Emploi Regulation district de Boudry NE

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Celgene Corporation Temps plein Il y a un mois

monster.ch   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...Engineering. Operational experience supporting risk management and/or analytics activities in a pharmaceutical, medical device, or related regulated industry, is ; Minimum of 3 years of experience with risk management/analytics approaches. Advanced degree may be substituted for...  >>

il y a 2 jours

Perreux, Boudry, NE

Celgene   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...should have solid experience working in the pharmaceutical industry, including expertise interpreting and applying legislation and regulations in the EMEA region. Additional geographic experience would be welcome. This role requires an operational and strategic engagement...  >>

Celgene Temps plein il y a 11 jours

monster.ch   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...and direct experience of leading regulatory strategy development and execution required. • In depth knowledge of current global regulations and guidances ( EU, ICH etc) essential as they relate to the overall global regulatory strategy. • Regulatory experience and knowledge...  >>

Celgene Corporation Temps plein il y a 29 jours

monster.ch   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...implementation experience a plus. • Requires an in-depth knowledge of quality control systems, including FDA and EU compliance standards, regulations, and guidelines. • Requires experience with analytical development and validation in support of all stages of drug development...  >>

il y a 3 jours

Perreux, Boudry, NE

Celgene   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...discipline. ~ Some experience in pharmaceutical industry for QA/QC-related function is an asset ~ Knowledge of international GxP regulations, 21CFR11, and good documentation practices. ~ Knowledge of pharmaceutical facilities, manufacturing, and laboratory systems....  >>

il y a 2 jours

Celgene   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...development to ensure ongoing alignment with clinical, regulatory and commercial strategies; • Ensure compliance with current EU regulations, guidances and templates. Have confident ability to discuss these guidances in project meetings; • Act as the Subject Matter...  >>

il y a 19 jours

Celgene   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...for salaries, payroll-related taxes and social charges for EMEA. 3. Ensure compliance with governmental and local labor and tax regulations for multiple international affiliates, in cooperation with outsourced consulting services and Celgene Management. 4. Ensure timely...  >>

Il y a un mois

Celgene   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...processes, including labelling requirements throughout the product lifecycle. ~In-depth knowledge of health authority labelling regulations in Europe and ROW. ~Writing, editing, and proofreading skills, with attention to detail. ~In-depth knowledge of labelling layout...  >>

Il y a un mois

Celgene   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...willingness to challenge the status quo & take calculated risks • Understands contributions of other departments & external stakeholders • Understands & utilises knowledge of local regulations & business practices when working across cultures • Ability to travel...  >>

Il y a un mois

Celgene   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...budget management tools  Familiarity with the pharmaceutical industry¸ healthcare compliance, Principles of Good Clinical Practice, regulations and regulatory guidelines regarding clinical trials and non-interventional studies  Understand the drug development process ...  >>

il y a 14 jours

F freelance.de   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...Technical Profile Requirements: * Must be able to lead and give direction to Validation Projects. * Minimum of 2 years working in a regulated environment, a minimum 1 of which has been spent carrying out validation activities. * English and German spoken and written....  >>

il y a 3 jours

F freelance.de   -   [ Sauvegarder l’offre ] [ Supprimer ] [ Ouvrir un emploi enregistré ]

 ...suppliers in product life cycle management projects. * Support to ensure the design transfer is performed according to the QMS regulation. * Pragmatic but compliant application of the PLCM process. * Ensuring the Risk Management process is followed. * Improvement...  >>

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