Kenny-Whelan (a specialist division of the CPL group) are hiring a QC
Chemist to work at our clients pharma site in Ballydine, Tipperary
CONTACT JENN DINAN ON **APPLY ON THE WEBSITE** AND EMAIL (PLEASE
CONTACT US USING THE "APPLY FOR THIS JOB POSTING" BOX BELOW) 
Qualifications/ Skills Required:
Graduate of a science based disipline
? Minimum of BSc in Chemistry or related discipline
**Apply on the website** years experience in a similar position
EMPOWER experience is an advantage; HPLC/GC and Ion Chromotography
experience in addition to wet chemistry techniques.
CORE COMPETENCIES:
TECHNICAL:
? Have knowledge of GMP standards
? Have knowledge Laboratory safety standards
? Must have good communication skills, both written and verbal.
? Strong documentation skills are required.
? Must be motivated, focused and technically strong.
BUSINESS:
? To perform analytical testing with a high degree of precision and
accuracy
? To perform instrument maintenance and troubleshooting
? To maintain accurate records in compliance with GMP expectations
? To understand and internalise procedures relevant to GMP operations
? To communicate clearly and concisely on technical issues
? On assignment, to deliver project goals on time.
LEADERSHIP:
? Analytical chemistry ? demonstrated ability in all technical
elements relevant to Ballydine ADC IPT operation
? Technical lab skills (precision, etc)
? Strong aptitude for handling analytical instruments
? Mechanical and computer
? Communication - written, oral
? Team and interpersonal skills
? Leadership skills
PRINCIPAL ACCOUNTABILITIES:
1. The Laboratory Analyst has responsibility for Raw Material,
Intermediate and Drug Substance testing to meet compliance
requirements and customer targets. The Analyst may also take a
leadership role in change or improvement projects in ADC or at a site
level.
2. The Laboratory Analyst is responsible for ensuring all testing
activities comply with cGMP. The Laboratory Analyst assures compliance
with all safety and environmental requirements. Compliance with other
regulated areas such as HR policies are also responsibilities of the
role.
3. To test Raw Materials, Intermediates,Drug Substance, Drug products
in accordance with Quality Standard and/or other approved protocols.
4. To comply with all GMP and analytical procedures relevant to area
of work.
5. To adhere and comply with department High Performance Analytical
Behaviours
6. To document all testing activities and to input results into
computerised lab systems in accordance with department and MMD
standards.
7. To provide analytical support to product quality investigations and
new product demonstrations under the supervision of the Laboratory
Leader or designate.
8. Complete the investigation of laboratory OOSs in line with site and
divisional procedures.
9. Complete documentation checks (e.g. PCR?s, ACRs, Deviations) as
required for the Drug Substance/Drug Product test package prior to
release.
**APPLY ON THE WEBSITE**. To complete testing as required on samples
to support process changes.
**APPLY ON THE WEBSITE**. Accountable for own laboratory safety
practices.
**APPLY ON THE WEBSITE**. To provide lead analytical support to
product quality investigations and new product demonstrations using
own initiative and with minimum supervision.
**APPLY ON THE WEBSITE**. Provide leadership in the laboratory aspects
of OOS investigations.
**APPLY ON THE WEBSITE**. To identify and aid resolution of analytical
issues within the IPT laboratory.
**APPLY ON THE WEBSITE**. To be a resource for analytical testing for
the site as required.
**APPLY ON THE WEBSITE**. Execute specific assignments (e.g.
stability programme, instrument management and other systems) in a
comprehensive manner and under minimum supervision.
All applications will be treated wiht the strictest of confidence.
Contact Jenn Dinan on **Apply on the website** and email
JOB DESCRIPTION
Kenny-Whelan (a specialist division of the CPL group) are hiring a QC
Chemist to work at our clients pharma site in Ballydine, Tipperary
CONTACT JENN DINAN ON **APPLY ON THE WEBSITE** AND EMAIL (PLEASE
CONTACT US USING THE "APPLY FOR THIS JOB POSTING" BOX BELOW) 
Qualifications/ Skills Required:
Graduate of a science based disipline
? Minimum of BSc in Chemistry or related discipline
**Apply on the website** years experience in a similar position
EMPOWER experience is an advantage; HPLC/GC and Ion Chromotography
experience in addition to wet chemistry techniques.
CORE COMPETENCIES:
TECHNICAL:
? Have knowledge of GMP standards
? Have knowledge Laboratory safety standards
? Must have good communication skills, both written and verbal.
? Strong documentation skills are required.
? Must be motivated, focused and technically strong.
BUSINESS:
? To perform analytical testing with a high degree of precision and
accuracy
? To perform instrument maintenance and troubleshooting
? To maintain accurate records in compliance with GMP expectations
? To understand and internalise procedures relevant to GMP operations
? To communicate clearly and concisely on technical issues
? On assignment, to deliver project goals on time.
LEADERSHIP:
? Analytical chemistry ? demonstrated ability in all technical
elements relevant to Ballydine ADC IPT operation
? Technical lab skills (precision, etc)
? Strong aptitude for handling analytical instruments
? Mechanical and computer
? Communication - written, oral
? Team and interpersonal skills
? Leadership skills
PRINCIPAL ACCOUNTABILITIES:
1. The Laboratory Analyst has responsibility for Raw Material,
Intermediate and Drug Substance testing to meet compliance
requirements and customer targets. The Analyst may also take a
leadership role in change or improvement projects in ADC or at a site
level.
2. The Laboratory Analyst is responsible for ensuring all testing
activities comply with cGMP. The Laboratory Analyst assures compliance
with all safety and environmental requirements. Compliance with other
regulated areas such as HR policies are also responsibilities of the
role.
3. To test Raw Materials, Intermediates,Drug Substance, Drug products
in accordance with Quality Standard and/or other approved protocols.
4. To comply with all GMP and analytical procedures relevant to area
of work.
5. To adhere and comply with department High Performance Analytical
Behaviours
6. To document all testing activities and to input results into
computerised lab systems in accordance with department and MMD
standards.
7. To provide analytical support to product quality investigations and
new product demonstrations under the supervision of the Laboratory
Leader or designate.
8. Complete the investigation of laboratory OOSs in line with site and
divisional procedures.
9. Complete documentation checks (e.g. PCR?s, ACRs, Deviations) as
required for the Drug Substance/Drug Product test package prior to
release.
**APPLY ON THE WEBSITE**. To complete testing as required on samples
to support process changes.
**APPLY ON THE WEBSITE**. Accountable for own laboratory safety
practices.
**APPLY ON THE WEBSITE**. To provide lead analytical support to
product quality investigations and new product demonstrations using
own initiative and with minimum supervision.
**APPLY ON THE WEBSITE**. Provide leadership in the laboratory aspects
of OOS investigations.
**APPLY ON THE WEBSITE**. To identify and aid resolution of analytical
issues within the IPT laboratory.
**APPLY ON THE WEBSITE**. To be a resource for analytical testing for
the site as required.
**APPLY ON THE WEBSITE**. Execute specific assignments (e.g.
stability programme, instrument management and other systems) in a
comprehensive manner and under minimum supervision.
All applications will be treated wiht the strictest of confidence.
Contact Jenn Dinan on **Apply on the website** and email
We need : English (Good)
Type: Permanent
Payment:
Category: Others
