For our client, an international pharmaceutical company, we are in search for a Validation expert for temporary assignment until the end of 2019 with a possibility of extension.
What the company offers you:
An international environment
Company is easily reachable by car or public transport
Temporary assignment until the end of 2019 with a possibility of extension
Competitive salary
Your responsibilities:
Leading, facilitating, elaborating and authoring risk assessments for validation together with the site validation team (PU, QC, QA ) and external functions (TRD, DRA)
Authoring and reviewing process, packaging or cleaning validation protocols (e.g. launches, transfers, weak point remediation) and related reports, proposes and reviews MBRs and associated change controls
Supporting the strategy for continued process verification (CPV) and annual monitoring batches that ensures all critical process parameters and quality attributes are defined after validation activities
Providing technical expertise and participating in the improvement and remediation of products in the product improvement portfolio
Your profile:
BSc. in Chemistry, Pharmacy, Chemical Engineering or Pharmaceutical Technology
Fluent in English and in local language
Several years experience in manufacturing/ manufacturing science and technology/technical development/Quality
Strong working knowledge of quality systems and regulatory requirements across multiple health authorities
Experience in executing process validation
Welcome to nemensis!
We are looking forward to getting to know you!online bewerben
Ihr direkter Kontakt:
Anastasiya Sakalouskaya Kägenstrasse 18 4153 Reinach Jetzt per E-Mail oder telefonisch bewerben
Tel.: +41 61 205 98 70 E-Mail: Diese E-Mail-Adresse ist vor Spambots geschützt! Zur Anzeige muss JavaScript eingeschaltet sein!
