1. Examining and analyzing cells, tissues and blood by collecting samples. For example, collecting blood samples to conduct blood tests.

2. Performing tests to look for microorganisms, parasites or bacteria in body fluids and blood.

3. Matching blood for blood transfusions.

4. Making specimens or samples to examine the count of cells in blood and abnormal cells in blood or body fluids.

5. Using microscopes and other sophisticated laboratory equipment to conduct tests.

6. Maintaining the laboratory equipment and ensuring that the laboratory is stocked well with all the necessary instruments.

7. Interpreting results and submitting the initial tests to the superior for further analysis.

8. Procuring up-to-date knowledge on technical developments in medical science.

9. Following science lab safety rules.

10. Performing laboratory tests in order to produce reliable and precise data to support scientific investigations.

11. Carrying out routine tasks accurately and following strict methodologies to carry out analyses.

12. Preparing specimens and samples.

13. Constructing, maintaining and operating standard laboratory equipment, for example centrifuges, titrators, pipetting machines and pH meters.

14. Ensuring the laboratory is well-stocked and resourced.

15. Recording and sometimes interpreting results to present to senior colleagues.

16. Using computers and performing mathematical calculations for the preparation of graphs.

17. Keeping up to date with technical developments, especially those which can save time and improve reliability.

18. Demonstrating practical procedures if working in education.

19. Conducting searches on identified topics relevant to the research.

20. Following and ensuring strict safety procedures and safety checks.

21. Analyze and record test data to issue reports that use charts, graphs and narratives.

22. Perform medical research to further control and cure disease.

The Mint Hotel Manchester
1 Auburn Street
1 Piccadilly Place,
Manchester  
M1 3DG,
United Kingdom
Tel: +447024070839


The Mint Hotel is short of employees in some of our positions at several departments as we want to increase man power (employees) due to increasing number of customers in the Hotel so at the moment we seek to employ the serives of devoted and qualifeid employees to fill these vacant positions. interested applicants should contact us immediately for thorough and brief examination and qualified persons will be employed.
Interested persons should forward their CV/RESUME via email along with evidence of qualifications and a recent passport photogragh to Albart Jones, Human Resources Manager, Mint Hotel

EMAIL:2011employeesearch.minthotel@gmail.com

AVAILABLE POSITIONS
-------------------
CONFERENCE & BANQUETING OPERATIONS MANAGER
DEMI CHEF DE PARTIE
CHEF DE PARTIE
FOOD & BEVERAGE TEAM MEMBERS
STORE KEEPER
CONTINENTAL/INTERCONTINENTAL DISHES COOK & CHEF
ACCOUNT MANAGER
ACCOUNTANT
ACCOUNT AUDITOR
CASHIER
BANQUET SALES EXECUTIVE
BANQUET SALES COORDINATOR
CASINO F&B BAR CAPTAIN
WAITER/WAITRESS
BARTENDER
HOST/HOSTESS
ASSISTANT MANAGER OF FRONT OFFICE
RECEPTIONIST
CASINO & F&B FLOOR MANAGER
CASINO F&B BAR SUPERVISOR
CASINO F&B WASHER
SERVICE STYLIST
DOOR PERSON
LOBBY ASSISTANT
PART-TIME GUEST RELATIONS ASSISTANT
FIRST AID WARDER
QUALIFIED NURSES
ASSISTANT FLOOR HOUSEKEEPER
COMMIS
HOUSEKEEPING SERVICES COORDINATOR
ROOM ATTENDANT
CLEANER
SECURITY PERSONNEL
FOREIGN/INTERNATIONAL LANGUAGE TRANSLATORS AND TEACHERS
RESERVATIONS CLERK
RESERVATION MANAGER
BEAUTY THERAPIST
MASSEUR/MASSA GIST
SPA RECEPTIONIST
ELECTRICAL ENGINEER
MECHANICAL ENGINEER
MARKETING ASSISTANT
MARKETING ADVISER
BUSINESS ANALYST
CAFÉ ATTENDANT
CAFÉ MANAGER
COMPUTER OPERATOR
INTERNET SERVICE EXPERT

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Management Mint Hotel

Our client is a very profitable, pharmaceutical company who is looking for a QA Supervisor to come in and make an impact. You will need to help hire, train, manage and coach assigned QA employees. You will also approve various documents and records. Ensure compliance with cGMP and company procedures. Communicate potential problems to senior management. Review and execute Batch Records as required, as well as review validation documents and control non-conforming materials. Ensure cGMP compliance in manufacturing, packaging and warehouse through informal and formal audits. You will communicate to senior management about supplier quality and production related issues as well as others that could potentially affect the safety, identity, strength, quality or purity of any product. Candidates must posses a BS degree. Solid dosage experience is also preferred.

My progressive, growing global chemical client has an opportunity for a R&D Manager to lead a global team responsible for developing chemistries for extractive metallurgy processes on a global basis. This is an attractive opportunity for a number of reasons:
 
1) this business segment has the top level support, global reach, and the technical and commercial capabilities to dramatically grow     
 2) you will be adding several members to your team in the coming months to meet strategic growth initiatives in this segment   
 3) you will be based at their new, state of the art, best in class, research facility (just opened June 2009) which will enhance your group’s research capabilities  
4) as technical leader you will closely align with marketing and sales globally, to commercialize new products and add clients, so there will be an opportunity for enhancing your business development skills
5) within five years you will have been a key part of a business that will have substantially grown globally with an opportunity for career advancement along the way
 
Salary is $100-120k and full benefits are included. Please refer to EWE when responding to this position.

Entity:  Spectrum Health Grand Rapids

Shift Length:  8 hours

Schedule: 80 hours per two-week pay period, Monday-Friday, 8:30 a.m. to 5:00 p.m.Maintains 24 hour responsibility for the implementation and ongoing maintenance of clinical research studies, making certain that all concerned are aware of new / ongoing / closing studies, changes in protocol, and preliminary results when possible. Collects, records and makes clinical judgments about data and develops system changes to facilitate efficiency and effectiveness of processes. Maintains clinical nursing responsibilities while carrying out requirements of research protocols.- Critically analyzes / evaluates research study protocols for efficacy, applicability to the setting and ethical nature.- Identifies potential subjects for study participation, assessing eligibility and appropriateness and enrolls them in the study per protocol.- Collects, documents, and reviews patient data / status in the study file utilizing the appropriate case report forms and other documents according to study protocols. Obtains, randomizes, distributes / administers, inventories, documents and returns study medications.- Develops internal and external system supports, in collaboration with other members of the health care team, to facilitate adherence to identified protocols and to streamline the research process.- Develops consent forms, imprinted physician orders, and other materials for study according to study guidelines and regulatory requirements. Prepares study documents for IRB presentation and communicates required information to the appropriate people.- Performs clinical skills including such things as administering study medications, drawing blood, performing assessments, etc.- Assesses the educational needs of study participants / significant others / community / members of the health care team within and outside the Health System and develops, implements and evaluates educational methodologies to meet identified needs.- Communicates, collaborates, networks with, and acts as a consultant to research study centers, the primary investigator(s), physicians / physician offices and other members of the health care team within and outside of the Spectrum Health System.

Pharmaceutical company looking for a dynamic Sr. Analytical Chemist that has experience with chromatographic data to facilitate key decision-making regarding the quality of drug products.  This chemist must have a broad range of instrumentation and analytical techniques, a understand the importance of deadlines, and the impact that accessibility to analytical data has on clinical and drug product submissions.
 
The chemist must have and demonstrated a full range of stability testing services that includes various long term, accelerated, and stress stability assessments performed according to ICH guidelines.  Stability studies are essential to our clients for systematic investigation of the conditions necessary to maintain a product’s quality characteristics, and for establishment of the analytical methods necessary to identify and quantitate product degradants.  Results from the stability study projects are presented in a final stability data summary report.  Some other criteria may include knowledge of chromatographic process, HPLC theory, stationary phases, method development, method validation, reference standards certification, impurity profiling and identification.

The Scientific Associate II will provide technical expertise in the R&D, design, measurement, installation, and commissioning of insertion devices for the National Synchrotron Light Source II Project.  Responsibilities will include designing and testing the electrical systems and controls interface for insertion device magnetic measurement facility.  Candidate will report to the NSLS-II Insertion Devices Group Leader.
 

R&D Manager - Food BA05617Indiv desiring to lead a prod/dev team for an expanding co. Seeking self starting Indiv w exp in R&D working w spices & seasoning blends. Involves new prod devel to protein processors. HACCP cert & Genesis knowledge a plus. Submit resume to info@olddominionspice.com Source - Baltimore Sun

A world-renowned Water Quality and Analytical testing equipment company, located in Northern Colorado, is seeking an Analytical R&D Chemist, experienced in spectroscopy, to join their team. This is a direct placement opportunity. Salary begins at $75K and is commensurate upon experience. Global travel will total a combined 4 weeks/year.

You will be responsible for the application of advanced knowledge of chemistry principles towards the development of chemical products and product applications within the Product Realization Group.

Working with little supervision and guidance, you will be heavily involved in the design and test of Optical Spectroscopic and Electroanalytical techniques, pure reagent synthesis, dry and liquid mixture formulation and product performance testing. Youwill also be very involved in the development of CFD systems, processes and procedures.

During the initial project scope and definition you are highly involved in market research and product definition with the intent to provide the technical prospective.

Must be experienced working within ISO 9001 guidelines and local, state and federal EPA regulatory requirements.

Mentoring and guiding junior chemists or scientists is also expected, as is the leadership of cross-functional teams.

Other Key Responsibilities:
Shows teaching level experience with methods for gathering and interpreting customer VOC. Monitors technical and competitive trends in the field. Investigates technical concepts and market needs then defines product requirements for new analytical products.
Uses expert technical knowledge to develop new applications for existing products to expand market and product base. Exhibits solid practical experience while working closely with marketing in commercialization of new product or application launches.
Writes chemical analysis procedures for incorporation into methods manuals. Supports efforts to write and/or edit product manuals and procedures

Background and Skill Requirements:
Bachelor's degree in chemistry or degree in related field with minimum of 12 years of directly relevant experience or an MS with 10 years of directly relevant experience or Ph.D. with 5 years of experience.

While we appreciate the interest of all, we will only be contacting those that meet the qualifications of the position.

Kelly Scientific Resources® has grown into a $300 million global business as the scientific business unit of Kelly Services. We employ more than 700 clinical research professionals and 4,500 scientists on an average workday on a temporary, project and full-time basis in a broad spectrum of industries and disciplines. KSR has more than 100 locations in North America, Europe and the Pacific Rim. Our staff of scientists provides scientific staffing to a broad spectrum of industries including: chemical, cosmetics, food science pharmaceutical, biomedical, consumer products, environmental, medical device, clinical, petrochemical, and clinical research.

Kelly Services is an Equal Opportunity Employer

We are seeking a Researcher for a federal government agency located in Washington DC.
 
Provide general research and administrative staff support to Manager and Director for mapping project and other high priority projects.
 
Will Research contacts, conduct data entry and check accuracy of data for H1N1 outreach and communications
 
Conduct internet research for contact with organizations and phone inquiries to test validity of contact information.
 
70% research and 30% administrative