Microbiology Shift Analyst (24 months Fixed Term) at Alexion PharmaceuticalsInc
Dublin, County Dublin, Ireland -
Full Time


Start Date

Immediate

Expiry Date

07 Sep, 25

Salary

0.0

Posted On

10 Aug, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Communications, Regulatory Requirements, Microbiology, Hazardous Materials, Sterility Assurance, Testing

Industry

Pharmaceuticals

Description

QUALIFICATIONS:

  • Minimum of 1 year experience in cGMP Quality environment.
  • Experience in testing of 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.
  • The duties of this role are generally conducted in an lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and
    Microbiology Shift Analyst
    Location: Alexion Dublin Manufacturing Facility
    Reports To: Siobhan Devoy, QC Microbiology Senior Manager
    around biological, infectious, and hazardous materials; 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.

EDUCATION:

  • Degree in Microbiology or related science.
Responsibilities

THIS IS WHAT YOU WILL DO:

The QC Microbiology Analyst will support the Bulk Drug Facility in Dublin with emphasis on microbiological testing such as Environmental Monitoring, Water sampling, TOC, Bioburden and Endotoxin. This is shift role 12h/7 days with two rotating shift patterns.

YOU WILL BE RESPONSIBLE FOR:

  • Environmental and Facilities monitoring sampling and testing.
  • Testing to support release and stability programs on site.
  • Ensuring high cGMP, GLP standards are maintained while testing and adherence to schedules and targets to meet regulatory and business requirements.
  • To ensure a high standard of housekeeping and safety is maintained in the Laboratory.
  • Completion of project work and implementation of initiatives designed to improve the efficiency of the laboratory function/department.
  • To keep management updated on issues arising within the laboratory.
  • Investigate out of specification/limit results utilizing Structured Problem Solving, Root Cause Analysis tools in conjunction with the Microbiology Laboratory Supervisor, QA and other relevant departments and to implement effective corrective and preventative actions while ensuring all investigations are closed with the specified lead-time.
  • To train laboratory personnel and play appropriate role in the development, operation and evaluation of training/re-training programs.
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