トレンド企業

BioNTech
BioNTech

Develops immunotherapies and vaccines, particularly for cancer and infectious diseases.

(Associate) Director Protein & ADC Drug Substance

職種エンジニアリング
経験ディレクター級
勤務オンサイト
雇用正社員
掲載2週間前
応募する

Shanghai, China | full time | Job ID: 11127

About the role:

  • The main responsibility of this role is to provide project overarching drug substance support (mainly protein purification and ADC bioconjugation) 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 Drug Substance may also take dedicated responsibility as drug substance lead within global development projects.
  • Specific tasks of this position include engaging directly with local collaboration partners, CDMOs, vendors, etc. to support drug substance development and GMP manufacturing for protein and ADC projects. This role also involves supporting operational & troubleshooting activities on-site
  • The (Associate) Director Protein & ADC Drug substance 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 Drug substance 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 Drug Substance process development and clinical GMP production (person in plant, ad-hoc site visits for troubleshooting etc.)
  • Review project documentation, including development reports, risk analysis, qualification/validation reports, batch records and release documentation according to regulatory guideline
  • Translation of technical documents for technical transfer as well as due diligence activities
  • Organization of technical visits at collaboration partners or CDMOs (project-related visits, technical transfers, due diligence, etc.)
  • Subject matter expert support for internal audits and Health Authority inspections

A good match:

  • Master’s degree in 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 m Ab and ADC Drug Substance process technologies with preferably specific operational experience in m Ab DSP or ADC bioconjugation
  • Sound experience in CMC development of early- and late-stage projects, including strategy definition and strategy execution, with a sound understanding of all stages 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 in a clear and concise way 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

BioNTech

Public

BioNTech 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

10件のレビュー

4.0

10件のレビュー

ワークライフバランス

2.8

報酬

3.7

企業文化

4.2

キャリア

3.5

経営陣

3.3

78%

知人への推奨率

良い点

Innovative and cutting-edge technology projects

Supportive and collaborative team environment

Meaningful and impactful work with strong mission

改善点

Long working hours and high workload

Fast-paced environment can be stressful

High pressure and expectations

給与レンジ

38件のデータ

L2

L6

Mid/L4

Intern

L3

L4

L5

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

面接レビュー

レビュー1件

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