Job Description
Our Manufacturing Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that is devoted to delivering a high-quality, reliable supply to customers and patients on time, every time.
Our site in 1210 Vienna is a strategic location for solid drug manufacturing including tablets, coated tablets, granules and implants for the health provision and treatment of livestock and domestic animals. Most of our products are exported. To ensure sustainable company growth we continually strive to offer attractive career opportunities for more than 450 employees at our Vienna site. In support of our existing team, we are currently looking for a:
Qualified Person /
Senior Specialist Quality Assurance (m/f/d)
We are looking for a Qualified Person (m/f/d) according to AustrianArzneimittelbetriebsordnung 2009 and EU “Guide to Good Manufacturing Practice Annex 16
Responsibilities
- Batch Release
- Usage Decision for Bulk, FPU and FPP based on product specific training
- Assure that each batch was manufactured according to GMP and all other applicable regulations including respective marketing authorization
- Issue CoAs and CoCs for Bulk, FPU and FPP
- Routine:
- Assess product quality related deviations and CAPAs
- Assess product impact in change control
- Mange, review and approve product quality complaints
Review and approve product quality reports
- Manage QP and QAO related document creation, review and approval
- Product Quality support in site and global projects
- General:
- Contribute to Inspection Readiness for the Vienna site
- Attend conferences and trainings as required to maintain proficiency
- Compliance with EHS regulations, reporting of dangerous situations, near misses and sources of danger in the working environment
- Compliance with companys ethical guidelines and global standards as applicable
- Additional role
- Perform any other duties as assigned management on an as-needed basis
Qualifications, Experience Skills
- Master’s degree in scientific education
- QP certification
- Significant work experience in quality department and GMP knowledge
- Strong knowledge of regulatory and governance requirements
- Understanding of product quality and compliance
- Broad industry knowledge
- Excellent internal and external communication skills
- Strong written and verbal communication skills in German and English
- Solid organizational and planning skills
- Strong problem-solving and analytical abilities
- Good judgment, discipline, and confidence
We offer
- Exciting and varied field of work in a modern, internationally operating company
- Annual bonus and employee recognition bonuses
- Employee referral program
- Attractive company pension
- Paid parental leave up to 12 weeks provided by company
- Company medical care and vaccination program
- Discounted fitness offer
- Fruit, coffee tea
- MassageWork
- Modern company canteen with generous company subsidy
- Annual ticket for Wiener Linien or subsidy for climate ticket and/or bike leasing
- Various employee discounts and benefits and much more!
We offer an attractive salary, outstanding social benefits and an exciting work environment with varied tasks in an international environment. The minimum annual salary for this position isEUR 61.300and varies according to the qualifications and experience of the successful candidate. We are looking forward to receiving your application.
Required Skills:
Adaptability, Adaptability, cGMP Regulations, Change Management, Deviation Management, German Language, GMP Compliance, Good Automated Manufacturing Practice (GAMP), Inspection Readiness, Manufacturing Quality Control, Oral Communications, Pharmaceutical Quality Assurance, Problem Solving, Product Disposition, Quality Assurance (QA), Quality Assurance Monitoring, Quality Assurance Processes, Quality Assurance Review, Quality Assurance Testing, Quality Auditing, Quality Control Management, Quality Management, Quality Management Standards, Quality Standards, Regulatory Compliance {+ 2 more}
Preferred Skills:
Current Employees applyHERE
Current Contingent Workers applyHERE
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:
Not Applicable
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
NA
Job Posting End Date:
08/18/2026*A job posting is effective until 11:59:59PM on the dayBEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFORE the job posting end date.
Requisition ID: R407270
