Senior Micro Analyst – QC & Microbiology Lead

AbbVie; Sligo; In loco; EUR 45.000 - 65.000; Tempo pieno

Descrizione del lavoro

AbbVie Inc. in Ballytivnan, Sligo is seeking a Senior Micro Analyst to join our QC team on a 12-month contract, on site in Ballytivnan, Sligo. You will ensure testing and release of materials meet specifications, supporting plant quality and safety goals.

The role requires 2+ years in Pharma, 5+ years in a lab setting, and strong regulatory knowledge, with expertise in HPLC, GC, LCMS, GCMS and related techniques.

Competenze

• Minimum 2 years’ experience in Pharma industry.
• 5 years in a lab-based role.
• Strong knowledge of regulatory requirements.
• Strong knowledge of HPLC, GC, LCMS, GCMS, Automatic titration, Identification techniques.

Mansioni

• Maintain and align with Laboratory Documentation and Computerized Systems Data Integrity requirements.
• Understand Regulations and business processes required to maintain Laboratory Data Integrity and ensure implemention.
• Carry out environmental and product microbiological tests as required.
• Define and update procedures for plant relative to microbiological and environmental testing.
• Lead validation of equipment and test methods for microbiological tests.
• Lead Test method transfer of microbiological methods.
• Further develop and streamline microbiological laboratory procedures.
• Maintain and approve up-to-date and detailed records of all tests performed.
• Adheres to and supports all EHS & E standards, procedures and policies.
• Lead and support any lab related investigations.

Conoscenze

Regulatory knowledge

Lab testing procedures

Strumenti

HPLC

GC

LCMS

GCMS

Automatic titration

Identification techniques

Descrizione del lavoro

AbbVie Inc. in Ballytivnan, Sligo is seeking a Senior Micro Analyst to join our QC team on a 12-month contract, on site in Ballytivnan, Sligo. You will ensure testing and release of materials meet specifications, supporting plant quality and safety goals.

The role requires 2+ years in Pharma, 5+ years in a lab setting, and strong regulatory knowledge, with expertise in HPLC, GC, LCMS, GCMS and related techniques.