Recruitment

 Senior Analytical Chemist

QUALIFICATIONS / EXPERIENCE REQUIRED:

  • Must have a minimum of three years industrial experience in a GMP regulated QC chemistry laboratory.
  • A degree in Analytical chemistry, Pharmaceutical Chemistry or other related qualification is required. 

The Candidate:

  • Must be strong on analytical techniques including HPLC/GC/GC-MS/ICP-MS
  • Have technical knowledge in the development and validation of analytical methods ad per ICH guidelines
  • Possess the ability to troubleshoot instrumentation/methodology/data validation issues systematically and utilise strong technical knowledge in resolving issues.
  • Must be motivated, focused and technically strong.

Reporting to: Quality Manager

Salary: A good remuneration package is available for the suitable candidate.

Please send applications with cover letter to: hr@cls.ie by 03rd May 2013

 MICROBIOLOGY TECHNICIAN

QUALIFICATIONS / EXPERIENCE REQUIRED:

• A primary qualification in Microbiology coupled with 1 years working experience in a GMP Quality Control Laboratory.
• Must be a team player with excellent communication skills – both written and verbal
• Full Driving Licence
 

JOB FUNCTIONS / RESPONSIBILITIES

• Generation of documentation to support test method transfers from clients
• Execution of microbiology testing as per approved protocols and test method etc
• Write up of all test results as per GMP and in accordance with the Quality System including Out of Specification results and Laboratory Deviations
• Method Validation
• Participation in self inspections audits
• GMP review of Laboratory log books
• Participate in Laboratory audits e.g. Regulatory / Customer
• Trending of results
• Issue and review of Certificate of Analysis for clients.
 

 Suitable applicants are invited to email their application with CV to amolloy@cls.ie

This job is based in our Galway city facility.

PHARMACEUTICAL CHEMIST

REPORTING TO:

The Head of Contracts

qualifications / experience required:

  • Must have a minimum of three years industrial experience in a GMP regulated QC chemistry laboratory.
  • A degree in Analytical chemistry, Pharmaceutical Chemistry or other related qualification is required.
     

THE CANDIDATE:

  • Must be strong on HPLC and familiar & fluent with Empower software.
  • Must have good communication skills, both written and verbal.
  • Strong documentation skills are required.
  • A strong team player is essential.
  • Must be motivated, focused and technically strong.

SALARY:

A good remuneration package is available for the suitable candidate.

Pharmaceutical Chemistry Analyst

 qualifications / experience required:

  • Minimum of 1-2 years experience working in a GMP environment.
  • Mminimum of an Honours BSc in a Chemistry related course.
  • Industrial experience in HPLC using Empower an advantage.
  • Knowledge in some of the following an advantage: GC, TLC, Viscosity, Penetrometry, Ph, Density,: KF, IR and UV.
  • Protocol writing, data analysis, and report writing skills are a requirement.
  • Must have good communication skills, both written and verbal.
  • Strong documentation review skills are required.
  • A strong team player is essential.
  • Must have a full driving licence.

LOCATION:

Sligo

SALARY & ADDITIONAL BENEFITS:

  • Generous remuneration for the right candidate.
  • Paid Holidays.
  • The successful candidate will gain valuable experience working in the GMP environment of a leading Pharmaceutical company.

 

VALIDATION CHEMIST

Qualifications/Experience Required:

  • A primary qualification in Chemistry coupled with 5-7 years working experience in a GMP Quality Control Laboratory.
  • A good working knowledge of HPLC / GC Systems with Empower software is required with particular emphasis on method validation.
  • A complete understanding of the applicable GMP/ICH requirements is desirable
  • Must be a team player with excellent communication skills – both written and verbal

JOB FUNCTIONS / RESPONSIBILITIES:

  • Development and validation of analytical methods for raw materials and finished products as per ICH guidelines.
  • Interpreting data and adhering to strict guidelines when recording data.
  • Working with other analysts to ensure timely closure of validation.
  • Prioritizing and scheduling validation work.
  • Familiarization with report writing on the basis of ICH and FDA/USP guidelines.
  • Solving instrumentation or method issues when they arise.
  • Ensuring activities are documented and archived appropriately.
  • Applying statistical concepts to data and test results.
  • Strong communication skills.
  • Liaising with customers, staff and supplier.

 

PhaRmaceutical Microbiology Analyst.

Qualifications/Experience Required:
 

  • Must have a primary qualification in Microbiology
  • 3-5 years work experience within in a GMP Quality Control Laboratory within Pharmaceutical Industries.
  • Previous experience in Endotoxin / Bioburden/ Sterility /PET testing is required in addition to their validations

JOB FUNCTIONS / RESPONSIBILITIES:

  • Set up, maintenance and review of the Laboratory Quality system to ensure compliance to GMP as defined in European Directives, CFR Parts 210 and 211.
  • Selection, installation, qualification and ongoing maintenance of laboratory equipment in accordance with the CLS laboratory Quality system and GMP.
  • Generation of documentation to support test method transfers from clients.
  • Execution of Microbiology testing as per approved protocols ,test method etc
  • Write up of all test results as per GMP and in accordance with the Quality System including Out of Specification results and Laboratory Deviations.
  • Review and approval of Laboratory quality records.
  • Training of junior Microbiology staff.
  • Participation in self inspections audits.
  • Communicate with customers in relation to technical queries, forecasting etc.
  • GMP review of Laboratory log books.

 

Contract Pharmaceutical Analyst:

Qualifications/Experience Required:

  • Minimum of one year analytical laboratory experience in a GMP operated QC lab with a good working knowledge of quality management systems,
  • A degree in Analytical chemistry, Pharmaceutical Chemistry or other related qualification.
  • Must have a full driving licence, must be motivated focused and technically strong.
  • Good working knowledge of HPLC and GC and Karl Fisher.
  • Experience with Empower software is a big advantage.
  • Must have good communication skills both written and verbal.
  • Must be willing to travel and relocate at short notice. 

JOB FUNCTIONS / RESPONSIBILITIES:
 

The selected candidate will be required to travel and relocate at short notice.

  

Contract Chemist:

Qualifications/Experience Required:

  • A degree in analytical chemistry, Pharmaceutical Chemistry or other related qualification.
  • Must have a full driving licence
  • Good working knowledge of quality management systems
  • Must have good communication skills both written and verbal
  • Must be motivated focused and technically strong.

JOB FUNCTIONS / RESPONSIBILITIES:

The selected candidate will be required to travel and relocate at short notice.
 

 

Suitable applicants are invited to email their application with CV to HR@cls.ie

 

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