QC Chemistry Senior Shift Analyst (2yr Contract) Job

Date: Feb 13, 2018

Location: Cork, IE

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Requisition ID: QUA006447

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where MSD has codified its 125-year legacy. MSD’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

MSD Manufacturing Division, MMD, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe.

The purpose of the QC Senior Analyst is to support the Quality release of our products.

The teamworking style is one of collaboration, coaching and facilitating to provide solutions to the Quality team to support a High Performance Organisation.

The candidate will contribute to the High Performance culture by providing an inclusive environment to enable team members to achieve their best work.

The QC Senior Analyst is an active member of the cross functional Team, providing expertise to ensure compliance.

The QC Senior Analyst will model the MSD Leadership behaviours and understand the MPS principles to drive a culture of continuous improvement building a High Performance Organisation.

The QC Senior Analyst will participate and comply with the MSD Manufacturing Division Quality Management System (QMS) requirements, including ownership, as relevant to you.

Primary activities/responsibilities:

  • Ensure highest Quality & Compliance standards.

  • Review and coordination of testing

  • Documentation in compliance with GMP and GDP standards.

  • Support Laboratory Investigations.

  • Problem solving to get to root cause of issues.

  • Compliance with 6S standards.

  • Responsible for supporting a culture of Continuous Improvement by using MSD Six Sigma tools in your daily work.

  • Coaching and collaborating with others by sharing your skill-set and expertise.

At least 3 years’ experience in the Pharmaceutical industry or a similar operating environment

Candidates must have :

  • Knowledge of working practices required for a Chemistry laboratory. 

  • Good knowledge of basic computer programs such as MS Word and Excel. 

  • Good verbal and written communication skills. 

  • Good understanding of quality principles and good attention to detail.

  • Excellent work ethic required.

  • Problem solving skills.

  • A good knowledge of cGMP, GLP, Quality Management Systems.

  • Training of area personnel.

  • Participate in corporate/regulatory audits.

  • Participate in risk assessments, inspections, audits, incident investigations, etc. and implement and follow-up CAPA’s assigned to you
Your role at MSD is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At MSD, we’re inventing for life.

Job: Quality Lab Related
Other Locations:
Employee Status: Regular
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: MSD

Job Segment: Medical, CAPA, Law, Compliance, Pharmaceutical, Healthcare, Management, Legal, Science

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