.... Als Ergänzung für unser Team suchen wir per sofort oder nach Vereinbarung eine motivierte Persönlichkeit als
Mitarbeiter:in Drug Regulatory Affairs, 80 - 100% (w/m/d)
Helfen Sie uns, Arzneimittel für die integrative Onkologie auf den Markt zu bringen, indem Sie, dank...
Empfohlen
...Development is responsible for the development and support of drug delivery devices for the product portfolio. The activities span... ...products and medical devices to the market
Apply knowledge of the regulatory landscape to ensure standard compliant designs (e.g. ISOCFR820...
Empfohlen
Vollzeit
Homeoffice
Remote job
...Adecco
Injectable Drug Packaging Engineer 100% (m/f/d/)
Location Basel, Basel
Category
Life Sciences
~ Contract Type... ...JN-032024-573523
Are you driven by a passion for ensuring regulatory compliance within the pharmaceutical industry? Our client in Basel...
Empfohlen
Vollzeit
Temporär
Adecco
Basel BS
Vor einem Monat
...We have an exciting opportunity for a Drug Safety Physician (m/w/d) in Switzerland
Tasks
You are responsible for safety aspects... ...of safety reports (DSUR PSUR/PBRER).
Contributes to key regulatory safety documents including RSI in the IB and RMP/REMS.
Review...
Empfohlen
Vollzeit
...covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for a:
Drug Regulatory Affairs Clinical Trial Manager 100% – 5716 LBD
10-month contract based in Basel area with possibility for extension....
Empfohlen
...13 major submissions and 2,000 associates worldwide. That was Regulatory Affairs in 2020. We are a culturally diverse, global team of talented... ...negotiations
• 2-4 years involvement in regulatory and drug/biologic development spanning activities in Phases I-IV in the...
Empfohlen
Invalidenversicherung
...industry and the academic sphere.
Job Description
One of Sobi’s four strategic pillars is to “Go Global”. The Manager, Regulatory Affairs International supports our ambitious geographical expansion plans. Sobi is seeking to register some of our existing...
Empfohlen
Vollzeit
...Zum Inhalt springen Siegfried Menü Siegfried
~ Siegfried
~ Current lang
Programm Manager Drug Substance (PM)
Allgemeine Informationen
Land Schweiz
Stadt Zofingen...
Empfohlen
Vollzeit
Unbefristete Arbeit
Siegfried AG
Zofingen AG
Vor einem Monat
Technical Project and Product Leader in Drug Subst
~Salary: CHF 86.44 – CHF 94.91 ph all-in
~REF Number: 00056626
~Consultant: Adrien Guimard
~Contact: (***) ***-****
~Date Published: 13.02.2024
~Sector:
~Location: Basel,
~Discipline:
QLS are recruiting...
Empfohlen
Homeoffice
Job Purpose
Be a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Canada, perform product registration in EU, US & Canada.
Main Tasks and Responsibilities...
Empfohlen
Vollzeit
...Lonza AG
QA Expert / Senior QA Specialist Instrument Qualification, Drug Product Services (m/f/d)
Switzerland, Basel
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how...
Empfohlen
Lonza AG
Basel BS
Vor 11 Tagen
...approaches and ground breaking technology, IMM strives to develop drugs that improve the lives of individuals suffering from autoimmune... ...will include:
• Contribute to the Biomedical Research drug discovery process with the goal to discover and develop novel therapeutic...
Empfohlen
Vollzeit
Postdoc Stelle
Beschreibung
- Ensure compliance with regulations throughout product development.
- Conduct regulatory research and prepare documentation for submissions.
- Support regulatory audits and assist in strategy development.
Motivation
Would you like to be part of a pharmaceutical...
Empfohlen
Temporär
...Tätigkeitsgebiet
Mitarbeit im Regulatory Affairs Bereich
Chargenfreigabe medizinischer Gase
Schulung und Qualifizierung von Mitarbeitern auf arzneimittelrechtliche Inhalte
Lokaler Pharmakovigilanz-Beauftragte
Anforderungsprofil:
Berufserfahrung im GMP...
Empfohlen
Selbständige Tätigkeit
Ferienjob
Homeoffice
...Omya AG
Group Regulatory Affairs Manager & Quality Management for Consumer Goods 100%
Establish and maintain strategy to ensure regulatory compliance of new as well as already marketed food additive, pharmaceutical and cosmetic raw materials
Coordinate Regulatory...
Empfohlen
Omya AG
Oftringen AG
Vor einem Monat
Senior Consultant Regulatory Affairs MedTech (SaMD, AI, Robotics)
Compliance Services - Basel, Frankfurt
Apply now
About Arcondis
Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries. Headquartered...
...Recruiter: Anil Dahiya
Technical Project & Product Lead – Drug Product (Oral Dosage) – 5752 ADA
Our client, an innovative... ...execution of the overall CMC strategy.
~Ensure compliance with regulatory guidelines.
Qualifications and Experience:
~Relevant Swiss...
...Inflection Points (on time and on budget)
Establish and oversee the execution of robust integrated drug development plans that are patient focused and address regulatory commercial and access considerations
Drive decisionmaking for budget and resource commitments....
Vollzeit
...products across various stages of clinical development to facilitate regulatory submissions.
Your tasks:
Develop a thorough understanding... ...regulatory submissions.
Comprehensive understanding of the drug development process.
Knowledge of GCP and ICH Guidelines....
Soforteinstellung
...the CHAD department (internal/external).
Assist the Technical Regulatory Department and the New Chemical Entities Department with paper... ...regulatory knowledge in a specific area.
Basic knowledge of drug development.
Detailed knowledge of Good Manufacturing...
Temporär
...diverse, ambitious and innovative environment, the path to bring drug candidates from early research into development.
We... ...deficiencies, propose solutions, and effectively interpret and apply regulatory requirements; excellent communication skills; ability to collaborate...
...diverse, ambitious and innovative environment, the path to bring drug candidates from early research into development. We collaborate... ..., propose solutions, and effectively interpret and apply regulatory requirements.
You demonstrate excellent communication skills...
...external guidelines regarding quality and safety (Quality Manual, regulatory cGMP guidelines, Health Authority guidances, SOPs etc.).... ...regulatory knowledge in a specific area.
Basic knowledge of drug development.
Detailed knowledge of cGMP, working knowledge of...
Soforteinstellung
...Ridgeline has assembled an international team of 50 highly experienced drug discovery and industry professionals and built and operated... ...versed in Swiss Code of Obligations
Experience with Swiss regulatory requirements, VAT filings, Stamp Tax filings, and other tax...
Vollzeit
Unternehmer
Weihnachten
Flexible Arbeitszeit
RIDGELINE Discovery GmbH
Basel BS
Vor 11 Tagen
...Commissioning & Qualification (C&Q) compliance of an aseptic fill-finish drug product manufacturing facility CAPEX project. Key responsibilities: - Responsible for the quality oversight and regulatory aspects of the assigned CAPEX project - Ensuring C&Q compliance of GMP...
Vollzeit
Swisslinx
Aarau AG
Vor 10 Tagen
...in future.
This specific role will take care of biological Drug Substance activities, mainly related to Upstream.
Key Responsabilities... ...and be an effective decision maker.
Experience of regulatory guidelines, regulatory authorities’ communication and file...
Vollzeit
Flexible Arbeitszeit
...Quality Agreements where needed.
Interface between quality/regulatory/compliance personnel and operations to identify applicable regulatory... ...as a Lead Auditor.
Knowledge and understanding of drug product development, manufacturing processes, quality control,...
...of patients and to be in compliance with GVP, GCP and worldwide regulatory requirements. You will also be working cross functionally... ...pharmaceutical industry, preferably in Patient Safety and/or Clinical/Drug Development, or at a regulatory agency
Previous experience...
Vollzeit
...reviewing GMP-relevant deliverables to ensure compliance with regulatory guidelines and project quality standards
Maintaining strict... ...environmental regulations and guidelines
~ Basic understanding of drug development processes and regulatory requirements
~...
...supplier selection input.
Candidate Requirements:
- Knowledge of GMP/regulatory requirements, a strong background in analytical chemistry is required.
- Basic knowledge in synthetic chemistry, drug substance processing and/or formulation development.
- Experience in...
Vollzeit
Soforteinstellung