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Associate Scientist QC Release & Stability
We believe health is everything at Johnson & Johnson. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured. Through our expertise in Innovative Medicine and MedTech, we innovate across the full spectrum of healthcare solutions today to deliver breakthroughs tomorrow and profoundly impact health for humanity.
Main Responsibilities:
The Quality Control department involves validation and transfer of test methods and routine release and stability tests for novel clinical phase materials and ENVM/CVAL samples. Chemical methods range from RP, SEC, IC, TOC, Conductivity, and biochemical methods like SDS-PAGE and Capillary Electrophoresis.
Your Impact:
* Work according to general guidelines, procedures, and processes in QC, adhering to internal regulations.
* Be compliant with general guidelines, procedures, and processes in QC, following internal rules.
* Contribute to building a strong team to expand, strengthen, and maintain current knowledge base and expertise within QC.
* Adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance.
* Perform timely and cost-effective testing of samples at required cGMP level.
* Create and process ETS records as needed, and support investigations when required.
* Maintain devices and technical aids used in QC, including coordination of maintenance and calibration dates.
* Write technical reports and documents as needed.
* Perform laboratory duties to support department objectives.
* Review and evaluate analytical assays (cGMP) according to given timelines.
* Contribute to validation and verification of analytical methods.
* Work in a clean and tidy manner to be ready for inspection at all times.
* Obtain necessary materials and reagents for assigned tests, including ordering laboratory consumables.
* Assist in achieving departmental goals and commitments despite obstacles.
* Support implementation of new equipment in QC Release & Stability team.
* Drive continuous improvement projects in operational efficiency and GMP compliance.
* Train employees and coordinate employee qualification and re-qualification.
* Additional tasks may be given by the team leader.
* Achieve annual goals and objectives guided by Our Credo and Leadership Imperatives.
* KPI, release, and stability testing performed in defined time period.
* KPI, release, and stability no overdue ETS record.
You Bring:
We are looking for candidates with the following essential requirements:
Education & Experience:
* Profound working understanding of laboratory operations and practices.
* University degree in natural sciences, applied sciences, or equivalent.
Skills & Competences:
* Good communication abilities.
* Time and self-management skills.
* Good language skills in German and English, written and spoken.
* Analytical thinking and problem-solving abilities.
Your Mark:
By joining Johnson & Johnson, you will find opportunities to craft your path and amplify your impact inside and outside our walls. With our commitment to being the world's healthiest workforce, you can strengthen your body as well as your mind. When you work at Johnson & Johnson, you can touch over a billion lives worldwide every day. And when you apply your talent to our collective purpose, there's no end to the lasting impact we can make together.
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