Hengrui Pharma
:
Process Development & Optimization
////Lead downstream purification process development and optimization for biologics, including depth filtration, chromatography (affinity/ion exchange/hydrophobic interaction), ultrafiltration/diafiltration, virus inactivation/removal, etc.
CQACPPAnalyze Critical Quality Attributes (CQA) and Critical Process Parameters (CPP) during purification, addressing challenges in yield, purity, host cell protein (HCP) residues, etc.
Technology Transfer & Regulatory Submissions AKTAGMPParticipate in pilot-scale purification process development (e.g., operation of AKTA systems), complete process scale-up and technology transfer to GMP manufacturing. SOPIND/BLADevelop technical documentation (process protocols, SOPs, validation protocols) and support IND/BLA submission dossier preparation.
Platform Development & Management Evaluate novel purification technologies (e.g., continuous flow chromatography, membrane chromatography) for potential implementation. Oversee daily instrument maintenance and other downstream process development-related tasks.
Masters degree or above in Bioengineering, Biochemistry, Pharmaceutical Engineering, or related disciplines.
Research projects involving protein purification experiments, with hands-on experience in operating relevant instruments.
Strong English proficiency (listening, speaking, reading, writing), capable of fluently interpreting English technical literature and conducting technical communication with international peers.
///Shanghai / Suzhou / Guangzhou / Lianyungang
1Western BlotAKTAProficient in fundamental experimental techniques (e.g.,
column packing ,
Western Blot );
Priority given to candidates with AKTA system operation experience . 2Understanding of downstream purification workflows (e.g., affinity chromatography, ion exchange). 3Excel/UNICORNBasic data analysis capabilities (Excel/UNICORN software).
Strong learning agility and deep interest in biopharmaceutical process development. Systematic thinking and data analysis skills, adaptable to fast-paced R&D environments. Independent problem-solving skills and cross-departmental collaboration mindset.
Technology Transfer & Regulatory Submissions AKTAGMPParticipate in pilot-scale purification process development (e.g., operation of AKTA systems), complete process scale-up and technology transfer to GMP manufacturing. SOPIND/BLADevelop technical documentation (process protocols, SOPs, validation protocols) and support IND/BLA submission dossier preparation.
Platform Development & Management Evaluate novel purification technologies (e.g., continuous flow chromatography, membrane chromatography) for potential implementation. Oversee daily instrument maintenance and other downstream process development-related tasks.
Masters degree or above in Bioengineering, Biochemistry, Pharmaceutical Engineering, or related disciplines.
Research projects involving protein purification experiments, with hands-on experience in operating relevant instruments.
Strong English proficiency (listening, speaking, reading, writing), capable of fluently interpreting English technical literature and conducting technical communication with international peers.
///Shanghai / Suzhou / Guangzhou / Lianyungang
1Western BlotAKTAProficient in fundamental experimental techniques (e.g.,
column packing ,
Western Blot );
Priority given to candidates with AKTA system operation experience . 2Understanding of downstream purification workflows (e.g., affinity chromatography, ion exchange). 3Excel/UNICORNBasic data analysis capabilities (Excel/UNICORN software).
Strong learning agility and deep interest in biopharmaceutical process development. Systematic thinking and data analysis skills, adaptable to fast-paced R&D environments. Independent problem-solving skills and cross-departmental collaboration mindset.