Overview
Sr. Tech, Quality Control role at MSD Ireland in Dunboyne, County Meath. This position is part of the Global Quality Large Molecule Analytical Sciences QC team. The Senior QC Analyst will support the Quality Control testing function, ensuring compliance with cGMP and corporate regulations. This is a key role within the Quality organisation to establish the Laboratories as a hub for specialised analytical testing and create value for patients.
Responsibilities
* A proven ability to deliver on tight timelines.
* Excellent influencing/collaboration skills and a teamwork mindset.
* Excellent troubleshooting and problem-solving skills.
* Ability to challenge the status quo with a continuous improvement mindset.
* Ability to think logically and be proactive under pressure.
* Proven ability in using a wide variety of lean tools and building capability within teams.
* Act as a change agent to support the organisation with good change management tools and techniques.
* Support creation of a focus on creating a continuous mindset organisation through active coaching.
* Effective communicator with a proven ability to develop capabilities of others in a team.
* Demonstrated ability to give and receive feedback; excellent troubleshooting and problem-solving skills.
* Ability to work as part of a team and on own initiative in a constructive manner.
* Flexible and self-motivated.
* Promoting a culture where diversity and inclusion is part of the DNA.
* Establishes stretch goals for self to deliver on priorities for the SDWT or Hub Team.
* Identifies and communicates risks in area of responsibility and across the site.
* Collaborates across the Network and continuous improvement teams across the Organisation.
* For product quality, collaborates with Process Development Technical Services (PDTS) and Manufacturing Operations but is responsible for providing information to support the QMR decision.
* For safety, the individual is accountable to drive a culture of “everyone owns safety”
Qualifications
* Degree Qualification (Science/Technical/Quality or related)
* 1-2 years’ experience in the biotechnology and/or pharmaceutical industry
* Excellent written and oral communication skills
* An understanding of cGMP requirements for Laboratory Operations and/or systems and compliance
* Ability to work on their own initiative in addition to working as part of a team
* Excellent time management and organisational skills
* An understanding of analytical methodology
* An understanding of GMP, ICH, USP and global compendia regulations and guidance
* Demonstrated understanding of continuous quality/process improvement tools (e.g., DMAIC, Lean, 5S) desirable
* Proven ability to work cross-functionally, focusing on meeting and tracking to schedules in an interdependent work culture
* Strong organisational skills with ability to manage multiple priorities and escalate issues when needed
Evidence of continuous professional development is desirable. We are committed to inventing for life and keeping the patient at the heart of everything we do. We are an equal opportunity employer and value diversity and inclusion. Please contact the Talent Acquisition Advisor assigned to this role if you need support during the recruitment process.
If you are ready to invent solutions to meet unmet healthcare needs, please apply today.
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