Lab Sales Rep required

We have a fantastic new job in for a Diagnostic/Laboratory Sales Specialist for Dublin -

Role Function -

This Laboratory Sales Rep will be responsible for the management of territory sales for a diverse range of Laboratory diagnostic equipment and kits, within a specified territory area.

Expertise within the area of Life Sciences and Molecular Pathology would be desirable but not essential.  

 The current customer base is in the Clinical and Industrial markets.

It includes but is not exclusive of the following contact groups: Laboratory/Pathology Managers; Medical Technician decision makers; Medical Consultants and Nurses; Phlebotomy/Infection control Managers; Purchasing/ Supply Managers; QA/QC/R & D Managers

Essential Requirements -

A third level qualification in a scientific field which incorporated exposure to a laboratory environment
2-3 years Sales experience working in a similar environment, preferably within the Laboratory Market

A proven successful track record in Hospital  sales in Ireland
A full, clean drivers license
IT literacy: Microsoft Office skills (Word, PowerPoint, Excel)
Ability to work independently and self-reliantly where strong flexibility and time management skills will be key
Excellent communication and interpersonal skills
Drive and self-motivation
The ability to close out opportunities and develop them into budget achievements and long term business

 
The ability to establish and maintain high quality partnerships with Customers
Flexible approach to working hours during busy periods
For further information or to apply, contact us -

http://www.jackiebrownmedical.ie/jobs_ireland.php?url=jobs

Fantastic new development for Cystic Fibrosis!

Fantastic new development for Cystic Fibrosis!

EU Approval for TOBI Podhaler comes as great news for cystic fibrosis patients across the country. TOBI Podhaler, an inhaled therapy for patients with cystic fibrosis, is to be used with patients 6years+ for suppression of chronic lung infections.

“With the approval of the TOBI Podhaler in Europe, and innovative version of an established treatment has become available that will improve the delivery of tobramycin and should have a positive impact on patients’ quality of life”,  said Professor Stuart Elborn, President of the European Cystic Fibrosis Society and Professor of Respiratory Medicine at Queens University.

Dr. Greg Hays of Novartis said “It is an important symbol of our long term commitment to improving the quality of care for patients with this serious and potentially life-threatening disease.”

Qualified Senior Mechanical Facilities Engineer 

Requirements:

•Degree in Marine/Mechanical/Process Engineering

 •6 -7 years experience in similar role, ideally in high volume manufacturing and/or Medical Device industry

. •Understanding of GMP, commissioning and validation activities

•Strong people & project management skills, and be able to manage multiple vendors and contractors.

•Experience with CAD tools and drawing change control.

•Structured approach to operation/capacity optimization, failure analysis and problem solving

. •Practical application of statistical analysis techniques. Knowledge of lean and 6-Sigma methodologies an advantage

Responsibilities:

This is a significant role within the Facilities organization and requires a person to lead the operation and maintenance group and drive the development and reliability improvement programs of existing utilities and facilities systems.

Responsibilities of this role will include the operation and management of maintenance facilities and utilities systems including; high pressure steam systems, nitrogen generation systems, vacuum conveying systems, HVAC, HEPA and clean room services, DI water, compressed air, solvent storage and distribution systems, chilled water systems, CHP systems and software control systems including BMS, QBMS and CMMS.

The successful candidate for this role will have proven experience in applying trouble shooting and diagnostics techniques on the above systems, generating corrective and improvement plans, implementing these plans and ensuring that the stated objectives are achieved.
 
These plans may include some of the following elements: capacity threshold analysis, reliability/ mean time to failure analysis, equipment efficiency, downtime reduction, preventative maintenance, condition monitoring, change control and training etc

If you want more information or wish to apply, go to -

http://www.jackiebrownmedical.ie/jobs_ireland.php?url=jobs&page=2

Quality Engineer - Complaints

Our Medical Device Client based in the Midlands is seeking a

 Quality Engineer for a Complaints Coordinator job.

Essential Skills / Experience

 
• Engineering/Science qualification 
• 2/3 years of working within a Quality environment
• Excellent technical writing skills – essential
• Attention to detail and accuracy – essential
• Ability to work well under deadlines and pressure
• Problem solving skills for developing creative solutions and meeting objectives are required.
• Skills that enable coordination of data, including MS-Office (primarily PowerPoint, Word, MD Project, Outlook and Excel);
• Excellent analytical ability
• The ability to prioritize tasks and be able to manage several projects and tasks simultaneously; and the ability to interface with all levels of management.

Job Purpose

 
The successful candidate will act as the primary contact within the EMEA region for Field Actions associated within the EMEA region.  He/She will be responsible for ensuring activities associated with Field Actions are approved, communicated, written and delivered as appropriate.  This will include initiation of Field Actions, ensuring compliance to associated regulatory requirements, creation and completion of the necessary paperwork required to complete the Field Action.  The role will also involve multi-site collaboration with local Company offices in addition to Customer Services and Legal Manufacturers.  The candidate will be responsible for providing regular status reports to Management and Regulatory Authorities as required.

For more information on this role, or to apply, go to -

http://www.jackiebrownmedical.ie/jobs_ireland.php?url=jobs&page=2

Engineers come together!

Engineers we need you!

Are you a fully qualified Engineer with experience in

• Medical Device
• Pharmaceutical
• High Volume Manufacturing
• Facilities

If so then we need to speak to you!

Everyday we have more and more jobs in Engineering and Science coming in the door so we may have the right career move for you!

So whether you are looking for your next career move, or move back into the Engineering field, please do get in touch!

http://www.jackiebrownmedical.ie/contact_us.php?url=contact

Science, Engineering and Validation

We have a flurry of Science jobs in the Munster region -

Aseptic Supervisor -

* Supervise all aspects of Aseptic formulation, filling and packaging
* Supervise warehouse operation including receiving and shipping of material

Requirements

* Bachelors degree or equivalent from an accredited college or university, preferably in Engineering or a science discipline. .
* Minimum of 3 years of supervisory experience of teams
* Experience with Aseptic manufacturing background

Senior Electrical Engineer – Facilities

-     Take responsibility for general electrical safety throughout the plant
-     Management of electrical maintenance personnel.
-     Development of electrical maintenance strategy, including manpower skills     development and appropriate preventative maintenance systems
-     Ensure compliance with best practice electrical standards.

Requirements -

• 5+ years in similar role.
• Experience in high volume manufacturing and/or Medical Device industry.
• Understanding of GMP, commissioning and validation activities

Validation Engineer – Software

·         Co-ordination, implementation and active participation in the site validation programme for  computer systems and cleaning
·         Provide input into all project phases i.e. from design through to the commissioning and qualification execution phases of the project.
·         Develop validation documentation as required (e.g. specifications, plans, protocols, procedures etc.).

Requirements –

·         Relevant 3rd Level Qualification in science or engineering
          A minimum of 3 years software validation experience in an established QA function preferably in the healthcare industry
·         Strong knowledge of CSV/GAMP,21CFR Part 11,Project Life Cycle and cGMP Regulations

Validation Manager

·               Manage all of the validation engineering functions at the site
·               Lead, integrate & project manage validation tasks from initial concept through to successful completion and delivery.
·               Continue to seek, support & drive cost saving initiatives where validation is involved or accountable for the functions

Requirements –

·            Bachelors degree from an accredited college or university, preferably in an Engineering discipline
·            In-depth knowledge of Validation processes, Medical Product Manufacturing, especially high automated processes or aseptic operations.
·            Experience in FDA or IMB regulated manufacturing and proven management experience in a Quality organization
·            Strong project management skills and Competent validation knowledge with good organizational/administrative skills

If you meet the above requirements and would like to apply for any of these roles, go to -

http://www.jackiebrownmedical.ie/job-tags/limerick-jobs.htm

We look forward to hearing from you!

Calling all Mad Chemists!

Mad Scientists we need you! Whether your passion lies in organic or inorganic chemistry, our question to you is have you 5 years experience in Raw Materials Testing,  Test Method Transfers or Aseptic Media Fills?

We have two Chemist positions available for a Medical Device company in Limerick, one dealing solely with Raw Materials Testing and introducing new techniques and the other is in a newer lab dealing with media fills, lab validation, set ups and Test Method Transfers!

Quite obviously you know what a HPLC is and the inner workings of the instrument itself, having clocked up infinite working hours on the main machine! But the instrumental requirements for these positions are the HPLC, GC, Mass Spec – you know the rest!

 We are now looking for your help!

PhD standard is desirable but not essential, but if you are Degree, Masters or PhD qualified in Chemistry/ Analytical Chemistry with 5 years experience in the med device or pharmaceutical industry (i.e. aseptic environements and procedures)  then we want to hear from you.

Contact us for further information on the link below

http://www.jackiebrownmedical.ie/contact_us.php?url=contact

Quality Jobs!

Hi everyone! I thought I would take advantage of MyScienceJobs this weeks to give you an update on the Engineering end of the Medical Device jobs.

Unfortunately the Kitting Director position has been put on hold due to restructuring, but nevertheless the

• Software Quality Engineer

role is still open amongst others!

If you have a background in Software Validation or QA Software or something similar in a high volume manufacturing plant/ indeed Medical Device then we want to hear from you!

Get in touch!

Celebrating Medical Device Jobs!

Good Morning good people of the Medical Device World!

I have another two jobs in for Med Device!

• Software Quality Engineer – Munster
• Aseptic Supervisor – Munster

Once again, should you want to have a look at the full job description then please forward your CV to elaine@jackiebrownmedical.ie or goto

http://www.jackiebrownmedical.ie/jobs_ireland.php?url=jobs

for more information!

New Jobs in!

Contrary to news reports of certain medical device companies offering voluntary redundancies due to restructuring to keep the company afloat, there are other medical device companies in the country that are in fact taking people on! Validation or Engineering anyone?

The following are the openings within Med Device at the moment:

• Quality Validation Manager – 7-8 yrs exp Med Device or high volume manufacturing
• Senior Mechanical Eng – 5-8 yrs exp Med Device or high volume manufacturing
• Senior Electrical Facilities Eng – 5-8 yrs exp with high volume facility
• EMEA Procedural Kitting Director – 10yrs++ exp in manufacturing and medical kits

So whether you are working at the moment or being offered redundancy and want a fresh look at the med device market at the moment, contact us here for a full job description or to register your interest in future medical device jobs!

Speak Soon!