QC Chemistry Analyst - Ireland - Kenny-Whelan & Associates

Description

Kenny-Whelan (a specialist division of the CPL group) are hiring a QC Chemistry Analysts to work on contract atJanssen Pharmaceutical Sciencesin Little Island Cork

MUST ALREADY BE ELIGIBLE TO WORK ON CONTRACT IN THE REPUBLIC OF IRELAND- i.e have a valid work permit with 12 months permission + on it

NEW VACANCIES MARCH 24

Contact Jenn Dinan on or email - the link below

QC Chemistry Analyst

This position is responsible for carrying out tasks and duties related to analysis, material release, lab utilities and testing procedures at Janssen Pharmaceutical Sciences UC as required by Good Manufacturing Practice (GMP). Partners with other Departments to ensure that all QC testing activities are completed in an efficient manner.

GENERAL SCOPE OF RESPONSIBILITIES:

• Achieves competency in laboratory methods and procedures, specifically compendial Wet Chemistry techniques and Chromatography

• Performs analytical testing activities in relation to material release.

• 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 and WIs as directed by company policy.

• Ensures QC activities are carried out in compliance with product licence 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 Team Leader and Manager.

• Deals with non-conformances/ deviations in an accurate and timely manner.

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

KEY COMPETENCIES REQUIRED:

• Facilitate an environment of continuous improvement

• Carries out all duties in a Safety conscious manner

• Collaboration and teamwork

• Strategic Thinker

• Credo value of integrity

• To work as a strategic partner with all other departments within the company

• Interface with all site departments as required.

• Excellent interpersonal skills

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

• Customer focus

• Innovative

• Excellent communication skills both written and verbal

• Attention to detail

• Good problem solving skills

• Results and performance driven

• Adaptable and flexible

QUALIFICATIONS AND EXPERIENCE:

• A level 8 qualification in a scientific/technical discipline required.

• Knowledgeable of FDA/EMEA regulatory requirements applicable to pharmaceuticals.

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

• A minimum of 2 years experience in a laboratory-testing environment within the pharmaceutical industry would be an advantage.

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 behaviour

• Treats people with dignity and respect

MUST ALREADY BE ELIGIBLE TO WORK ON CONTRACT IN THE REPUBLIC OF IRELAND- i.e have a valid work permit with 12 months permission + on it

All applications will be treated with the strictest of confidence.

Contact Jenn Dinan on or email the link below