Position: CD Process Integration Officer
The Clinical Development Process Integration Officer is responsible for developing, implementing, maintaining and improving the CD Quality System (QS) documents in close collaboration with all CD Functions, for driving the management of process-related QS documents and CAPAs, for ensuring Inspection readiness, and for monitoring regulatory compliance of our CD QS documents.
Key Factors for Decision making:
Musts: 10 year experience in pharma including cross functional disciplines, experience of driving business process improvement projects
Education: University degree
Work Experience:
*10 or more years experience in the pharmaceutical industry, must include cross functional disciplines
*Proven prior experience in the management of clinical Quality System documents
*Extensive facilitation and presentation skills
*Experience of driving business process improvement projects
*Excellent verbal and written communication skills
*Demonstrated analytical skills
*Proven track record of effective persuading and influencing skills
*Ability to manage people and to provide clear direction and coordinating actions
*Computer systems and software experienced user
€130 - €150 per annum + CHF
Basel, Switzerland
Main requirements:Ten (10) plus years of experience in clinical requirement: development and the pharmaceutical industry preferably with at least 3 years in Quality Assurance/ Compliance roles. Thorough and extensive knowledge of international GCP regulations including FDA/EU GCP, ICH, pharmacovigilance, new drug regulations, other key HA guidance’s, and current industry practice. Main responsibilities:Support Development Project Teams with adequate quality and compliance guidance /Provide quality and compliance guidance for the development and implementation of corrective and preventive actions/ Monitor their status and timely closure /Ensure adequate regulator y inspection and audits preparation
€700 - €900 per day
Basel, Switzerland
*3 – 5 years previous experience in a labeling role or vendor management role with some of that specifically related to translations *Experience working in global/multi-national pharmaceutical environment and working in drug development.*Must be able to work independently in complex matrix team environments and have demonstrated ability to manage cross-functional teams
For more information please contact with: Agness +44 2072556665 or Agness.Slomska@secpharma.com
£40000 - £45000 per annum + negotiable
England
SEC is working closely with a major global Pharma company to find highly motivated individuals for a business critical assignment. Are you looking for a new opportunity to develop your professional skills in a dast paced learning environment? Would the chance to work in the Paris area suit your current needs? An assignment has recently
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Paris, France
I have a great permanent senior opportunity – Senior Quality Development for Pediatrics based in Basel, Switzerland in one of the biggest international pharmaceutical companies specialized in vaccines. For more informations please contact directly with Agness Maria Slomska + 044 207 255 6665 or Agness.Slomska@secpharma.com
€80000 - €81000 per annum
Basel, Switzerland
Minimum requirements:
Education: PhD or MSc or Technician or BTA/MTA/CTA in pharmacy/biotechnology/chemistry, biology or related.
Experiance with proteins or sterile liquids /lyophilised pharmaceuticals/
Excellent knowledge of laboratory tools/
Experiance and knowledge of drug product developement activities and cGMP’s/
Overall avarage time distribution of tasks:
- People management: 25%/ Work at production sites (in case of ongoing transfer): 15%
– Office work: 30%/ Meetings & trainings: 30%
€70000 - €71000 per annum
Austria
Minimum requirements:
-Experience and expert knowledge in the development process of new vaccines or other pharmaceuticals,
-Experience and/or trained in project management
-Clear understanding of GCP regulations and knowledge of international and national regulations
For more information’s please contact directly with Agness Maria Slomska +4402072556665 or Agness.Slomska@secpharma.com
€70000 - €71000 per annum
Amsterdam, Netherlands
An independent and globally operating Swiss-based biotechnology company with a comprehensive range of services for pharmaceutical and biotechnology companies seeks to hire a QA Manager to work on site close to Basel. This is an ideal opportunity to apply for a position where you will see the effect your work has on the companies quality
€70000 - €90000 per annum + Benefits
Switzerland
My client, a leading pharmaceutical manufacturing organisation, is looking for a Qualified Person (QP) to function as Quality Manager, with overall responsibility for quality management and batch release, reporting directly to the Quality Director for France. Accountabilities/Responsibilities: – Member of the Senior Management Team (SMT) and reporting to the Company Managing Director – Overall responsibility
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Sens, France
Our client is a leading global pharmaceutical specialising in the discovery, development and marketing of innovative products to prevent and treat diseases, to ease suffering and to enhance the quality of life. Their mission is is to provide healthcare solutions that address the evolving needs of patients and societies worldwide. Due to the growth of
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Mulhouse, France
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