Scientific  - Pharmaceutical Jobs Listings in UK

Application Deadline: 16.08.2010
Job Profile:

Work on the project: the approval system of clinical trials and performance evaluations of medical devices. Specifically, the following tasks in the project are met:

Implementation of the legal requirements in proceedings of the department
Preparation of the work flow and the accompanying computer technical implementation of the approval process and t...

Application Deadline: 23.08.2010
Job Profile:

Focus of the task lies in the participation in the project "Adaptation and revision of the informative text of generic oncology products to the current state of knowledge and alignment with European decentralized and centralized approvals.

Another task is the prospective Nutzen-/Risikoabschätzung new drugs by medical evaluation of therapeutic efficacy and...

Application Deadline: 30.08.2010
Job Profile:
Formal scientific evaluation of the regulatory requirements under the validation of requests for re-registration of a medicine in decentralized procedure (DCP) and national procedures:
Review of the authorization and responsibilities, clarification of the European regulatory status, decision on the possibility of processing in the requested procedures and examinati...

Develop and implement product launch / conversion events, marketing activities, key account management, key initiative projects to align with business plan.
-Provide product training to distributor sales team and support marketing activities.
-Coordinate the external and internal market information to evaluate the market opportunity for the project.
-To collect and analyze market intelligences: customer inform...

Responsibilities:
This position will be responsible for managing Chemical synthesis programs in Exelgen China located in Taizhou China. Key activities include project assessment, resource allocation, and recruiting, professional development for employees, comprehensive project updates, and exceeding customer expectations.
Requirements:
• Ph.D. in Chemistry and a strong scientific track record
•...

The director is responsible for building sample library, sample donation, storage and service system with high-quality ethical standard. And the director will also be responsible for establishing sample library and donations service system with famous hospitals. He or she will report to Vice-president.

Responsibilities:
Develop more hospitals to become members of our Bio-bank; Ensure more and more qualified s...

Your responsibilities
Leadership of the staff of the area hospital care
Ensure the supply of the Hospital in medicines and pharmaceutical-care professional of the central and decentralized services
Establishment and development of decentralized pharmaceutical services
Content Management SAP
Quality assurance in hospital care
Planning of the area in the project process including hospital care, repai...

Application Deadline: 31st July 2010

Conditions
• completed medical school
• good IT skills and English
• scientifically oriented professional presentation
• interest, over several years with clinical pharmacology
to address issues and patient-oriented research.
• years of clinical experience is desirable

The Department of Clinical Pharmacology and Pharmacoepidemiology is ISO90...

Application Deadline: 07/12/2010

Responsibilities:
- Pharmacological and toxicological evaluation of new and existing medicines with focus on the areas of "Genetic and Reproductive Toxicology"
- Project-work topics for the International Conference on Harmonisation (ICH) and / or project level assessment of toxicological studies related to indications for children.

Requirements:
- University...

We are looking for time to strengthen our team as

Staff in Microbiology
- Limited for 12 months -

Its tasks are:
- Testing for microbiological purity of medicinal products, cosmetics, raw materials and packaging
- Hygiene controls in production, packaging and Microbiology
- Cleaning, maintenance and qualification of equipment and rooms
- Testing for sufficient conservation
- Parti...

To enhance our scientific team in the area of regulatory science,
we are looking for a scientist in the field of
Toxicology.
Your duties will include:

planning and monitoring studies
preparation of expert statements and dossiers as well as risk assessments
coordination of regulatory projects
co-operation with German and international authorities.

Our requirements:


y...

Scientific supervision and participation in technical committees and working groups of the German Homeopathic Pharmacopoeia (HAB-Commission), particularly in the area of analytics
Representation of Germany in homeopathic working groups of the Arzneituchkommission the EDQM
scientific support of the Secretariat of the HAB-Commission.
Requirements:
degree in Pharmacy or equivalent qualification, preferably wi...

scientific evaluation of the documentation of requests for approval for drugs with indications in neurology and psychiatry in proceedings of the European Community and national procedures of change indicators, and in opposition and litigation
Assessment and verification of documentation of ready in terms of their raw materials, production, quality specification, description and validation of test methods and stability...

Participation in the establishment of the preferred initial treatment of generics after the expiry of data exclusivity for originator ("Flying Team Project") in European approval procedure:

Assessment of pharmaceutical quality and the Formalpharmazie of drugs, mainly in the areas of endocrinology, diabetes, gynecology, andrology
Testing and evaluation of documents for the pharmaceutical quality of medicinal p...