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AM - Bioanalytical Technology Laboratory
15000-20000元 應(yīng)屆畢業(yè)生 本科
  • 全勤獎
  • 節(jié)日福利
  • 不加班
  • 周末雙休
上海羅氏制藥有限公司 2026-02-12 23:57:38 735人關(guān)注
職位描述
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在羅氏,我們鼓勵每位同事展現(xiàn)真實的自己;我們欣賞獨(dú)特且出眾的品質(zhì)。羅氏的文化鼓勵積極的表達(dá)、開放的對話和真誠的連結(jié),在這里,你將因為做自己而被重視、接納和尊重,并得到個人的提升和職業(yè)的發(fā)展。所有的這一切,都是為了更好地預(yù)防、阻止和治愈疾病,并確保醫(yī)療資源的可及性和可持續(xù)性。歡迎加入羅氏,一個重視每種聲音的地方。
職位
1. Lab Establishment and Setup:
Lead the setup and validation of the new QC laboratory:


Define the scope and requirements for lab infrastructure and layout.

Select appropriate lab equipment and instruments, ensuring they meet the necessary technical specifications and compliance standards.

Arrange the installation and qualification of lab equipment including IQ/OQ/PQ (Installation Qualification/Operational Qualification/Performance Qualification).

Oversee laboratory layout design:


Develop an efficient and compliant lab layout that adheres to GMP requirements and supports optimized workflow.

Ensure that lab workstations, storage areas, and other lab spaces are designed to prevent cross-contamination and ensure safety.

Develop and implement standard operating procedures (SOPs):


Create and document SOPs covering all aspects of lab operations, including equipment use, maintenance, safety protocols, and testing procedures.

Ensure that SOPs are regularly reviewed and updated in line with regulatory changes and best practices.

2. GMP System Development:
Establish and maintain a robust GMP system:


Develop and implement a comprehensive GMP framework that includes all aspects of lab management and operations.

Ensure that QC processes align with GMP requirements to guarantee product quality and safety.

Develop and implement quality control procedures and protocols:


Design and document detailed QC procedures for sample testing, handling, and storage.

Implement protocols for method validation, calibration, and testing consistency.

Ensure proper documentation practices:


Maintain accurate and complete records of all lab activities, including test results, equipment logs, and compliance documentation.

Establish data integrity practices to ensure that all records are reliable and traceable.

3. Regulatory Compliance and Quality Assurance:
Ensure compliance with regulatory requirements:


Ensure all lab operations comply with relevant regulatory standards (e.g., FDA, EMA, and other international guidelines).

Stay updated on changes in regulations and industry standards to ensure ongoing compliance.

Coordinate and support for audits and inspections:


Prepare the lab for internal and external audits and inspections by regulatory bodies.

Collaborate with the quality department to manage audit findings and implement corrective actions.

Investigate and resolve quality-related issues:


Perform root cause analysis for any deviations, out-of-specification results, or laboratory incidents.

Develop and implement corrective and preventive actions (CAPAs) to address and prevent quality issues.

4. Collaboration and Communication:
Collaborate with cross-functional teams:


Work closely with RA, Manufacturing, engineering and QA teams to support the transfer and commercialization of biological drug products.

Provide QC expertise to support product development, process optimization, and troubleshooting.

Communicate effectively with stakeholders

Provide regular updates to internal and external stakeholders on lab activities, project progress, and compliance status.

Foster strong relationships with external partners and regulatory authorities to facilitate cooperation and compliance.

5. Other business activities:
Understand and support day-to-day operations of the QC lab:


Regularly review lab performance metrics and KPIs to identify areas for improvement.

Implement continuous improvement initiatives to enhance lab processes and productivity.

Leadership and project management

Promote members to complete tasks according to project goals

Have project node awareness and risk awareness, and actively communicate with project-related personnel, such as project stakeholders and project members.

As the project manager, manage project conflicts, manage risks, and drive project implementation.

Education/Qualifications

● Bachelor of Science Degree or above
● Pharmacy, Chemistry, Biochemistry and equivalent
● Master at analytical science of Biological Product;
● At least 4 years’ experience in analytical testing and method validation of biologics
● At least 2 years’ experience of project management.

Leadership Competencies

● Models Integrity
● Focus on value and customer
● Align for success
● Deliver results
● Learn for the future

Job Required Competencies

● Project management skills
● Leading team capability
● Language skills – English
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工作地點(diǎn)
地址:羅氏診斷產(chǎn)品(上海)有限公司
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