Senior Validation Engineer
Senior Validation Engineer
Senior Validation Engineer
Senior Validation Engineer
Thermo Fisher Scientific
Medizintechnik
Lengnau BE
- Art der Anstellung: Vollzeit
- 98.000 CHF – 103.500 CHF (von XING geschätzt)
- Vor Ort
Senior Validation Engineer
Über diesen Job
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Loud Noises (Equipment/Machinery), Office, Rapid flashing lights, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materialsJob Description
When you join us at Thermo Fisher Scientific, you’ll be part of an inquisitive team that shares your passion for exploration and discovery. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the world.
The Senior Validation Engineer is responsible for the definition and implementation of qualification & validation processes in collaboration with Quality. He defines and implements processes for equipment and process qualification & validation to ensuring GMP standards are met.
Position Responsibilities & Accountabilities
Technical Responsibilities
- Prepares, reviews and approves production, validation, audit reports documents, procedures, and rationales.
- Evaluates new regulations, changes to existing regulations and regulatory trends; prepares inspections and customer audit responses and reports; performs gap analysis to resolve efficiencies and take appropriate actions.
- Defines, in collaboration with other partners (Quality Assurance, System Owner…) the requalification strategy of GMP systems and implements it, including maintaining the quality system and complete practical activities.
- Coordinates execution of activities by external contractors.
- Performs requalification and revalidation Work Orders, including routine and non-routine operations, and documents in forms and OMX following Good Documentation Practices
- Participates in the culture of continuous improvement and development of technologies.
- Identifies training needs and develop training programs.
- Works in a safe and responsible manner in order to build an injury-free and incident-free workplace.
- Participates in calibration activities
Quality
- Adheres to general cGMP rules, Quality policies, procedures and instruction as rolled out by the Quality function and endorsed by the site management (Deviations, CAPAs, Change Control, etc.).
- Actively chips in to continuous quality improvement initiatives and deviation reporting and follow-up.
- Represent the department as SME for the responsible area in audits and regulatory inspections.
EHSS
- Adheres to general safety rules, policies, procedures and instructions as rolled out by the EHSS functions and endorsed by the site management.
- Actively supplies to safety initiatives and issues as well as near miss reporting and follow-up.
Values & Behaviour
- Maintains dedication to Thermo Fisher Scientific values and alignment with ethics and legal compliance standards.
- Takes personal accountability for their presence, performance, and efficiency for the achievements of defined objectives.
- Thinks and acts with a customer-centric mentality.
- Is intellectually curious and accepts Practical Process Improvement (PPI).
Position Qualifications
Education
- Bachelor’s degree in Biotechnology, Quality, Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or a related field.
Experience & Competences
- Experience in the pharmaceutical industry for qualification & validation is required
- Experience working in validation activities of steam sterilization processes and cleanroom qualification.
Additional Requirements
- Ability to work independently and demonstrate job ownership.
- Analytical and concept-based thinking and acting.
- Physical ability to perform tasks that may require prolonged standing, walking, and lifting of materials and equipment.
- Proficiency in working in cleanroom environments and adhering to all GMP and safety laws.
- Proficient in the use of computerized office applications (e.g. Word, Excel, Outlook) and systems/business applications, project management and confirmed scientific writing skills.
- Knowledge of cGMPs and FDA/industry expectations.
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Apply today! http://jobs.thermofisher.com
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482 Mitarbeitende haben abgestimmt: Sie bewerten die Unternehmenskultur bei Thermo Fisher Scientific als ausgeglichen zwischen traditionell und modern.Der Branchen-Durchschnitt tendiert übrigens in Richtung modern