Biochemist Salary in USA

Eurofins Lancaster Laboratories PSS is searching for a Biochemist in Branchburg, NJ. Biochemist responsibilities include, but are not limited to, the following : • Perform biochemical testing on proteins and antibodies including, but not limited to, Capillary Electrophoresis, HPLC techniques such as SEC and CEX, SDS-PAGE, UV, Protein A titer, ELISA, qPCR and/or Bioassays • Prior experience with maintaining or passaging cell lines is a plus • Enter data into laboratory information management systems • Participate in conducting investigations • Document test results in notebooks and reports The ideal candidate would possess : • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications : • Bachelor's degree in biology, biochemistry, chemistry, engineering or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) • At least three months related laboratory experience • Authorization to work in the United States indefinitely without restriction or sponsorship Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of Branchburg, NJ are encouraged to apply. As a Eurofins Lancaster Labs employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. To learn more about Eurofins, please explore our website www.eurofinsus.com . Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Job DescriptionAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.Discover Impactful Work:Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.A day in the Life:Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing.Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines.Communicates project status to project leader.Maintains a laboratory notebook and completes all laboratory documentation in clear and accurate language and according to SOP and GLPs.Performs daily work assignments accurately, and in a timely and safe manner.Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.Keys to Success:EducationEducation and Experience:Bachelor's degree or equivalent and relevant formal academic / vocational qualificationExperiencePrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 years).In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered enough for an individual to meet the requirements of the role.Knowledge, Skills, AbilitiesKnowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelineKnowledge of applicable regulatory authority, compendia and ICH guidelinesExcellent manual dexterity skillsGood written and oral communication skillsTime management and project management skillsProven problem solving and troubleshooting abilitiesAbility to cross-train on sample preparation techniques with another laboratory groupAbility to work in a collaborative work environment with a teamWork EnvironmentThermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.Able to work upright and stationary and/or standing for typical working hours.Able to lift and move objects up to 25 pounds.Able to work in non-traditional work environments.Able to use and learn standard office equipment and technology with proficiency.May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.Apply today! http://jobs.thermofisher.comThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.Accessibility/Disability AccessJob Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Job no: 933466Work type: Faculty/Academic StaffMajor Administrative Unit / College: College Of Osteopathic MedicineDepartment: Pharmacology Toxicology 10034646Sub Area: FAS- Fac./Acad StaffSalary: Salary Commensurate with ExperienceLocation: East LansingCategories: Research/Scientific, Fixed Term Academic Staff, Full Time (90-100%), Non-UnionPosition SummaryWe are seeking a highly motivated and productive chemical biologist/biochemist to conduct daily research on exciting recently funded projects to 1) investigate how lipid metabolites affect neurodegeneration and 2) discover novel molecules to treat diseases with no effective intervention. Key functions:To investigate how lipid metabolites affect neurodegeneration with novel model organisms and cell models.Apply, develop, and conduct high-throughput screenings in novel model organisms and cell lines to identify novel compounds and protein targets to treat diseases with unmet medical needs. Adapt new technologies and solutions to program studies.Ensure laboratory compliance with safety regulations and maintain routine day-to-day laboratory operations.Training project team members for running specific in vitro assays developed in the lab.Assist in the preparation of presentations, manuscripts, and proposals.Equal Employment Opportunity StatementAll qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, age, disability or protected veteran status.Required DegreeDoctorate -Chemical Science/Pharmacology/BiochemistMinimum RequirementsKnowledge equivalent to that which normally would be acquired through completing a PhD program in chemical science/pharmacology or related fields (Chemistry, biochemistry, chemical biology, chemical engineering, Pharmacology and Toxicology etc); highly experience in C. elegans or cell-model research; experience in metabolomics research; one to three years of related and progressively more responsible or expansive work experience in overseeing research projects and laboratory operations, operating and maintaining a variety of laboratory equipment, performing specialized and difficult analytical and research techniques and assays, and designing research experiments; or an equivalent combination of education and experience. Experienced in scientific communications including but not limited to manuscript and proposal preparations.Desired QualificationsPh.D. in Chemistry or Biochemistry or Pharmacology or related field with at least 3 years of relevant research experience. Sound knowledge of high throughput assays and or experience in C. elegans research or high-performance liquid chromatography coupled with mass spectrometry (HPLC-MS) would be considered a strength. Excellent interpersonal and communication skills. Works independently and leads from the bench. Demonstrates creative initiative and successful in securing grants/fellowships. Results oriented with effective problem-solving skills. Open to suggestions and able to critically evaluate and embrace new or different ideas.Required Application Materials(1) CV(2) Cover letter(3) List of three references. The search committee will not contact references without first notifying the candidate. (4) Diversity, Equity, and Inclusion (DEI) statement. Submit a description of your past experiences and contributions to inclusive excellence including a brief description of your ideas for future initiatives that you would like to implement to support MSUCOM's commitment to inclusive excellence. (https://com.msu.edu/about-us/diversity-inclusion-safety/initiatives). Review of Applications Begins On03/25/2024Summary of Health RisksExposure to blood, tissue and other fluids; work with animals or unfixed animal tissue.MSU StatementMichigan State University has been advancing the common good with uncommon will for more than 160 years. One of the top research universities in the world, MSU pushes the boundaries of discovery and forges enduring partnerships to solve the most pressing global challenges while providing life-changing opportunities to a diverse and inclusive academic community through more than 200 programs of study in 17 degree-granting colleges.Advertised: Mar 15, 2024 Eastern Daylight TimeApplications close: Mar 15, 2026 Eastern Daylight Time

Company DescriptionThe work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.If you're looking for a rewarding career, a place to call home, apply with us today!Job DescriptionGathers data and documents test results.Follows effective standard operating procedures to complete all job tasks.Reviews test results to ensure compliance with standards; reports any quality anomalies.Complies with all pertinent regulatory agency requirements.Operate inside a GMP regulated lab space supporting pharmaceutical clinical testing.Participates in required training activities.Maintains laboratory supplies.Completes test records and reviews data.Follows good documentation practices in both paper logbooks and electronic systems.Calibrates or verifies calibration of instruments/devices prior to use.Interacts with outside customers or functional peer groups.May assist in validation of methods.Strong computer, scientific, and organizational skills.Excellent communication (oral and written) and attention to detail.Ability to work independently and as part of a team, self-motivated, adaptability, andapositive attitude.Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.QualificationsMinimum Qualifications:Bachelor's degree in biochemistry or other science related degree concentration, orequivalent directly related experience.Authorization to work in the United States indefinitely without restriction or sponsorship.The Ideal Candidate would possess:Experience with biochemistry assays and techniques such as:Experience with ELISAsWorking with 96 well-platesSerial dilutionsWorking with small volumes with multi-channel pipetteAdditional InformationPosition is full-time, 1st shift Mon-Fri, 8am-4:30pm. Candidates currently living within a commutable distance of Rensselaer, New York are encouraged to apply. Pay is between $26.25-28.25/hr and isdetermined based on relevant education and/or experience.Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Company DescriptionThe work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.If you're looking for a rewarding career, a place to call home, apply with us today!Job DescriptionGathers data and documents test results.Follows effective standard operating procedures to complete all job tasks.Reviews test results to ensure compliance with standards; reports any quality anomalies.Complies with all pertinent regulatory agency requirements.Operate inside a GMP regulated lab space supporting pharmaceutical clinical testing.Participates in required training activities.Maintains laboratory supplies.Completes test records and reviews data.Follows good documentation practices in both paper logbooks and electronic systems.Calibrates or verifies calibration of instruments/devices prior to use.Interacts with outside customers or functional peer groups.May assist in validation of methods.Strong computer, scientific, and organizational skills.Excellent communication (oral and written) and attention to detail.Ability to work independently and as part of a team, self-motivated, adaptability, andapositive attitude.Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.QualificationsBachelor's degree in biochemistry or other science related degree concentration, orequivalent directly related experience.Authorization to work in the United States indefinitely without restriction or sponsorshipAdditional InformationPosition is full-time, 1st shift Mon-Fri, 8am-4:30pm. Candidates currently living within a commutable distance of Rensselaer, New York are encouraged to apply. Pay is between $26.25-28.25/hr and isdetermined based on relevant education and/or experience.Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Biochemist Scientist Employee Responsibilities: Perform assays on vaccine products, process intermediates, and related experimental samples using one or more of the following techniques HPLC, UPLC, ELISA, SDS-Page, Capillary Electrophoresis, or other biochemical/analytical tests (e.g., spectrophotometric, electrophoretic, immunochemical methods) Support Critical Reagent activities including sample management shipments (~50%of the time) Prepare solutions and reagents Technical document preparation and review Laboratory data review Maintain records and test results following good manufacturing practices (GMP) The Ideal Candidate would possess: Minimum of 1 year GMP related laboratory experience General laboratory skills, experience with pipettes, HPLC equipment, and other automated instrumentation Experience using Empower III Excellent communication skills- with oral and written Strong organization and attention to detail Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies (GMP knowledge a plus) Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Minimum Qualifications: Bachelor's degree in biology, chemistry, or other related degree concentration Authorization to work in the United States indefinitely without restriction or sponsorship What we offer: Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays As a part of Eurofins BioPharma Product Testing - the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide - Eurofins Lancaster Laboratories provides comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies. Our service offering includes comprehensive chemistry, biochemistry, microbiology, molecular and cell biology and biosafety testing of drug substances, final products, intermediates, and starting materials for both small and large molecule drug products. To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com . Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer .

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionSupports clinical testing of pharmaceutical productsGathers data and documents test results.Reviews test results to ensure compliance with standards; reports any quality anomalies.Complies with all pertinent regulatory agency requirements.Participates in required training activities.Maintains laboratory supplies.Completes test records and reviews data.Calibrates or verifies calibration of instruments/devices prior to use.Interacts with outside customers or functional peer groups.May assist in qualification and validation of methodsStrong computer, scientific, and organizational skillsExcellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivated, adaptability, andapositive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesQualificationsThe Ideal Candidate would possess:Laboratory experience (chemistry/biochemistry preferred)Exposure to working in a GMP environmentExcellent communication (oral and written) and attention to detailKnowledge of ELISAExperience of capillary electrophoresisFamiliaritywith LIMS preferredMinimum Qualifications:Bachelor's degree in Chemistry, Life Sciences, Engineering, or other science-related degree concentration, orequivalent directly-related experienceExperience in Gel ElectrophoresisAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesAuthorization to work in the United States indefinitely without restriction or sponsorshipWhat to Expect in the Interview Process:10-15 Minute Phone Interviewwith the Recruiter45 Minute Virtual Interview with Hiring Manager30 Minute Virtual Interview with Regional DirectorAdditional InformationThe position is full-time,Monday-Friday 8 am - 4:30 pm.Candidates currently living within a commutable distance ofRensselaer, NYand the surrounding areas are encouraged to apply.What we offer:Excellent full-time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysBase compensation is $60k-70kper hour based on experience.2nd and 3rd shift positions will add a 10% and 15% differential to the base pay.Eurofins Lancaster Laboratories Professional Scientific Services®(PSS) is a global, award-winning insourcing solution that places our people at our clients' site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client's quality systems and equipment.To learn more about Eurofins Lancaster Laboratories, please explore our websitewww.eurofinsus.com.#LI-EB1Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Apply now for the position of Staff Biochemist in Technical Operations, Walpole MA, and you will support the manufacture and improvement of our immunoassay diagnostic products at our world class manufacturing facility that deliver diagnostic products to millions of patients globally. Your role: You will utilize your scientific and technical expertise to lead and participate on teams that investigate manufacturing issues with Immunoassay products and respond to changing priorities to meet business demands. You will coordinate and complete multiple simultaneous complex investigations supporting change projects while meeting business timelines. You will produce compliant documents associated with investigations, technical studies, verification/validation activities, and CAPAs. You will identify cost savings measures that can be implemented with no impact to product quality and supply. You will mentor and coach less experienced staff. You will serve as a technical leader and represent our team in cross-functional initiatives, while proactively keeping up to date with product and technology knowledge. Your expertise: PhD with 6+ years, in diagnostics, immunoassay, chemiluminescent technology, or medical device or equivalent Superior understanding and knowledge of polyclonal and monoclonal antibodies Superior understanding of the principles of chemiluminescent based immunodiagnostic technology plus extensive experience with diagnostic immunoassays. Demonstrated ability to design experiments, interpret data, troubleshoot and resolve technical issues Well-versed in the application of cGMP as applied to Medical Devices: CFR 21 Part 820 and ISO 13485. Strong command of PC skills (MS Office 365 software like Word, PowerPoint, Excel, and Outlook) and statistical methods (Minitab preferred) Who we are: We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Check our Careers Site at https://jobs.siemens-healthineers.com/careers Beware of Job Scams Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers Career Site. "Successful candidate must be able to work with controlled technology in accordance with US export control law." "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations." As an equal opportunity employer, we welcome applications from individuals with disabilities. We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities. To all recruitment agencies: Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated. Equal Employment Opportunity StatementSiemens is an Equal Opportunity and Affirmative Action Employer encouraging diversity in the workplace. All qualified applicants will receive consideration for employment without regard to their race, color, creed, religion, national origin, citizenship status, ancestry, sex, age, physical or mental disability unrelated to ability, marital status, family responsibilities, pregnancy, genetic information, sexual orientation, gender expression, gender identity, transgender, sex stereotyping, order of protection status, protected veteran or military status, or an unfavorable discharge from military service, and other categories protected by federal, state or local law.EEO is the LawApplicants and employees are protected under Federal law from discrimination. To learn more, Click here .Pay Transparency Non-Discrimination ProvisionSiemens follows Executive Order 11246, including the Pay Transparency Nondiscrimination Provision. To learn more, Click here .California Privacy NoticeCalifornia residents have the right to receive additional notices about their personal information. 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Scientist, Antibody Expression and PurificationWe are looking for a highly motivated and talented protein biochemist with quality mindset to join our Biologics Expression Team (BET) team. The successful candidate will play a critical role in a dynamic group responsible for performing expression and purification of a wide variety of antibodies, multi-specifics, and complex modality biologics. He/She will be a key player in providing high quality, well-characterized proteins to support biologics discovery across multiple therapeutic indications. The successful candidate will be a well-organized and a highly productive scientist that can design and execute experiments efficiently, analyze, interpret, and present data to multidisciplinary project teams.AstraZeneca is an exciting company with long-standing tradition of excellence in drug discovery that offers a fantastic culture and great opportunities to enhance your skills and grow your career. At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.ResponsibilitiesPerform expression and purification of mono- and multi-specific antibodies and complex modalities fusion proteins from sub-milligram to gram scale to support antibody discovery, characterization, and pre-clinical validation of leads.Purification of recombinant proteins and antibodies using affinity-based and/or conventional chromatographic separation techniques; use of automated purification platforms including AKTA.Perform biologics quality assessment utilizing a variety of techniques, such as CE-SDS, SEC-HPLC, endotoxin assay, etc.Proven ability to work independently, effectively plan and organize work activities and prioritize task completion to meet project deadlines.Collaborate and work with a diverse group of scientists across all therapeutic areas to ensure timely progress of research projects.Maintain complete and updated records in electronic lab notebook.Required SkillsBachelor's with 3+ years or Masters with 1+ years of experience in Biologics production at Biotech/Pharma industryExtensive hands-on experience with transient mammalian expression (HEK293 and CHO) and purification of mono- and bi-specific antibodies, Fab fragments, scFv, VHH, and various antibody-fusion formats. Demonstrated proficiency with various modes of chromatography, including affinity, IEX, mixed mode, HIC, and SEC. Deep and current knowledge of resigns, membranes and suppliers.Extensive hands-on experience with chromatography instrumentation as AKTA. Experience with automation is preferred.Strong protein characterization and QC skills including analytical SEC, CE-SDS, endotoxin assays, etc.Proven ability to work independently, effectively plan and organize work activities, and prioritize task completion to meet project deadlines in a fast-paced industrial environment.Strong interpersonal and communication skills, ability to collaborate and communicate across disciplines.About AstraZenecaAstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies.At AZ, we're proud to have an exceptional workplace culture that encourages innovation and collaboration. Here, employees are empowered to express diverse perspectives - and made to feel valued, energized and rewarded for their ideas and creativity. AZ is a place where passionate people can immerse themselves in their work and make significant contributions to scientific excellence and medicines - does this describe a place where you would like to work?Our Gaithersburg, Maryland facility creates life-changing medicines for people around the world. This campus employs more than 3,500 experts in our field and is only a short drive from Washington, DC. This modern and vibrant scientific campus is the home of R&D and Oncology in the US. Here, we play host to some of the most cutting-edge technology and lab spaces, all designed to inspire collaboration and cross-functional science. We believe employees benefit from being challenged and inspired at work. We are dedicated to creating a culture of inclusion and collaboration.The Gaithersburg site offers a variety of amenities to help boost productivity and help keep our employees happy and healthy. This includes a fitness center, employee healthcare clinic, electric vehicle charging stations, dry cleaning, full-service cafeteria and copy center. This is where you'll find newly-designed, activity-based work spaces to suit a variety of working styles while increasing collaboration between teams."When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world." AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.

Company DescriptionEurofins PSS Insourcing provides tailored laboratory solutions for companies seeking to outsource their analytical testing needs. By partnering with Eurofins PSS Insourcing, businesses can access state-of-the-art laboratory facilities, equipment, and expertise without the burden of maintaining their own in-house labs. This allows companies to focus on their core competencies while ensuring the quality and reliability of their analytical testing processes. Eurofins PSS Insourcing offers a range of services including method development, validation, and sample analysis across various industries such as pharmaceuticals, food and beverage, environmental, and more.Job DescriptionLaboratory ResponsibilitiesExecute assigned/trained assays, constituting 80-90% of working hours.Fulfill all duties pertinent to the Quality Control Chemist role as necessary.Manage inventory of laboratory supplies, media, and reagents.Maintain and update relevant databases, and generate monthly reports.Conduct laboratory investigation reports as required.Utilize Laboratory Information Management System (LIMS) for sample and test result tracking.Leadership ResponsibilitiesProvide support and supervision to a team of analysts.Participate in new hire interviews.Assist in the onboarding process of new employees.Contribute to the training of team members.Conduct peer review of data.Coordinate equipment maintenance and calibration.Be available for overtime and weekend shifts as needed.Adapt quickly to changing priorities to accommodate immediate testing requirements and assist team members in refocusing as necessary.QualificationsThe Ideal Candidate Would Possess:Laboratory experience, with a preference for chemistry/biochemistry backgrounds.Exposure to working in a GMP (Good Manufacturing Practice) environment.Strong communication skills, both verbal and written, with a keen attention to detail.Proficiency in ELISA and experience with capillary electrophoresis.Familiarity with LIMS is advantageous.Minimum Qualifications:Bachelor's degree in Chemistry, Life Sciences, Engineering, or a related scientific discipline, or equivalent directly relevant experience.Proficiency in Gel Electrophoresis.Ability to acquire new techniques, manage multiple tasks simultaneously, maintain accurate records, follow instructions, and adhere to company policies.Authorization to work in the United States indefinitely without sponsorship or restriction.Additional InformationThe position is full-time,Monday-Friday 8 am - 4:30 pm.Candidates currently living within a commutable distance ofRensselaer, NYand the surrounding areas are encouraged to apply.What we offer:Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysYearly goal-based bonus & eligibility for merit-based increasesBase compensation is $25-$35per hour based on experience.2nd and 3rd shift positions will add a 10% and 15% differential to the base pay.Eurofins Lancaster Laboratories Professional Scientific Services®(PSS) is a global, award-winning insourcing solution that places our people at our clients' site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client's quality systems and equipment.To learn more about Eurofins Lancaster Laboratories, please explore our websitewww.eurofinsus.com.#LI-EB1Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.