Job Details: QC Scientist


JobsIreland
Jervis Street
Dublin 1
jobsireland.ie
QC Scientist
Johnson & Johnson Worksense (via Randstad Sourceright) is responsible
for finding, engaging and contracting talent for the Johnson & Johnson
contingent workforce.

We are currently recruiting a QC Scientist to join our contingent
workforce on a growing team in Johnson and Johnson. This will be an
initial **Apply on the website** month contract. About Janssen
Pharmaceuticals:

Janssen Sciences Ireland UC, (previously Janssen Biologics), is part
of the Johnson & Johnson family of companies, the world&#**Apply on
the website**;s most comprehensive and broadly-based manufacturer of
healthcare products and related services. Our site in Ringaskiddy was
established in **Apply on the website** on a **Apply on the
website**-acre site with an investment of ?**Apply on the website**
million. We manufacture a range of biopharmaceutical products
indicated for the treatment of conditions that include rheumatoid
arthritis, psoriasis and cancer.

We are expanding our site to allow us to meet the critical needs of
patients around the world. The expansion plans involve an investment
of more than ?**Apply on the website** million that will increase
the existing manufacturing space by an additional **Apply on the
website**,**Apply on the website**m2, provide employment for up to
**Apply on the website** people during construction and an extra
**Apply on the website** people once completed.

The

ROLE:

Reporting to the QC NPI Manager, this position is responsible for
delivery of the NPI and Commercial Product Portfolio projects to QC
Key

RESPONSIBILITIES:

Coordination and project management of Clinical product introduction
to QC Acts as a Single Point of Contact for introduction of new
products and/or technologies to QC Participate in Site NPI teams,
attend Work Cells Collaborate with global and local stakeholders in
Analytical development, Technical Operations, QC & Operations
Investigating and resolving challenges relating to Method Transfer
activities in QC Participate in/lead Cross Functional activities with
JSC NPI teams/AD/QC Coordination, Support of Co-validation/PPQ
activities Completion of assigned tasks to support the introduction of
testing associated with new or existing projects
Authoring/Review/Approval of documents associated with NPIs or
Commercial product lifecycle management and analytical method transfer
in QC Deputise for QC NPI manger where appropriate Candidate

REQUIREMENTS:

A relevant third level qualification in either Microbiology,
Biochemistry, Pharmacy, Biotechnology, Science or Engineering Proven
experience of leading projects involving multiple stakeholders
Experience/understanding of the Analytical Method Transfer process
**Apply on the website** years of relevant experience working in a
laboratory setting within a GMP regulated environment
? Proven experience of leading projects involving multiple
stakeholders

_EXPERIENCE WITH_ Regulatory filings

_EXPERIENCE OF_ Microsoft Word, Excel and Outlook Experience in eLIMS,
TruVault and/or other business systems Problem solving/decision making
methodology training If you meet our requirements and are interested
in hearing more about our QC Scientist role, please do not hesitate to
apply through the provided link today and a member of our recruitment
team will be in touch! Johnson & Johnson Worksense (via Randstad Sourceright) is responsible
for finding, engaging and contracting talent for the Johnson & Johnson
contingent workforce.

We are currently recruiting a QC Scientist to join our contingent
workforce on a growing team in Johnson and Johnson. This will be an
initial **Apply on the website** month contract. About Janssen
Pharmaceuticals:

Janssen Sciences Ireland UC, (previously Janssen Biologics), is part
of the Johnson & Johnson family of companies, the world&#**Apply on
the website**;s most comprehensive and broadly-based manufacturer of
healthcare products and related services. Our site in Ringaskiddy was
established in **Apply on the website** on a **Apply on the
website**-acre site with an investment of ?**Apply on the website**
million. We manufacture a range of biopharmaceutical products
indicated for the treatment of conditions that include rheumatoid
arthritis, psoriasis and cancer.

We are expanding our site to allow us to meet the critical needs of
patients around the world. The expansion plans involve an investment
of more than ?**Apply on the website** million that will increase
the existing manufacturing space by an additional **Apply on the
website**,**Apply on the website**m2, provide employment for up to
**Apply on the website** people during construction and an extra
**Apply on the website** people once completed.

The

ROLE:

Reporting to the QC NPI Manager, this position is responsible for
delivery of the NPI and Commercial Product Portfolio projects to QC
Key

RESPONSIBILITIES:

Coordination and project management of Clinical product introduction
to QC Acts as a Single Point of Contact for introduction of new
products and/or technologies to QC Participate in Site NPI teams,
attend Work Cells Collaborate with global and local stakeholders in
Analytical development, Technical Operations, QC & Operations
Investigating and resolving challenges relating to Method Transfer
activities in QC Participate in/lead Cross Functional activities with
JSC NPI teams/AD/QC Coordination, Support of Co-validation/PPQ
activities Completion of assigned tasks to support the introduction of
testing associated with new or existing projects
Authoring/Review/Approval of documents associated with NPIs or
Commercial product lifecycle management and analytical method transfer
in QC Deputise for QC NPI manger where appropriate Candidate

REQUIREMENTS:

A relevant third level qualification in either Microbiology,
Biochemistry, Pharmacy, Biotechnology, Science or Engineering Proven
experience of leading projects involving multiple stakeholders
Experience/understanding of the Analytical Method Transfer process
**Apply on the website** years of relevant experience working in a
laboratory setting within a GMP regulated environment
? Proven experience of leading projects involving multiple
stakeholders

_EXPERIENCE WITH_ Regulatory filings

_EXPERIENCE OF_ Microsoft Word, Excel and Outlook Experience in eLIMS,
TruVault and/or other business systems Problem solving/decision making
methodology training If you meet our requirements and are interested
in hearing more about our QC Scientist role, please do not hesitate to
apply through the provided link today and a member of our recruitment
team will be in touch!

We need : English (Good)

Type: Permanent
Payment:
Category: Others

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