Analytical Chemist: Global Impact Lab & Tech Transfer

LSNE Contract Manufacturing; Stamullen; On-site; EUR 42,000 - 56,000; Full time

Job summary

PCI Pharma Services in Stamullen is seeking an Analytical Chemist to join our lab on a rotational three-day-per-week shift. You will perform routine analytical testing with a right-first-time approach, support technical transfer activities, and assist in preparing and reviewing technical documentation within the department.

The role requires meeting testing schedules, maintaining inventory and logbooks, and taking ownership of samples across projects while ensuring compliance with cGMP/GXP and

Qualifications

• Experience performing routine analytical testing with accuracy and first-pass compliance.
• Solid understanding of cGMP/GxP requirements in a regulated lab.
• Ability to prepare and review technical documentation and SOPs.
• Experience identifying and addressing out-of-specifications and deviations.
• Familiarity with technical transfer activities and collaboration with QA.
• Ability to train team members and deputise for management when needed.

Responsibilities

• Perform routine testing with a right first time approach.
• Assist in technical transfer activities.
• Prepare and review department documentation.
• Meet testing deadlines and support team members as required.
• Monitor inventory levels and maintain logbooks for analytics and equipment usage.
• Own sample handling for different project work.
• Adhere to cGMP and GXP guidelines and comply with customer/regulatory requirements.
• Participate in continuous improvement projects to maintain testing standards.

Skills

Analytical testing

cGMP knowledge

Quality documentation

OOS handling

Technical transfer

Lab equipment handling

Job description

PCI Pharma Services in Stamullen is seeking an Analytical Chemist to join our lab on a rotational three-day-per-week shift. You will perform routine analytical testing with a right-first-time approach, support technical transfer activities, and assist in preparing and reviewing technical documentation within the department.

The role requires meeting testing schedules, maintaining inventory and logbooks, and taking ownership of samples across projects while ensuring compliance with cGMP/GXP and