Pharmaceutical Jobs
Laboratory Leaders:
Our client, based in the Dublin 15 area, is engaged in the synthesis,
purification and isolation of peptide based active ingredients for
two of the company's leading products. They are now looking recruit
additional laboratory Leaders to join their team due to expansion.
Purpose of the role:
Responsible for the achievement of the production plan for the laboratory
area.
Duties include:
· Implement site production Plan and cascade to detailed batch
schedule plan.
· Owner of batch records for designated lab to guarantee compliance
to GMP documentaion standards.
· Equipment owner for designated lab to ensure compliance to
calibration, testing and preventative maintenance schedules.
· Contribute to the design, updating and implementation of
SOPs
· Report unplanned events and support CAPA process
· Train and motivate lab team and contribute to the recruitment
of new team members, ensuring that appropriate training modules and
assessments are available.
· Schedule frequent lab area meetings and contribute to production
meetings.
· Promote a strong EHS culture in the lab area.
· Assist with technical services in the execution of projects
that may lead to process improvement.
· Manage budget for Lab area.
Candiate :
· Will hold a BSc in Chemistry/Analytical Chemistry/Pharmaceutical
technology or similar.
· Will have 3-5 yrs experience in a GMP Pharmaceutical lab
Environment.
Should have supervisory experience and be capabl;e of planning staff
and work within the lab.
Clinical Data Co-ordinator – Dublin
Based within easy access of the City Centre, our client is an Internation
contract clinical research company.
Role
The successful candidate will perform a wide range
of data management tasks in accordance with SOPs.
Duties include:
- Data Validation
- Discrepancy review
- Query Generation
- Quality Control
- Database Testing.
- Consistency check Validation.
- Reconciliation of Serious Adverse Advents.
- Coding of clinical data.
- Project Planning.
Candidate:
- Will hold a Degree in Science/Clinical or Nursing.
- Familiarity with medical terminology and/or the clinical drug
development process would be an advantage.
- Will have excellent organisational, communication and interpersonal
skills and a strong attention to detail.
- Will have good PC skills and have an ability to work to deadline.
- Previous Data Management skills an advantage.
Formal Training and Development:
Our client has a formal career development plan that offers a visible
training and development plan that recognises employee progress.
Salary €23.5k + benefits
Analytical Lab Analysts – North Dublin:
Our client is a leading pharmaceutical manufacturer, currently exploying
more than 600 people at it's ultra modern manufacturing facility in
North Dublin. Due to continued growth, they are currently looking
to recruit additional Analytical Lab Analysts.
Duties include:
· Chemical and biochemical analyses of samples utilising techniques
including; Wet Chemistry, TLC, HPLC, GC, Spectroscopy, EIA, IEF and
SDS gels.
· Recording and documenting all data and relevant info onto
worksheets in batch file/logbooks.
· Inputting of Data onto LIMS system.
· Cleaning and production process validation, Method transfer
of new test methods.
· Comply with GLP and GMP regulations.
· Train other analysts as required.
· Involvement in preparation for audits.
Candidate:
· Will hold a 3rd level qualification in a relevant science
discipline.
· Will have a minimum of 1-2 yrs experience of working in a
regulated environment.
Will have excellent organisational skills, ability to work on own
initiative, meet deadlines and have good attention to detail and interpersonal
skills.
Formulation Scientist – Dublin City Centre:
Our client is a high growth company focused on delivering innovative
drug products to the world market. Due to expansion they are now looking
to recruit an additional Formulation Scientist.
The Role:
The candidate will carry out formulationdevelopment of controlled
release solid oral dose drug delivery technologies from initial research
to Phase I and Phase II clinical development.
Duties include:
· Experimental Design for the drug formulation strategy.
· Excecuting experiements and deciding next steps based on
results.
· Interaction with Analytical during formulation development,
optimisation and scale-up.
· Complying with cGMP, Environmental and Safety Legislation.
Candidate:
· Will hold a BSc/Msc in relevant discipline.
· Will have 2-3 yrs hands on experience in solid oral dosge
forrmulation in a commercial environment.
· Should be self motivated with a sound knowledge of pharmaceutical
formulation and design.
· Excellent problem solving and communication skills.
· Working knowledge of formulation process equipment including
but not limited to Tablet presses, granulators and coating machines.
Product evaluation, product license requirements and cGMP quality
standards.
Research Chemists – Cork:
Our client is a recognised market leader in the area of Biopharmaceuticals
and due to continued growth they are looking to recruit additional
Research Chemists.
Duties include:
· Undertake lab Work - both chemistry and analytical, to develop
new processes and technology.
· Continually contribute a range of innovative ideas for PDC
and Global Process Development projects.
· Implement scale-up trials from Kilo Lab and Pilot Plant to
full scale qualification batches in different API Facilities.
· Ensure all regulatory, quality, safety, financial and planning
aspects of the project are addressed to meet the schedule.
· Actively participate in the work of the team to maximise
efficiency of the unit.
Candidate:
· Will hold a PHD in Chemistry.
· Should have 1 years experience in industry in a Process Development
role.
Have demonstrated skills in Chemistry, reactiona analysis and innovation.
QA Specialist – Dublin
Our client is recognised as one of the worlds leading Biopharmaceutical
companies. Due to a large expansion they are now looking for an experienced
QA Specialist to join their team.
Duties include:
- Review and approval of transfer documentation, e.g. Validation/Technical
Services/QC protocols, Master Batch Records, Material Specifications.
- Preparation of Quality Agreements.
- Review and Approval of SOP's.
- Prep of SOP's in accordance with company policies.
- Review of QC and Manufacturing batch records.
- Review of failure/deviation Investigations.
- Preparation of documentation to support regulatory submissions.
Candidate:
- Will hold a Degree/Diploma in relevant Science/Engineering discipline.
- Will have 2-3 years experience in QA preferably in Pharmaceutical/healthcare
role.
CHEMISTRY ANALYST - PEGYLATION:
Our client, a world leader in pharmaceuticals, are looking to recruit
an additional Chemistry Analyst on contract for a site expansion project.
The contract will be for a 9-12 month period.
Duties include:
· Testing of raw materials, in process and finished product
samples.
· Monitoring of site water systems for chemical and/or micro
attributes.
· Assist in the completion of Lab Ivestigation reports.
· Training of lab colleagues on current testing procedures.
· Equipment and process Qualification protocol execution.
· Method Validation Protocol Execution.
· Cleaning Validation protocol Execution.
· Transfer of analytical methods.
Candidates:
· Will hold a Diploma/Degree in Chemistry or related discipline.
· Will have 1-2 yrs experience in a Pharmaceutical/healthcare
lab.
· A working knowledge of Electrophoresis(SDS-Page), Capilliary
Electrophoresis, Cell Culture and/or HPLC would be an advantage.
Be PC literate and have good keyboard skills.
Apply
for this position?
QC CHEMISTS - Tipperary:
Our client, an international pharmaceutical manufacturer based
in South Tipperary, are looking to recruit additional QC Chemists.
Duties include:
· Under general direction perform routine and non routine
testing.
· Review analytical documentation related to lot release,
raw materials and stability.
· Evaluate analytical methods and procedures with a view
to continuous improvement.
· Carry out problem solving, troubleshooting under direction
of QC Supervisor.
· Compile SOPs and other Lab documents.
· Provide training and technical guidance as required.
· Ensure all work is carried out in accordance with cGMP
and company guidelines.
Candidate:
· Will hold a Diploma/Degree in a Science related subject.
· Will ideally have 6 months experience in a similar role.
· Have a thorough knowledge of HPLC & GC.
Knowledge of Quality Systems required to support a lab.
Apply for this position?
