採用
Shanghai, China | full time | Job ID: 11126
About the role:
- The main responsibility of this role is to provide project overarching analytical support within the China organization and serve as a local interface for all clinical CMC project teams with Chinese collaboration partners, CDMOs, and vendors. In addition, the (Associate) Director Protein & ADC Analytics may also take dedicated responsibility as analytical lead within global development projects.
- Specific tasks of this position include engaging directly with local collaboration partners, CDMOs, vendors, etc. to support analytical development and quality control for protein and ADC projects. This role also involves supporting operational & troubleshooting activities on-site.
- The (Associate) Director Protein & ADC Analytics will also support technical transfers to in-China and ex-China sites (focus clinical phase), internal audits, and Health Authority inspections.
- As cultural and operational facilitators for the CMC teams, the (Associate) Director Protein & ADC Analytics will leverage his/her language skills and local knowledge to resolve issues promptly. This role will also closely collaborate with Product Supply and Quality counterparts to enable efficient technical project handover to commercial operations.
Your main responsibilities are:
- On-site operational support at collaboration partners and CDMOs for analytical development and quality control for clinical GMP production (ad-hoc site visits for troubleshooting etc.)
- Review project documentation, including method development reports, method qualification/validation reports, and release documentation according to regulatory guidelines
- Independently drive assigned analytical packages within global development projects
- Translation of technical documents for technical transfer activities
- Organization of technical visits at collaboration partners, CDMOs or vendors
- Subject matter expert support for internal audits and Health Authority inspections
A good match:
- Master’s degree or preferably PhD in Pharmacy, Chemistry, Biopharmaceuticals, Biochemistry, Biology, or a comparable field with at least 5 years of relevant professional experience in an international and highly regulated environment
- Proven experience in protein and ADC analytical technologies (physico-chemical assays, functional assays, quality control); knowledge in small molecule analytics is considered a plus
- General experience in CMC development of early- and late-stage projects, including strategy definition and strategy execution, with a sound understanding of all stages in the drug development process
- Sound GMP knowledge and experience with regulatory filings for biologicals (IND/IMPD, BLA/MAA)
- Excellent project management skills, capable of working in cross-functional CMC teams and with external stakeholders
- Excellent communication and negotiation skills as well as ability to communicate complex technical matters concisely to various stakeholders
Your Benefits:
BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.
Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.
How to apply:
Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.
Please note:
Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘Hire Right’. You will be informed accordingly by your BioNTech-Recruiter.
We are looking forward receiving your application.
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BioNTechについて

BioNTech
PublicBioNTech SE is a German multinational biotechnology company headquartered in Mainz that develops immunotherapies and vaccines, particularly for cancer and infectious diseases.
1,001-5,000
従業員数
Mainz that develops immunotherapies
本社所在地
$21.7B
企業価値
レビュー
4.0
10件のレビュー
ワークライフバランス
2.5
報酬
3.8
企業文化
4.2
キャリア
3.5
経営陣
3.2
75%
友人に勧める
良い点
Innovative and cutting-edge projects
Great team and collaborative environment
Excellent benefits and flexible schedule
改善点
Long working hours and high workload
Fast-paced and high-pressure environment
Management and communication issues
給与レンジ
70件のデータ
L2
L3
L4
L5
L6
Mid/L4
Intern
L2 · Data Scientist L2
0件のレポート
$53,767
年収総額
基本給
$21,507
ストック
$26,884
ボーナス
$5,377
$37,637
$69,897
面接体験
1件の面接
難易度
3.0
/ 5
期間
14-28週間
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Panel Interview
5
Final Interview
6
Offer
よくある質問
Behavioral/STAR
Technical Knowledge
Past Experience
Culture Fit
Problem Solving
ニュース&話題
BioNTech’s BNT323 Achieves Strong Phase 2 Response Rates in Endometrial Cancer - Oncodaily
Oncodaily
News
·
3d ago
BioNTech And Boehringer Trial Adds Dimension To Small Cell Lung Cancer Story - simplywall.st
simplywall.st
News
·
5d ago
Biontech prepares FDA application after strong phase II results in endometrial cancer - medwatch.com
medwatch.com
News
·
1w ago
BioNTech and DualityBio report positive data for trastuzumab pamirtecan - Clinical Trials Arena
Clinical Trials Arena
News
·
1w ago