Quality Control Analyst II Wet Chemistry

1100 Mylan Pharmaceuticals Inc.; Galway; On-site; EUR 32,000 - 42,000; Full time

Benefits offered by this job

Bonus scheme

Health insurance

Pension

Job summary

Viatris is seeking a Quality Control Analyst I in Ireland to perform wet chemistry analyses of raw materials, in-process, finished products and stability samples. You will document results per GMP and support sampling, validations and continuous improvement initiatives within the QC team.

Ideal candidates hold a Science degree (Chemistry preferred) with 0–2 years of relevant experience, strong analytical skills, good communication, and the ability to work in a collaborative team environment.

Qualifications

• Bachelor's degree in science (chemistry preferred) with 0–2 years of relevant industrial experience.
• Strong analytical skills with excellent attention to detail.
• Excellent verbal and written communication abilities.
• Ability to work as part of a team and manage time effectively.
• Ability to read and interpret general business documents and write routine reports.
• Knowledge of basic chemistry and proficiency with MS Office tools.

Responsibilities

• Perform wet chemistry analysis of raw materials, in-process, finished product and stability samples and document results in GMP-compliant records.
• Conduct routine wet chemistry testing in line with GLP and cGMP procedures.
• Assist QC Sampling Technician with material and water sampling when required.
• Support validation activities including process and method validations.
• Contribute to department projects and continuous improvement initiatives (6S/lean).
• Carry out additional duties as assigned by QC leadership.

Skills

Analytical skills

Attention to detail

Communication

Teamwork

Time management

Education

Bachelor's degree in Science

Tools

MS Office

Job description

Viatris is seeking a Quality Control Analyst I in Ireland to perform wet chemistry analyses of raw materials, in-process, finished products and stability samples. You will document results per GMP and support sampling, validations and continuous improvement initiatives within the QC team.

Ideal candidates hold a Science degree (Chemistry preferred) with 0–2 years of relevant experience, strong analytical skills, good communication, and the ability to work in a collaborative team environment.