations that effectively communicate the findings of the data flow in a project.  
    -Skilled at working on projects with high-dimensional data and/or clinical data is a plus.  
    -Proficiency in English is required. 

    Qualifications: 
    -Pursuing a BA/BS/MS/MA/MD in any Science, Technology, Engineering, and Mathematics (STEM), Systems Engineer, Social Scientist or other. 

    * Salary is negotiable depending on experience and academic background.

    Cargos relacionados

    Matemático, Ingeniero de sistemas, Científico de datos
- Hibrido

  • Clinical operations associate

    COP

  • industry IGC PHARMA SAS

  • $5,5 a $6 millones Bogotá country Publicado 7 Abr 2025
  • Trabajo en equipo Comunicación asertiva Liderazgo

  • Clinical operations associate

    COP
  • $5,5 a $6 millones
  • IGC Pharma is a USA-based pharmaceutical company dedicated to advancing innovative treatments to improve patient outcomes. As part of our commitment to advancing pharmaceutical innovation, we are currently seeking a motivated Clinical Operations Associate to support our clinical trial operations team in Bogotá, Colombia. This is a great opportunity to start or advance your career in clinical trial operations in an exciting and impactful industry.

    Job Description:
    The Clinical Operations Associate will play a key role in supporting the clinical trial process, ensuring smooth and compliant trial operations. Working closely with senior clinical staff, including Clinical Trial Managers, this position provides essential support in the day-to-day management of clinical trials.

    Key Responsibilities:
    -Trial Support: Assist with the preparation, execution, and oversight of clinical trials, ensuring adherence to trial protocols and regulatory guidelines.
    -Documentation and Compliance: Support the management of essential clinical trial documentation, ensuring completeness, accuracy, and compliance with regulatory requirements (e.g., GCP, ICH).
    -Communication: Serve as a liaison between the clinical trial team, external partners, and clinical trial sites to ensure smooth communication and prompt resolution of issues.
    -Logistical Coordination: Coordinate logistics related to clinical trials, including trial supplies, equipment, and site visits.
    -Monitoring Support: Assist with the monitoring of clinical trial progress, including tracking milestones and reporting to senior staff on any trial delays or issues.
    -Regulatory Support: Ensure compliance with regulatory requirements and assist with the preparation for site audits or regulatory inspections.

    Qualifications:
    -Bachelor’s degree in Life Sciences, Health Sciences, Pharmacy, pharmaceutical chemistry, chemistry, microbiology or a related field.
    -1-2 years of experience in clinical trials, healthcar

    Cargos relacionados

    Microbiólogo, Químico, Farmacéutico
- Hibrido

  • Quality control analyst

    COP

  • industry IGC PHARMA SAS

  • $5,5 a $6 millones Bogotá country Publicado 26 Mar 2025
  • Trabajo en equipo Comunicación asertiva Atención al detalle

  • Quality control analyst

    COP
  • $5,5 a $6 millones
  • Job Description:
    The Quality Control Analyst will coordinate and oversee all quality control activities at IGC Pharma, working closely with our third-party laboratory to ensure that all raw materials, in-process samples, and finished pharmaceutical products meet the required internal specifications. The role involves reviewing analytical data, managing product release processes, and ensuring compliance with cGMP 211, regulatory requirements, and company quality standards. This position will report to the Quality Assurance (QA) lead and collaborate cross-functionally with manufacturing and regulatory teams.

    Key Responsibilities:
    -Coordinate third-party laboratory interactions, ensuring timely and accurate testing of raw materials, intermediates, and finished products.
    -Review and translate from English to Spanish Method Validations /Verifications/Scopes/Challenges
    -Review and approve laboratory test results, certificates of analysis (CoAs), and investigations related to out-of-specification (OOS) results or deviations.
    -Ensure compliance with GMP, regulatory guidelines (e.g., FDA, EMA), and internal quality policies by monitoring QC activities.
    -Coordinate product release processes by verifying all quality documentation and ensuring specifications are met before distribution.
    -Assist in stability studies by coordinating testing schedules and reviewing reports from the third-party laboratory.
    -Develop and maintain Standard Operating Procedures (SOPs) related to quality control activities.
    -Participate in audits and inspections, providing necessary documentation and ensuring QC-related compliance.
    -Support quality investigations and CAPAs (Corrective and Preventive Actions) related to analytical testing issues.
    -Assist in the creation of Specifications and Quality Course Trainings for the Company.
    -Work closely with the QA team to implement continuous improvement initiatives in quality control processes.

    Qualifications:
    -Bachelor’s de

    Cargos relacionados

    Microbiólogo, Químico, Farmacéutico, Farmacólogo
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