Location: King Of Prussia, PA
Company: Center For Breakthrough Medicines
medicine and 767 vaccine doses in 2021. We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change.
For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together. As a QC Scientist, you will west drug product and drug substance samples for release and stability as well as sample, test,
and release raw materials for production use. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following.
Perform and train others on physical testing of laboratory samples (drug product, drug substance, in-process, etc) utilizing various chemical and biochemical techniques including Immunoassay (see Section C for details). Prepare laboratory samples for analysis and prepares laboratory standards and solutions. Perform sampling and laboratory testing (instrumental and wet chemistry) for quality disposition in support of manufacturing operations, technical transfers, and special studies within the product
supply chain. Manage samples and associated documentation for duration of sample lifecycle, both physically and electronically.
Participate in and/or lead laboratory investigations. Author, review, and revise SOP's and support Electronic Notebook template development (testing electronic lab notebook templates, author user requirement specifications, etc) Reviews and approves laboratory data. Performs routine departmental GMP activities (lab instrument calibrations, preventive maintenance, audits, work orders, etc) Support analytical and instrument lifecycle, technical transfer, and/or validation Laboratory upkeep and maintenance (5S, routine equipment/glassware cleaning, etc) Why you?
Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Bachelor's degree in Chemistry, Biochemistry, or science related field 2+ years experience in the pharma industry Preferred Qualifications: If you have the following characteristics, it would be a plus: Biomedical testing experience is preferred, ability to learn various techniques and assays techniques Experience with techniques performance Bioassay, cell culture, aseptic techniques, and other potency analysis, use of micro pipettes, Wet Chemistry, use of BSCs, etc.
System experience preferred - SAP/ERP, LES, Webstatistica, Empower, analytical instrument software (softmax, Molecular devices plate readers, Hamilton automated liquid handler, Biacore, etc)Experience with MS Excel, Word, Powerpoint Working knowledge of c GXP, ICH guidelines, FDA, USP/EP/JP and data integrity guidelines and regulations Why GSK? GSK is a global biopharma company with a special purpose -to unite science, technology and talent to get ahead of disease together -so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns -as an organization where people can thrive.
Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves -feeling welcome, valued and included. Where they can keep growing and look after their wellbeing.
So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. #LI-GSK Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why Us? GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at -xyz X (US Toll Free) or xyz X (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, interaction, pregnancy, marital status, interactionual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK.
In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.
This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site. PDN-9ae5f1a0-dcc7-497b-bc55-97e7d0393cd0
tirelessly to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Arterial Hypertension.
Visit us: The successful candidate for this position will join the upstream process development team within the therapeutic protein process development group in Malvern, PA. The candidate will be responsible to perform upstream process development studies including: Participate in design of experiments Perform study
execution Participate in control strategy development Participate in tech transfer, facility fit, and process scale up/ scale down Record and analyze data Author technical reports Additional duties include: Participate in scientific investigations and trouble-shoot process issues that arise during development, technology transfer, or scale-up Collaborate on regulatory filings The candidate is expected to work effectively in a team environment and well as contributing individually to meet project objectives and timelines.
Other duties will be assigned, as necessary. Education: A Master's in Chemical Engineering or Biological Sciences or Biochemistry or related field with 4 years
of relevant experience OR bachelor's with 8 years of experience performing progressively advanced duties is required Requirements: Knowledge of and hands-on experience performing large molecule drug substance (API) upstream manufacturing process development is required Highly organized and capable of managing/ pursuing multiple projects with some supervision is required Good written and verbal communication skills are required Experience maintaining written records of work in the form of laboratory notebooks (paper or electronic) is required The ability to report data, present findings to management is required Experience with team-based collaborations and direct management of staff is required Occasional weekend work may be required Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
according to appropriate study protocols/plans Preparing samples for analysis Operation of standard laboratory equipment General laboratory maintenance (preparing buffer and pipette calibration) Maintaining documentation for all areas of study Conducting routine maintenance of the instruments Maintain current knowledge of Standard Operating Procedures Follow scientific developments in the area of expertise Work on other assignments as directed by Management Required Education & Experience: Bachelor of Science 0-2-year lab experience in biology, life sciences, or biochemistry Cell culture experience preferred Benefits: Pharmaron cares about our work community and offers a variety of benefits allowing
employees the opportunity to customize a benefits package that meets their personal needs.
Company benefits include the following: Medical, Dental & Vision Insurance Plan with Employer Contribution Health Reimbursement Account Funded by Employer Healthcare & Dependent Care Flexible Spending Accounts Employee Life and AD&D Insurance 100% Employer Paid Voluntary Life and AD&D Insurance for Employee, Spouse & Child(ren) Short and Long Term Disability 100% Employer Paid 401k with Employer Match Employee Assistance Program About Pharmaron Pharmaron (Stock Code: 300759.
SZ/3759. HK) is a premier R&D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested
in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products.
With over 19,000 employees, and operations in China, the U. S. and the U. K. Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China. Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer.
Scientist II will play a role in the design and validation of study methodologies to support DMPK studies that make in vitro assays more relevant to in vivo outcomes while supervising a team of up to 3 scientists. Primary responsibilities : Designing studies that meet sponsors' needs or internal needs in a scientifically sound manner.
Executing HPLC and LC-MS studies that follow developmental and GLP guidelines. Author and execute study protocols governing definitive transporter studies, bioanalytical studies, and sample analysis. Take an active role in solving problems and trouble-shooting studies. Analyzing and reporting study data. Peer review of data and reports. Interacting with
different teams daily including other scientists, management, vendors, and sales/marketing team. Interacting with study sponsors. Mentoring and organizing the work schedules of up to 3 scientists.
Qualifications : Bachelor's degree in medical sciences, life sciences or a related analytical field required. Master's or a Ph D in a related field preferred. 5+ years of Development or GLP bioanalytical testing experience. 5+ years of HPLC or UPLC experience (Agilent or Waters experience preferred). Knowledge across other analytical platforms such as HPLC is also preferred. Position requires strong professional communication skills and attention to detail. Strong work ethic, self-motivation,
and ability to adapt in a dynamic team environment are keys for success.
Benefits: Pharmaron cares about our work community and offers a variety of benefits allowing employees the opportunity to customize a benefits package that meets their personal needs. Company benefits include the following: Medical, Dental & Vision Insurance Plan with Employer Contribution Health Reimbursement Account Funded by Employer Healthcare & Dependent Care Flexible Spending Accounts Employee Life and AD&D Insurance 100% Employer Paid Voluntary Life and AD&D Insurance for Employee, Spouse & Child(ren) Short and Long Term Disability 100% Employer Paid 401k with Employer Match Employee Assistance Program About Pharmaron Pharmaron (Stock Code: 300759.
SZ/3759. HK) is a premier R&D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products. With over 19,000 employees, and operations in China, the U. S. and the U. K. Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China.
Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer.
materials, especially polymers. The candidate will utilize NMR spectroscopy to determine molecular identity and structure of materials to help create solutions for client problems. The individual performing this role also has a key responsibility with communication.
The individual must communicate clearly and effectively with his/her colleagues and internal and external clients. What you'll do: Collaborates with members of the organic analysis and other teams to solve problems for clients using NMR Analyzes wide variety of materials including polymers, organic molecules, and complete unknowns Uses NMR to determine identity and structure of materials Designs experiments, collects and
interprets data, authors, and issues formal reports Able to distinguish good measurements from poor ones, identify appropriate next steps, and modify methods to produce accurate results Ensures compliance of company/client SOP, protocols, safety policies, methods, or other procedures with government rules and regulations What it takes to be successful in this role: BS in Chemistry or related field with 5+ years industrial experience in NMR or Ph.
D. with direct research experience relating to NMR Working knowledge of the fundamentals of NMR Demonstrated ability to apply chemical and analytical knowledge and experience to a broad range of materials for non-standard analysis. Must
be able to think beyond standard analytical approaches Excellent organization/multitasking, project management, and communication skills Excellent teamwork ability to integrate expertise into multi-technique solutions to complex problems Why work at Intertek?
Intertek is a world leader in the $250 billion Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. At Intertek, we exercise our spirit of innovation, the passion of our people and our unmatched customer commitment to realize our purpose of making the world an ever better, safer, and more sustainable place for all.
Learn more about Our History and What We Do. What we have to offer: When Working with Intertek , you can expect salary and benefit package competitively placed within the local market, including medical, dental, vision, life, disability, 401(k) with company match, tuition reimbursement and more. Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed. Intertek believes that Our People are our strongest tool for success. We are an Equal Opportunity Employer and do not discriminate against applicants due to veteran status or on the basis of disability.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, interactionual orientation, or gender identity. For individuals with disabilities who would like to request an accommodation, or who need assistance applying, please email xyz X@ or call -xyz X (option #5) to speak with a member of the HR Department. #LI-DNIIntertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers' operations and supply chains.
Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.
home to five clinical institutes. Each serve as a hub for innovation, collaboration and education. Our institutes include Lehigh Valley Topper Cancer Institute, Lehigh Valley Heart and Vascular Institute, Lehigh Valley Institute for Surgical Excellence, Lehigh Valley Fleming Neuroscience Institute and Lehigh Valley Orthopedic Institute.
LVHN is also home to Lehigh Valley Reilly Children's Hospital, which is the only children's hospital in the region. This hospital gives our community access to more than 30 pediatric specialties, Children's Express CARE locations and a dedicated Children's ER. nn We've been consistently recognized by U. S. News & World Report as the top hospital in the
region and among the best in the state. We're also Great Place to Work-Certified TM, which means an overwhelming majority of our colleagues have a positive experience at LVHN.
nn These designations tell you that LVHN is a great place to work from hire to retire. If you are someone who aligns with LVHN's core values - Compassion, Integrity, Collaboration and Excellence – you will have a rewarding and successful career here. nn Hemodialysis is now hiring. nn n Summaryn Provides professional nursing care through skillful backssment, diagnosis, outcomes identification, planning, implementation, and evaluation in accordance with facility or department policies and procedures. Directs and manages
the care of designated patients. Utilizes effective and appropriate communication styles.
Assists in maintaining a safe work environment and maintains clinical and professional competency as appropriate to the population of patients served. nn Job Dutiesnnnt Assesses, plans, implements, and evaluates the care for designated patients. Recognizes the need for and initiates collaboration/communication with physicians, interdisciplinary team members, and takes actions to proactively resolve patients needs. - Synthesizes available data, information, and knowledge relevant to the situation to make decisions which optimize patient outcomes based on ANA Scope and Standards of Practice and the Code of Ethics.
nt Demonstrates commitment to quality and safety, in accordance with established policies and procedures, utilizing evidence-based practice. Participates in evidence-based practice and research projects as applicable. nt Uses effective and appropriate verbal and non-verbal communication styles with patients, significant others, visitors, staff, and professional colleagues. nt Coordinates and provides patient and family education throughout treatment course to facilitate an effective transition of care. nt Functions as a department team member to support unit and hospital goals and objectives.
Participates in all phases of the performance improvement process, including organizational and unit-based patient experience goals. nt Performs validated technical skills based upon clinical specialty and unit practice. nt Utilizes technology and incorporates technology to optimize alternative modes of care delivery. nt Demonstrates leadership and team building skills including: - Teaching and mentoring new colleagues and department interns. Additional precepting, as assigned. - Delegating on the basis of skills and expertise of team member, acuity and specific needs of the patient, and time availability of team members.
- Providing input as requested for performance appraisals of care delivery team members. nnn Minimum Qualificationsnnnt Graduate of accredited Nursing program. nt Knowledge and competence that reflects current nursing practice. nt Ability to organize and prioritize assignments in the delivery of patient care. nt Successful completion of additional orientation programs related to specialty. nt Attainment and maintenance of unit-specific competencies. nt Basic computer skills. nt Registered Nurse State of Pennsylvania Upon Hirent BLS - Basic Life Support Upon completion of orientation Upon Hire andnnn Preferred Qualificationsnnnt Bachelor's Degree Nursingnt As per Clinical specialty within 2 yearsnnn Physical Demandsn Lift and carry 40-50 lbs.
Examples: Push/pull patients on bed, stretcher (requires 29 lbs. push force), lateral transfers up to 50 lbs. of the patient's weight. Frequent to continuous standing/walking. Patient transporters can walk 8-10 miles per shift. Patient care providers may be required to perform activities specific to their role including kneeling, bending, squatting and performing CPR. nn Job Description Disclaimer: This position description provides the major duties/responsibilities, requirements and working conditions for the position.
It is intended to be an accurate reflection of the current position, however management reserves the right to revise or change as necessary to meet organizational needs. Other responsibilities may be assigned when circumstances require. For more details: jobs-search. org/hemodialysis-nurse_allentown-c445985/hemodialysis-nurse-hemodialysis-allentown_i1966129930
pediatric care at Lehigh Valley Reilly Children’s Hospital, minimally invasive and open heart services, comprehensive inpatient and outpatient burn care, and a dedicated inpatient rehabilitation center that will help you maximize your recovery. nn Additionally, LVH–Cedar Crest is the home to many specialty physician practices, outpatient cancer care and the Diagnostic Care Center, where you may receive tests ranging from lab work to heart monitoring to X-ray imaging.
nn If you or a loved one suffers a stroke, our certified Comprehensive Stroke Center offers rapid diagnosis of the type of stroke, targeted therapies – such as clot-busting medication (intravenous thrombolytic) or interventional
clot retrieval – and follow-up rehabilitation, when needed. We have been recognized by the American Heart Association/American Stroke Association’s Get With The Guidelines-Stroke Gold Plus Quality Achievement Award.
nn nn Multiple Neuroscience positions open at Cedar Crest Hospital! nn We have Full-Time. Part-Time, Weekend-Only and Per Diem roles available. Day, Evening and Night shifts available! nn Limited time; OFFERING A $30k Welcome Bonusnn n Summaryn Provides professional nursing care through skillful backssment, diagnosis, outcomes identification, planning, implementation, and evaluation in accordance with facility or department policies and procedures. Directs and manages the
care of designated patients. Utilizes effective and appropriate communication styles.
Assists in maintaining a safe work environment and maintains clinical and professional competency as appropriate to the population of patients served. nn Job Dutiesnnnt Assesses, plans, implements, and evaluates the care for designated patients. Recognizes the need for and initiates collaboration/communication with physicians, interdisciplinary team members, and takes actions to proactively resolve patients needs. - Synthesizes available data, information, and knowledge relevant to the situation to make decisions which optimize patient outcomes based on ANA Scope and Standards of Practice and the Code of Ethics.
nt Demonstrates commitment to quality and safety, in accordance with established policies and procedures, utilizing evidence-based practice. Participates in evidence-based practice and research projects as applicable. nt Uses effective and appropriate verbal and non-verbal communication styles with patients, significant others, visitors, staff, and professional colleagues. nt Coordinates and provides patient and family education throughout treatment course to facilitate an effective transition of care. nt Functions as a department team member to support unit and hospital goals and objectives.
Participates in all phases of the performance improvement process, including organizational and unit-based patient experience goals. nt Performs validated technical skills based upon clinical specialty and unit practice. nt Utilizes technology and incorporates technology to optimize alternative modes of care delivery. nt Demonstrates leadership and team building skills including: - Teaching and mentoring new colleagues and department interns. Additional precepting, as assigned. - Delegating on the basis of skills and expertise of team member, acuity and specific needs of the patient, and time availability of team members.
- Providing input as requested for performance appraisals of care delivery team members. nnn Minimum Qualificationsnnnt Graduate of accredited Nursing program. nt Knowledge and competence that reflects current nursing practice. nt Ability to organize and prioritize assignments in the delivery of patient care. nt Successful completion of additional orientation programs related to specialty. nt Attainment and maintenance of unit-specific competencies. nt Basic computer skills. nt Registered Nurse State of Pennsylvania Upon Hirent BLS - Basic Life Support Upon completion of orientation Upon Hire andnnn Preferred Qualificationsnnnt Bachelor's Degree Nursingnt As per Clinical specialty within 2 yearsnnn Physical Demandsn Lift and carry 40-50 lbs.
Examples: Push/pull patients on bed, stretcher (requires 29 lbs. push force), lateral transfers up to 50 lbs. of the patient's weight. Frequent to continuous standing/walking. Patient transporters can walk 8-10 miles per shift. Patient care providers may be required to perform activities specific to their role including kneeling, bending, squatting and performing CPR. nn Job Description Disclaimer: This position description provides the major duties/responsibilities, requirements and working conditions for the position.
It is intended to be an accurate reflection of the current position, however management reserves the right to revise or change as necessary to meet organizational needs. Other responsibilities may be assigned when circumstances require. For more details: jobs-search. org/neuroscience-specialist_allentown-c445985/job_i1966129769
Requirements for a Pharmacist with Phoebe Allentown shop: Must have a shop degree (Bachelor’s of Science in shop, or Pharm. D) from the Pennsylvania Board of shop, or be Board eligible for shop Licensure in Pennsylvania. Possess a valid Pennsylvania State License.
Successful candidates are those who thrive in a positive and respectful Customer Driven Culture and exemplify the organization’s Faith in Action Mission, Vision, and Values. Apply today! We can’t wait to meet you! Phoebe is an equal opportunity employer. IIFxesg0ly For more details: jobs-search. org/sciences_allentown-c445985/pharmacist-per-diem-allentown_i1966602573
