Job Details: Biopharmaceutical Senior Scientist


JobsIreland
Jervis Street
Dublin 1
jobsireland.ie
Biopharmaceutical Senior Scientist
Position: ?Biopharmaceutical Senior Scientist ?Joining bonus
?**Apply on the website**)
* Biopharmaceutical Senior Scientist - Athlone, Ireland ( Joining
bonus ?**Apply on the website** )
* We are vital links between an idea for a new medicine and the people
who need it. We are the people of PPD - thousands of employees in
locations worldwide connected by tenacity and passion for our purpose:
to improve health .

_YOU WILL_ be joining a truly collaborative and winning culture as we
strive to bend the time and cost curve of delivering life-saving
therapies to patients.

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.

The role of Biopharm Senior scientist 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).

* QUALIFICATIONS:

* Experience and

_QUALIFICATIONS_

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

* 5+ years&#**Apply on the website**; relevant industry experience
within a GMP laboratory (with experience in the following lab testing
areas HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA,
spectrophotometry.

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

* 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

As well as being rewarded a competitive salary, we have an extensive
benefits package based around the health and well-being of our
employees. We have a flexible working culture , where PPD truly value
a work-life balance. We&#**Apply on the website**;ve grown sustainably
year on year but continue to offer a collaborative environment, with
teams of colleagues eager to share expertise and have fun together.

We are a global organisation but with a local feel.

* Joining Bonus

* Pension scheme

* Annual Leave **Apply on the website** days

* Medical Health care cover

* Life Insurance

* We have a strong will to win - We earn our customer&#**Apply on the
website**;s trust - We are gamechangers - We do the right thing
-We are one PPD ** - **
* If you resonate with our five principles above, and ultimately wish
to accelerate the delivery of safe and effective therapeutics for some
of the world&#**Apply on the website**;s most urgent health needs,
then please submit your application - we&#**Apply on the website**;d
love to hear from you. 1

As we are likely to receive many applications, sometimes we are unable
to provide feedback to everyone.

#LI-MG1 G1

#LI-MG1 Position: ?Biopharmaceutical Senior Scientist ?Joining bonus
?**Apply on the website**)
* Biopharmaceutical Senior Scientist - Athlone, Ireland ( Joining
bonus ?**Apply on the website** )
* We are vital links between an idea for a new medicine and the people
who need it. We are the people of PPD - thousands of employees in
locations worldwide connected by tenacity and passion for our purpose:
to improve health .

_YOU WILL_ be joining a truly collaborative and winning culture as we
strive to bend the time and cost curve of delivering life-saving
therapies to patients.

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.

The role of Biopharm Senior scientist 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).

* QUALIFICATIONS:

* Experience and

_QUALIFICATIONS_

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

* 5+ years&#**Apply on the website**; relevant industry experience
within a GMP laboratory (with experience in the following lab testing
areas HPLC, UPLC, Electrophoresis (CE, iCE, SDS-PAGE), ELISA,
spectrophotometry.

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

* 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

As well as being rewarded a competitive salary, we have an extensive
benefits package based around the health and well-being of our
employees. We have a flexible working culture , where PPD truly value
a work-life balance. We&#**Apply on the website**;ve grown sustainably
year on year but continue to offer a collaborative environment, with
teams of colleagues eager to share expertise and have fun together.

We are a global organisation but with a local feel.

* Joining Bonus

* Pension scheme

* Annual Leave **Apply on the website** days

* Medical Health care cover

* Life Insurance

* We have a strong will to win - We earn our customer&#**Apply on the
website**;s trust - We are gamechangers - We do the right thing
-We are one PPD ** - **
* If you resonate with our five principles above, and ultimately wish
to accelerate the delivery of safe and effective therapeutics for some
of the world&#**Apply on the website**;s most urgent health needs,
then please submit your application - we&#**Apply on the website**;d
love to hear from you. 1

As we are likely to receive many applications, sometimes we are unable
to provide feedback to everyone.

#LI-MG1 G1

#LI-MG1

We need : English (Good)

Type: Permanent
Payment:
Category: Others

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