Director of Bioconjugation
at MabPlex International
China, Maine, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Jan, 2025 | Not Specified | 31 Oct, 2024 | 5 year(s) or above | Biology,Organic Chemistry,Regulatory Filings,Conjugation | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
WHAT WE OFFER
- Competitive Salary and Welfare
- Performance Incentives
- Share option
- Two Way Development
- Talent Selection Mechanism
- Additional Benefits
TYPE: Full-Time
LOCATION: Yantei, China
JOB DESCRIPTION
The Director of Bioconjugation will assume responsibility for the following activities:
- Daily management of the department and coordination with other groups.
- Definition and execution of work plans for each project.
- Training and assessment of staff, improvement and retention of technical expertise.
- Process development of antibody drug conjugates (ADCs).
- Developing novel conjugation platforms, keeping pace with novel technologies.
- Execution of manufacturability assessments supporting Client’s early needs.
- Supporting business development; serving as a subject matter expert (SME).
- Troubleshooting conjugation processes that fall outside of platform-able design spaces.
- Drafting technology transfers, development reports, and CMC sections.
- Assisting other groups (AD, QC, QA, MFG) with method development and confirmation.
The desired requirements for this position are as follows:
- PhD in Organic Chemistry, Pharmaceutical Synthesis, Biology, or related field.
- At least 5 years of direct experience in downstream process development, including antibody purification and conjugation.
- At least 5 years of experience directly managing reports.
- Experience with regulatory filings is desirable.
- Experience with commonly used toxins and antibody-drug conjugates.
- Working knowledge of small molecule registration, shipment, and declaration.
How To Apply:
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Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Information Technology/IT
IT Software - Other
Software Engineering
Phd
Proficient
1
China, ME, USA