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Open Positions

We are looking for a “hands-on “ experienced and enthusiastic researcher, to join our  Analytical department

 

Job Description:
Development and validation of analytical, biological and biochemical methods.
Analytical support for the process development department, alongside with the product release under GMP requirements.
Scientific writing of protocols, reports, SOP’s, analytical methods and validations.

 

Requirements:
At least M.Sc. degree. Priority to Biochemistry/Biology/ biotechnology
Experience in the development of biological and biochemical methods: Tissue culture and cell-based assays, ELISA, CgE, SDS-PAGE, q-PCR, IEF, etc.
Knowledge and experience in protein analysis and characterization.
Experience in working under GMP/GLP requirements.
A Team player with excellent human relations that can work also independently.
Very good English (reading writing and speaking).

We are looking for a “hands-on “ experienced and enthusiastic researcher, to join our  Analytical department

Job Description:

-Development and validation of analytical and physicochemical methods.

-Analytical support for the process development department, alongside the product release under GMP requirements.

-Scientific writing of protocols, reports, SOP’s, analytical methods and validations.

Requirements:

-At least M.Sc. degree. Priority to Biochemistry/Biology/ biotechnology

-Experience in the development of physicochemical methods: HPLC/UPLC methods such as SEC, RP and normal HPLC, CEX, peptide mapping, HIC, HILIC, GC, etc.

-Knowledge and experience in protein/mAb analysis and characterization.

-Experience in working under GMP/GLP requirements.

-A Team player with excellent human relations that can work also 

independently.

-Very good English (reading writing and speaking).

We are looking for an experienced and highly motivated QA Engineer, to join our QA department.

Job Description:

– Manage all aspects of QA work delegated by the head of QA

– Writing, reviewing, and approving controlled documents, such as SOPs, WIs, Batch Records, Protocols, reports, etc.

– Conducting deviations and investigations, corrective and preventive actions managing.

– Performing internal audits, accompanying external audits.

Requirements:

– Relevant academic degree

– At least 3 years of experience working in QA in a GMP environment and pharmaceutical companies. 

-Excellent English (reading, writing and speaking).

We are looking for an experienced and knowledgeable RA CMC manager, for a significant and challenging position

Job Description:

  • Formulate and lead the Company’s CMC regulatory strategy.
  • Author and review high-quality CMC documentation for Dossiers.
  • Represent the Company at the corporate’s global cross-functional project teams.

Requirements:

  • Ph.D. in Life Sciences/chemistry
  • Demonstrated experience in Regulatory Affairs and Regulatory Submission within a biopharmaceutical company.
  • Profound knowledge of biologic s processes, CMC content and regulations.
  • Fluent in English (speaking and writing).