ACCOUNTABILITIES:

• Conduct environmental and facilities monitoring sampling and testing.
• Perform testing to support release and stability programs on site.
• Maintain high cGMP and GLP standards while adhering to schedules and targets to meet regulatory and business requirements.
• Ensure a high standard of housekeeping and safety in the laboratory.
• Complete project work and implement initiatives to improve laboratory efficiency.
• Keep management updated on issues arising within the laboratory.
• Investigate out-of-specification/limit results using Structured Problem Solving and Root Cause Analysis tools, collaborating with relevant departments to implement effective corrective and preventative actions.
• Train laboratory personnel and contribute to the development, operation, and evaluation of training/re-training programs.

ESSENTIAL SKILLS/EXPERIENCE:

• Experience in testing sterile/non-sterile pharmaceutical/biopharmaceutical products.
• Good knowledge of current regulatory requirements for Microbiology/Sterility Assurance in support of cGMP operations supporting clinical and commercial manufacturing.
• Degree in Microbiology or related science.
• Ability to work in a lab environment with biological, infectious, and hazardous materials; lift/carry 15/30 pounds unassisted/assisted; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem-solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

DESIRABLE SKILLS/EXPERIENCE:

• Experience with aseptic techniques. AstraZeneca offers an environment where you can work on diversified tasks with a global team. Collaborate with knowledgeable colleagues across multiple business functions, exposing yourself to new ways of thinking that foster growth both collectively and individually. Here, every voice is heard and matters, creating an inclusive atmosphere where you feel part of the conversation!
  If you are ready to take the next step in your career, apply now to join our team and make a real difference!
  We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Are you ready to make a difference in the world of pharmaceuticals? As a QC Microbiology Analyst, you’ll play a crucial role in supporting the Bulk Drug Facility in Dublin. Your expertise in microbiological testing, including Environmental Monitoring, Water sampling, TOC, Bioburden, and Endotoxin, will ensure the highest standards of quality and safety are maintained. Dive into a dynamic environment where your skills will be valued and your contributions will have a direct impact on patient care.