Job detail for Head of Quality Control

Job Description

The stated goal of our Production & Supply business unit is to operate as the world’s most reliable manufacturer and supplier of . Together with our external contractors, suppliers, and partners, our production sites form a closely interconnected global manufacturing network that has made it its mission to supply customers and patients reliably and on time with high-quality products in every single case.

Our Quality Assurance ensures that all materials and substances contained in our products are manufactured, processed, tested, packaged, stored, and delivered in compliance with our strict quality standards and all regulatory requirements. Through close collaboration among our in-house production sites and cooperation with external manufacturers and suppliers, we create a closely interconnected global manufacturing network that has made it its mission to supply customers and patients worldwide reliably and on time in every single case with products that meet high quality standards.

Our site in 1210 Vienna is a strategic location for solid dosage forms such as tablets, film-coated tablets, granules, and implants for the protection and treatment of livestock and companion animals. The vast majority of products are exported. To ensure sustainable company growth, we are always committed to offering attractive career opportunities for the more than 450 employees in our company. To strengthen our team, we are currently looking for the following for our production site in Vienna:

Head of Quality Control (m/f/d)

The Head of Quality Control reports directly to the Quality Head and is responsible for a department of approximately 70 employees and an annual budget of around EUR 7 million, as well as a project budget of around EUR 1.5–2 million.

Scope of :

• Lead and further develop the QC department, including workforce planning, team leadership, coaching, and training
• Ensure the implementation and ongoing effectiveness of quality systems and regulatory requirements in the QC laboratory
• Qualification to act as a control laboratory manager in accordance with TAMBO (Tier-) and support compliance with applicable Austrian veterinary pharmaceutical requirements
• Oversee the tracking and closure of deviations, change controls, CAPAs, and other quality-related actions
• Serve as the central point of contact for internal and external inquiries, audits, and inspections
• Support budget and investment planning for the quality unit in collaboration with the Site Quality Head
• Drive continuous improvement of analytical systems, test methods, laboratory equipment, laboratory infrastructure, and key laboratory interfaces
• Promote a strong culture of compliance, accountability, safety, and continuous improvement
• Support a high-performing and engaged QC organization that contributes to site reliability and business success

Requirements:

• University degree in natural sciences, pharmacy, chemistry, biotechnology, or a related field
• Extensive experience in quality control within a regulated pharmaceutical environment
• Proven leadership experience with large teams and budget responsibility
• Sound GMP knowledge and a deep understanding of quality systems, audits, and regulatory expectations
• Experience with deviations, CAPAs, change management, and inspection readiness
• Ability to lead, motivate, and develop teams in a structured and collaborative manner
• Strong communication skills in German and English
• Qualifications required to serve as a control laboratory manager pursuant to TAMBO
• Resilience, self-motivation, sense of responsibility, and a solution-oriented working style
• Experience with US FDA inspections or in veterinary pharma, analytical modernization, or laboratory transformation is an advantage

What we offer you:

We offer a challenging and rewarding leadership role in a growing international company, with modern technologies and a high level of responsibility. You can expect:

• A strategically important leadership position with real impact
• The opportunity to shape and further develop a large QC organization
• A highly regulated, scientifically interesting environment in veterinary pharma within an international setting
• Collaboration with strong internal and external stakeholders
• Attractive compensation and a broad range of additional benefits, including:
• Company pension plan
• Hybrid working models
• Subsidized meals
• Support for public transportation
• Employee recognition programs

Why join us?

This is an excellent opportunity for a strong QC leader who truly wants to make a difference in quality, compliance, and team development. If you are motivated by leadership, scientific excellence, and the opportunity to help shape a critical function in the veterinary pharmaceutical industry, we would be very pleased to receive your application.

The collectively agreed minimum salary for this position is EUR 91.000 gross per year. Depending on the qualification profile and professional experience of the successful candidate, willingness to overpay is provided.

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.

Required Skills:

Budget Control, Budget Management, Continuous Development, Cost Modeling, Driving Continuous Improvement, Improvement Projects, Onboarding, Partner Relationship Management (PRM), Product Costing, Quality Control Management, Quality Management, Standards Compliance

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description:

The stated goal of our Production & Supply business unit is to operate as the world’s most reliable manufacturer and supplier of . Together with our external contractors, suppliers, and partners, our production sites form a closely interconnected global manufacturing network that has made it its mission to supply customers and patients reliably and on time with high-quality products in every single case.

Our Quality Assurance ensures that all materials and substances contained in our products are manufactured, processed, tested, packaged, stored, and delivered in compliance with our strict quality standards and all regulatory requirements. Through close collaboration among our in-house production sites and cooperation with external manufacturers and suppliers, we create a closely interconnected global manufacturing network that has made it its mission to supply customers and patients worldwide reliably and on time in every single case with products that meet high quality standards.

Our site in 1210 Vienna is a strategic location for solid dosage forms such as tablets, film-coated tablets, granules, and implants for the protection and treatment of livestock and companion animals. The vast majority of products are exported. To ensure sustainable company growth, we are always committed to offering attractive career opportunities for the more than 450 employees in our company. To strengthen our team, we are currently looking for the following for our production site in Vienna:

Head of Quality Control (m/f/d)

The Head of Quality Control reports directly to the Quality Head and is responsible for a department of approximately 70 employees and an annual budget of around EUR 7 million, as well as a project budget of around EUR 1.5–2 million.

Scope of :

• Lead and further develop the QC department, including workforce planning, team leadership, coaching, and training
• Ensure the implementation and ongoing effectiveness of quality systems and regulatory requirements in the QC laboratory
• Qualification to act as a control laboratory manager in accordance with TAMBO (Tier-) and support compliance with applicable Austrian veterinary pharmaceutical requirements
• Oversee the tracking and closure of deviations, change controls, CAPAs, and other quality-related actions
• Serve as the central point of contact for internal and external inquiries, audits, and inspections
• Support budget and investment planning for the quality unit in collaboration with the Site Quality Head
• Drive continuous improvement of analytical systems, test methods, laboratory equipment, laboratory infrastructure, and key laboratory interfaces
• Promote a strong culture of compliance, accountability, safety, and continuous improvement
• Support a high-performing and engaged QC organization that contributes to site reliability and business success

Requirements:

• University degree in natural sciences, pharmacy, chemistry, biotechnology, or a related field
• Extensive experience in quality control within a regulated pharmaceutical environment
• Proven leadership experience with large teams and budget responsibility
• Sound GMP knowledge and a deep understanding of quality systems, audits, and regulatory expectations
• Experience with deviations, CAPAs, change management, and inspection readiness
• Ability to lead, motivate, and develop teams in a structured and collaborative manner
• Strong communication skills in German and English
• Qualifications required to serve as a control laboratory manager pursuant to TAMBO
• Resilience, self-motivation, sense of responsibility, and a solution-oriented working style
• Experience with US FDA inspections or in veterinary pharma, analytical modernization, or laboratory transformation is an advantage

What we offer you:

We offer a challenging and rewarding leadership role in a growing international company, with modern technologies and a high level of responsibility. You can expect:

• A strategically important leadership position with real impact
• The opportunity to shape and further develop a large QC organization
• A highly regulated, scientifically interesting environment in veterinary pharma within an international setting
• Collaboration with strong internal and external stakeholders
• Attractive compensation and a broad range of additional benefits, including:
• Company pension plan
• Hybrid working models
• Subsidized meals
• Support for public transportation
• Employee recognition programs

Why join us?

This is an excellent opportunity for a strong QC leader who truly wants to make a difference in quality, compliance, and team development. If you are motivated by leadership, scientific excellence, and the opportunity to help shape a critical function in the veterinary pharmaceutical industry, we would be very pleased to receive your application.

The collectively agreed minimum salary for this position is EUR 91,000 gross per year. Depending on the qualification profile and professional experience of the successful candidate, willingness to overpay is provided.

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.

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

NA

Job Posting End Date:

10/5/2026

***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.