Staff Engineer MSAT Bio DP
vor 13 Stunden
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex 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
Job Function
Supply Chain Engineering
Job Sub Function
Process Engineering
Job Category
Scientific/Technology
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description
Cilag AG, part of Johnson & Johnson, is recruiting for a
Staff / Senior Engineer, LM DP STO
within Manufacturing Science and Technology (MSAT) team, located in
Schaffhausen, Switzerland.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex 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
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at
Come and join us to create a future where disease is a thing of the past. At our Schaffhausen Site we launch new products with focus on Parenteral Products (e.g., Prefilled Syringes and vials).
We belong to the Manufacturing, Science & Technology (MSAT) organization for the MTO (Manufacturing and Technical Operations) Large and Small Molecule Manufacturing Platform. We support Small Molecule API and Drug Product operations and the Parenteral small and large molecule Filling, visual inspection, device assembly and pack operations at JSC Schaffhausen, Janssen Supply Chain and currently we are looking for a MSAT Validation Staff Engineer to be based in Schaffhausen, Switzerland to join our team.
Position Summary
You will be the Site MSAT representative on cross functional teams owning the responsibility for the reliability of product processes of commercial product and new product introductions for non-biologic and biologic parenteral liquids, suspensions, and lyophilized products at the Schaffhausen Fill Finish site. You will provide the following:
- Technical support and leadership to top line growth
- Enhance reliability, compliance & efficiency of product value chains end to end
- Integrate Manufacturing Operations and Pharmaceutical Development in partnership with Product and Customer Management
Responsibilities
- Site Technical Owner for New Product Introductions, Tech Transfer Projects and specific commercial product
- Own and coordinate validation activities with internal partners
- Lead cross functional project teams
- Implement Process Capability/Quality/Cost Improvement Changes
- Provide Technical Assessments to Change Controls/CAPAs and Deviations
- Active participation in inspections as Subject Matter Expert
- Maintain excellent partnership with all business partners
- Execute statistical analyses on production data
Qualifications
- You have a Degree in Chemistry or Pharmacy or equivalent
- You have 4+ years of experience in the pharmaceutical sector overall with past proven field experience in the following areas:
- Parenteral drug product manufacturing
- Quality Assurance and Regulatory Compliance cGMP
- Leading GMP Investigations
- Experience in the following fields are of advantage, but not a must:
- DP manufacturing process validation
- Leading cross-functional teams and project
- Leading GMP investigations
- You have strong decision making and problem-solving competencies
- You are a flexible, motivated, and innovative team player
- You are open to new ideas and driving innovation
- You are proficient in English and you have basic German knowledge
We are offering
a multifaceted challenge in a dynamic, international environment with attractive terms and career opportunities as well as a good infrastructure at the Janssen site Schaffhausen.
- Many opportunities to work on exciting projects and assignments.
- Childcare benefit
- A broad spectrum of training opportunities to grow further for personal as well as professional development
- The Johnson & Johnson Pension Fund Switzerland offers attractive performance
- A range of benefits for insurance, products, sport, culture and much more
- 1 year limited contract to start with
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