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Job DescriptionCompany Description At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries. PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees. Job Description We are seeking an Analytical Clinical Chemistry Scientist to set up, execute, and troubleshoot HPLC and UPLC instrumentation. Responsibilities include preparing protein samples, mobile phases, and cleaning solutions, handling micropipettes, and documenting procedures and test data. The ideal candidate will ensure compliance with quality standards, participate in training activities, and maintain lab supplies and equipment. • Set up, execution, and troubleshooting on HPLC and/or UPLC instrumentation., • Preparation of protein samples, standards, and controls, • Preparation of organic and salt mobile phases as well as acidic cleaning solutions., • Handling and use of micropipettes, • Gathering, processing, and recording data in an electronic database, • Thorough and complete documentation of standard operating procedures followed and resulting test data., • Review of test results to ensure results meet validity, suitability, and specification acceptance criteria; report any quality anomalies., • Complies with all quality, integrity, and safety standards outlined through effective policies and procedures., • Participates in required electronic and in-person training activities, • Maintains laboratory supplies., • Routine calibration and/or verification of instruments and other lab equipment prior to use., • Interacts with outside customers or functional peer groups.Qualifications, • Bachelor’s degree in chemistry, related field with 2-4 years of HPLC, GMP experience OR, • MS with 1+ years of HPLC, GMP experience, • Experience maintaining HPLCs/UPLCs, • Experience with MCE and iCEIF assays, • Knowledge of cGMP, • Strong technical, computer, 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., • Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information The position is full-time, Monday - Friday, with the hours of 8:00 am - 4:00 pm with overtime as needed. Candidates living within a commutable distance of Rensselaer, New York, are encouraged to apply. 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, • Hourly rate is between $26.25-$33.50 dollars per hour. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionCompany Description At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries. PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees. Job Description This position is designed for candidates with an Associate degree in Biology, Microbiology, Biotechnology, Chemistry, or a related laboratory science field and hands-on laboratory experience. This is an entry-level laboratory technician position with limited advancement into scientist-level roles. • Perform environmental monitoring of GMP manufacturing and process areas., • Collect samples from high-purity water, clean steam, and compressed gas systems to support quality and compliance requirements., • Conduct routine utility testing in accordance with established procedures., • Use the Laboratory Information Management System (LIMS) to track samples, test results, and laboratory activities., • Maintain inventory of laboratory supplies, microbiological media, and reagents to ensure uninterrupted operations., • Support the coordination of equipment maintenance, calibration, and laboratory readiness activities., • Assist with the training and onboarding of team members by sharing knowledge and best practices., • Perform basic microbial identification and data review, as assigned., • Conduct acceptance testing of commercially prepared microbiological culture media, as applicable., • Participate in an on-call, overtime, and weekend rotation to support business and operational needs. What You'll Gain • Hands-on experience with microbiological testing and environmental monitoring programs., • Exposure to regulated laboratory and manufacturing environments., • Opportunities to develop expertise in LIMS, utility monitoring, GMP compliance, and laboratory operations., • Collaboration with experienced scientists and quality professionals in a team-oriented environment.Qualifications, • Associates Degree in Life Sciences, • Relevant experience, preferably in the pharmaceutical or biotechnology industries, • Environmental Monitoring experience preferred, • Microbial identification procedure knowledge, • Knowledge cGMP is a plus, • 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, • Experience with LIMS preferred, • Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information • Position is full-time, Sunday-Wednesday 12:30 PM - 11:00 PM., • Pay range: $17.50 - $19.00 per hour based on experience level, • 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 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Position Summary: The Senior Scientist will work closely with the Center for Biopharmaceutical Education and Training (CBET) and College faculty and staff to provide expertise and continuous support to achieve CBET’s objectives. This position reports to the Director of CBET. Interested candidates should submit a resume and cover letter. Major Duties & Responsibilities: • Lead upstream laboratory development activities in coordination with CBET team, • Participate effectively in teaching and training programs designed for industry professionals, • Work directly with industry partners to execute projects under confidentiality and in accordance with good laboratory practices (GLP), • Generate project data and assist in analyzing laboratory results while maintaining data integrity standards, • Author and review technical documents, technical reports, Batch records, and SOPs Knowledge, Skills and Abilities: • Expertise in cell culture (e.g., CHO, mammalian) and fermentation (E. coli, yeast), • Proven expertise bioreactor processes scale-up and scale-down (single-use and stainless steel), • Strong knowledge of aseptic techniques and GMP compliance, • Skills in process parameter control (pH, DO, temperature, agitation), • Data analysis, experimental design, and troubleshooting abilities, • Experience in bioanalytics and downstream processing is a plus., • Experience in downstream purification, chromatography, and TFF are desirable., • Effective written and verbal communication skills with a respect for confidential material, • Strong organizational and problem-solving skills with attention to detail., • Work independently and with other members of the team to execute required tasks, • Excellent time management and task prioritization skills, • Comfort managing multiple projects at the same time – i.e., multitasking, • Ability to interact collaboratively with a diverse team of professionals both from academia and industry, • Demonstrated ability to meet deadlines on accelerated timelines in a fast-paced work environment Education and Experience: • Ph.D. in life sciences, biochemical engineering, biomedical engineering, or related discipline, • Minimum of 2 years of experience in an academic or industry environment, • Experience in downstream processing related to the biopharmaceutical industry, preferred, • Experience in a GMP/GLP environment, preferred Physical Demands: While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to stand; walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, and the ability to adjust focus. Work Environment: While performing the duties of this job, the employee is not substantially exposed to adverse environmental conditions. Additional Information: This position is based in Albany, NY. The duties and responsibilities of this particular role require the need for consistent, in-person collaboration and/or interaction with our community, requiring all work to be performed full-time on-site. Standard work hours are from 8:30 AM – 4:30 PM EST, Monday through Friday. Additional details pertaining to this position will be discussed during the interview process. Benefits: Albany College of Pharmacy and Health Sciences (ACPHS) offers a comprehensive benefits package for full-time employees including medical, dental and vision benefits, free life insurance and disability programs, tuition assistance programs, retirement plan with employer match and contribution, and generous time off including 20 paid holidays plus paid sick and vacation time. Additional perks include wellness rewards, free gym access, free parking, identity theft protection and many others. Please note, benefits and benefits eligibility can vary by position, and exclusions may apply for some roles. ACPHS is an Equal Opportunity Employer and does not discriminate against any protected class of job applicant or employee in our hiring and employment practices.

Job Description SummaryYou will work within an interdisciplinary team to innovate and push the technical envelope in all aspects of magnetic resonance imaging. You will have opportunities to work both on MRI systems hardware as well as algorithms and pulse sequence development. The research and development work will be across 1.5T-3.0T whole body and 3.0T-7.0T high-performance, head-only MRI platforms.Job DescriptionJob DescriptionAs a Magnetic Resonance Research Scientist, you will:Apply deep knowledge in MR physics, mathematics, engineering and chemistry to conceptualize and prototype novel MR systems and applications that address key clinical needs.Develop impactful applications that leverage next-generation MRI sub-systems that have enhanced imaging capabilities. Examples are in high-performance gradient coils, RF coils, receiver sub-systems, gradient drivers, etc.Develop and deploy investigational MR applications and systems in clinical and preclinical environments for tests and validation.Determine the impact of systems hardware performance on image quality and safety.Develop algorithmic and/ or systems hardware solutions for MR-guided therapy and interventional applications.Grow external collaborations with academic and industry partners through joint publications, grant submissions and advanced technology development.Work with clinicians to refine emerging technologies for clinical applications.Create intellectual property by generating invention disclosures and filing patents.Maintain external visibility through conference presentations and peer-reviewed journal publications.Required QualificationsPh.D. degree in Physics, Electrical Engineering, Biomedical Engineering, Chemistry, Computer Engineering, or other related fields, with at least 3 years of research experience.A demonstrated record of research and development outcomes as evidenced by peer-reviewed conference proceedings and journal publications.Strong fundamentals in MR imaging physics and sub-systems, signal processing and electromagnetic theory.Demonstrated strong problem-solving skills, including the ability to understand and address root causes of MR image quality issues in investigational prototypes.Proficiency in programming in C, Python and/ or simulation tools.Legal authorization to work in the U.S. is required. You will need to have valid, on-going authorization to work in the U.S.Must be willing to work out of an office located in Niskayuna, NY.You must submit your application for employment on the careers page at to be considered.Desired CharacteristicsDemonstrated ability to originate and follow through on ideas.High levels of curiosity, independence and adaptability.Strong interpersonal skills.Excellent written and verbal communication skills.Experience in writing and executing grant proposals.Experience in developing or modifying components of MR sub-systems leading to measurable changes in image quality and new applications.Experience in EM and multi-physics modeling, especially for analysis of RF transmit and gradient field bioeffects.Experience in pulse sequence programming on a GE HealthCare MRI scanner and/ or developing new image reconstruction algorithms.For U.S. based positions only, the pay range for this position is $100,000.00-$150,000.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement.GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.Relocation Assistance Provided: YesJob SummaryJob number: R4040298Profession: Engineering / Technology