Ich Q7 Jobs in Abu Dhabi

Qualifications Master scientific degree or equivalent experience. 4 - 6 years' experience in pharmaceutical or chemical industry. Knowledge of cGMP/Qualification compliance (21 CFR Parts 211; EU Directive 2003/94/EC and annex 15; ICH Q7,...) Experience with Equipment Quali More...

Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: BSc in Scientific Discipline Minimum 5 years' demonstrated experience in the Pharmaceutical Industry in leading the technical aspects of the product li More...

Uses regulatory guidance and industry best practice, and scientific and technical experience, to develop innovative approaches to process or viral clearance or process validation. Plans, executes and reports process or viral clearance validation studies through process sciences More...

Role Requirements Sound knowledge (10-12 years) of tablet dosage with subject matter expertise in FBP granulation (Top spray, bottom spray) & Sugar-coated tablet techniques, Hard Gelatine capsules dosage form, Injection dosage form is a needed skill for the role. Ex More...

Hallo liebe Freiberufler, für ein Kundenprojekt suche ich aktuell nach einem freiberuflichen Coach für den Bereich Data Analytics (M/W/D), der einen Kurs in Berlin auf Basis eines bereits feststehenden Curriculums leiten soll. Eckdaten: Start: asap Dauer: 3-6 Monate (+ V More...

Für ein renommiertes Unternehmen suche ich zur Erweiterung des Teams einen erfahrenen Auditor (m/w/d) im Raum Frankfurt. Ihre Aufgaben Vorbereitung, Planung und Durchführung von Prüfungen gemäß internen und externen Anweisungen und Vorschriften Mitwirk More...

Job Description Job Description Pharmaron is a leading clinical research company, and we are currently looking for a Clinical Research Nurses to join our team on a part-time basis in Baltimore, Maryland. The Clinical Research Nurse participates throughout the entire clinical trials More...

Develop and perform assays that support development, release and stability testing of pharmaceutical drug substance and drug products. Documents laboratory work in accordance with GxP expectations, company policy, and legal requirements. Review of experiments, stability protoc More...

Key Duties And Responsibilities Lead Quality Event Management activities related to the investigation, root cause analysis and development of corrective action/ preventive action plans for GCO assigned events, including unplanned deviations, corrective/ preventive actions and ef More...

Principal InvestigatorLady Lake, FLThe Principal Investigator (PI) promotes International Council for Harmonization - Good Clinical Practice (ICH-GCP) in the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of study s More...

Job Description: Our client is seeking a Clinical Systems Administrator to lead the User and Site Account Administration within all clinical systems across the clinical platform. This position will initiate best practices and processes related to user and site account managemen More...

Description: Performs site qualification, initiation, interim and close-out monitoring visits. This role ensures compliance with clinical trial protocols and regulations. Conducts monitoring visits at sites to perform source data verification and study file (regulatory) review More...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Apex Systems, is seeking the following. Apply via Dice today! Job#: Job Description: Clinical Scientist (Part-Time) Location: Cambridge MA (Hybrid) Science: CRISPR/Cas9 Therapeut More...

How you will contribute: Leads the Early Development Pharmaceuticals GRA CMC regulatory team in the development and implementation of global CMC regulatory strategies during development ,commercialization and post approval LCM stages Combines knowledge of scientific, regulatory More...

Overview:The QC department is responsible for microbiological and analytical cGMP testing of sterile and non-sterile products, raw materials, components and utilities. This includes routine microbiological and analytical testing of products for release and stability, development and More...

Responsibilities: Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring the recording of trial in compliance with project goals. Creating and implementing study-specific clinical monitoring tools and documents. Creating and overseeing the t More...

Develop complete technical/, functional understanding of existing IT solutions from support, continuity and development perspective and use that understanding in ensuring continuity, enhancing existing systems and delivering new solutions while working in coordination with all stakeho More...