Job Description

A fantastic opportunity has arisen for a Technical Specialist.

Bring energy, knowledge, innovation to carry out the following:

Ensure the highest Quality, Compliance and Safety standards relating to all activities, including process robustness changes and continuous improvement projects.Work within our team to enable our team’s overall performance within the Tech Ops organization.Responsible for providing technical guidance to the site teams in support of commercial vaccine drug substance manufacturing.Project lead for technical projects.Development and execution of protocols to support process robustness changes and any associated qualifications.Technical Review of Global Change management records as required.Recommend technical approaches in line with global and local standards.Benchmark and remain current with development of new technologies in the vaccine and biopharmaceutical processing field of expertise and seek to deploy process improvements through innovation and utilization of these technological advances.Contribute for driving a culture of Continuous Improvement through MPS within Tech Ops on projects such as: problem solving, reducing cycle time, Lean principles within the new processes.Stakeholder management of multiple decision makers, corporate colleagues, cross-functional team by demonstrating the ability to maintain and strengthen trust relationships with people on all levelsParticipate and comply with our Manufacturing Division Quality Management System (QMS) requirements, including ownership, as relevant.Support Knowledge Management efforts within the team.

What skills you will need:

In order to excel in this role, you will more than likely have:

Hon. Degree or Masters in a Science or Engineering discipline (preferably Biotechnology).3-5 years’ experience in biopharmaceutical/vaccines environment would be an advantage.Prior experience with managing process changes.Demonstrated knowledge in pharmaceutical / biopharmaceutical technical / manufacturing operations. Experience of involvement in a technical project an advantageKnowledge of Regulations and applicable standards for Quality, Safety, Regulatory within the biopharmaceutical/vaccine area.Prior experience with change management would be an advantage.Managing projects and aligning key stakeholders.Evidence of Continuous Professional Development

As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about our hybrid working model

So, if you are ready to:

Invent solutions to meet unmet healthcare needs, please apply today.

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:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

02/15/2025

*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:R334064