Job Details: Senior GMP Scientist/Pharma


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Jervis Street
Dublin 1
jobsireland.ie
Senior GMP Scientist/Pharma
Position: Senior GMP Scientist (Pharma)

Location: Not Specified

*At PPD, we help our client delivers life-changing therapies that
address the world&#**Apply on the website**;s most challenging health
concerns. Due to continued growth we are looking to expand our team
across all areas of our GMP facility. *

*We hire the best, develop ourselves and each other, and recognize the
power of being one team!*

*

*

Our GMP laboratory based in Athlone, Ireland offers fully integrated
solutions for product development and analytical development,
including analytical testing services in method development, method
validation, method transfer, release and stability studies. Our highly
qualified GMP lab staff work across our 3 laboratory groups: Biopharm,
Small Molecule, and Inhalation.

Athlone is one of PPD&#**Apply on the website**;s fastest-growing
laboratory locations. Due to this continued expansion, we are
recruiting *Senior Analytical Chemists *to join our Small Molecule
group.

*Senior Analytical chemist -*

The role of Senior Analytical chemist is to perform complex laboratory
analysis of pharmaceutical products and proficiently uses analytical
instrumentation, calculates and analyses data and records data.
Routinely acts as the project leader on multiple projects, interacts
with clients, reviews and evaluates data, writes reports and
protocols. Responsible for the scientific conduct of the project and
communication of regulatory issues with senior level team members.

* *

*Key responsibilities:*

* Independently performs method validations, method transfers and
analytical testing of pharmaceutical compounds in a variety of
formulations.

* Designs and executes experiments with minimal supervision.

* Prepares study protocols, project status reports, final study
reports and other project-related technical documents.

* Communicates data and technical issues to the client and responds to
client needs

* Mentors, trains and coordinates laboratory activities of other team
members and assists in troubleshooting instrument and analytical
problems.

* Assists in designing method validation or method transfer protocols
and establish project timelines.

* Reviews data for technical, quality and compliance to protocols,
methods, SOPs, client criteria and Good Manufacturing Practices (GMP)
or Good Laboratory Practices (GLP).

*Qualifications:*

* Key Experience *

* Education to a Bachelors or higher level in related subjects ie;
Chemistry.

* 5+ years&#**Apply on the website**; relevant industry experience
within a GMP laboratory (with experience in the following lab testing
areas HPLC, GC, MS, Dissolution testing, Karl Fischer, UV-vis, FT-IR,
TOC.

* Experience in Method Validation, Method Transfer and Analytical
testing.

* *

* Additional Requirements *

* Detailed knowledge of method validation; method development would be
an advantage.

* The ability to plan, schedule and carry out work for successful
project completion

* A positive attitude and ability to work well with others

* Excellent attention to detail

* The successful candidate can look forward to job stability with a
leading CRO that has experienced year-on-year growth. With future
expansion plans, there is the opportunity to progress in your career
with PPD at our Athlone labs. *

*LI-VK1

#IndeedPPDEMEA1 Position: Senior GMP Scientist (Pharma)

Location: Not Specified

*At PPD, we help our client delivers life-changing therapies that
address the world&#**Apply on the website**;s most challenging health
concerns. Due to continued growth we are looking to expand our team
across all areas of our GMP facility. *

*We hire the best, develop ourselves and each other, and recognize the
power of being one team!*

*

*

Our GMP laboratory based in Athlone, Ireland offers fully integrated
solutions for product development and analytical development,
including analytical testing services in method development, method
validation, method transfer, release and stability studies. Our highly
qualified GMP lab staff work across our 3 laboratory groups: Biopharm,
Small Molecule, and Inhalation.

Athlone is one of PPD&#**Apply on the website**;s fastest-growing
laboratory locations. Due to this continued expansion, we are
recruiting *Senior Analytical Chemists *to join our Small Molecule
group.

*Senior Analytical chemist -*

The role of Senior Analytical chemist is to perform complex laboratory
analysis of pharmaceutical products and proficiently uses analytical
instrumentation, calculates and analyses data and records data.
Routinely acts as the project leader on multiple projects, interacts
with clients, reviews and evaluates data, writes reports and
protocols. Responsible for the scientific conduct of the project and
communication of regulatory issues with senior level team members.

* *

*Key responsibilities:*

* Independently performs method validations, method transfers and
analytical testing of pharmaceutical compounds in a variety of
formulations.

* Designs and executes experiments with minimal supervision.

* Prepares study protocols, project status reports, final study
reports and other project-related technical documents.

* Communicates data and technical issues to the client and responds to
client needs

* Mentors, trains and coordinates laboratory activities of other team
members and assists in troubleshooting instrument and analytical
problems.

* Assists in designing method validation or method transfer protocols
and establish project timelines.

* Reviews data for technical, quality and compliance to protocols,
methods, SOPs, client criteria and Good Manufacturing Practices (GMP)
or Good Laboratory Practices (GLP).

*Qualifications:*

* Key Experience *

* Education to a Bachelors or higher level in related subjects ie;
Chemistry.

* 5+ years&#**Apply on the website**; relevant industry experience
within a GMP laboratory (with experience in the following lab testing
areas HPLC, GC, MS, Dissolution testing, Karl Fischer, UV-vis, FT-IR,
TOC.

* Experience in Method Validation, Method Transfer and Analytical
testing.

* *

* Additional Requirements *

* Detailed knowledge of method validation; method development would be
an advantage.

* The ability to plan, schedule and carry out work for successful
project completion

* A positive attitude and ability to work well with others

* Excellent attention to detail

* The successful candidate can look forward to job stability with a
leading CRO that has experienced year-on-year growth. With future
expansion plans, there is the opportunity to progress in your career
with PPD at our Athlone labs. *

*LI-VK1

#IndeedPPDEMEA1

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Type: Permanent
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Category: Others

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