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Company: Amavita Chemical & Pharmaceutical industry
Associate Scientist QC Raw Materials
Johnson & Johnson Innovative Medicine in Bern is recruiting for an Associate Scientist QC Raw Materials.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where sophisticated diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at www.jnj.com.
For our site in Bern, we are looking for an open-minded, goal-driven, motivated Associate Scientist QC Raw Materials.
The QC Raw Materials team is involved in the qualification and validation of various test methods and the performance of sampling and routine release tests for raw materials used in both clinical and commercial production phases. The methods used for routine release tests include qualitative and quantitative analysis tests, ranging from wet chemistry tests (e.g., Ion ID test, TLC, Titration) to instrumental analysis tests (e.g., FTIR, pH, Conductivity, Density, Refractometry, Osmometry).
Responsibilities
* Perform timely and cost-effective analytical tests of raw materials according to internal (TMDs) and/or external (e.g., EP, USP, JP, ISO) requirements.
* Operate analytical instruments efficiently and support equipment periodic maintenance and calibration tasks.
* Support raw material sampling activities, including sampling, cleaning, and monitoring.
* Assist in training and qualifications of team personnel.
* Ensure timely and effective completion of lab events, investigations, and CAPAs related to OOS and non-conformances.
* Perform laboratory duties to support department objectives.
* Support method qualification, verification, and validation activities as required.
* Write technical documents, including Verification/Validation plans and Reports.
* Support laboratory management activities, including planning activities covering end-to-end raw materials processes.
* Lead and support continuous improvement projects within Quality Control for operational efficiency and GMP compliance.
* Comply with all applicable health, safety, and environmental regulations, processes, and guidelines.
* Provide support to analytical development, process development, and other stakeholders as needed.
* Assist in inspection preparations, execution, and follow-up.
* Support building and expanding a strong team.
Minimum Requirements
* University degree in natural sciences, applied sciences, or equivalent with work experience in the pharmaceutical, biotech, or vaccine industry.
* At least 3 years of experience in a cGMP regulated environment and competence in microbiology techniques.
* Sound knowledge of analytical laboratory operations and practices.
* Well organized, self-starter, results-oriented individual with multitasking ability in a fast-paced team environment, attention to detail, and good documentation practice.
* Strong strategic and conceptual skills, analytical thinking, and problem-solving ability.
* Good communication abilities.
* Proactive attitude that challenges the status quo; team player and team builder.
* Ability to manage multiple projects, tasks, and assignments simultaneously and prioritize accordingly.
* Able to work independently and take ownership of assigned tasks to plan and execute according to agreed deadlines.
* Good verbal and written skills in English and German.
Why Join Us
* Be part of a world-leading healthcare company committed to improving the lives of patients worldwide.
* Collaborate with a highly skilled and dedicated team in a state-of-the-art facility.
* Contribute to our sustainability goals by ensuring efficient and balanced facility operations.
* Opportunity for career growth and professional development. Apply now to join our team and contribute to our mission of advancing health and well-being through innovative solutions!
Diversity, Equity & Inclusion at Johnson & Johnson means “YOU belong”!
For more than 130 years, diversity, equity & inclusion have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.
That is why we are working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued, and every one of our people feels that they belong and can reach their potential. No matter who they are.
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