( AST ) is a function of the Sanofi Global Manufacturing Science and Analytical Technology organization. AST is a partner of Process Sciences within MSAT, Biologics Quality, and Manufacturing Departments. AST provides support to2nd generation process development for biologics DSCommercial product and analytical LCMImplementation of digital tools and infrastructure Advancement of analytical automation, high throughput capabilities, and PATPartner with internal and external functions for technology transfer Develop analytical control strategy and support regulatory filings POSITION OVERVIEW/KEY RESPONSIBILITIES: Key Responsibilities Lead analytical method development activities Lead technical transfers
of analytical and characterization methods Provide analytical testing support and serve as analytical subject matter expert to Process Science, R&D and other groups Support second generation projects, process improvement, investigations, Degradation Pathway, Comparability and Technical Transfer studies Author protocols, technical memos and reports, data analysis summaries, process investigations and procedures Lead initiatives for new analytical techniques and technologies Serve as representative on cross functional teams including Sanofi network teams, technology transfer teams and project teams Interact cross-functionally with colleagues from various Sanofi Genzyme functions including QCTS,
QC, g MSAT to implement best practices BASIC QUALIFICATIONS BS in related discipline with at least 6 years of industrial experiences in relevant fields.
MS in related discipline with at least 4 years of industrial experiences in relevant fields. Ph. D. in related discipline with limited to no industrial experiences in relevant fields. PREFERRED QUALIFICATIONS: Experience with method development for recombinant proteins Knowledge of mammalian cell culture and commercial protein purification processeinteractionperience with Empower analytical control software Experience with statistical tools and high-level data analysis Ability to design experiments and troubleshoot probleminteractioncellent communication and writing skills Ability to work effectively in a highly collaborative and dynamic environment SPECIAL WORKING CONDITIONS: Ability to work in a laboratory environment Sanofi Inc.
and its U. S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; interaction, gender, gender identity or expression; affectional or interactionual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SG#LI-GZAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers.
We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. DEPARTMENT DESCRIPTION: The MSAT function within Specialty Care Operations ( SCO ) is responsible for leading technology transfer, implementing control strategy, providing technical process and analytical support, and driving process and analytical lifecycle management ( LCM ) for biologics drug substance operations. Analytical Science and Technology ( AST ) is a function of the Sanofi Global Manufacturing Science and Analytical Technology organization.
AST is a partner of Process Sciences within MSAT, Biologics Quality, and Manufacturing Departments. AST provides support to2nd generation process development for biologics DSCommercial product and analytical LCMImplementation of digital tools and infrastructure Advancement of analytical automation, high throughput capabilities, and PATPartner with internal and external functions for technology transfer Develop analytical control strategy and support regulatory filings POSITION OVERVIEW/KEY RESPONSIBILITIES: Key Responsibilities Lead analytical method development activities Lead technical transfers of analytical and characterization methods Provide analytical testing support and serve as analytical subject matter expert to Process Science, R&D and other groups Support second generation projects, process improvement, investigations, Degradation Pathway, Comparability and Technical Transfer studies Author protocols, technical memos and reports, data analysis summaries, process investigations and procedures Lead initiatives for new analytical techniques and technologies Serve as representative on cross functional teams including Sanofi network teams, technology transfer teams and project teams Interact cross-functionally with colleagues from various Sanofi Genzyme functions including QCTS, QC, g MSAT to implement best practices BASIC QUALIFICATIONS BS in related discipline with at least 6 years of industrial experiences in relevant fields.
MS in related discipline with at least 4 years of industrial experiences in relevant fields. Ph. D. in related discipline with limited to no industrial experiences in relevant fields. PREFERRED QUALIFICATIONS: Experience with method development for recombinant proteins Knowledge of mammalian cell culture and commercial protein purification processeinteractionperience with Empower analytical control software Experience with statistical tools and high-level data analysis Ability to design experiments and troubleshoot probleminteractioncellent communication and writing skills Ability to work effectively in a highly collaborative and dynamic environment SPECIAL WORKING CONDITIONS: Ability to work in a laboratory environment Sanofi Inc.
and its U. S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce.
All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; interaction, gender, gender identity or expression; affectional or interactionual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. #GD-SG#LI-GZAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.
We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. PDN-9ae3d4d3-aaeba-acf35a33d81c
collaborate very closely with our Genomic Medicine Bioprocess Analytics, Characterization and Analytical Development groups, based in Framingham and Waltham MA. The applicant must have strong industry experience in developing automated liquid handler methods for common DNA/RNA sample prep workflows on Hamilton and/or Tecan platforms.
The successful candidate should have working knowledge in integrating liquid handlers to analytical instrumentation via robotic arms and scheduler software. Key Responsibilities: Automate sample preparation methods for GMP release of AAV or lentivirus gene therapy drug products. Design and establish integrated platforms for end-to-end automation of workflows.
Develop and implement new automated methods and data solutions. Perform maintenance on robotic platforms. Present results in cross-functional meetings. Develops job aids, SOPs and JSAs for lab equipment.
Participate in CMC meetings as an automation representative for improving current and future analytical methods. Mentor junior lab members in all areas of laboratory automation. Basic Qualifications: Ph. D. in Molecular Biology, Biotechnology or related discipline degree with a minimum of 4 years or MS degree with a minimum of 6 years of relevant experience in the biotechnology/medical industry. Proven experience in developing and qualifying automated methods to support gene therapy drug
development. Working knowledge of liquid handlers. Experience with integrating instruments.
Experience with robotic systems and scheduling software. Experience with computational analysis of biological data using program languages (R, Python, MATLAB, etc.). Preferred Qualifications: Experience with gene therapy specific analytical methods. Ability to troubleshoot mechanical issues associated with liquid handlers. Experience in evaluating, developing and implementing new automation technologies. General working knowledge of common data science tools; Python, R, SQL/no-SQL databases, AWS, Docker, etc. Ability to write tools and scripts to automate repetitive tasks.
Familiarity with networking (TCP/IP), or Serial Communications Sanofi Inc. and its U. S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; interaction, gender, gender identity or expression; affectional or interactionual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
The Bioanalytics Automation lab, part of the Global CMC Development organization, uses robotic workstations and general-purpose programming languages to accelerate and streamline analytical workflows. The lab supports analytical groups responsible for drug development, from pre-candidate selection through commercialization. The incumbent will collaborate very closely with our Genomic Medicine Bioprocess Analytics, Characterization and Analytical Development groups, based in Framingham and Waltham MA. The applicant must have strong industry experience in developing automated liquid handler methods for common DNA/RNA sample prep workflows on Hamilton and/or Tecan platforms.
The successful candidate should have working knowledge in integrating liquid handlers to analytical instrumentation via robotic arms and scheduler software. Key Responsibilities: Automate sample preparation methods for GMP release of AAV or lentivirus gene therapy drug products. Design and establish integrated platforms for end-to-end automation of workflows. Develop and implement new automated methods and data solutions. Perform maintenance on robotic platforms. Present results in cross-functional meetings.
Develops job aids, SOPs and JSAs for lab equipment. Participate in CMC meetings as an automation representative for improving current and future analytical methods. Mentor junior lab members in all areas of laboratory automation. Basic Qualifications: Ph. D. in Molecular Biology, Biotechnology or related discipline degree with a minimum of 4 years or MS degree with a minimum of 6 years of relevant experience in the biotechnology/medical industry. Proven experience in developing and qualifying automated methods to support gene therapy drug development. Working knowledge of liquid handlers.
Experience with integrating instruments. Experience with robotic systems and scheduling software. Experience with computational analysis of biological data using program languages (R, Python, MATLAB, etc.). Preferred Qualifications: Experience with gene therapy specific analytical methods. Ability to troubleshoot mechanical issues associated with liquid handlers. Experience in evaluating, developing and implementing new automation technologies. General working knowledge of common data science tools; Python, R, SQL/no-SQL databases, AWS, Docker, etc. Ability to write tools and scripts to automate repetitive tasks.
Familiarity with networking (TCP/IP), or Serial Communications Sanofi Inc. and its U. S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; interaction, gender, gender identity or expression; affectional or interactionual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. PDN-9ad5bf42-a439-4aac93cd7180d
Morse Hospital in Natick, and the Metro West Wellness Center. Metro West Medical Center has been named to the 2019 America’s 100 Best Hospitals List by Healthgrades. Position Summary Under the supervision of the V. P. of Perioperative Services and the OR Nurse Manager according to established policies and procedures, the OR RN plans, coordinates, implements, and evaluates nursing care provided to patients of all ages, whose protective reflexes or self-care abilities are potentially compromised during a surgical or invasive procedure.
Performs any other specialized nursing duties as assigned. The OR RN possess clinical knowledge, judgment, and critical thinking skills based upon scientific
principles and evidenced based practice to address the patient’s physical, psychological, and spiritual needs. Practice follows all regulatory agencies including: The Joint Commission, Department of Public Health, CMS, CDC, and OSHA.
The OR RN ensures a safe environment for patients and staff and serves as a resource to healthcare team members. The OR RN collaborates and consults with Management, Service Leaders, physicians, educator, staff nurses, and technical staff to ensure patient and family-centered perioperative nursing care. Although the OR RN collaborates with professional and technical providers, the OR RN is accountable for patent outcomes resulting from the nursing care provide
during a surgical or invasive procedure. Onboarding Process: Please be advised that candidates must successfully complete a background check and pre-employment health screening which includes a drug screen.
KNOWLEDGE, EXPERIENCE, AND OTHER JOB REQUIREMENTS: Bachelor of Science Degree Current RN licensure in the state of Massachusetts Certified Perioperative Nurse (CNOR) preferred BLS – American Heart Association Ability to arrive with 30 minutes when called in for an emergent or urgent procedure Three years of related nursing experience preferred Tenet complies with federal, state, and/or local laws regarding mandatory vaccination of its workforce. If you are offered this position and must be vaccinated under any applicable law, you will be required to show proof of full vaccination or obtain an approval of a religious or medical exemption prior to your start date.
If you receive an exemption from the vaccination requirement, you will be required to submit to regular testing in accordance with the law. 210502xyz X Employment practices will not be influenced or affected by an applicant’s or employee’s race, color, religion, interaction (including pregnancy), national origin, age, disability, genetic information, interactionual orientation, gender identity or expression, veteran status or any other legally protected status.
Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship. For more details: jobs-search. org/sciences_framingham-c434656/rn-or-full-time-rotate-framingham_i1942932814
