MSAT Intern 4640

MSAT Intern

As an MSAT Intern you will be responsible for supporting various aspects of the manufacturing process. This includes assisting in the documentation and optimization of manufacturing procedures conducting data analysis contributing to technology transfer activities and participating in validation processes. The intern collaborates with crossfunctional teams to troubleshoot issues identify opportunities for process improvement and actively engages in continuous improvement initiatives. Additionally the intern plays a role in ensuring compliance with regulatory requirements supporting safety protocols and contributing to the overall success of MS&T projects. The position requires a combination of technical knowledge analytical skills effective communication and a proactive approach to learning and problemsolving in a dynamic manufacturing environment.

Organization Description

WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. Were one of the worlds top three contract development and manufacturing companies for biopharmaceuticals we provide our clients with a worldleading open access technology platform. We enable our clients to research develop and manufacture from the concept phase to commercial manufacturing.

Our mission is to accelerate and transform discovery development and manufacturing in the rapidly growing field of biologics to benefit patients worldwide. We have sites/offices in China the US the EU Asia and Ireland. We currently employ over 10000 people and provide services to more than 600 customers worldwide including the top 20 biopharmaceutical companies.

Department Description

As an MSAT Intern youll be joining an organization where people of all backgrounds and experiences are respected and where we work together focused on changing our lives.

In this role youll be reporting to the MSAT Associate Director.

Your Responsibilities

In this role you will act on the following tasks:

Process Documentation and Optimization:

• Assist in the creation review and revision of manufacturing batch records standard operating procedures (SOPs) and other documentation.
• Collaborate with the MS&T team to identify opportunities for process optimization and efficiency improvements in bioprocessing.

Data Analysis and Reporting:

• Collect and analyze data from manufacturing processes to identify trends deviations and areas for improvement.
• Generate comprehensive reports summarizing key performance indicators (KPIs) and present findings to the MS&T team.

Technology Transfer Support:

• Support the technology transfer of new processes or modifications from development to manufacturing.
• Work closely with crossfunctional teams to ensure a seamless transition of processes into the production environment.

Validation Activities:

• Assist in the and documentation of validation protocols for manufacturing processes and equipment.
• Collaborate with the validation team to ensure compliance with regulatory requirements and industry standards.

Troubleshooting and Issue Resolution:

• Participate in investigations related to deviations nonconformances and outofspecification results.
• Work with the MS&T team to identify root causes and implement corrective and preventive actions (CAPAs).

Continuous Improvement Initiatives:

• Contribute to continuous improvement projects aimed at enhancing manufacturing processes reducing costs and increasing product quality.
• Provide input and recommendations for the implementation of best practices in bioprocessing.

Collaboration with CrossFunctional Teams:

• Work closely with research and development (R&D) quality assurance (QA) and production teams to foster effective communication and collaboration.
• Participate in crossfunctional meetings and provide input on processrelated matters.

Training and Development:

• Engage in ongoing learning and development opportunities to enhance knowledge of bioprocessing technologies and industry trends.
• Actively participate in training sessions and workshops offered by the MS&T department.

Compliance and Regulatory Support:

• Assist in ensuring compliance with regulatory requirements cGMP (current Good Manufacturing Practice) and other relevant standards.
• Contribute to the preparation of documentation for regulatory submissions and inspections.

Safety and Environmental Compliance:

• Adhere to safety protocols and guidelines in the manufacturing environment.
• Contribute to initiatives promoting environmental sustainability and compliance with relevant environmental regulations.

Project Management:

• Support project management activities including timeline tracking resource allocation and milestone achievement.

Your Profile

The ideal candidate for this position will have the following:

Education

• Currently pursuing a bachelors or masters degree in chemical engineering Biochemical Engineering Biotechnology or a related field.
• Strong academic performance with coursework relevant to bioprocessing and pharmaceutical manufacturing.

Knowledge/Experience

Technical Knowledge:

• Understanding of bioprocessing principles including upstream and downstream processing techniques.
• Familiarity with current Good Manufacturing Practices (cGMP) and regulatory requirements in the pharmaceutical industry.
• Proficiency in data analysis tools and software commonly used in bioprocessing.
• Ability to analyze complex data sets and draw meaningful conclusions.
• Problemsolving skills with a focus on identifying and addressing root causes.
• Proficiency in Microsoft Office Suite (Word Excel PowerPoint).
• Familiarity with data analysis and visualization tools (e.g. MATLAB R Python) is a plus.

Personal skills

• Excellent written and verbal communication skills.
• Ability to articulate ideas and findings clearly and concisely.
• Comfortable collaborating with crossfunctional teams and presenting information to various stakeholders.
• Demonstrated ability to work collaboratively in a teamoriented environment.
• Willingness to contribute actively to team discussions and share insights.
• Strong attention to detail ensuring accuracy in data analysis and documentation.
• Commitment to maintaining highquality standards in all aspects of work.
• Ability to adapt to a dynamic and fastpaced work environment.
• Openness to learning new technologies and techniques in bioprocessing.

As we extend our global reach we need colleagues interested in change in challenge and in building a new future together. Reach beyond yourself and discover your true potential!

If you have the ability to thrive in a dynamic and fastpaced environment and feel that the moment has come for you to be part of such an exciting journey towards accomplishing our vision Any drug can be made and any disease can be treated dont miss out on this opportunity to join us and reach beyond yourself and discover your true potential.

Apply now!

Would you like to know more before you apply Please visit us athttps:// contact us via

WuXi Biologics is an equal opportunities employer.