Biologics Technician

AbbVie; Sligo; On-site; EUR 40,000 - 55,000; Full time

Job summary

AbbVie is seeking a Biologics Technician for its new team in Ballytivnan, Sligo. The role involves ensuring the efficacy of biologics production, documentation compliance, and quality assurance. Candidates are expected to have a 3rd level qualification in a relevant Science discipline and at least 2 years of experience in GMP manufacturing, with preference for experience in antibody drug purification. Shift work is required, alongside collaboration with various departments to ensure operational excellence.

Qualifications

• Minimum 2 years experience in GMP manufacturing.
• Experience with antibody drug and drug substance purification preferable.

Responsibilities

• Operate daily production equipment efficiently.
• Document activities in line with cGMP requirements.
• Perform visual inspection of final products.
• Conduct in process testing and comply with regulations.

Skills

GMP manufacturing

Process testing

Equipment operation

Documentation

Education

3rd level qualification in a relevant Science discipline

Job description

Job Description

We are recruiting a Biologics Technician to join our site in Ballytivnan, Sligo on a brand new team, working on a new groundbreaking drug. This role will require shift work.

A snapshot of your key responsibilities as a Biologics Technician would be:

• You will be assigned to the daily production operations, operating different equipment.
• Efficiently operate all biologics processes minimizing material loss.
• Documentation of all activities in line with cGMP requirements.
• Perform final product visual inspection.
• Perform product intermediary packaging, as applicable.
• Perform all in process testing methods.
• Material receipt from warehouse, verifying all pertinent documentation.
• Transfer of final material to warehouse inventory.
• Perform process tests and participate in qualification and validation activities as required.
• Diagnose and resolve events or exceptions of production equipment and processes.
• Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulations, following the procedures and policies of the plant, division, and the corporation.
• Keep detailed records, manual or electronic, of the operations carried out during the work shift.
• Adhering to all relevant policies relating to Quality & Safety.
• Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures.

Qualifications

What you will need:

• 3rd level qualification in a relevant Science discipline
• 2 years experience in GMP manufacturing
• Antibody drug, ADC and drug substance purification experience preferable

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.