Job Description
QC Laboratory Technician
- 18 month Fixed-Term role with competitive remuneration and benefits
- Based on site at Upper Hutt, Wellington, New Zealand
- Global Animal Health Manufacturing organisation
- Work in a quality-focused QC Laboratory environment supporting safe, effective and compliant product release
- Join a collaborative team dedicated to reliable supply and continuous improvement
- Report to the QC Manager
As a QC Laboratory Technician, you will play a key role in performing and documenting activities within the assigned QC Laboratory area. You will support assay performance, manage your workload effectively and help ensure smooth laboratory operations to meet schedules for release of intermediate and final products.
What You Will Do
QC Laboratory Operations
- Perform, document and coordinate activities within the assigned QC Laboratory area
- Monitor assay performance and support the timely release of intermediate and final products
- Ensure adequate stocks of reagents, test materials and equipment are available to perform testing on time
- Plan, conduct, report and interpret routine laboratory assays in accordance with SOPs
Documentation and Data Integrity
- Accurately document all tasks, test data and observations in test records, worksheets and logbooks in accordance with Good Documentation Practice (GDP)
- Peer review the work of team members on procedures you are fully trained in
- Develop and maintain documentation in line with company and quality standards
- Assist with SOP and worksheet development and updates
Housekeeping and Equipment Maintenance
- Perform housekeeping tasks in accordance with SOPs and GLP
- Complete assigned housekeeping inspections
- Maintain laboratory equipment in a fully operational state of calibration and validation
- Perform routine calibrations as required
- Refer to, understand and follow applicable Global Quality Policies
Event Management and Continuous Improvement
- Monitor assay outcomes for unusual occurrences and review trends
- Investigate and report events
- Notify the supervisor of potential failures, record faults and rectify common faults independently
- Implement assigned CAPAs arising from investigations
- Perform routine test method or equipment validations under direction
- Author or technically review SOPs for procedures you are fully trained in
Team Contribution and Reporting
- Complete training in assigned areas and tasks
- Support team initiatives and collaborate with other team members
- Follow global and local procedures for reporting Events, Adverse Events and Product Quality Complaints within required timelines
What You Must Have
- Bachelor’s degree in a scientific discipline or equivalent experience
- Experience working in a QC, laboratory or quality-focused manufacturing environment
- Strong understanding of SOPs, GLP and Good Documentation Practice
- Ability to plan and coordinate your workload to meet schedules
- Strong attention to detail and accuracy in documentation
- Ability to investigate issues, identify faults and support corrective actions
- Good communication and teamwork skills
- Willingness to complete training and support broader team initiatives
- Ability to maintain high standards of housekeeping and equipment care
What You Can Expect
- The opportunity to contribute to the release of safe, effective and compliant products
- A collaborative QC team environment with a focus on quality and continuous improvement
- A role where your attention to detail and laboratory skills make a real impact
We are proud to be a company that embraces the value of bringing talented and committed people together. The fastest way to breakthrough innovation is when 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 workplace.
Required Skills:
Calibration Procedures, Controls Management, Equipment Testing, Inventory Management, Laboratory Operations, Laboratory Safety, Microbiology Lab Techniques, Pipetting, Production Quality Control, Quality Standards, Recordkeeping, Regulatory Compliance, Safety Measures, Statutory Compliances, Test Data Management
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Temporary (Fixed Term)
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
No Travel Required
Flexible Work Arrangements:
Not Applicable
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
10/24/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
