location_0_addressRegionName

location_0_addressCountryName

ONSITE

PERMANENT

FULL_TIME

jobPosting hiringOrganization as json hashed.

ADAPTED_NOW

UNKNOWN

YEAR

Regional Sales Manager

Based on precise feeding analysis you will advise farmers on a suitable balanced diet in the form of silage additives , enzymes & yeast and minerals. Known for its precise feed analyses, highly fortified products the business strives to help livestock producers get the most out of each pound of feed and each head of livestock.

KBSkills

ACTIVE

<img height="1" src="https://counter.adcourier.com/am9obm0uODg0MDAuNDc5QGZycy5hcGxpdHJhay5jb20.gif" width="1"/> FRS Recruitment is currently looking to recruit and Area Sales Manager for a leading animal nutrition company.This is a full-time permanent role. Our client is a leading animal nutrition company committed to the success and profitability of livestock producers worldwide. Known for its precise feed analyses, highly fortified products the business strives to help livestock producers get the most out of each pound of feed and each head of livestock. Reporting to the Regional Manager you will be responsible for building relationships with dairy & beef farmers in County Waterford and East Cork. My client offers a highly fortified balanced diet range that aims to improve herd health. You will be inheriting an existing customer base that has been well developed over the past 3-4 years. You will be expected to maintain and account manage these customers but you will also expected to grow the business. Based on precise feeding analysis you will advise farmers on a suitable balanced diet in the form of silage additives , enzymes & yeast and minerals. Duties <ul><li>Provide technical and sales support to Dairy & Beef farmers.</li><li>Maintain existing business</li><li>Develop and grow business</li><li>Work to agreed sales targets</li><li>Attend national agricultural shows throughout the year.</li></ul> Candidate profile <ul><li>Previous on farm sales experience an advantage</li><li>3rd level degree in Agriculture / Green Cert a distinct advantage</li><li>A strong knowledge of farming</li><li>Strong communication and interpersonal skills.</li></ul> Remuneration Attractive Basic salary + commission & expense's, laptop, phone etc To apply Please email your cv through the attached link Please note FRS offer 100 % confidentiality at all times. All cv application and phone inquiries will be processed in the strictest of confidence. For further information please call John Miller on 087 9955439

FRS Recruitment

Area Sales Manager ( Animal Nutrition )

Agriculture

Analysis Skills

Animal Nutrition

Business Development

Business Growth

Communication Skills

Dietary Management

Farming

Interpersonal Skills

Profit & Loss

Regional Sales

Sales

Sales Management

Sales Support

Technical Sales

Technical Support

monster

TEMPORARY

CONTRACTOR

Validation Engineer

If you choose to apply to this opportunity and share your CV or other personal information with eir evo talent, eir evo and our clients, these details will be held by us in accordance with our privacy policy used by our recruitment team to contact you regarding this or other relevant opportunities at eir evo talent and eir evo. Candidates must be eligible to work full time and long term in the location specified or currently hold a valid appropriate long term work Visa to apply.

Role: Validation Engineer Type :12 month contract Location:Waterford Work Model : Fully Onsite The Role In the Validation Engineer role, you will be required to support a new project The Validation Engineer has a key role in ensuring the on-going validation and compliance of new equipment, systems and processes Job Responsibilities: <ul><li>Executing FAT/SAT/IOQ protocols including generation of protocols and reports. Designing, executing and reporting on validation studies for equipment, systems and processes.</li><li>Ensuring validation studies are managed in conjunction with all required standards and legal requirements (Health & Safety, cGMP, construction, environmental etc.)</li><li>Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation and depyrogenation</li><li>Ensuring that the validation status of equipment and systems are in compliance with cGMP at all times</li><li>Maintaining validation documentation through the validation lifecycle</li><li>Participation in external regulatory inspections</li><li>Support Site Change Control process</li></ul>Skills : <ul><li>Experience: 3-5 years’ experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector.</li><li>Capable of troubleshooting validation issues associated with projects, process development etc.</li><li>Competent technical knowledge of pharmaceutical plants.</li><li>Previous validation/product development experience would be highly advantageous for the role.</li><li>Knowledge of Process Validation regulations, current process validation and technical transfer industry practices, and experience of interpretation and application of guidelines and regulations.</li><li>Knowledge of requirements for of GAMP, ISPE Baseline guides.</li><li>Knowledge of steam and dry heat validation publications such as AAMI/ANSI, PDA and ISO guidelines.</li><li>Full understanding of relevant quality and compliance regulations</li><li>Able to execute projects to plan.</li><li>Good knowledge of quality management systems.</li><li>Good communication skills at organisation, team and individual levels.</li><li>Ability to use MS Project and SPC packages an advantage</li><li>Understands KPI’s for the site.</li><li>Previous Equipment knowledge for example pack lines, Autoclaves, Isolator Technology and fill lines would be an advantage.</li></ul>EET7156 If you would like to discuss this role in confidence, contact Harleen Tora/harleen.tora@eirevo.ie      Candidates must be eligible to work full time and long term in the location specified or currently hold a valid appropriate long term work Visa to apply.    eir evo talent, eir evo and our clients are equal opportunity employers who seeks to recruit and appoint the best available person for a job regardless of marital / civil partnership status, sex (including pregnancy), age, religion, belief, race, nationality and ethnic or national origin, colour, sexual orientation or disability. eir evo talent, eir evo and our clients apply all relevant Data Protection laws when processing your Personal Data.    If you choose to apply to this opportunity and share your CV or other personal information with eir evo talent, eir evo and our clients, these details will be held by us in accordance with our privacy policy used by our recruitment team to contact you regarding this or other relevant opportunities at eir evo talent and eir evo

eirevo talent

American National Standards Institute (ANSI)

Asepsis

Association for the Advancement of Medical Instrumentation (AAMI)

Autoclave

Biotech and Pharmaceutical

Change Control

Current Good Manufacturing Practice (cGMP)

Data Processing

Equipment Validation

FDA (Food and Drug Administration)

Green Construction

Healthcare

ISO (International Organization for Standardization)

Identify Issues

Information/Data Security (InfoSec)

Legal Standards

Manufacturing

Microsoft Project

Mobile Devices

Order Picking/Packing

Performance Metrics

Process Development

Process Validation

Product Development

Product Testing

Project Planning

Publications

Quality Management

Regulations

Regulatory Compliance

Regulatory Requirements

Requirements Validation/Verification

Safety/Work Safety

Sterilization

Validation Documentation

Quality Control Engineer

QC Analytical Expert Location : Waterford Duration : 6+months Main Responsibilities: <ul><li>Providing his/her analytical experts for any project, troubleshooting, investigation on analytical methods and lab technologies.</li><li>Coordinate analytical testing on projects (validation/transfer), ensuring adherence to the committed scheduled plans</li><li>Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasks</li><li>Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements</li><li>Writing/reviewing protocols and reports related to analytical validation/transfers and qualification activities</li><li>Writing/reviewing and maintaining accurate analytical methods procedures</li><li>Informing his/her manager of any quality or HSE event (deviations or OOx) in a timely manner to ensure investigation and impact assessment are performed appropriately</li><li>Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately</li><li>Performing periodically trend analysis on method performance in order to determine the need to revalidate, optimize or replace the method</li><li>Ensuring that his/her lab/facilities, lab instruments, are kept in a quality and safety status to ensure that they can be used appropriately</li><li>Supporting QC teams during internal, external audits and inspections</li></ul> Skills and Experience <ul><li>Experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements.</li><li>Ability to analyse complex data and laboratory results to make informed decisions and identify areas for improvement.</li><li>Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.</li><li>Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.</li></ul> Qualifications <ul><li>Higher Level degree in science or equivalent technical discipline</li><li>3years + experience within Pharmaceutical Development, Analytical and/or Manufacturing department</li></ul>  Candidates should hold appropriate RTWs for Ireland i.e. Stamp1G, Stamp 4, Irish/British/EU passport.   For more information please apply here or contact Agnes Reena/agnes.reena@eirevo.ie  Contact: 0858564199      Candidates must be eligible to work full time and long term in the location specified or currently hold a valid appropriate long term work Visa to apply.    eir evo talent, eir evo and our clients are equal opportunity employers who seeks to recruit and appoint the best available person for a job regardless of marital / civil partnership status, sex (including pregnancy), age, religion, belief, race, nationality and ethnic or national origin, colour, sexual orientation or disability. eir evo talent, eir evo and our clients apply all relevant Data Protection laws when processing your Personal Data.    If you choose to apply to this opportunity and share your CV or other personal information with eir evo talent, eir evo and our clients, these details will be held by us in accordance with our privacy policy used by our recruitment team to contact you regarding this or other relevant opportunities at eir evo talent and eir evo

itContracting

QC Analytical Expert

Data Analysis

Data Quality

Detail Oriented

Drug Development

External Audit

GMP (Good Manufacturing Practices)

Internal Audit

Maintain Compliance

Performance Analysis

Pharmaceutical Analysis

Precision Testing

Problem Solving Skills

Quality Control

Time Management

Trend Analysis

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