Wien, Österreich
Onsite
Not Available
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 Austrian "Arzneimittelbetriebsordnung 2009" and EU “Guide to Good Manufacturing Practice Annex 16"
Responsibilities
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 company's 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
Massage@Work
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 is EUR 61.300 and 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 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:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
Not ApplicableShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
NAJob Posting End Date:
08/18/2026*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.