This is a stellar opportunity responsible for leading tech transfers with major BioPharma industry clients for ADC conjugation processes. This is a once-in-a-lifetime Global Expat leadership opportunity within the World's Largest biologics CMO expanding to 784,000L total mammalian cell culture manufacturing capacity across 5 plants with commercial monoclonal antibody, Antibody Drug Conjugate and mRNA manufacturing capabilities. You will be charged with overseeing the following activities:
* Leading and performing tech transfers for ADC conjugation and downstream manufacturing processes.
* Working directly with external client partners for ADC Manufacturing troubleshooting and tech transfers with clients during tech transfer project meetings and PIP visits.
* Leading site client visits and supporting technical process clarification with clients.
* Driving the generation of GMP documents for ADC conjugation and ADC manufacturing tech transfers such as SOPs, Quality Risk Assessment and Manufacturing Batch Records.
* Analyzing risk assessments for ADC conjugation processes.
* Working cross functionally with Manufacturing, Quality, Supply Chain Management, Project Management and other internal teams.
* Providing input on the improvement of tech transfer workflows for ADC conjugation processes.
* Supporting quality audits and global regulatory inspections.
Desired Skills & Experience
* 5+ years working experience with ADC biopharmaceuticals, including manufacturing process development.
* BS, MS or Ph.D. in Biochemistry, Biology, Organic Chemistry, Chemistry, or related Biological Sciences degree.
* Experience performing tech transfers for the manufacturing and conjugation of Antibody Drug Conjugates.
* Proven experience with ADC conjugation processes, tech transfer and manufacturing operations for commercial ADCs and monoclonal antibody therapeutics.
* Knowledge of ADC conjugation or downstream purification processes for GMP biologics manufacturing.
* Expertise generating and authoring cGMP documentation including PCS, QRA, MBR, BPR, SOP and PQR documents.
* Experience supporting FDA, EMA and other Global regulatory audits and inspections.
*** Please note that this is a full-time Expat Opportunity Based in South Korea. It is not based in the US or remote from the US. A full Expat Benefits package is provided including a company paid apartment, international school tuition and relocation assistance. ***
Expatriate Benefits Package:
* Competitive base salary, target bonus, retirement allowance and excellent medical benefits.
* Company paid luxury apartment in Songdo.
* International school tuition paid for children at the top rate Chadwick International School in Songdo, 3 miles from SBL - There are also excellent English speaking preschools.
* Company paid airfares to visit the US (or country of origin).
* 3 weeks of vacation time.
* Opportunity to rapidly advance your career within the World's Largest Biologics CMO. A majority of Expats we have placed are now working in their 4th, 5th, 6th and even 9th years. Many have been promoted up to Sr. Director and VP levels.
* Work alongside a friendly team of over 100 US Expats and live within the amazing Songdo international community. Other Songdo community employers include the United Nations Green Climate Fund and Incheon Global Campus with University of Utah, SUNY Stony Brook and George Mason University.
* Opportunity to live and work in the ultramodern New Songdo city with excellent restaurants and an abundance of shopping. Just 20 minutes away from the Incheon ICN International Airport, trips to the US is easy and Asia travel opportunities are endless.
You can also view new photos of Korea and Songdo at
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