Descripción de la oferta
HIPRA is a pharmaceutical and biotechnological company focused on prevention and diagnosis for animal and human health, with a broad range of highly innovative vaccines and an advanced diagnostic service.
HIPRA has a solid international presence in more than 40 countries, with its own subsidiaries, 11 diagnostic centres and 6 production plants strategically located in Europe (Spain) and America (Brazil). Research and Development constitute the core of its knowledge.
HIPRA dedicates 15% of its annual turnover to R&D activities that concentrate on the creation and application of the latest scientific advances to the development of the highest quality innovative vaccines. To give added value to its vaccination experience, the company also develops medical devices and traceability services.
The R&D Animal Health department based in Amer (Girona) is actively seeking a highly skilled and driven R&D Researcher to join the Method Development unit.
This is a temporary position covering maternity leave, with a strong potential to transition into a permanent role.
We Are Looking For Candidates With
PhD or postdoc in Biochemistry or Analytical Chemistry with a specialization in Biological Products, or a related field.
A minimum of 3 years of experience with analytical methods to measure quality attributes from proteins.
Proven expertise in analytical techniques such as UV-Vis spectrophotometry, HPLC-MS, HPLC (SEC, IEX), MALS, peptide mapping, capillary electrophoresis (CE-SDS, cIEF).
Knowledge of proteomics will be valued.
Strong experience in using statistical analysis tools and data modeling for the design, optimization, and improvement of analytical techniques.
Proven ability to independently execute experimental protocols and interpret data.
Good communications skills, strong ability to work collaboratively within a multidisciplinary group and with external partners.
Knowledge of pharmaceutical quality standards (GLP, GMP, VICH) and regulatory standards and guidelines, including those established by the FDA and EMA would be appreciated.
Proficiency level of spoken and written English for daily task development.
At Hipra You Will Find
Continuous learning.
A rapidly expanding multinational company.
A multicultural environment open to new ideas.
Main Responsibilities
Development of analytical techniques for assessing the quality of biopharmaceutical products, including small molecules and biologicals such as proteins.
Collaborate with other development teams within the Company, as well as external partners including CROs.
Author and review protocols and technical reports that meet CMC requirements and expectations of regulatory agencies.
Display effective organization, verbal and written communication skills, and adhere to good documentation practices.
Optimize and adapt pre-existing analytical methods.
#J-18808-Ljbffr
