Technical Specialist QC

Job Role: Technical Specialist – Laboratory
About the Role:
We are seeking an experienced Technical Specialist to join a dynamic laboratory team. This role focuses on handling medium and high-quality compliance issues, maintaining cGMP compliance, and supporting new product introductions and lab operations. You will act as the Subject Matter Authority during audits and inspections and provide technical expertise for laboratory systems and processes.

Key Responsibilities:

Lead deviation management, acting as investigator for non-conformances and coordinating corrective and preventive actions (CAPAs).
Create, review, and update laboratory documentation, including supporting documents for new product introductions (NPI).
Provide technical support to the lab and contribute to cross-functional projects and services.
Act as technical system owner for analytical equipment and lab systems.
Serve as Subject Matter Authority during audits and inspections.
Lead and drive continuous improvement projects.
Promote and demonstrate safety, compliance, and reliability in daily operations.
Communicate effectively and build trusted relationships with team members, supervisors, and customers.

Key Competencies:

Strong analytical thinking and technical problem-solving skills.
Proven ability to work independently and collaboratively with cross-functional teams.
Knowledge of GMP and cGMP compliance requirements.
Experience in microbiological techniques such as bioburden, endotoxin, and sterility testing is a plus.
Excellent communication and interpersonal skills.
Experience with laboratory systems and equipment.

Requirements:

Bachelor’s degree (HLO) or higher in Life Sciences, Molecular Biology, or comparable field.
Fluency in English (written and spoken).
2–5 years of relevant laboratory or pharmaceutical experience.

Practical’s: