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Skill:Qualification and validation

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1–3 jobs· newest first

Sr. Specialist, Engineering
Merck · Rahway, US+1 more
$117K–$184KOn-site · Full-time · SeniorVisa
Packaging Technology Manager
Zentiva · Praha, Czechia
Associate Expert Qualification & Validation H/F - CDI
Octapharma · Lingolsheim, France
Full-time · Associate

+10K new in the last hour

Sr. Specialist, Engineering

Merck · Posted Nov 6, 2026

Rahway, New Jersey, United States +1 more
On-site
Full-time · Senior
$117K–$184K per year
5+ years

Visa sponsorship

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Senior Specialist, Technical Operations – Engineering in the FLEx Sterile Expansion Project

Locations (2)

Rahway, New Jersey, United States
Germany, Germany

Compensation

$117,000.00 - $184,200.00

Responsibilities

Collaborate with stakeholders to design and maintain equipment
Attend and complete Optima Super user training in Germany
Provide training on advanced troubleshooting
Support project assignments and facility innovation
Perform manual and automated operations

Requirements

B.A./B.S. in Mechatronics, Engineering, Automated Sciences, Computer Science, Biology, Chemistry or equivalent
Master’s degree with a minimum of 3 years relevant experience
Nice to have: Automated aseptic filling lines
Nice to have: Smart technologies
Nice to have: Robotics

Skills

Gowning and PPE Standard Operating Procedures Problem-solving Troubleshooting GXP compliance Drug product aseptic processing Equipment qualification Quality systems Commissioning, Qualification and Validation Optima Multi-use filler Optima Pharma and Isolator facilities Grade A barrier isolation systems

Benefits

Medical, dental, vision healthcare
Retirement benefits including 401(k)
Paid holidays
Vacation
Compassionate and sick days

See full job description

Packaging Technology Manager

Zentiva · Posted Nov 6, 2026

Praha, Czechia
5+ years

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Lead and develop a team of packaging technology specialists in a pharmaceutical manufacturing environment.

Compensation

Benefitní program 12 000 Kč ročně.

Responsibilities

Lead a team of technology specialists and Master Data experts
Set priorities and develop the team
Own process and packaging technologies for packaging lines
Improve line performance, OEE and solve recurring technical problems
Provide technical oversight for changes, transfers, new products and packaging materials

Requirements

SŠ/VŠ vzdělání technického směru

Skills

packaging technologies technical thinking team leadership Master Data OEE GMP SVP LEAN

Associate Expert Qualification & Validation H/F - CDI

Octapharma · Posted Nov 4, 2026

Lingolsheim, Grand Est, France
Full-time · Associate
2+ years

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Lead qualification and validation activities for equipment and processes at the Lingolsheim site, ensuring compliance with regulatory standards.

Responsibilities

Define and implement qualification/validation strategies (FAT, SAT, QI, QO, QP).
Coordinate and participate in tests with suppliers, automation, production, engineering, and PMO.
Manage deviations and conduct root cause analysis, impact assessment, and corrective/preventive actions.
Plan, monitor, and report on activities.
Draft risk analyses and criticality assessments based on technical documentation and regulatory requirements.

Requirements

Bac+5 (Ingénieur / Pharmacien / Master)

Skills

Qualification and validation FAT SAT QI QO QP Risk analysis Protocol writing

technical change management

qualification and validation

cross‑team collaboration

Benefits

25 days vacation
3 days health leave
Benefit program 12,000 Kč per year

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Process control

Regulatory knowledge (BPF, GMP)

Guidelines and technical guides

Benefits

Mutuelle d’entreprise
Primes d’intéressement
Participation
Restaurant d’entreprise
Micro-crèche d’entreprise

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