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Urgent! Technical Specialist 3 (Deviation Investigation) Job Opening In Singapore, Singapore – Now Hiring Lonza
Lonza is the pioneer and world leader in the CDMO industry operating across 5 continents, setting the pace with cutting-edge science, smart technology and lean manufacturing.
We turn our customers’ break-through innovations into viable therapies and manufacture the medicines of tomorrow.
At the heart of every scientific breakthrough are talented individuals collaborating to develop solutions that empower businesses to improve lives.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
As a Biotechnologist at Lonza Mammalian business, you’ll be part of our globally recognized network, driving the production of mammalian cell culture and treatments.
Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation, and make a difference from day one.
Learn new skills and capabilities, and grow your career with us in manufacturing therapeutic proteins under cGMP conditions.
Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.
The Technical Specialist is responsible for performing Readiness, Release and Run aspects of Manufacturing Operations as assigned.
This role will also be involved in driving continuous improvement initiatives within Manufacturing.
What you’ll get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Daily company bus from the MRT location near your home to and from the Tuas site.
Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
The full list of our global benefits can be also found on .
What you’ll do
Readiness
Lead and support all tasks associated with operational readiness for technology transfers and process campaigns.
Develop / revise the Master Batch Records (MBRs) in support of technology transfers/ process campaigns with technical information / instructions that meet the user requirements as well as approval of MBR template/ structures.
Initiate and complete the change request prior to the start of a required process run.
Support with creation / revision of risk assessments such as operational, safety and data integrity risk assessments.
Support equipment, material or supplier qualification activities related to Manufacturing.
Run
Prepare and support the assessment / rating of manufacturing deviations at the Deviation Review Board (DRB).
Handle rejected materials through defective material inspections, review and assess vendor reports for operational improvements.
Participate in Customer and Regulatory Audits to present relevant topics (e.g. Deviation, Change Requests, CAPA, etc.)
Support with follow-up audit requests such as follow-up action from audits.
Release
Lead investigations for deviations, non-conformities, trends and / or abnormalities which occur on product floor.
Conduct root cause analysis using standard methodologies such as 5 Whys, Ishikawa Diagrams, causal branching, event and causal factor charting, Failure Mode, Effect and Cause Analysis (FMECA).
Interact with customers in the form of face to face meetings and / or teleconferences to communicate investigation findings / outcomes to the customer.
Ensure timely investigation and closure of deviation reports in support of lot disposition.
Generic
Additionally participate or lead and facilitate continuous improvement initiatives pertaining to Manufacturing Technical Team (MTT) and / or Manufacturing operations.
Collaborate interdepartmentally to drive assigned tasks to completion
Perform other tasks assigned by your Lead / Manager.
What we are looking for
Preferably a degree in Chemical/ Biochemical/ Pharmaceutical Engineering or Science.
Over 5+ years of experience in Manufacturing or Biopharmaceutical processing, experience in Deviation Investigation and/or Technical Writing experience mandatory.
Familiarity FDA & EMA GMP and regulatory requirements.
Ability to lead and optimally facilitate discussion / projects in cross functional team
Proficient communication abilities with internal and external customers
Ability to lead projects under timelines
Advanced knowledge in navigating through Controlled Document Management System (DMS) and Quality Management system (Trackwise)
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically .People come to Lonza for the challenge and creativity of solving sophisticated problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a relevant difference.
✨ Smart • Intelligent • Private • Secure
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Unlock Your Technical Specialist Potential: Insight & Career Growth Guide
Real-time Technical Specialist Jobs Trends in Singapore, Singapore (Graphical Representation)
Explore profound insights with Expertini's real-time, in-depth analysis, showcased through the graph below. This graph displays the job market trends for Technical Specialist in Singapore, Singapore using a bar chart to represent the number of jobs available and a trend line to illustrate the trend over time. Specifically, the graph shows 11698 jobs in Singapore and 10267 jobs in Singapore. This comprehensive analysis highlights market share and opportunities for professionals in Technical Specialist roles. These dynamic trends provide a better understanding of the job market landscape in these regions.
Great news! Lonza is currently hiring and seeking a Technical Specialist 3 (Deviation Investigation) to join their team. Feel free to download the job details.
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An organization's rules and standards set how people should be treated in the office and how different situations should be handled. The work culture at Lonza adheres to the cultural norms as outlined by Expertini.
The fundamental ethical values are:The average salary range for a Technical Specialist 3 (Deviation Investigation) Jobs Singapore varies, but the pay scale is rated "Standard" in Singapore. Salary levels may vary depending on your industry, experience, and skills. It's essential to research and negotiate effectively. We advise reading the full job specification before proceeding with the application to understand the salary package.
Key qualifications for Technical Specialist 3 (Deviation Investigation) typically include Life, Physical, And Social Science Technicians and a list of qualifications and expertise as mentioned in the job specification. Be sure to check the specific job listing for detailed requirements and qualifications.
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Here are some tips to help you prepare for and ace your job interview:
Before the Interview:To prepare for your Technical Specialist 3 (Deviation Investigation) interview at Lonza, research the company, understand the job requirements, and practice common interview questions.
Highlight your leadership skills, achievements, and strategic thinking abilities. Be prepared to discuss your experience with HR, including your approach to meeting targets as a team player. Additionally, review the Lonza's products or services and be prepared to discuss how you can contribute to their success.
By following these tips, you can increase your chances of making a positive impression and landing the job!
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