QC Chemistry Analyst (12 Month Temporary Contract)

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

QC Chemistry Analyst is required for a new purification and aseptic manufacturing plant for the blood protein albumin at Grifols Worldwide Operations (GWWO).

This role offers a chance to work in a state of the art facility, in an innovative Biotechnology company with excellent career development opportunities and a clear and committed patient focus. Reporting directly to the Quality Control (QC) Manager of Grifols Worldwide Operations (GWWO).

The Core working hours are currently:

Mon - Thursday 7am - 4pm

Friday 8am - 3pm

Please note, In the near future, this role will transition to a shift-based schedule. Candidates interested in the position must be flexible and willing to work various shifts

Key Responsibilities

• Carry out raw material, in-process and finished product chemistry and immunochemistry analysis.
• In-process and finished product QC including protein and excipient analysis including analytical techniques such as Spectrophotometry, Immuno-electrophoresis, HPLC, GC, AA and Flame-photometry.
• Raw material QC including Karl-Fischer, FT-IR and NIR techniques.
• Testing carried out in relevant fumehoods / safety cabinets as required.
• Ensure laboratory processes, equipment and services are installed and qualified appropriately.
• Ensure laboratory equipment and services maintained in an operational (and safe) state.
• Participate in the verification, validation and technical transfer of analytical testing procedures.
• Ensure that all cGMP, company specifications, procedures and guidelines are followed.     
• Investigate Out of Specification (OOS) and Out of Trend (OOT) results as required.
• Investigate Non Conformances and actively lead subsequent corrective actions as required.
• Participate in and responsible for QC related CAPA’s.
• Adhere to QC documentation system and prepare and review document change requests as required.
• Develop, improve and implement QC procedures, processes and systems.
• Support projects and continuous improvement initiatives within the Quality department and other functional areas.
• Participate in international project teams relating to QC and wider quality activities and travel maybe required.
• Adhere to safety standards to ensure a safe working environment while ensuring the laboratory is kept clean, tidy and safe at all times.
• Prepare for, and support regulatory and internal inspections/audits.
• Provide hands-on guidance and training when needed.
• Ensures area of responsibility is maintained in a state of compliance and audit readiness.
• Maintain current knowledge of regulatory and industry standards, trends and advancements through independent reading and training. 
• Flexibility and willingness to carry out shift work when required.

Knowledge And Skills 

• Knowledge of and proficiency in a wide array of current analytical techniques including HPLC and UV Spectrophotometry,.
• Knowledge of and proficiency in the use of analytical instruments including troubleshooting skills.  
• Ability to carry out a wide array of Standard Operating Procedures.
• Experience with investigating and determining root cause of Out of Specification and Out of Trend events, and writing thorough reports regarding the investigational findings. 
• Interpret and apply applicable regulatory guidelines.
• Excellent verbal and written communication.  Must be able to read, write, and speak English.
• Must have strong technical writing skills. 
• Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner. 
• Strong organizational, analytical and problem-solving skills.  Ability to analyze details and perform structured decision-making on a daily basis.

Our Benefits Include:

• Highly competitive salary
• Group pension scheme - Contribution rates are 5% employer and 5% employee
• Private Medical Insurance for the employee
• Ongoing opportunities for career development in a rapidly expanding work environment
• Succession planning and internal promotions
• Education allowance
• Wellness activities - Social activities eg. Golf, Padel, Summer Events

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

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Location: Grange Castle (Dublin) 

Learn more about Grifols