release and characterization testing of different cell therapy candidates. The group supports c GMP-compliant in-process Quality Control (QC) support of c GMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround c GMP testing of in-process materials.
In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. Responsibilities Execute
test methods following established procedures, compliant with c GMPs and in some cases turning data around in a rapid manner Manage test deliverables and training activities to defined test schedules Collaborate with colleagues to align on test requests Maintain compliance of a c GMP environment ranging from instruments, to reagents, data packs, etc.
Manage analytical databases and perform data analysis to support assay performance and control Contribute to assay investigations for out of expectation results or test failures Lead or support internal assay transfers from analytical development teams Write simple technical reports & SOPs, including clear and concise technical data presentation
and discussion. Generate of materials for internal/external presentations as needed Participate in interdepartmental meetings and project specific sub-team meetings Train on new approaches needed for incoming programs and act periodically as the lead to train colleagues.
Plan, prioritize and execute simple and complex experiments with the relevant controls with little guidance from their supervisor. Acquire, compile, analyze, and interpret data with minimal supervision. Work within a broader team to support the development and implementation of new ways of working and methodologies. Basic Qualifications Master's degree in Biology/Biochemistry or related discipline or Bachelor's degree with a minimum of two years of relevant experience in the Biotechnology/medical industry.
Experience with molecular biology techniques, cell culture and cellular based assay development Preferred Qualifications Experience using and developing molecular techniques such as residual, identity, and strength assays (including platforms ranging from flow cytometry, ELISAs, and cell counting). A minimum of 1 year experience in a c GMP environment. Experience validation and transfer analytical methods. Experience using Quality by Design (Qb D) principles and have used Design of Experiment (DOE) approaches for method development/optimization.
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-SA#LI-SAAt 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.
Position Overview/Department Description This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi's CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports c GMP-compliant in-process Quality Control (QC) support of c GMP Manufacturing cutting edge methods such as flow cytometry.
The selected candidate will execute rapid turnaround c GMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month. Responsibilities Execute test methods following established procedures, compliant with c GMPs and in some cases turning data around in a rapid manner Manage test deliverables and training activities to defined test schedules Collaborate with colleagues to align on test requests Maintain compliance of a c GMP environment ranging from instruments, to reagents, data packs, etc.
Manage analytical databases and perform data analysis to support assay performance and control Contribute to assay investigations for out of expectation results or test failures Lead or support internal assay transfers from analytical development teams Write simple technical reports & SOPs, including clear and concise technical data presentation and discussion.
Generate of materials for internal/external presentations as needed Participate in interdepartmental meetings and project specific sub-team meetings Train on new approaches needed for incoming programs and act periodically as the lead to train colleagues. Plan, prioritize and execute simple and complex experiments with the relevant controls with little guidance from their supervisor. Acquire, compile, analyze, and interpret data with minimal supervision. Work within a broader team to support the development and implementation of new ways of working and methodologies. Basic Qualifications Master's degree in Biology/Biochemistry or related discipline or Bachelor's degree with a minimum of two years of relevant experience in the Biotechnology/medical industry.
Experience with molecular biology techniques, cell culture and cellular based assay development Preferred Qualifications Experience using and developing molecular techniques such as residual, identity, and strength assays (including platforms ranging from flow cytometry, ELISAs, and cell counting). A minimum of 1 year experience in a c GMP environment. Experience validation and transfer analytical methods. Experience using Quality by Design (Qb D) principles and have used Design of Experiment (DOE) approaches for method development/optimization.
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-SA#LI-SAAt 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.
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home environment. We are affiliated with the UMass Memorial Health system and receive significant support from them. This support helps to provide stability in these challenging times. We love working in a learning environment and have a great deal of longevity in our agency.
We have created a team-oriented, and patient focused atmosphere. You will have the opportunity to make a positive impact on patient care. Enjoy working close to home and maintain work/life balance while giving excellent care to our community based patients. Health Alliance Home Health and Hospice has competitive compensation, quality Health Insurance at a good cost and free parking. MAJOR RESPONSIBILITIES: Assures
case coordination and provides direct nursing care to patients and families. Collects comprehensive data pertinent to the patient's health or the situation. Analyzes backssment data to determine the diagnoses or issues.
Identifies expected outcomes in a plan individualized to the patient, family and/or caregivers and the situation. Develops a plan that prescribes strategies and alternatives to attain expected outcomes. Implements the individualized patient plan of care. Employs strategies to promote health, comfort, and a safe environment. Evaluates progress towards attainment of outcomes. Attains knowledge and competency that reflects current nursing practice. Evaluates one's own nursing
practice in relation to professional practice standards and guidelines, relevant statutes, rules, and regulations.
Interacts with peers and colleagues, and contributes to their professional development. Collaborates with the patient, family, and others in the conduct of nursing practice. Integrates ethical principles into all areas of practice. Integrates best practices and/or research findings into practice. JOB REQUIREMENTS EDUCATION: Graduate of an accredited school of nursing required. LICENSES, CERTIFICATIONS, ETC. Valid and unrestricted licensure as a Registered Nurse in the Commonwealth of Massachusetts required. Valid and unrestricted driver's license recognized by the Commonwealth of Massachusetts and access to a reliable, insured vehicle required.
EXPERIENCE: Experience is preferred but not required. For more details: jobs-search. org/insurance_leominster-c434638/job_i1949647879
additional critical care services for medically complex conditions such as trauma, infectious diseases, wound healing, cardiovascular disease, stroke, amputation and ventilator weaning. As a smaller, specialized hospital, we offer an opportunity to work in a fast-paced and friendly work environment where you really get to know your patients and their families.
Responsibilities The RN develops, implements, evaluates and revises a plan of care of assigned patients and families while promoting the mission and values of Vibra Healthcare. The provision of care includes direct care along with the delegation and supervision of all nursing care in accordance with the applicable Nurse Practice
Act. Specific components of the Registered Nurse role include demonstrating clinical competence; managing patient care; improving quality of care; establishing professional relationships and utilizing professional skills; fulfilling responsibilities of the role of the hospital; and developing clinical expertise per specialty.
Required Skills: Current, valid, and active license to practice as a Registered Nurse in the state of employment required. Current BLS certification from a Vibra-approved vendor required. Current ACLS certification from a Vibra-approved vendor required within six (6) months of hire. Additional Qualifications/Skills: Previous acute care experience is strongly preferred.
Ability to project a professional image. Knowledge of regulatory standards and compliance requirements.
Strong organizational, prioritizing and analytical skills. Ability to make independent decisions when circumstances warrant. Working knowledge of computer and software applications used in job functions. Freedom from illegal use of and effects of use of drugs and alcohol in the workplace Benefits At Vibra Healthcare, employees are our priority. We are passionate about patient care and consider it a privilege to be able to provide services to patients and their family members. Below is a brief summary of our benefits. Medical PPO high and low deductible plans / HSA options as well as HMO options in some markets FREE prescription plans Dental and Vision coverage Life insurance Disability Benefits Employee Assistance Plan Flex Spending plans, 401K matching Additional Critical Illness, Accident, and Hospital plans Company discounts for mobile phone service, electronics, cell phones, clothing, etc Pet Insurance Group legal - provides legal assistance with personal legal matters Tuition and continuing education reimbursement Work life balance At Vibra Healthcare, our patients are family.
Healthcare is constantly evolving, our growing organization is devoted to ensuring that each person in our care feels safe.
Our world-class team of driven, passionate healthcare professionals are always focused on service excellence and providing top quality care at the bedside. Our culture fosters engagement, diversity and advocacy. Our goal is to empower our employees and support them in their professional growth while leading them on a path to success within our organization. For more details: jobs-search. org/information-technology_rochdale-c434263/job_i1949786393
