Our client is one of the leaders in global pharmaceuticals and is
growing substantially. We are looking for QC Analysts, QA Specialists,
Analytical Scientists, Production Operatives, Process Scientists and
Technical Reviewers to join this fantastic team. Why work for this
company?
Our client discovers, develops, manufactures and commercialises
medicines, vaccines and diagnostic products, which are complemented by
bio-devices, genetic tests and a range of services. They serve
veterinarians, livestock producers and people who raise and care for
farm and companion animals in more than **Apply on the website**
countries.
Company Profile
**Apply on the website**+ years of experience in animal health.
Nearly $6 billion annual revenues.
**Apply on the website** manufacturing sites around the world.
**Apply on the website**,**Apply on the website** employees worldwide
of which 1,**Apply on the website** employees are committed to R&D.
POSITION SUMMARYProvide scientist level expertise to support
analytical technology covering a range of active pharmaceutical
ingredients.
POSITION RESPONSIBILITIES Key objectives of this position include:
Perform testing of in-process, final product, and stability of drug
substance and drug product samples using a suite of protein-specific
analytical methods (CGE, SEC-HPLC, cIEF, ELISA) and general analytical
methods (appearance analysis, pH, conductivity, etc.).Microbiological
analysis including Environmental Monitoring, Endotoxin and Bioburden
testing, growth promotion, and other associated tests.
Support the technical transfer of analytical test methods to and from
the Tullamore facility.
Creation and revision of documents including test methods, SOPs,
material requirement specifications, forms, and other quality system
documentation to allow the execution of the analysis in a GMP
environment. This will include trending data, monitoring Out of
Specifications and participating in laboratory investigations.
Work closely with the process development group to support the
development of a robust manufacturing process.
Work closely with specialist contract testing service providers to
ensure excellent collaboration is maintained throughout the project.
Support raw material testing (and outsourcing activities) to E.P./USP
monographs when required for GMP manufacture.
Input into the identification of equipment requirements and work with
vendors to ensure execution of all deliverable, including equipment
qualification and validation.
Provide technical reports upon completion of QC projects.
Participate in Quality and Safety regulatory audits. EDUCATION AND
EXPERIENCE BS degree in chemistry, or analytical / chemical
engineering is required; a post-graduate qualification within
analytical sciences may be advantageous.
Industry experience, minimum of 1 years of process chemistry
experience.
Mastery of scientific principles, practices and theories with broad
analytical experience, such as method development / troubleshooting
Familiarity with commercial scale processes and analytical techniques
is desired
Skilled in applying statistical methods to analytical method
performance characteristics Demonstrated ability to work effectively
in a cross functional and culturally diverse work environment. ?This
is a **Apply on the website** month contract role with a view to
permanency and progression.
If you would like to learn more about this opportunity please contact
Dannielle or Lisa, our Life Science Specialists. dannielle.beggs
lisa.mccarrollquinnandstad encourage applications from individuals of
all ages & backgrounds. Whilst appointments will be made on merit
alone candidates must be able to prove their right to work in the UK
or the Republic of Ireland (as relevant). Randstad acts as an
employment agency for permanent recruitment & an employment business
for temporary recruitment as defined by the Conduct of Employment
Agencies & Employment Business Regulations **Apply on the website** We are currently recruiting for a number of exciting roles in Offaly.
Our client is one of the leaders in global pharmaceuticals and is
growing substantially. We are looking for QC Analysts, QA Specialists,
Analytical Scientists, Production Operatives, Process Scientists and
Technical Reviewers to join this fantastic team. Why work for this
company?
Our client discovers, develops, manufactures and commercialises
medicines, vaccines and diagnostic products, which are complemented by
bio-devices, genetic tests and a range of services. They serve
veterinarians, livestock producers and people who raise and care for
farm and companion animals in more than **Apply on the website**
countries.
Company Profile
**Apply on the website**+ years of experience in animal health.
Nearly $6 billion annual revenues.
**Apply on the website** manufacturing sites around the world.
**Apply on the website**,**Apply on the website** employees worldwide
of which 1,**Apply on the website** employees are committed to R&D.
POSITION SUMMARYProvide scientist level expertise to support
analytical technology covering a range of active pharmaceutical
ingredients.
POSITION RESPONSIBILITIES Key objectives of this position include:
Perform testing of in-process, final product, and stability of drug
substance and drug product samples using a suite of protein-specific
analytical methods (CGE, SEC-HPLC, cIEF, ELISA) and general analytical
methods (appearance analysis, pH, conductivity, etc.).Microbiological
analysis including Environmental Monitoring, Endotoxin and Bioburden
testing, growth promotion, and other associated tests.
Support the technical transfer of analytical test methods to and from
the Tullamore facility.
Creation and revision of documents including test methods, SOPs,
material requirement specifications, forms, and other quality system
documentation to allow the execution of the analysis in a GMP
environment. This will include trending data, monitoring Out of
Specifications and participating in laboratory investigations.
Work closely with the process development group to support the
development of a robust manufacturing process.
Work closely with specialist contract testing service providers to
ensure excellent collaboration is maintained throughout the project.
Support raw material testing (and outsourcing activities) to E.P./USP
monographs when required for GMP manufacture.
Input into the identification of equipment requirements and work with
vendors to ensure execution of all deliverable, including equipment
qualification and validation.
Provide technical reports upon completion of QC projects.
Participate in Quality and Safety regulatory audits. EDUCATION AND
EXPERIENCE BS degree in chemistry, or analytical / chemical
engineering is required; a post-graduate qualification within
analytical sciences may be advantageous.
Industry experience, minimum of 1 years of process chemistry
experience.
Mastery of scientific principles, practices and theories with broad
analytical experience, such as method development / troubleshooting
Familiarity with commercial scale processes and analytical techniques
is desired
Skilled in applying statistical methods to analytical method
performance characteristics Demonstrated ability to work effectively
in a cross functional and culturally diverse work environment. ?This
is a **Apply on the website** month contract role with a view to
permanency and progression.
If you would like to learn more about this opportunity please contact
Dannielle or Lisa, our Life Science Specialists. dannielle.beggs
lisa.mccarrollquinnandstad encourage applications from individuals of
all ages & backgrounds. Whilst appointments will be made on merit
alone candidates must be able to prove their right to work in the UK
or the Republic of Ireland (as relevant). Randstad acts as an
employment agency for permanent recruitment & an employment business
for temporary recruitment as defined by the Conduct of Employment
Agencies & Employment Business Regulations **Apply on the website**
We need : English (Good)
Type: Permanent
Payment:
Category: Others
