Exciting Fixed-Term Contract until end of December 2024
To be based at our expanding manufacturing site in Upper Hutt, New Zealand
Opportunity to bring your knowledge and grow your Validation skills
Be part of our collaborative Validation team in the country!
Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate.
With our extensive range of facilitaies and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.
Reporting to the Validation Manager , you will work on several business-critical projects to complete validation of new equipment, processes, and buildings within project timelines on a fixed-term contract until 31 December 2024.
WHAT YOU WILL DO
Ensures all equipment qualification work is carried out to meet the site requirements
Manage the planning, execution and documentation of qualification studies on new and legacy equipment
Complete all assigned re-validation tests in accordance with established procedures
Write validation protocols and summary reports for complex items of equipment (eg. autoclaves, fermenters).
Accurately record data and observations on test execution worksheets in accordance with Good Documentation Practices.
Complete all ancillary documentation (eg deviation reports).
After one year, you will be supporting the manufacturing site to maximise the use of company assets and complete the qualification studies and validation tests to the agreed schedule.
WHAT YOU MUST HAVE
You may be an experienced Validation Engineer who is looking to join an innovative biopharma and utilise your skills and experience on an exciting project.
Alternatively, you may have solid knowledge & prior exposure to aspects of validation in previous roles and looking to further grow your career as a Validation Engineer.
We will provide you with the support to develop your skills in this role & you will bring with you your motivation and ability to learn on the job.
To be successful in this role, you will :
Hold a relevant tertiary qualification in Engineering or related discipline
Demonstrate prior validation experience working on equipment, facilities & / or utilities
Experience in biotechnology or the pharmaceutical industry is highly regarded
Have a solid understanding of GMP requirements
Hold the ability to work well under pressure and achieve results often to tight deadlines
Have excellent communication and interpersonal skills with the ability to inspire others towards a common goal
Take a proactive approach to your own learning and development and find creative ways to solve problems
Demonstrate strong documentation skills including the creation and implementation of protocols
WHAT YOU CAN EXPECT
Be part of a leading global organisation with long standing history in NZ
Opportunity to work on an exciting project relating to site expansion
Comprehensive & Attractive Total Rewards package on offer
Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time.
Who we are
We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases.
Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
What we look for
In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come.
We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth .
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
Current Contingent Workers apply
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, 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 :
Project Temps (Fixed Term)
Relocation : No relocation
VISA Sponsorship :
Travel Requirements :
Flexible Work Arrangements :
Valid Driving License :
Hazardous Material(s) :