Regulation Bezirk Solothurn SO Jobs

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Biogen Vor 13 Tagen

successfactors.com   -   [ Job speichern ] [ Aus der Liste entfernen ] [ gespeicherte Jobs zeigen ]

 ...Department in accordance with current guidelines on equipment, utilities, and facilities validation, in compliance with pertinent regulations (e.g., FDA, EMA). 2. Assesses overall validation workload, staffs accordingly, and deploys resources to attain Manufacturing...  >>

Vor 14 Tagen

Michael Bailey Associates   -   [ Job speichern ] [ Aus der Liste entfernen ] [ gespeicherte Jobs zeigen ]

 ...bespoke validation. * Process knowledge and documentation. Desirable: * In depth knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry * High understanding of GMP, Compliance, Validation Practices including the system...  >>

Biogen Vor 17 Tagen

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 ...guidelines. MAIN ACCOUNTABILITIES: 1. Compiles updates and analyzes programs and data to ensure proper compliance with government regulations and to provide for a safe and healthy workplace, community and environment. 2. Oversees the development, implementation and...  >>

Biogen Vor 5 Tagen

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 ...implementation of EHS procedures and programs required. - Advanced knowledge of EHS Management Systems, technical programs and swiss regulations required. - In-depth knowledge of drug development process with particular emphasis on large scale bioprocessing highly...  >>

Biogen Vor 3 Tagen

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 ...strong partnerships, and the ability to lead and execute globally. Practical knowledge of GxP practices and experience working in a regulated environment is preferred. Education Masters or doctorate in Business, Learning, Psychology, Engineering, or related field (or...  >>

Biogen Vor 4 Tagen

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 ...Operations, Technology & Innovation (PO&T) Requisition Number 30321BR Qualifications - Maintain knowledge of relevant FDA/EMA regulations and compliance. - Approximately 4 years of experience in pharmaceutical or biotech manufacturing environment. - Previous...  >>

Biogen Vor 27 Tagen

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 ...procedures and overall cGMP compliance. 3. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures all safety incidents are properly investigated and corrective / preventive actions are implemented. 4. Maintains the...  >>

Biogen Vor 19 Tagen

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 ...operator room and all utility areas. 3. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures all safety incidents in his/her area of responsibility are properly investigated and corrective / preventive actions are...  >>

Biogen Vor 19 Tagen

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 ...ensures compliance to EHS and cGMP’s. 6. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures all safety incidents are properly investigated and corrective / preventive actions are implemented. 7. Develop &...  >>

cBcon Vor einem Monat

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 ...or Life Science with additional IT qualification) with a broad technical/educational skills base ~Minimum of 2 years working in a regulated environment a minimum 1 of which has been spent carrying out validation and/or testing activities ~A degree in an appropriate...  >>

Vor 1 Tag

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 ...performance management duties for the site MS team * Ensure compliance of investigatory activities within the MS team with cGXP regulations, and maintain a high degree of regulatory compliance with the FDA, EMA, and other agencies by contributing to and reviewing relevant...  >>

Biogen Vor 13 Tagen

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 ...engineering and operation knowledge within electrical installation and equipment. - Practical knowledge and application of GMP’s and EMEA regulations. - Experience in a pharmaceutical or biotech manufacturing environment. - Proficiency in MS Word, MS Excel, MS Power Point and...  >>

cBcon Vor 4 Tagen

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 ...customer in Solothurn. Description Responsible for supporting Computer Systems Compliance activities applicable to country specific regulations (e.g. FDA, Health Canada), international standards (e.g. MDD, ISO) and as appropriate best business practices (e.g. GAMP 5). This...  >>

Biogen Vor 19 Tagen

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 ...in conjunction with other trades 3. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures that HAZOP review suggestions are incorporated in the BMS design (if applicable) and participate in bi-annual Hazop reviews...  >>

Biogen Vor 4 Tagen

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 ...least 3 years of experience within Quality Assurance or related function is preferred - Maintain knowledge of relevant FDA/EMA regulations and compliance. - Prior experience with regulatory audits - Good communication skills in English, verbally and written. Dual language...  >>

Biogen Vor 26 Tagen

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 ...realize the facility certification against the timeline. The Microbiology manager is expected to possess expert level knowledge of regulations and guidance documents applicable to environmental, utility and water systems as well as the associated compendia based testing...  >>

Biogen Vor 21 Tagen

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 ...approval and into daily GMP operations. This function has the overall responsibility to ensure the requirements of the Quality System Regulations is effectively established and maintained and is also intended to take on the Responsible Person role for the Solothurn Site....  >>

Vor einem Monat

Solothurn SO

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 ...Description Quality & Compliance Conduction of internal audits according 21 CFR 820; ISO EN 13485:2012; MDD; other applicable regulations Writing of internal and reports and creation of relevant documentation Follow up of internal and external audit observation to...  >>

Vor 5 Tagen

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 ...documents and activities associated with change control *LI-POT4 Qualifications - Maintain knowledge of relevant FDA/EMA regulations and compliance. - Approximately 4 years of experience in pharmaceutical or biotech manufacturing environment. - Previous experience...  >>

Vor 12 Tagen

Michael Bailey Associates   -   [ Job speichern ] [ Aus der Liste entfernen ] [ gespeicherte Jobs zeigen ]

 ...Technical Profile Requirements: * Must be able to lead and give direction to Validation Projects. * Minimum of 2 years working in a regulated environment, a minimum 1 of which has been spent carrying out validation activities. * English and German spoken and written....  >>

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