Job Description
QC Senior Laboratory Technician
- Permanent, full-time role with competitive remuneration and benefits
- Location: New Zealand - Wellington - Upper Hutt, on-site with a supportive, collaborative team
- Career growth: Expand your expertise in a growing, successful industry
- Professional development: Gain valuable experience in a dynamic, evolving role
The primary responsibility of the Senior QC Laboratory Technician is to perform and document tests within the assigned QC Laboratory, monitor assay performance, plan and co-ordinate own workload and contribute to ensuring the smooth running of their area to meet schedules for release of final and intermediate products.
The QC Senior Laboratory Technician sits within the Global Animal Health Manufacturing organisation and reports to QC Manager.
What You Will Do
Responsibilities include, however not limited to:
Test antigen and/or vaccine to required standards, following set schedules/timelines by:
Planning, conducting, reporting, and interpreting routine laboratory assays per SOPs- Ensuring sufficient stocks of reagents, test materials, and equipment for timely testing
Accurately record all test data and observations by:
Documenting tasks in test records, worksheets, or logbooks per Good Documentation Practice- Peer reviewing work of fully trained team members
Maintain housekeeping standards by:
Performing housekeeping tasks per SOPs and GLP- Completing regular housekeeping inspections
- Keeping lab equipment calibrated, validated, and operational, including routine calibrations
- Following applicable Global Quality Policies
Minimise events/invalid assays by:
Monitoring assays for anomalies and preparing/reviewing assay result trends- Investigating and reporting events (deviations)
- Notifying supervisors of potential failures, recording faults, and independently resolving common faults
- Identifying technical problem resolutions
Contribute to continuous improvement and new method introduction by:
Implementing CAPAs from investigations- Performing routine test method and equipment validations
- Authoring and executing qualification protocols and reports
- Authoring or technically reviewing SOPs
What You Must have
- Science degree in Chemistry
- Extensive laboratory experience, essential for routine vaccine product and raw material testing (GMP, GLP OECD and/or ISO17025)
- Proficiency with AAS, UV-Vis, and titrator methods
- Understanding of cGMP/GLP and equipment/method validation
- Experience leading laboratory investigations and system improvements (e.g. deviations, CAPA, change management)
- Chromatography experience will be advantageous (e.g. HPLC, ICP-OES etc.)
- Skilled in writing technical procedures and troubleshooting
- Experience with laboratory software systems (e.g., LabX, Labware etc.)
What You Can Expect
- Autonomy with strong support within a trusted global Animal Health organisation
- Opportunities to upskill and develop your role
- Pathways to broaden your skills and career
- Joining a collaborative team of like-minded professionals
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.
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:
RegularRelocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
Valid Driving License:
Hazardous Material(s):
Required Skills:
Chemistry, Chemistry, Compound Management, GMP Compliance, GMP Laboratory, Keen Observation, Laboratory Analytical Techniques, Laboratory Information Management System (LIMS), Laboratory Investigations, Laboratory Operations, Liquid Chromatography-Mass Spectrometry (LC-MS), Method Validation, OOS Investigations, Pharmaceutical Microbiology, Process Verification, Quality Control Management, Quality Standards, Raw Material Preparation, Raw Materials, Recordkeeping, Reporting Management, Spectrophotometer, Spectrophotometry, Standard Operating Procedure (SOP) Writing, Sterility Testing {+ 4 more}Preferred Skills:
Job Posting End Date:
08/19/2025- 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.
Requisition ID:R352975