An experienced QC Analyst is required to join a global pharma in Dublin.
The primary purpose of the Analyst is to analyse raw material, in-process and finished product as well as stability samples according to the relevant specifications while ensuring the documenting and reporting of same is conducted in accordance with good laboratory practices.
The Analyst shall carry out most of his/her duties in the Quality Control Laboratory and the primary tasks and responsibilities of the position are as follows.
Working as directed by the Area Supervisor, in accordance with Company safety policies, cGMP and cGLP.
Receiving and logging samples into the Laboratory.
Analysing raw material, in-process, finished product and stability samples according to specifications, primarily HPLC and dissolution.
Analysing validation samples according to validation protocols and investigational samples as directed.
Recording results in a timely and accurate fashion.
Ensuring the Right First Time KPI with respect to Analyst's documentation are achieved.
Reviewing co-workers/analyst documentation
Ensuring that all Quality Systems within the department are adhered to on a daily basis.
Ensuring correct labelling of laboratory reagents and samples.
Troubleshooting any erroneous analytical data obtained (Involvement in Lab Investigations Reports)
Helping to ensure laboratory SOPs and specifications are kept up to date and in a state of compliance.
Training other laboratory staff as requested and appropriate.
A BSc Degree (life science) in conjunction with at least 12 months' work experience working within a pharmaceutical cGLP environment (HPRA and FDA approved).
A minimum of 6 months practical/working experience of HPLC, IC & GC testing methods.
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.