Senior Scientist QC mRNA
View: 169
Update day: 26-03-2024
Category: Pharmaceutical / Chemical / Biotech Consulting / Customer Service Information Technology
Industry:
Job content
Summary
As a part of the QC the Senior Scientist has the responsibility of the release analytics for a broad range of analytical methods regarding biopharmaceutical molecules. (usage for clinical and commercial purposes).
Accountabilities
- Coordination of projects and taking care for the technical realization of project steps during method transfer and consulting on projects after method transfer
- Reporting on project progress and the escalation of issues when they occur
- Initiation and completion of necessary process change controls, deviation and laboratory investigation reports
- Responsible for providing and organizing adequate training to QC associates in order to enhance the site level compliance cGMP knowledge
- Proactive follow-up on development activities within the applicable discipline as well building up and sharing of knowledge within the QC department
- Creation, revision and review of cGMP documentation (SOP’s, Quality Instructions, protocols, reports…) based on a standard format related to quality control activities.
- Participate in project related audits if applicable
Candidate profile:
- PhD degree in chemistry, biochemistry or equivalent education; or experienced professional with a Bachelor’s or Master’s Degree in a scientific discipline
- Experiences: o Expert scientific knowledge in the field of analytical chemistry, focus HPLC o Versed with regulations (GMP & ISO 9001)
- Languages: Good English skills, German beneficial
- IT skills: Software use in OC like LIMS, Empower, DMS etc.
- Soft skills:
o Good communication skills
o Ability to work independently and a deep sense of responsibility
Application open to any EU candidates, due to the competitive salaries, no relocation packages are included, the successful candidate will be required to relocate to the location.
Contract renewal and/or permanent contract is entirely dependent on the job performance.
Contract length: 12 months
Job Types: Full-time, Contract
Ability to Commute/Relocate:
- 3930 Visp, VS: Reliably commute or planning to relocate before starting work (Required)
Education:
- Doctorate (Required)
Experience:
- field of analytical chemistry, focus HPLC: 1 year (Preferred)
- GMP & ISO 9001: 1 year (Preferred)
- Software use in OC like LIMS, Empower, DMS etc: 1 year (Preferred)
- QC Mammalia in interdisciplinary project teams: 1 year (Required)
- Biopharm: 1 year (Required)
License/Certification:
- EU Passport (Required)
Work Remotely:
- No
Deadline: 10-05-2024
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