Description
The purpose of the Quality Analyst is to analyse/test samples to support the
Quality release of our products.
The teamworking style is one of collaboration, coaching and facilitating to
provide solutions to the Quality CoE team to support a High Performance
Organisation.
He/She will contribute to the High Performance culture within the Quality CoE
by providing an inclusive environment to enable team members to achieve their
best work.
The Quality Analyst is an active member of the cross functional CoE Team,
providing support, guidance and expertise to ensure the success of the IPT. The
Quality Analyst will model the Merck Leadership behaviors and understand the
MPS principles to drive a culture of continuous improvement building a High
Performance Organisation.
The Quality Analyst will participate and comply with the MMD Quality Management
System (QMS) requirements, including ownership, as relevant to you.
Responsible for supporting a culture of Continuous Improvement by using Merck
Six Sigma tools within the CoE in your daily work.
Coaching others by sharing your skill-set and expertise.
Key Behaviours
Focus on Customers, Including Patients
Focus the entire organization on delivering value for customers, including
patients, by understanding and meeting their needs.
Collaborate
Actively listen and seek to understand differing perspectives; work together to
achieve the common goals of the new Merck.
Act with Candor and Courage
Speak openly, honestly and with conviction; have the courage to take
appropriate risks and make difficult decisions.
Make Rapid, Disciplined Decisions
Make timely decisions at the right level with the right data, and support them
once made.
Drive Results
Set clear performance standards; overcome obstacles; hold ourselves and others
accountable for achieving results.
Demonstrate Ethics & Integrity
Adhere to the highest standards of trustworthy and ethical behavior in all
interactions and hold others to the same standards; comply with all laws,
policies and regulations; identify and address ethical issues without
hesitation.
Qualifications
Job Experience
· Demonstrated knowledge in more than one pharmaceutical and/or chemical
manufacturing operation (e.g. Quality, Science etc). Bioassay and/or cell
culture experience is highly desired.
· At least two years experience in the Pharmaceutical industry or a similar
operating environment which should include experience in a Bioassay laboratory.
A good knowledge of cGMP, GLP, site and corporate Quality Systems
Qualifications
· Degree or 3rd level qualification in Science or related discipline.
Preference for Lean Six Sigma Yellow Belt.
Expected Skill Set
Expected:
· Knowledge of working practices required for a Bioassay laboratory (e.g. good
aseptic techniques, cell culture, etc)
· Basic knowledge of computer programs such as MS Word, Excel and Access
· Good verbal and written communication skills
Good understanding of quality and good attention to detail
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