Micro Analyst Quality Control

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

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About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine 

We are searching for the best talent for Analyst Quality Control to be in Cork.

An pre-identified candidate for consideration has been identified. However, all applications will be considered.

You will be responsible for:

• Achieves competency in laboratory methods and procedures.
• Trains other QC analysts in laboratory methods and procedures when required.
• Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
• Executes validation, operation, maintenance, calibration and troubleshooting of equipment and its associated software.
• Writes, executes, reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
• Performs routine and non-routine analytical testing activities.
• Review and approval (where appropriate) of laboratory test results. Ensures that testing and results approval are completed within agreed turnaround times.
• Writes and reviews laboratory TMs, SOPs, TMDs and WIs as directed by company policy.
• Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
• Is an active member of the QC group and provide assistance with other group activities as required and communicates relevant issues to the QC Specialist, QC Team Leader and Manager.
• Deals with Quality Issues in an accurate and timely manner.
• Maintains and develops knowledge of analytical technology as well as cGMP standards.
• In process control testing and activities to support the production units.

Qualifications / Requirements:

• A third level qualification of a scientific/technical discipline is required.
• Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.

Key Individual Contributor Competencies

• Builds strong productive relationships.
• Demonstrates ability to work with teams and individuals.
• Asserts personal ideas and opinions using persuasion to influence others.
• Seeks opportunities to grow and develop professionally.
• Uses best practices to improve business operations.
• Holds self-accountable for compliant and flawless execution.
• Takes personal responsibility for decisions that successfully build customer value.
• Effectively manages and adapts to change.
• Demonstrates the courage to stand alone on ideas and opinions that differ from others.
• Listens effectively and remains open to other’s ideas.
• Works effectively with people that have diverse styles, talents and ideas.
• Maintains the highest standards of ethical behavior.
• Treats people with dignity and respect.

Significant Environmental, Health and Safety Considerations

• All employees are required to comply with the requirements of the company’s Environmental Health and Safety Policy, Safety Statement, associated EHS Procedures and local legislation.#RPOAMS