Quality Control Scientist

2 months ago

Upper Hutt, New Zealand MSD Full time

**Quality Control Scientist**
- ** Looking for a different challenge as a** **Quality Control Scientist **whereby you can still utilise your skills?
- ** Permanent Full-time **position with **competitive renumeration **and** benefits**:

- ** Located: NZ - Wellington - Upper Hutt**:

- Work with a **dedicated and welcoming team**:

- ** Upskill and growth in an area your passionate about**, whilst being fully supported and encouraged.
- Join a Trusted Global Leading** Animal Health **organisation

The primary responsibility of the QC Scientist is to perform and document tests within the assigned QC Laboratory, monitor assay performance, provide technical support in areas of expertise, plan and co-ordinate own and testing workload, review and release of test results and contribute to ensuring the smooth running of their area to meet schedules for release of final and intermediate products.

**What You Will Do**

**Responsibilities include, however not limited to**:
**Test antigen and / or vaccine, to required standards, according to set schedules/timelines by**:

- Conducting, reporting, and interpreting routine laboratory assays in accordance with Standard Operating Procedures (SOPs)
- Planning and coordinating the resources required to ensure achievement of the area outputs
- Working closely with logistics, production and engineering to set priorities when conflicts occur.

**Accurately record and report all test data / observations by**:

- Documenting all tasks in test records, worksheets or logbooks in accordance with Good Documentation Practice.
- Peer reviewing work of other team members on procedures in which they are fully trained.
- Performing test result release including SAP reporting and submission of documentation to QA.
- Ensuring test reporting and document reviews are performed to meet KPIs

**Minimise Events / invalid test assays by**:

- Monitoring assays for unusual occurrences including preparing and reviewing trends of assay results and recommending corrective action where necessary.
- Investigating and reporting on Events.
- Notifying Manager of potential failures, recording faults and rectifying common faults independently.

**Contribute to the continuous improvement and introduction of new methods in the department by**:

- Providing technical leadership in area of expertise
- Implementing assigned CAPA identified in investigations.
- Authoring or technically reviewing SOPs for procedures in which they are fully trained.
- Authoring and executing test method or equipment qualification protocols and reports.
- Involvement in the transfer of methodology from BTS or Global

**What You Must have**
- Science degree in relevant discipline preferred (Chemistry, Biology, Microbiology or related discipline)
- Experience in a laboratory (e.g. ISO17025, GLP OECD, GMP )
- Experience with GMP/GLP
- Previous method development and validation experience will be advantages.
- Demonstrated knowledge of relevant technical standards for laboratories e.g. VICH, ICH guidelines, EP and USP monographs
- Understanding of calibration requirements of laboratory equipment is desirable
- Previous experience with Laboratory LIMS systems
- Excellent technical written skills
- Computer Skills: Spreadsheet, Word, SAP

**What You Can Expect**
- ** Work** **autonomously whilst being supported, encouraged** and being part of a trusted Global Leading Animal Health organisation
- Flexibility and **opening doors to other opportunities** and skillsets
- Joining a **collaborative** team of **likeminded individuals**

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Regular

**Relocation**:
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Requisition ID**:R248433

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