Senior In-vitro Analyst | Mayo

Recruit Island; Calgary; On-site; CAD 70,000 - 90,000; Full time

Job summary

A leading Pharma Company is seeking a Senior In Vitro Analyst to establish a new laboratory in Ireland. The role involves qualifications, validations, and compliance with GMP standards, along with generating cell banks and drafting SOPs. Ideal candidates will have experience in scientific research, particularly in virology and biosafety testing.

Qualifications

• At least 1 year of relevant experience in scientific research.
• Experience in in-vitro bioassays and project management is highly desirable.

Responsibilities

• Qualification and validation of all equipment for the new laboratory.
• Drafting SOPs and implementing testing procedures.

Skills

Problem Solving

Independent Work

Job description

Leading Pharma Company in the West of Ireland

Excellent career progression opportunities along with a generous package.

Oradeo Recruitment is seeking a Senior Invitro Analyst to join our clients in Mayo to establish a new suite of laboratories within strict timelines and manage the laboratory operations post-establishment. Our client is expanding the Biosafety (In-Vitro Adventitious Agent) line of business, including Virology and Mycoplasma laboratories, to meet growing testing needs. These assays will include cell culture, viral, and mycoplasma methods.

We are recruiting an In Vitro (Cell Culture / Virology) Analyst to work in and help establish a new Cell Culture and Virology Laboratory in Ballina, Co. Mayo, Ireland. This role reports to the In-Vitro (Cell Culture / Virology) Supervisor, and the main responsibilities include:

1. Qualification and validation of all equipment for the new laboratory in accordance with GMP and validation standards.
2. Drafting SOPs and implementing testing procedures in strict compliance with these SOPs to ensure GMP regulatory adherence.
3. Generating and qualifying cell banks for client-specific testing.
4. Establishing test method SOPs and validating methods as appropriate.

Core duties include:

1. Understanding all regulatory guidelines relevant to the work.
2. Executing protocols and preparing reports.
3. Carrying out test method procedures.
4. Assisting in addressing departmental quality documents including audit responses, facility replies, and deviation reports.
5. Participating in laboratory investigations as needed.
6. Participating in training sessions.
7. Updating SOPs as required.
8. Assisting in generating risk assessments for laboratory activities and test items.

The minimum requirements for the In Vitro Analyst role are:

1. At least 1 year of relevant experience in scientific research, preferably within a GMP-regulated environment (EMEA / FDA), in the pharmaceutical, medical device, or CRO industry.
2. Experience in in-vitro bioassays and project management is highly desirable.
3. Experience in virology and biosafety testing is highly desirable.
4. Knowledge of biosafety classifications and relevant safety regulations is desirable.
5. Ability to problem-solve and work independently.

For more information about this position or other opportunities, contact Angela Haran at Oradeo Recruitment on [phone] or apply in confidence.

About Oradeo: We are specialists in life sciences, pharmaceutical, construction, and engineering sectors. We provide recruitment and managed labour services across Ireland, the UK, and Europe, serving sectors including construction, civil engineering, data centers, mechanical & electrical, life sciences, and renewable energies.