Job Description

We are looking for a Project Manager Biomaterial to strengthen our European team at our site in Boxmeer.

The department

The Global Analytical Technology Solutions (ATS) team, covering Small and Large Molecules, oversees analytical activities across the Animal Health network. The ATS-Bio Inline Support EU team (7 employees) provides essential support to the Animal Health Quality Control (QC) laboratories across Europe. The team supports the Animal Health Quality Control (QC) laboratories with remediation / improvement of analytical tests, site to site transfer of biomaterials and QC tests, and implementation of new technologies.

The position

We are looking for an enthusiastic and motivated Project Manager Biomaterial to work in our team (7 people). The position focusses on supporting the site-to-site transfer of biomaterials and setting up a life cycle management program for Biological Critical Reagents (BCRs) used for QC testing within the EU network. This primarily involves 150 different BCRs, including e.g. reference standards, internal standards, (coat) antigens, monoclonal/polyclonal antibodies, hyperimmune sera, F(ab)2 fragments, conjugates, which are used in a broad variety of biological assays used for Large Molecule vaccine release testing by our global Animal Health QC sites.

Your key tasks and responsibilities are:

Support site-to-site Biomaterial transfer activities including gap assessments and transfer documentation.Support the development and implementation of a life cycle management program (production/USP & purification/DSP, qualification, implementation, ongoing monitoring and stability testing) for Biomaterials.Participate in biomaterial-related QC method root cause investigations.Write protocols and reports for production and qualification of biomaterials, standard operating procedures for USP and DSP of biomaterials, and biomaterial specification forms.Present project progress to internal stakeholders and customers

Desired skills and experience

Completed Bachelor’s, Master’s or higher degree in Biology, Chemistry, Pharmacy or other related scientific disciplineAt least 5 years of relevant experience in the pharmaceutical industryExperience in manufacturing, production, purification, qualification and handling of biomaterials.Experience with various vaccine analytical technologies including ELISA, AlphaLisa, virus titration assays, immunofluorescence assays etc.Experience working under GLP and GMP requirementsAble to work independently and in a teamStrong communication, project management and problem-solving skillsSupport-oriented and continuous improvement mindsetAbility to work in a multi-disciplinary and international teamProficient in Dutch and English, both speaking and writing

What we offer

Being an Associate Director at our company means you will work together with a team on animal healthcare in an international environment. You will get the opportunity to develop yourself.
Our benefits are very competitive, and the summary below will give you an idea of what you can expect.
• Competitive salary and a 3% year-end allowance;
• 35,5 days of leave;
• Attractive collective health care insurance package with considerable reduction rates;
• Solid Pension Plan;
• Annual bonus based on own and company performance;
• Travel allowance for commuting;
• Numerous trainings, coaching and e-learning modules for long term job opportunities and development.
 

Animal Health Division

Our Animal Health division is a trusted global leader in veterinary medicine, dedicated to the health and well-being of animals. We are a global team of professionals working together to make a positive difference in animal care and the world’s food supply and have a deep sense of responsibility towards our customers, consumers, animals, society and our planet. We offer one of our industry’s most innovative portfolio of products, services and technologies that serve to prevent, treat, and control diseases across all major farm and companion animal species.

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:

Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

03/19/2025

*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:R335585