QC Executive

Back4good; Dublin (OH); On-site; USD 80,000 - 100,000; Full time

Job summary

Back4good is seeking a QC Executive in Dublin, Ohio, to ensure compliance with FDA and EMEA regulations for solid oral dosage pharmaceuticals. The ideal candidate will have over 5 years of experience in an analytical lab, strong organizational and technical writing skills, and the ability to lead a team. Expertise in GC/HPLC analysis is essential, alongside a BSc in a science-related field. The role emphasizes adaptability and knowledge of manufacturing processes.

Qualifications

• 5+ years of experience in an analytical laboratory in the pharmaceutical industry.
• Thorough knowledge of Good Manufacturing Practice current FDA & EMEA regulations.
• Good working knowledge of manufacturing processes and packaging processes.

Responsibilities

• Manage and lead a team of Analysts.
• Adapt to changing priorities.

Skills

Organisational skills

Technical writing skills

Investigation skills

Analytical skills

Interpersonal skills

Communication skills

Education

BSc in a science related discipline

Tools

GC

HPLC

Job description

back 4 Good -Your future in Ireland is working on an assignment to source a QC Executive.

This role requires a thorough knowledge of Good Manufacturing Practice current FDA & EMEA regulations for solid oral dosage pharmaceuticals and API intended for Human use.

The role requires good working knowledge of manufacturing processes, packaging processes and validation activities used in the Pharmaceutical industry.

Responsibilities

• Demonstrates experience managing, motivating and leading a team of Analysts.
• Ability to adapt to changing priorities.

Qualifications

• Excellent organisational supervisory, technical writing skills and investigation skills are necessary.
• BSc (minimum) in a science related discipline.
• More than 5 years of experience in an analytical laboratory in the pharmaceutical industry.
• Technical experience of GC/HPLC analysis is essential.
• Knowledge of Mircobiological testing is desirable.
• Excellent organisational, communications, interpersonal and report writing skills.
• Good working knowledge of manufacturing processes, packaging processes and validation activities used in the Pharmaceutical industry.
• Thorough knowledge of Good Manufacturing Practice current FDA & EMEA regulations for solid oral dosage pharmaceuticals and API intended for Human use.