Location: Zurich / Zug
Country: Switzerland
Role: Consultant, Subject Matter Expert
Team: Pharma/Biotech
Review of batch documents for label release of API, Safety Assessment or clinical supply lots (bulk and packaged) to ensure conformance to appropriate regulatory requirements
GMP review of batch documents and disposition of Clinical Batches for use in clinical trials
Deviation and change handling for packaging, lab investigations and related records
Act as contact person for complaints and temperature excursions
Ensure quality and compliance of all qualifications documents
On behalf of Manager Quality Systems, review and approval of specifications for clinical use and of method validation summaries
Preparation and implementation of procedures related core tasks
Responsible for metrics related equipment qualification
Issue reports summarizing deficiencies and work with areas to execute remedial action
Communicate and resolve audit comments with client areas
Under supervision, or as part of a team, perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards
Review and approval of SOPs
University degree in Quality, Engineering, Sciences or another relevant discipline
At least 1-3 years of experience within a GMP-regulated environment, preferably in the Pharmaceutical or Medical Devices industry
Broad working knowledge of cGMP regulations; basic understanding of manufacturing process
Analytical and structured working style; strong attention to detail
Ability to effectively work as part of a multidisciplinary, international team
Fluency in English is required, German, French or Italian would be a plus
Please submit your online application in English or German language.
For further information, please contact our local Human Resources department.
At Consultys we want to make it easy for you to find and apply for a job, which is why we have listed here the most commonly
asked questions we receive regulary.
No, Consultys is neither headhunter nor a job agency. We are providing our clients local, operational, compliances services within an integrated team-approach. Consultys always owns the direct relationships to the responsible line manager(s) within the organization.
We offering our compliance services for LifeScience clients mainly in Switzerland, Germany, France and Belgium, locally.
In addition we are offering our Medical Device clients dedicated services in Product Certification and Mock-Inspections for the US market (FDA).
Consultys offers it`s compliance services, tools and solutions for LifeScience organizations of all sizes, from small start-ups, spin-offs (ETH, EPFL, …) to mid-size (KMU) and global companies with thousands of employees.
Once you apply to the position, you will be provided with an automatic email confirming that your application has been successful. Timeframes differ by team but you should expect an answer within a few weeks, usually this will be faster. Once you have applied for the first time, your profile will be stored in the system. You might be contacted by our recruiters or by our automatic matching tool of job opportunities of interest to you.
In any case, your resume/CV will remain in our database for up to 4 years and we might contact you during that time. If you would like to be removed from the database, please review the FAQ "How can I delete my profile from the Consultys Talent Pool listed below.
When applying for a position, your information will be made available to our recruiters. They will analyse your skills & experience and will compare it to the requirements of the position for which you have applied (as well as any other open position).
If we believe you match the requirements, we will contact you and, in a first phase, we will invite you for a telephone interview or physical interview (or videoconference interview); further interviews will be fixed when evaluated positively.