Associate Scientist QC Raw Materials

vor 4 Stunden

Bern, Schweiz Johnson & Johnson Vollzeit

Job Description - Associate Scientist QC Raw Materials (2506230886W)

Associate Scientist QC Raw Materials - 2506230886W

Description

Johnson & Johnson Innovative Medicine Bern are 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 https://www.jnj.com/.

For our site in Bern, we are looking for an open minded, goal driven, motivated Associate Scientist QC Raw Materials.
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 phase. 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/tasks

  1. Performs timely and cost-effective analytical tests of raw materials according to internal (TMDs) and/or external (e.g., EP, USP, JP, ISO) requirements
  2. Operates efficiently analytical instruments and supports equipment periodic maintenance and calibration tasks timely execution
  3. Supports raw material sampling activities, i.e., sampling, cleaning, monitoring
  4. Supports training and qualifications of team personnel
  5. Supports timely and effective completion of lab events, investigations and CAPAs related to OOS and non-conformances
  6. Performs laboratory duties to support department objectives
  7. Supports method qualification, verification and validation activities, if required
  8. Writes technical documents, e.g., Verification/Validation plans, Reports, …
  9. Supports laboratory management activities, e.g., planning activities covering end-to-end raw materials process
  10. Leads and supports continuous improvement projects within Quality Control in operational efficiency and GMP compliance
  11. Complies with all applicable health, safety and environmental regulations, processes and guidelines
  12. Provides support to analytical development, process development and other stakeholders when the need arises
  13. Supports inspection preparations, execution and follow-up
  14. Supports to build and expand a strong team

Qualifications

We would love to hear from you, if you have the following essential requirements:

  1. University degree in natural sciences, applied sciences, or equivalent and work experience in the pharmaceutical, biotech or vaccine industry
  2. At least 3 years experience in a cGMP regulated environment and competence in microbiology techniques
  3. Sound knowledge of analytical laboratory operations and practices
  4. Well organized, a self-starter, results oriented individual with the ability to multitask in a fast-paced team environment with attention to detail and good documentation practice
  5. Strong strategic and conceptual skills, analytical thinking and problem-solving ability
  6. Good communication abilities
  7. Proactive attitude that challenges the status quo, team player and team builder
  8. Ability to manage multiple projects, tasks and assignments simultaneously and prioritize accordingly
  9. Able to work independently and take ownership of assigned task to plan and execute according to agreed deadlines
  10. Good IT user skills
  11. Good verbal and written skills in English and German

Why Join Us

  1. Be part of a world-leading healthcare company committed to improving the lives of patients worldwide.
  2. Collaborate with a highly skilled and dedicated team in a state-of-the-art facility.
  3. Contribute to our sustainability goals by ensuring efficient and balanced facility operations.
  4. 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.

Primary Location

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

If you are an individual with a disability, please check our page for information on how to request an accommodation.

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