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Applications close November 21st, 2026

Product and Validation Specialist – Pharma Tech Support

Auto-translated from Yoruba · original: Produkt - und Validierungsspezialist – Pharma Tech Support

5 day weekGenerous PTO€50kHybrid · Vienna, Austria

The 4-day week in Austria

About the role

Job Description

Our engineers ensure the uninterrupted operation of our internal and external production and drive its continuous improvement and innovation. Thanks to our diverse production sites and working environments, our engineers have broad opportunities in a wide range of areas such as biology, chemistry, automation, investment projects, maintenance & repair, safety, process development, technical services, energy supply and validation.

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

Product and Validation Specialist – Pharma Tech Support (m/f/d)

Responsibilities

  • End-to-end responsibility for a specific product/product group

  • Project leadership as a product expert

  • Ongoing optimization of production processes

  • Evaluation and implementation of process changes, alternative suppliers for APIs (Active Pharmaceutical Ingredients) and the selection of production equipment with regard to new technologies

  • Implementation of product transfers, design of experiments (DoEs) and execution of test batches, definition of process parameters

  • Ownership of change requests, CAPAs and events, preparation of registration documents

  • Point of contact for authority inspections (FDA, AGES,…) on process validations and production processes

Requirements

  • Completed technical or scientific education (at least HTL or a technical/scientific degree)

  • Experience in the pharmaceutical industry

  • Experience in process validation is an advantage

  • Appropriate GMP knowledge

  • Excellent German and good English skills are required

  • Very good IT skills (Microsoft Office)

  • Teamwork and communication skills

  • Accuracy and flexibility

What we offer:

  • Exciting and challenging field of work with modern "state-of-the-art" technologies in a growing organization

  • Varied work in an internationally active company

  • Attractive company pension

  • Free FSME and flu vaccinations

  • Company doctor

  • Massage@Work

  • Hybrid working possible

  • Dogs are welcome in the office

  • Modern company canteen with generous company subsidy

  • Annual public transport pass (Vienna) or subsidy towards the Klimaticket and/or bicycle leasing

  • Employee referral program

  • Annual bonus and employee recognition bonuses

  • Discounted fitness offer

  • Paid parental leave for mothers and fathers of 12 weeks

The collective agreement minimum salary for this position is EUR 50.300,- gross per year. Depending on the qualification profile and professional experience of the successful candidate, we are willing to pay above this amount.

We are proud to be a company built on the values of our diverse, talented and committed employees. The fastest way to advance innovative developments is to bring different ideas together in an inclusive environment. We encourage our colleagues to discuss their ideas objectively and to tackle problems together. We see ourselves as an equal opportunity employer and are committed to promoting inclusive, diverse workplaces.

Additional location(s) Compensation Information:

Required Skills:

Adaptability, Adaptability, Biopharmaceutical Industry, Budget Development, Cloud Storage, Data Analysis, FDA Regulations, Feasibility Studies, IT Competency, Manufacturing Process Improvements, Medical Communications, Medical Logistics Management, Operational Process Improvements, Performance Monitoring, Pharmaceutical Microbiology, Pharmaceutical Sciences, Pharmacogenomics, Process Optimization, Process Validation, Project Management, Project Management Improvement, Project Management Tools, Project Optimization, Project Planning, Resource Allocation {+ 2 more}

Preferred 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:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

11/22/2026

*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.

About Merck

Global pharmaceutical leader (NASDAQ: MRK) offering 25 vacation days from day one regardless of tenure, 12 paid US holidays, and a 4-day year-end shutdown — ~41 days off per year for US employees.

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