Drug Product Lead Parenteral Iron — CSL Behring
NewCHF 94'500 - 143'000
CSL Behring · Bern (BE)
- Location
- Bern
- Contract
- full-time
- Posted
- Yesterday
SalaryCHF 94'500 - 143'000
Role overview
We are looking for a DP Lead parenteral Iron, to join our team in Zurich or St.
Gallen, Switzerland.
As part of the Integrated Product Team Iron & Small Molecules within Technical Operations, you will be responsible the scoping and execution of technical work packages related to CMC Development, Continuous improvement, and Technology Transfer of parenteral pharmaceutical products and manufacturing processes, as well as providing continuous MS&T support to external partners and CMOs to support routine manufacturing operations.
- We are looking for a DP Lead parenteral Iron, to join our team in Zurich or St.
- Gallen, Switzerland.
- Key Responsibilities
- Scoping of technical work packages for different types of projects (e.g.
Main responsibilities
- Key Responsibilities
- Scoping of technical work packages for different types of projects (e.g.
- CMC Development, Tech Transfer, Continuous Improvement) by defining technical implementation strategies, deliverables and technical risks
- Contribute to and review project execution plans (e.g. technical transfer plans)
- Execute DP related project work packages and tasks as subject matter expert for aseptic and terminally sterilized parenteral products manufacturing as per the project plan
- Proactively engage in periodic cross functional calls and meetings with internal and external team members
- Prepare regular status updates on assigned work packages and tasks as part of regular project reporting and stakeholder management
- Serve as a key technical contact for external partners and CMOs for assigned projects as well as for defined topics in routine manufacturing (including coordination and support in case of technical issues, process changes, major deviations, and improvement initiatives)
- Serve as a key subject matter expert for internal stakeholders (e.g. perform Change Control impact assessments and support quality event investigations)
- Support the evaluation of alternative, cost-effective sourcing strategies for related products as technical SME, including attending technical due diligence visits at potential future CMOs
Application process
- Minimum 5 years experience in the pharmaceutical industry, direct experience in full scale commercial manufacturing (compounding, aseptic filling, sterilization, CCIT/Visual inspection) of parenteral products for intravenous application
Company and context
- Self-driven and fast learner with the ability to take ownership execute work packages and tasks independently in a matrix organization
- Confident and proactive team player who collaborates effectively while working autonomously.
- Solid expert knowledge in sterile and aseptic fill & finish CMC development, Equipment -/Process Qualification & Validation, Manufacturing
- High Flexibility and willingness to travel & Experience in External Manufacturing Environment Preferred Requirements
- Familiarity with GMP requirements and Guidelines related CMC LCM activities, including Annex 1
- Preferably, experience with non-transparent solutions
- Know-how across various parenteral product primary packaging solutions (vials, ampoules, infusion bags)
- Experience in other Drug Product and Finished Product manufacturing & Technology Transfer, e.g. oral solid dosage forms
- Ability to work effectively in a multicultural and international environment Strong communication skills
- Analytical thinking & problem-solving skills Ability
Additional details
- Contribute to the establishing of business cases and decision-making processes on implementation of change Minimum Requirements
- High Flexibility and willingness to travel & Experience in External Manufacturing Environment
- Ability to work effectively in a multicultural and international environment Strong communication skills
- Analytical thinking & problem-solving skills
Notes and original content
- Contribute to the establishing of business cases and decision-making processes on implementation of change
- Skills & Experience
- Minimum Requirements
- Ability to work effectively in a multicultural and international environment
- Strong communication skills
