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Document Preparation Jobs In 上海 - 94 Job Positions Available

1 – 20 of 94 jobs
Novotech jobs

Responsibilities Performing site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations. Supporting the development of a subject recruitment plan. Establishing regular lines of communication

Novotech  27 days ago
Sanofi jobs

Clinical Operations Study Country Lead I (COSCL) is the country level operational lead in clinical studies. He/she owns, and is accountable for, the strategic planning, management and performance of their assigned clinical trials, for his/her country(ies),

Sanofi  26 days ago
KLA jobs

Company Overview KLA is a global leader in diversified electronics for the semiconductor manufacturing ecosystem. Virtually every electronic device in the world is produced using our technologies. No laptop, smartphone, wearable device, voice-controlled gadget, flexible screen,

KLA  26 days ago
Pfizer jobs

Responsibility: -· Leads China clinical development strategy and delivery, as part of global early development. · Ensures that early oncol clinical trials for their program are designed and executed to the highest scientific and quality standards,

Pfizer  26 days ago
Koch jobs

Location(s) Shanghai, Shanghai Company Molex Career Field Quality Job Number 191994 Your Job 1. Manufacturing AQP for projects awarded to 4/5 suppliers 1) Summarize lesson learn documents and conduct gauge/fixture review 2) Review important process/documents with suppliers, including

Koch  26 days ago
Koch jobs

Location(s) Pudong, Shanghai, Shanghai Company Molex Career Field Quality Job Number 191990 Your Job Support Quality Excellence (QEX) and Digital Quality Transformation initiatives through data analysis, process mapping, dashboard development, and quality system digitization projects to

Koch  26 days ago
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Alfa Laval jobs

Every day, we get opportunities to make a positive impact – on our colleagues, partners, customers and society. Together, we’re pioneering the solutions of the future and unlocking the full potential of precious resources. Trusted to

Alfa Laval  25 days ago
Fortrea jobs

Job Overview: The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their

Fortrea  25 days ago
Bristol Myers Squibb jobs

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.

Bristol Myers Squibb  25 days ago
Blue Education jobs

Academic Lead (across all subjects) Teaching Excellence | Academic Mentoring | Curriculum Contribution | Tutor Leadership Salary: £50,000-£60,000 per year, plus performance-based bonuses and potential equity options Locations: London or Shanghai Contract: Full-time | Hybrid |

Blue Education  25 days ago
NBBJ jobs

NBBJ is an award-winning design firm recognized as a TIME100 Most Influential Company, a Fast Company Most Innovative Architecture Firm and a two-time 2025 AIA National Honor Award recipient. These recognitions reflect our purpose-driven approach that,

NBBJ  24 days ago
PSI CRO jobs

Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials

PSI CRO  24 days ago
AstraZeneca jobs

Typical Accountabilities: - In partnership with AZ enablement team, other AZ clinical experts and external service providers, the GSAM provides oversight to ensure study delivery. - Leads/contributes to the preparation of delegated study documents (e.g. Informed Consent Form,

AstraZeneca  23 days ago
Fortrea jobs

Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation

Fortrea  24 days ago
Abbott jobs

JOB DESCRIPTION: 核心工作职责:Core Job Responsibilities: 一、技能操作 制粒Granulation 严格按照标准操作规程和制造指令单/工艺操作规程进行制粒操作。 Operate strictly as SOP and MO/MD. 严格执行清场。生产前仔细按照制造指令单复核原辅料。 Properly carry out line clearance. Before production, carefully check raw materials as MO. 严格执行中控检查(颗粒外观、LOD等),确保产品质量。 Properly carry out in-process checks such as

Abbott  23 days ago
Clifford Chance jobs

Company Description Who we are We are one of the largest international law firms in the world. With over 30 offices across the globe, we strive to exceed the expectations of our clients, providing them with

Clifford Chance  22 days ago
Abbvie jobs

Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on

Abbvie  22 days ago
Evonik jobs

What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you

Evonik  21 days ago
Abbvie jobs

Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on

Abbvie  20 days ago

Intern, Sales Assistant, HNC GC Shanghai, China Join our Flavor team as a Sales Assistant Intern in Shanghai, where you will support account managers with daily coordination, sample preparation, documentation and communication. This is a great opportunity

Dsm-firmenich  19 days ago

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