Principal Scientist Stability - Boudry, Schweiz - Interiman

Interiman

Geprüftes Unternehmen

Boudry, Schweiz

vor 2 Wochen

Geschrieben von:

Lena Schneider

beBee Recruiter

Beschreibung

INTRODUCTION:

For our client, a leading international Pharmaceutical company, we are searching for a:

Principal Scientist Stability - 100% - 12 months temporary contract

English & French

This position is responsible for stability product strategy and oversight of product stability programs for commercial small molecules Drug Substances and Drug Products Oral and Sterile.

**DESCRIPTION DE LA MISSION: - Participates on transfer team for new products to internal and external sites (as required), reviews registrational stability studies and conducts gap analysis against Global Manufacturing & Supply requirements. Develops stability data where gaps exist

Develops and maintains expertise on the overall stability performance of products manufactured in the global supply chain, including maintaining a working knowledge of the attributes that impact the products' performance/stability profile
Serves as stability representative on project teams covering postapproval changes, designs and executes required premarket stability program in support of the change
Perform change control impact assessments and document the stability assessment in change controls
Review and endorse change controls as an expanded reviewer. Initiate change controls related to stability operations
Provide the technical requirements in a Master Stability Protocol, review and approve study specific protocols and /or batch enrollment forms
Responsible for the handling of annual commercial stability program for assigned products in coordination with sample management groups
Authors stability sections of CTD dossiers for postapproval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related responses to health authority inquiries
Serves as stability representative for OOT/OOS investigations, Market Action Fact Finding, and other investigations related to potential quality issues and/or deviations from standards
Leads work activities involving Change Controls and CAPA's
Identify information regarding stability program that may impact lab capacity, product studies or regulatory commitments directly, escalate promptly to management and act as required

PROFIL ATTENDU:

8 years of relevant work experience required, preferable in a Pharmaceutical environment
Expert Knowledge of US/EU/ROW Requirements, Corporate Directives and industry best practices
Knowledge of Drug Substance and Drug Product manufacturing and good understanding of analytical and/or Microbiology methods
Very good skills to drive development of technical or scientific initiatives for solving complex problems/issues; recommending and drive sciencebased decisions/ implementation of solutions
Experience with authorship and able to critically review investigations,interpret results, and generate technical conclusions consistent with Quality management principles
Good Knowledge of evaluation and interpretation of stability data using statistics software. Review data and demonstrated ability to recognize anomalous trends or results
Experience to oversee external service providers involved in stability studies
Significant experience on health authorities inspections on stability programs
Exhibit strong leadership and decision making skills
Advanced ability to work independently and collaboratively in a team matrix environment, contribute to a team based environment, promoting a high commitment to business goals and objectives
Advanced ability to prioritize objectives from multiple projects and ability to adapt to quick changes in schedules in order to accommodate priority requests

- ** Advanced knowledge in English and French