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Associate Scientist QC Release & Stability
At Johnson & Johnson, we believe health is everything.
We are committed to building a world where complex diseases are prevented, treated, and cured through our expertise in Innovative Medicine and MedTech.
Our strength in healthcare innovation empowers us to deliver breakthroughs today and profoundly impact health for humanity.
Learn more at www.jnj.com.
Key Responsibilities:
The Quality Control department plays a crucial role in validating and transferring various test methods.
They also perform routine release and stability tests for novel clinical phase materials as well as ENVM and CVAL samples.
The chemical methods applied in-house range from RP, SEC, IC methods, TOC, Conductivity, and a broad range of biochemical methods such as SDS-PAGE and Capillary Electrophoresis.
Your Impact:
* Work according to general guidelines, procedures, and processes in the QC in accordance with internal regulations.
* Be compliant with general guidelines, procedures, and processes in the QC in accordance with internal rules.
* Help build a strong team to expand, strengthen, and maintain the current knowledge base and expertise within QC to reflect changing business needs.
* 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 resulting from operational activities, stability programs, and monitoring.
* Create and process ETS records if needed, and support investigations when required.
* Maintenance, care, and GMP-compliant handling of devices and technical aids used in the QC.
* Write technical reports and documents if needed.
* Perform laboratory duties to support department objectives.
* Periodic review and evaluation of analytical assays (cGMP) according to given timelines if needed.
* Contributing to the 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.
* Assist in and drive achievements of departmental goals and commitments.
* Support implementation of new equipment in the QC Release & Stability team.
* Drive continuous improvement projects within Quality Control in operational efficiency and GMP compliance.
* Training of employees and coordination of employee qualification and re-qualification.
* Additional tasks can be given by the team leader.
* Delivery on annual goals & 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.
About You:
We are looking for an individual with the following essential requirements:
Education & Experience:
* A profound working understanding of laboratory operations and practices.
* A university degree in natural sciences, applied sciences, or equivalent.
Skills & Competences:
* Good communication abilities.
* Time and self-management.
* Good language skills in German and English, written and spoken.
* Analytical thinking and problem-solving abilities.
Your Opportunity:
By joining Johnson & Johnson, you will find boundless opportunities to craft your path and amplify your impact inside and outside our walls.
And 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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