Wallace Myers International
are recruiting
Analytical Chemists
for our client, a leading global Contract Development and Manufacturing organisation (CDMO).
The role is site based onsite in
Swords, Co Dublin
.
Contact
Jenn Dinan
on **********.
Analytical R&D Chemist – 12 MONTH CONTRACT – Dublin
This position is based at the R&D Centre in Swords, Co Dublin.
The R&D Centre has co-located technical and operational expertise, including analytical expertise that supports the development and manufacture of clinical and commercial products (small molecule APIs).
Position Description
The Analytical Chemist will be responsible for providing technical support for all aspects of analytical methodology, method development, transfer, qualification and troubleshooting pertaining to the manufacture of small molecule APIs and intermediates.
The successful candidate will also provide support in the day-to-day running and maintenance of the AR&D laboratories, including equipment.
They will collaborate closely with other functions, including PR&D, Operations, Quality (QA/QC), SHE and external stakeholders/customers working towards the flawless, compliant and right-first-time manufacture of existing and new products.
In addition, they will provide mentorship, where applicable, to more junior analytical staff.
Key responsibilities include:
Carry out analytical method development, specifically for HPLC and GC.
Perform analytical testing in a timely manner for method development, validation and qualification to ensure project deadlines are achieved for campaign support, material release, PR&D support, reference standard qualification and analytical investigations.
Prepare, review and execute analytical protocols.
Prepare and review analytical reports.
Ensure all documentation is completed to the required standard, right-first-time, in compliance with local procedures and in a timely manner.
Ensure all instrumentation is within calibration and correctly maintained.
Liaise with AR&D Senior Analytical Chemists for technical support with instrumentation, methodology and laboratory investigations or quality events.
Ensure training is completed before execution of a task.
Attend weekly team meetings and participate in a culture committed to high performance, innovation, continuous improvement and idea sharing.
Meet with manager to discuss performance, provide feedback and identify development opportunities.
Ensure CGMP compliance of laboratory operations and documentation, including testing, write-ups, review and approval of protocols, reports and change controls.
Ensure a safe work environment for oneself and all employees.
Maintain high standards of housekeeping in the laboratory.
Required Key Skills and Experience
Ideally a BSc/MSc in analytical chemistry or equivalent, preferably a minimum of 3–5 years' experience in analytical activities and method development within a pharmaceutical manufacturing environment.
Demonstrable expertise in developing analytical methods, particularly for HPLC and GC.
Excellent core competencies such as teamwork, communication skills and technical writing.
Strong technical background in chemistry, particularly analytical chemistry.
Ability to work to tight timelines.
Openness to change and receptiveness to new ideas.
Knowledge of FDA and European GMP requirements, particularly pertaining to laboratory operations.
All applications will be treated with the strictest of confidence.
Contact
Jenn Dinan
on **********.
At Wallace Myers International Recruitment Agency we specialise in sourcing professionals for key industries and services.
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