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Applicants should have experience and be competent in Good Laboratory Practises such as dilutions, titrations and operation of general analytical test equipment which is required to perform routine chemistry analytical techniques - Ensuring that all required testing is completed in the chemistry department
Be the Chemistry technical expert for the technology transfers of products to the site to ensure that the processes are run right first time - B.Sc / MSc / PhD in Chemistry preferably in the area of synthetic organic chemistry. Knowledge of Organic Chemistry, Process Development, Process Optimization and GMPs.
Our client, a major player in the food/beverage industry, is looking to recruit a Research Scientist. This exciting, challenging and career advancing opportunity requires a PhD (Analytical Chemistry/Forensic Science/related) qualifications coupled with 5 years experience gained in a Food Beverage company (production research facility).
Degree in Analytical Chemistry or related discipline. QC and Stability Chemist - County Waterford - My client is a large Pharmaceutical company who are actively looking for a chemist to support QC and Stability by ensuring all raw materials, packaging, finished products and Stability samples are analysed in accordance with cGxP.
Degree in Chemical/Process or Chemistry is essential - We now wish to recruit a Process Engineer / Chemist with MSAT Lab experience ideally for a multi-product API Facility. This position will be based on an API Clients site in Cork.
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A degree in Analytical chemistry, Pharmaceutical Chemistry or other related qualification is required. 3 – 5 years’ Experience in a GMP accredited Chemistry Laboratory is required. Pharmaceutical Chemist working primarily to identify unknown impurities using HPLC. 3 - 5 years experience required.
Qualified to a minimum of honours degree level in Analytical Chemistry, Pharmaceutical science or related discipline. The QC and Stability Chemist will ensure all raw materials, packaging, finished products and Stability samples are analyzed in accordance with cGxP. The Opportunity - The Role
As the QC Chemist you will analyse Raw Materials, In-Process Intermediate and Finished Product, using instrumental and wet chemistry test methods. As the QC Chemist you hold a Degree in Chemistry and are familiar with HPLC, GC and other analytical instrumentation.
This role is responsible for analysing Raw Materials, In-Process Intermediate and Finished Product, using instrumental and wet chemistry test methods - The purpose of this role will be to have responsibility for analysing Raw Materials, In-Process Intermediate and Finished Product, using instrumental and wet chemistry test methods
Improve knowledge in Analytical Chemistry area in terms of new technologies and new methodologies. - 2 years+ industrial experience in a GMP regulated chemistry laboratory -BSc. in Analytical Chemistry, Pharmaceutical Chemistry or other related qualification is required. -A good knowledge of wet chemistry, Karl Fisher, FTIR, particle size analysis desirable
Minimum qualification B.Sc. or M.Sc./ M.Eng Degree in Chemical or Biochemical Engineering or equivalent discipline; equivalent is defined as a Biotechnology or Industrial Chemistry Degree with basic the elements of chemical/biochemical engineering fundamentals as applied to biotechnology/bioprocessing
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Check out all our open jobs on our HERO Recruitment website - Our client, a medical device company in Galway are currently looking to recruit a Chemical Manufacturing Engineer for their site. Contact: Caroline Kingston - Our Offer - You will be responsible for researching and developing new and improved chemical manufacturing processes.
Degree in Chemistry, Biochemistry, Biotechnology or other scientific discipline with relevant practical experience. QCL Analyst - We have one goal: to deliver more than our clients expect first time, every time. We’ve been serving industry around the world for 40 years plus, relied on for our agility, original thinking, sound judgment and high-caliber people.
The Job: Chemistry Analyst. Must have a minimum of Three years industrial experience in a GMP operated QC chemistry laboratory, with a strong working knowledge of quality management systems. The Job: Pharmaceutical and Medical Device Chemistry Analyst. A degree in Analytical chemistry, Pharmaceutical Chemistry or other related qualification is required.
QC Analyst, Chemistry QC Chemistry Manager - BSc in Chemistry or a biological science, with 3 – 6 years’ experience, or equivalent combination of education and experience. The individual in this position should have a working knowledge of the cGMP QC laboratory environment and laboratory equipment associated with biopharmaceutical analysis. Dublin
We are now looking for students who are interested in QC Chemistry Programme. Experience life inside Sanofi where you will quickly become part of the team. During your placement you will have the opportunity to work on real projects that challenge you and help you develop the skills for a great career. About our Work Placement
We have a fantastic opportunity for a Section Manager (Chemistry) to join our team in Dungarvan Co Waterford. Due to the expansion of our operations here in Dungarvan, we have a new and fantastic opportunity for a Section Manager (Chemistry) to join our team in Dungarvan Co Waterford.
We have fantastic opportunities for Chemistry Analysts to join our team in Dungarvan Co Waterford - Minimum BSc in Science, preferably chemistry Eurofins is the world leader in food and bio/pharmaceutical product testing.
CHEMISTRY LABORATORY SUPERVISOR required for mulitnational biopharma client in Co. Cork. The CHEMISTRY LABORATORY SUPERVISOR role will involve supervision and co-ordination of a team within Quality laboratories to ensure the timely and efficient testing and reporting of QC samples. This is a permanent role. * Co-ordination of area resources.
QC Chemistry laboratory experience is highly desired. Knowledge of working practices required for a Chemistry laboratory. 2-year contract - Ensure highest Quality & Compliance standards. Analysis, release and testing of samples. Documentation in compliance with GMP standards. Compliance with 6S standards. Problem solving to get to root cause of issues.