QC Chemistry Analyst

GRIFOLS, S.A.; Dublin; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Competitive salary package

Group pension scheme

Private medical insurance

Career development opportunities

Succession planning

Job summary

Grifols Worldwide Operations (GWWO) is seeking a QC Chemistry Analyst to support purification and aseptic manufacturing in a state-of-the-art facility. You will report to the QC Chemistry Supervisor and enjoy strong career development opportunities within a global biotechnology company.

You will perform raw material, in-process and finished product analyses using HPLC, spectrophotometry and related techniques, participate in method transfer and validation, and ensure compliance with cGMP.

Qualifications

• Bachelor’s degree in Chemistry or Biochemistry.
• Minimum of 2 years of related experience.
• Knowledge of analytical techniques/instruments including HPLC and spectrophotometry.
• Experience with biologics or protein-based therapeutics is desirable.

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 using analytical techniques (HPLC, Spectrophotometry, etc.).
• Raw material QC including Karl-Fischer, FT-IR and NIR techniques.
• Ensure laboratory processes, equipment and services are installed, qualified and maintained appropriately.
• Participate in verification, validation and technical transfer of analytical testing procedures.
• Ensure adherence to cGMP and company specifications.

Skills

Chemistry

Biochemistry

Analytical thinking

Verbal communication

Team collaboration

Problem-solving

Education

Bachelor’s degree in Chemistry/Biochemistry

Tools

HPLC

Spectrophotometry

Electrophoresis

Karl-Fischer

FT-IR

NIR

GC

Flame-photometry

AA

Job description

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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.

Position Summary:

Quality Control (QC) Chemistry Analyst is required for the purification and aseptic manufacturing plant at Grifols Worldwide Operations (GWWO), reporting to the QC Chemistry Supervisor.

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.

What You Will Do:

• 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
• Ensure laboratory processes, equipment and services are installed, qualified and maintained appropriately
• Participate in the verification, validation and technical transfer of analytical testing procedures
• Ensure that all cGMP, company specifications and procedures are followed.
• Investigate Out of Specification (OOS) and Out of Trend (OOT) results as required
• Participate in and responsible for QC related CAPA’s.
• Adhere to QC documentation system and prepare 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 work area is maintained in a state of compliance and audit readiness
• Flexibility and willingness to carry out shift work when required

What You Will Bring:

• Bachelor’s degree in Chemistry, Biochemistry or closely related scientific field
• Requires a minimum of 2 years of related experience.
• Knowledge of a wide array of analytical techniques/instruments including HPLC, Spectrophotometry and Electrophoresis.
• Knowledge of specific product analysis (e.g. IC, AA, GC, Flame-photometry and Kjeldahl techniques) desirable
• Knowledge of raw material analysis (e.g. Karl-Fischer, FT-IR and NIR techniques) desirable
• Experience with investigating Out of Specification and Out of Trends.
• Experience in method transfer and verification/validation desirable.
• Knowledge of analytical techniques for biologics or protein-based therapeutics desirable.
• Excellent verbal and written communication.
• Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner.
• Strong organizational, analytical and problem-solving skills.

Our Benefits Include:

• A highly competitive salary package
• Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
• Private medical insurance for the employee
• Ongoing career development opportunities within a rapidly growing organisation
• Strong focus on succession planning and internal promotion
• Dedicated education and professional development allowance
• Wellness and social initiatives, including activities such as padel and summer events