Allergan
Scientist II (Cleaning Validation) (Temporary Position)
Allergan, Lincoln, Nebraska, United States, 68511
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .Job Description
PurposeSupport the AbbVie Technical Operations Functions and the AbbVie Technical Center. Resolve issues associated with commercial and research & development API’s and drug products. Provides technical support to cross-functional teams within and outside of the site during development, commercial launch or problem solving for a given API or drug product. Accountable for test results, project reports and experiments in support of process development, validation activities and Technical Transfers while maintaining and meeting the highest standards in quality, customer service and regulatory compliance.ResponsibilitiesSupport site Cleaning Validation strategy documents.Develop Cleaning Validation protocol and reports.Investigate and document investigations.Independently design, execute and interpret critical experiments to answer scientific questions. Understand the broad objectives of the project as well as their role in achieving those objectives, and modify experimental plan when required, to respond.Learn, understand and master new experimental techniques, and act as a resource or mentor for others.Innovate and implement new experimental protocols.Demonstrate a high level of proficiency in his/her field.Set and meet experimental timelines.Effectively organize and present scientific plans and data.Contribute to writing and conceptual framework of publications, presentations, and patents.Routinely read and apply relevant scientific literature. Impact projects mostly through lab and/or pilot plant based activities where applicable.Demonstrate writing skills and strong verbal communication skills.Qualifications
Bachelor's Degree in Science with 6 or more years of experience or MS or equivalent education with 5 or more years of experience.Experience in Oral Solid Dosage processes and equipment is highly desirable.Background performing Cleaning Validation activities is necessary.Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions.Demonstrated ability to learn, understand and master new experimental techniques.Ability to multitask and work within timelines.Demonstrated scientific knowledge.Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html
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AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .Job Description
PurposeSupport the AbbVie Technical Operations Functions and the AbbVie Technical Center. Resolve issues associated with commercial and research & development API’s and drug products. Provides technical support to cross-functional teams within and outside of the site during development, commercial launch or problem solving for a given API or drug product. Accountable for test results, project reports and experiments in support of process development, validation activities and Technical Transfers while maintaining and meeting the highest standards in quality, customer service and regulatory compliance.ResponsibilitiesSupport site Cleaning Validation strategy documents.Develop Cleaning Validation protocol and reports.Investigate and document investigations.Independently design, execute and interpret critical experiments to answer scientific questions. Understand the broad objectives of the project as well as their role in achieving those objectives, and modify experimental plan when required, to respond.Learn, understand and master new experimental techniques, and act as a resource or mentor for others.Innovate and implement new experimental protocols.Demonstrate a high level of proficiency in his/her field.Set and meet experimental timelines.Effectively organize and present scientific plans and data.Contribute to writing and conceptual framework of publications, presentations, and patents.Routinely read and apply relevant scientific literature. Impact projects mostly through lab and/or pilot plant based activities where applicable.Demonstrate writing skills and strong verbal communication skills.Qualifications
Bachelor's Degree in Science with 6 or more years of experience or MS or equivalent education with 5 or more years of experience.Experience in Oral Solid Dosage processes and equipment is highly desirable.Background performing Cleaning Validation activities is necessary.Demonstrated ability to independently design, execute and interpret critical experiments to answer scientific questions.Demonstrated ability to learn, understand and master new experimental techniques.Ability to multitask and work within timelines.Demonstrated scientific knowledge.Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html
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