Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Senior AD Chemist
Location:
This role is based at our Cork, Ireland API site.
How will you make an impact?
The AD chemist will function as a key member of the Team. You’ll be responsible for providing technical support for all phases of drug development. This will include high quality analytical and technical support to internal and external customers, to ensure that analytical infrastructure is in place to support the introduction of new products and support development activities.
What will you do?
* Provide analytical support, including method development, validation/qualification and transfer of methods to clients.
* Prepare, review, update analytical methods and specifications as appropriate.
* Prepare QC handover package. Present training sessions to QC as agreed with QC and provide technical support during method familiarisation and validation period.
* Support external audits as appropriate.
* Support innovative idea of new analytical methods as well as improvement and optimisation of current methods.
* Complete analytical data collection, interpretation and characterization of compounds while ensuring accurate documentation of experimental data is adhered to.
* Preparation, review change controls, study protocols, project status report, final reports and other internal documentation relevant to the role.
* Develop/Expand scientific, technical knowledge by reading the peer reviewed scientific literature, attending scientific conferences and via relevant training.
* Ensure the delivery of projects in the required timeframe and ensure that the site’s technical, quality and safety metrics are all achieved.
* Work with due care and attention, perform all quality, regulatory and safety duties whilst acting always with the Dignity at Work Policy, Code of Business Conduct and Ethics and our values: Integrity, Intensity, Innovation and Involvement.
* Candidate should have hands on experience in handling HPLC, GC and other basic instruments (FTIR, UV spec, Balance, pH etc). Experience in LC-MS, GC-MS and NMR will be added advantage.
Quality Responsibilities
* Perform duties in an accurate manner and behave in accordance with our Quality Management System requirements.
* Participate fully in our site’s quality initiatives and ensure all relevant quality standards are adhered to.
* Maintain GMP standards.
* Read relevant Standard Operating Procedures and Global Quality Policies, Management Procedures and Guidelines relevant to your job role.
* Attend training and complete assessments.
* Work in a GMP quality compliance manner.
* Be inspection ready.
Behaviours
* Demonstrate behaviours that we value.
* Good Communication
* Good facilitation and presentation Skills
* Leadership, Influencing and Negotiating Skills.
* Positive, can-do approach and passion.
Ability to coach, empower, train and mentor others.
Education: Bachelor’s Degree in Chemistry or Analytical Chemistry. Preferred master degree.
Job-Related Experience required: A minimum proven experience within the pharmaceutical industry.
About us:
Thermo Fisher Scientific Inc. is a leading global provider in the science sector, generating more than $30 billion in revenue annually. Our mission is to empower our customers in promoting global well-being and safety. Whether our customers are propelling scientific research, addressing complex analytical challenges, enhancing medical diagnostics and treatments, or improving laboratory efficiency, we are dedicated to assisting them.
Apply today!
http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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