BTS Associate Scientist
Wellington - New Zealand
Job Summary
Job Description
BTS Associate Scientist - Specialist
2-Year Fixed Term ContractwithCompetitive Remuneration
Opportunity toupskill and growin advanced vaccine and bioprocess science working withcutting-edge technologiesandglobal experts
Based in Upper Hutt New Zealand contributing locally while collaborating with our global Animal Health network
Join atrusted global-leading Animal Health organisationwhere your work directly supports thereliable supply of life-saving vaccines for animals worldwide
Biotechnology Solutions (BTS) within Animal Healthis responsible for remediation improvement and project management for commercial vaccines and process and analytics work across manufacturing and quality. Based atUpper Hutt BTS also supports process development for immunological analytical and biological methods used to test antigens and vaccines production processes for bacterial antigens vaccine manufacturing/formulation processes for new vaccines in the R&D pipeline and technology transfers.
The BTS team works closely with Manufacturing Quality and R&D colleagues worldwide.
As aBTS Associate Scientist - Specialist you will develop and validateELISA methodsand support otherin vitro antigen assaymethod development manage assigned projects and support improvements to antigen and vaccine production processes as needed.
What You Must have
Responsibilities include but are not limited to:
Leadership and Improvement Activities
Develop a strong working knowledge of assigned projects and workstreams contributing to related activities as required
Work closely with project leads and stakeholders to plan deliver monitor and report on assigned activities escalating risks and issues when needed
Communicate clearly and effectively to maintain alignment encourage collaboration and support timely decision-making
Contribute toOn-Point8-Step Problem Solving and continuous improvement initiatives taking ownership of defined actions where appropriate
Collaborate with colleagues locally and globally acrossBTS Manufacturing Quality R&D Regulatory and Supply Chain
Contribute to trials experiments method development and process development through accurate execution documentation and reporting
Support vaccine process development technology development and technology transfer by completing assigned tasks and preparing technical documentation
What You Must Have
Qualifications
Bachelors degree or equivalent inImmunology Protein Biology Biotechnology Microbiology or a related field
Demonstrated critical thinking and analytical skills
Required Skills and Experience
Strong team player with clear communication organisational and interpersonal skills.
Able to work effectively in amatrix GMP biopharma / biological / vaccine manufacturing environmentwith appropriate guidance
Developing project management skills with the ability to plan organise and track assigned work to meet agreed timelines
Knowledge and developing experience inimmunological and biological methodsused to measure antigens and vaccines including method execution data review and documentation
Familiarity with developing and executingin vitro methodsto measure antigens and vaccines with support from technical leads or senior scientists as required
Experience inELISA method development including assay design support optimisation execution data review and documentation in a regulated laboratory environment
Experience or exposure to abiopharmaceutical production laboratory bioprocessing or other regulated environment
Developing working knowledge ofGMP GDP data integrity and EHSexpectations in a regulated biological/pharmaceutical manufacturing environment
Foundational theoretical and practical understanding ofupstream and downstream processing technologiesfor biopharmaceuticals at laboratory or manufacturing scale
Ability to work accurately and with attention to detail while understanding how assigned tasks contribute to broader project or site outcomes
Ability to analyse routine technical information identify anomalies and escalate appropriately with proposed next steps where possible
Hands-on scientist able to execute assigned laboratory or technical activities safely accurately and within agreed timelines
Fluent in English with the ability to write clear technical notes protocols records and reports
What You Can Expect
Autonomyon complex vaccine and process challenges with strongsupportfrom BTS Manufacturing Quality and R&D
Avisible impactful rolewhere yourproblem-solvingdirectly supports reliable antigen and vaccine supply
Broadexposureacross the vaccine lifecycle creating futurecareerandskill developmentopportunities
Exposure tobiopharmaceutical productionorbioprocessing in aregulated laboratory or manufacturing environment
Broader understanding ofupstream and downstream processing
Acollaborative multidisciplinary team thatshares knowledgeencourages innovationandvalues your ideas
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 anothers thinking and approach problems collectively. We are an equal opportunity employer committed to fostering an inclusive workplace.
Required Skills:
Biological Sciences Biological Sciences Data Monitoring Data Recording GMP Compliance Good Laboratory Practices (GLPs) Health Sciences Immunoassays In Vitro Studies Legal Compliance Manufacturing Quality Control Method Validation Microbiology Pharmaceutical Manufacturing Pharmaceutical Sciences Physical Sciences Production Operations Production Process Development Production Processes Research Techniques Scientific Communications Scientific Literature Reviews Strategic Planning Team Collaboration Teamwork 1 morePreferred 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:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not ApplicableShift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
07/25/2026*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
IC
About Company
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more