QC Analyst

QC Micro Analyst 

Location: Cork, Ireland (onsite)

Duration: 12 months 

Hours: 2 & 4 cycle shift 

Imagine your next project working in the position of a QC Micro Analyst where you will be responsible for carrying out tasks and projects related to raw material, utility, in process, release and stability testing of biotechnology products as required by Good Manufacturing Practice (GMP).

roles and responsibilities

• Achieves a high level of competency in laboratory methods and procedures to support raw material, utility, in process, release and stability testing of biotechnology products.

• Performs routine and non-routine Microbiological and or Biochemical/Chemical testing activities as required.

• Ensures that all testing is completed, reviewed and approved within agreed turnaround times.

• Ensures QC activities are carried out in compliance with product licence commitments, cGMP and company quality standards.

• Trains other QC analysts and Manufacturing personnel in laboratory methods and procedures when required.

• Writes/updates and reviews TMs, SOPs and WIs as required.

• Writes and reviews invalid assays, non-conformances and deviations as required.

• Initiates and drives change controls to completion to implement process improvements.

• Actively participates in JBIL lean initiatives such as Kaizen, 5S and Gemba.

• Is an active member of the QC group and provides assistance with other group activities as required.

• Communicates relevant issues to the QC Team Leader promptly.

• Deputises for the QC Team Leader as appropriate.

• Maintains and develops knowledge of analytical technology as well as cGMP standards.

• Partners with other departments to ensure that all QC testing activities are completed in a compliant and efficient manner

how to succeed

The ideal candidate should have a minimum of 1 to 3 years of experience working in a dynamic microbiology environment

You will also bring:

• BSc (Honors) in a scientific/technical discipline.

•  Demonstrated knowledge and testing experience in an FDA/HPRA approved QC laboratory

• Previous aseptic techniques (desirable)

• knowledge of LIMS, Track wise and Electronic documentations systems. (desirable)

• Excellent interpersonal skills

• Ability to operate as part of a team is critical.

• Excellent communication skills both written and verbal

• Good knowledge of Microsoft Office applications such as word, excel, PowerPoint

• Excellent technical writing skills

• Customer focus

• Attention to detail

• Good problem solving skills

• Results and performance driven

• Adaptable and flexible

Benefits

This role offers a very competitive hourly rate. This contract will run for a minimum of 12 months with a strong possibility of extending.

you are welcome here

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Janssen

Janssen is the Pharmaceutical Companies of Johnson & Johnson - the world's most comprehensive and broadly-based healthcare Company. At Janssen, we bring together top scientists and researchers to pursue the most promising science and drive collaboration to create visionary medicines and healthcare solutions covering five priority therapeutic areas - Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience and Oncology. Contribute to the next pharmaceutical breakthrough with your next project at Janssen. 

Janssen UK: https://www.janssen.com/uk/

Janssen Ireland: https://www.janssen.com/ireland/

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, Limited & Umbrella options are available. 

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.