RJ Lee Group jobs - 126 jobs

RJ Lee Group is hiring a Strategic Project Applications Manager to support our Industrial Hygiene/Environmental division. This full-time role, based in Monroeville, PA, involves 50% travel and offers a unique opportunity to work directly with our VP of Emerging Contaminants. The ideal candidate will combine technical expertise in air quality instrumentation with strong project management and business development skills. Responsibilities include operating advanced mobile platforms, supporting strategic initiatives, and managing client-facing projects. Candidates with a background in Materials Science, Chemistry, or related disciplines and experience in PTR-MS and AIM instrumentation are encouraged to apply.Key ResponsibilitiesBusiness Development & Strategic Planning Assist in identifying and qualifying new business opportunities Conduct market research and competitive analysis Help prepare proposals, presentations, and client communications Contribute to special initiatives and strategic planning efforts Technical Operations & Data Management Assist with data collection, instrument operation, method development, reporting, and quality control Track leads, opportunities, and client interactions in CRM systems Project Management & Coordination Support project planning, scheduling, and documentation Monitor project milestones and deliverables Coordinate meetings, take notes, and follow up on action items Process Improvement & Internal Support Help streamline workflows and improve internal process Qualifications Bachelor's degree in Materials Science, Chemistry, Geology, Physics, or a closely related scientific discipline is required; advanced degrees (Master's or Ph.D.) are preferred 5-7 years of professional experience in environmental science, industrial hygiene, or related technical fields Demonstrated expertise in volatile organic compound (VOC) and combustion analysis Hands-on experience with air quality monitoring systems and instrumentation Strong understanding of relevant analytical methods and industry standards Exceptional communication, organizational, and analytical problem-solving skills Preferred Skills Strong mass-spectrometry PTR MS, and AIM instrumentation Strong client relationship and technical writing abilities Join RJ Lee Group as a Strategic Project Applications Manager and help shape the future of environmental innovation! We're looking for a proactive leader with a passion for emerging contaminants, mobile platform instrumentation, and strategic growth. If you thrive in a fast-paced, collaborative environment and want to make a real impact, apply today!

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Manufacturing Associate II - O'Hara - M -TH 5:30am - 3:50 pm Manufacturing Associate II - O'Hara - M -TH 5:30am - 3:50 pm - Multiple positions available We are currently seeking motivated colleagues to contribute to meaningful work in our local manufacturing plants. Our positions perform meaningful work and includes exposure to advancing technologies, having a voice to challenge our status quo, and training for career advancement. We offer on the job training to start you on your journey with Bayer! Our O'Hara, PA location operates Monday to Thursday from 5:30 am to 3:50pm with Friday overtime sometime available. We also offer a breadth of benefits, included (but not limited to) 120 hours of vacation, 128 hours of holiday time, 40 hours sick time, full medical/dental/vision, educational assistance, annual bonus and MORE! Pay is $18.00 per hour. This position also has up to a 5% yearly bonus. Learn more by clicking the Bayer benefits link! Bayer Benefits Purpose: This advanced position exists to provide experienced resources to assemble and support the various medical device manufacturing processes. It also provides a supporting role in the way of quality control in combination with advanced assembly, performed in a timely manner to meet quality and productivity goals of the department. This role will also assist the process coordinator or group lead in any training or cross training efforts as needed. The role will also interact between many departments to transmit information and recommend solutions to design, process and quality problems/non-problems. Leadership, a positive attitude and willingness to support teamwork is key! This role provides mentorship and support to the Manufacturing Production floor personnel in any way possible! This position will incorporate both Assembly and Quality inspections and requires more than one years' experience at Bayer or in a position with related work experience. YOUR TASKS AND RESPONSIBILITIES A day in the life of a Manufacturing Associate II includes: You will use your advanced mechanical assembly skills to integrate circuit boards, wiring harness, units and mechanical assemblies using the appropriate tooling equipment in an FDA regulated facility. You will use your knowledge of statistical process control (SPC), good manufacturing practices (GMP), traceability and material review board (MRB) while working independently with little direction to perform automated testing and other requirements. You will professionally interact with the lead, the supervisor, engineers and coworkers to enhance teamwork and to foster positive working relationships. You may also support production or quality control inspections, You will use your attention to detail and understanding of continuous improvement/lean initiatives to collaborate with them to resolve line issues and suggest improvements. Training: You will support Group Lead/Process Coordinator with their training needs providing guidance to new trainees and assemblers on complicated aspects of the assembly work. You will guide them on the how to collect data, maintain accurate records/documentation related to quality, work in progress, test results, labor and special products. Testing: You will perform Quality Control measurements and functions and support new product builds and testing them as required. WHO YOU ARE Bayer seeks an incumbent who possesses the following: Required Qualifications * High School Diploma/GED; * At least 1 year experience performing Medical Device assembly or technical assembly experience performing in a solid and consistent level; * Understanding of or the ability to quickly learn BAYER's quality systems policies; * Ability to perform technical writing; * Ability to adapt quickly to fast-paced changing situations; * Proven sound judgment, continuous improvement, and customer focus; * Demonstrated adaptability and teamwork skills; * Ability to interpret technical drawings and visual work instructions. Preferred Qualifications * Associate's Degree * The ability to perform all major tasks and at least 50% of all operations within the Bayer manufacturing cells/lines with no assistance. Employees can expect to be paid a hourly wage of $18.00 per hour. Additional compensation may include, shift differential pay, a bonus or incentive compensation (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 9-15-24. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location:United States : Pennsylvania : Pittsburgh Heilman Division:Pharmaceuticals Reference Code:860112 Contact Us Email:hrop_*************

**At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.** **Senior Medical Science Liaison, Stroke/Thrombosis (Pittsburgh, PA)** The Senior Medical Science Liaison (MSL) serves as a trusted scientific expert and partner representing Bayer in the medical community through the dissemination of and education on scientific data related to Bayer products across the product lifecycle. The MSL establishes proactive long- term scientific/strategic relationships with key, influential healthcare providers, and stakeholders, and with major medical associations and academic centers of excellence. These relationships will ensure that healthcare providers and organizations have access to relevant scientific information and that pertinent information is shared with the medical community. The MSL serves as technical and scientific support in the field for healthcare providers ensuring safe and effective use of Bayer products including timely adverse event reporting and responses to unsolicited requests for detailed product and disease state information. The MSL also develops a complete understanding of national, regional, and local experts and stakeholders in specific therapeutic categories and the healthcare environment in which they work. The MSL is an expert in specific therapeutic areas covering a specific region and Area Business Unit, collaborating with internal business partners and external contacts addressing specific scientific and educational needs. The Territory will cover: **YOUR TASKS AND RESPONSIBILITIES** The primary responsibilities of this role, Senior Medical Science Liaison, Stroke/Thrombosis (Pittsburgh, PA) are to: **Scientific Expertise** + Complete core training curriculum and basic MSL and Therapeutic Area (TA) Certification; + Demonstrated accountability to continuous learning and growth (Franchise data, MSL role, Soft Skills, Personal Development). Completes recertification where applicable; + Professional licensure with CEU documentation where applicable; + Depth of knowledge within the therapeutic area exceeds that of peers and/or Medical Affairs experience in multiple therapeutic areas; + Coordinates and lead TA updates, team discussions, training initiatives (i.e. journal clubs); + Attend and report on local, regional and national medical conferences and other meetings of value; + Coordinate team coverage of major regional or national meetings including program evaluation, required attendance and coordination of high quality meeting reports; + Identifies educational gaps and provides subsequent recommendations for educational resource, content, or initiative development. **External HCP and Stakeholder Engagement** + Establishes robust long-term relationships with Thought Leaders and other key stakeholders through education on up to date scientific information in alignment with US, Global, and Area Business Unit definitions and strategies; + Impactful proactive engagement with TLs, HCPs, research sites, associations, societies, & other stakeholders according to defined scope and engagement plans. Actively seeks future stakeholders and emerging Thought Leader groups in alignment with local health care system and medical strategy; + Leverage knowledge of US and Global definitions and strategies to develop and pull through local Area Business Unit strategy; + Responsible and Accountable for driving medical strategy by translating the local medical plan into implementable TL and stakeholder engagement strategies with cross-functional teams and identify synergies with the interests of Bayer and the general medical community; + Approach accounts, customers, and Area Business Unit strategically, utilizing key metrics to ensure alignment to territory plan and medical objectives; + Compliantly supports speaker training and evaluation and medical evaluation of scientific merit; + Advisory Board or other Bayer Program coordination or support during meeting; + Coordinates TL engagement with Franchise Medical Affairs team and relevant internal stakeholders. **Education** + Delivers educational presentations to external audiences, stakeholders, and customers groups. Proactive identification of educational opportunities within assigned Area Business Unit to stakeholders or customers groups; + Responsible for timely, accurate, specific and balanced responses to Medical Inquires in collaboration with Medical Communications; + Adherence to SOP and FDA guidance for distribution of scientific information; + Adherence to SOP and compliance guidelines for all external contacts; + Prepares and presents data to internal audiences including MA and Commercial partners. **Research** + Responsible for supporting research projects aligned with medical and brand strategy; including facilitating investigator-initiated research (IIR) and research site identification; + Responsible for supporting clinical trial team and engaging with appropriate stakeholders for Bayer sponsored clinical trials. Support with data collection, feasibility & initiation visits, and study support as appropriate. **Insights** + Responsible and Accountable for generating relevant HCP and stakeholder insights that deepen understanding of patients, HCPs, consumers, or treatment landscape. Document and communicate them accordingly within system or to stakeholders to inform, refine, and enhance tactics and strategy; + Report new compound development information and potential collaborations when appropriate or requested in line with corporate strategy. **Collaboration** + Compliant active strategic partnership and collaboration with territory cross-functional stakeholders (i.e. Area General Manager, Area Business Unit team, Field DGOS, etc.) as part of Area Business Unit team; + Presentations to internal audiences including Therapeutic Area Medical Affairs (MA) or commercial partners; + Lead project teams or task forces as appropriate within Franchise Medical Team; + Initiates best practice discussions for MSL team and internal partners; + Responsible and accountable as MSL mentor as appropriate. **New Ways of Working (Data Collection / Analysis / Interpretation)** + Internal champion of new ways of working including platforms, systems, capabilities. Train, mentor, and empower Field Medical team to leverage new ways of working; + Complete all required customer activity documentation, training, expense reporting, and other administrative responsibilities in a timely, accurate, and compliant manner; + Responsible for reviewing and interpreting interaction analytics related to TL engagement and take appropriate actions to execute stakeholder plans; + Use data and analytics to seek out and maximize customer engagement opportunities within the territory; + Leverage evolving country and Global platforms and systems to ensure data driven tailored approach to customer engagement; + Leverage omnichannel methods of engagement with stakeholders to ensure customer-centric approach to data dissemination and education. **WHO YOU ARE** Bayer seeks an incumbent who possesses the following: **Required Qualifications:** + BA/ BS Degree is required; + Experience in a scientific or healthcare clinical setting; or pharmaceutical industry experience in Medical Affairs, Sales, Marketing or Clinical Development; or post-graduate fellowship experience in a hospital or industry setting; Rotations or fellowships do not contribute to above requirements; + MSL experience is required; + Demonstrated project management ability; + Demonstrated expertise in communicating scientific information; + Demonstrated project management ability; + Excellent oral and written communication skills; + Excellent interpersonal skills; + Demonstrates understanding of clinical trial design; + Ability to critically evaluate the medical literature; + Ability to work in a team environment; + Established ability to build productive work relationships both internally and externally; + Travel 50+% and manage a demanding schedule; + Valid Driver's License and eligibility to drive a company car or pooled vehicle (driving record must meet guidelines base on the company's Risk Screening for Hiring Drivers and MVR will be reviewed as part of pre-employment screening). **Preferred Qualifications:** + Advanced terminal Doctorate degree in medical or health sciences (e.g M.D., PhD, PharmD, DPH, EdD) or an advanced degree in Pharmacology, Pharmacy, Medicine, Nursing or equivalent experience is preferred; + Working knowledge of FDA, OIG requirements; + A minimum of 1 year MSL experience or 2 years experience working within the pharmaceutical/biotech industry or post-graduate fellowship experience in a hospital or industry setting. + Area of expertise in neurology, stroke, thrombosis, or anticoagulation, preferred. Employees can expect to be paid a salary of between $156,000 to $234,000. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This position is eligible for Bayer's enhanced Referral Bonus. This posting will be available for application until at least: 1/22/2026. \#LI-US **YOUR APPLICATION** Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. **Location:** United States : Pennsylvania : Pittsburgh || United States : Pennsylvania : Residence Based **Division:** Pharmaceuticals **Reference Code:** 859960 **Contact Us** **Email:** hrop_*************

Full-time Description Ready to look forward to going to work every day? Want to be a part of a service driven culture where employees are appreciated? Check out our opportunity with Bayer Heritage Federal Credit Union! A BSA and Compliance Specialist ensures that a financial institution adheres to the Bank Secrecy Act (BSA), anti-money laundering (AML) regulations, and other compliance requirements. The role involves monitoring transactions for suspicious activity, conducting investigations, preparing regulatory reports such as SARs and CTRs, and supporting audits and risk assessments. Essential Functions & Responsibilities: Reviews all regulations pertinent to Credit Union Operations and make recommendations for procedure and policy changes to assure BHFCU complies with such regulations. Regulations include, but are not limited to: - The Privacy Act, The SAFE Act, and FACT Act - The Bank Secrecy Act - Regulation Z: Truth in Lending - Regulation CC: Availability of Funds & Collection of Checks - Regulation B: Equal Opportunity Act - Assist the compliance officer with compliance questions or issues from credit union employees. - Assist the compliance officer with ongoing reviews of the various compliance areas including risk assessments, Red Flags - Gathers necessary documentation for exams and audits which pertain to areas of compliance and BSA. - Utilizes Verafin to ensure we maintain a comprehensive BSA program. - Work alerts associated with BSA. - Respond to and initiate 314(b) conversations regarding suspicious member activity. - Review and schedule high risk member reviews (HRC). - Review reporting exemptions to ensure continued qualifying activity. - Review resolved cases for potential BSA reporting. - Upload and work 314(a) lists and alerts. Performance of daily tasks: - Review member transactions for BSA compliance utilizing Verafin. - Complete CTRs and author SARs for timely submission. - Research and act upon suspicious incidents received by the branch. - Gather and submit documentation for subpoenas received. - Perform other job-related duties as assigned. Requirements Experience Two years of experience in a credit union environment. BSA/compliance experience preferred. Education High school diploma or equivalent. Interpersonal Skills Courtesy, tact, and diplomacy are essential elements of the job. Work involves much personal contact with others inside and/or outside the organization for purposes of giving or obtaining information, building relationships, or soliciting cooperation. Other Skills Ability to read, comprehend, and interpret technical documents. Work Environment Office setting. EEO Statement Bayer HFCU is an equal opportunity employer. We are committed to our policy of providing equal employment opportunity in a manner consistent with applicable laws and regulations, including federal laws prohibiting employment discrimination on the basis of race, color, creed, national origin, sex, age, disability, sexual orientation or genetic information. *Some states are ineligible for remote work.

We are seeking a detail-oriented and experienced Transmission Electron Microscopy (TEM) Supervisor to oversee the daily operations of our asbestos TEM laboratory. This role focuses on supervising lab personnel, maintaining equipment, ensuring compliance with safety and analytical protocols, and supporting consistent, high-quality sample analysis. The ideal candidate will have a strong background in electron microscopy and asbestos analysis, along with proven leadership and organizational skills. Key Responsibilities TEM Lab Operations Supervise daily TEM lab activities, ensuring safe and efficient workflows Oversee operation, calibration, and routine maintenance of TEM instruments (e.g., JEOL, FEI, Hitachi) Monitor instrument performance and coordinate service with vendors as needed Staff Supervision & Training Train and mentor lab staff in sample preparation, instrument use, and data handling Ensure adherence to lab protocols and regulatory standards Manage user scheduling and maintain usage logs Lab Management & Compliance Maintain inventory of lab supplies and consumables Ensure compliance with safety procedures and waste disposal regulations Keep documentation up to date, including SOPs, maintenance records, and training logs Reporting & Communication Support preparation of client reports and internal documentation Communicate effectively with the Program Manager and other departments Stay informed on TEM and asbestos analysis best practices Required Qualifications: Bachelor's or Master's degree in Materials Science, Geology, Chemistry, Biology, or related field. 3+ years of hands-on experience with transmission electron microscopy. 3+ years of hand-on experience with asbestos analysis Prior experience in a supervisory, training, or core facility support role. Proficiency in sample preparation, instrument operation, and digital image analysis. Strong communication and organizational skills. Powered by JazzHR Y8XhQgtGa9

**At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.** **Senior Corporate Counsel** **YOUR TASKS AND RESPONSIBILITIES** The primary responsibilities of this role, Senior Corporate Counsel are to: Provides overall direction and leadership in provision of legal services in order to meet the business needs of the Business Group's operations and business, consistent with Corporate legal policy. Provides legal counsel directly to senior management with respect to highly complex issues concerning the obligations of the company as it relates to contracting, drug and medical device advertising, promotion and healthcare compliance. + Provides legal advice to the Bayer Pharmaceuticals Oncology, Women's Health, or Cardio franchises and platform functions within Bayer's pharmaceutical business; + Drafts, reviews and negotiates all contracts (such as consultation, licensing, clinical studies, supply, advertising and non-disclosure agreements) relating to the relevant business units; + Ensures compliance with all US laws and regulations governing the Pharmaceutical industry and such global laws that impact US business. Advise on anti-kickback and fraud and abuse issues, data privacy issues, and provide legal advice on FDA, FTC and other regulatory agency matters; + Provides counsel and advice regarding existing and future collaborations and interactions with healthcare providers; + Reviews promotional materials involving the marketing of pharmaceutical products; + Partner with Legal and Compliance colleagues in the development of policies, procedures, legal guidance documents and related training materials; + Represents the legal department on various committees, teams, etc.; + Active member of Promotional Review Team that supports business strategy; + Provides Proactive legal advice to senior management on key legal and business issues; + Lead regular training of clients on relevant legal issues; + Handles such other legal matters as may be assigned by the incumbent's direct supervisor and/or the head of the legal department. **WHO YOU ARE** Bayer seeks an incumbent who possesses the following: **Required Qualifications:** + Juris Doctor (J.D.) from an accredited school; + Admission to a state bar (with the ability to become licensed as an in-house counsel in NJ if not otherwise licensed in NJ); + The incumbent must develop and apply a comprehensive understanding of the policies and ethics of the company to assure that the management and personnel are adequately counseled and trained. **Preferred Qualifications:** + A minimum 8 years of experience practicing law with at least five years' experience as an attorney with a pharmaceutical company or directly involved in the representation of the pharmaceutical industry at a law firm. Employees can expect to be paid a salary between $132,240 to $198,360. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 1/22/2026. **YOUR APPLICATION** Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. **Location:** United States : Missouri : Creve Coeur || United States : Missouri : St. Louis || United States : New Jersey : Whippany || United States : Pennsylvania : Indianola **Division:** Enabling Functions **Reference Code:** 859949 **Contact Us** **Email:** hrop_*************

**At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.** **Director of Software Architecture, Cevego** This position is global and leads the technical aspects of the Cevego software development team as part of the software element team led by the Cevego software Lead. The Cevego injector offers users the ability to program and execute injections of contrast media and flushing solutions for Interventional Radiology (IR) and Interventional Cardiology (IC) procedures. The role requires directing the technical implementation and architectural design work of teams of developers familiar with medical device user interfaces, as well as embedded hardware control and enterprise platform integration. The position reports into the Head of Radiology R&D Software Architecture. As the Director of Software Architecture - Cevego, you have technical leadership responsibility within the Cevego product team and work closely with the Cevego Software Lead who directs the week-to-week activities of the team. You are responsible for ensuring that the Cevego architecture remains maintainable and in line with the overall architectural vision of the Radiology Software Architecture Board. The role is expected to be on-site at Bayer's R&D center in Pittsburgh. Specifically, you are responsible for steering the technical direction of the Cevego software team, optimizing the use of development tools and the integration of advanced UI, micro-services, connectivity, embedded and workflow solutions into the device and connectivity software domains. **YOUR TASKS AND RESPONSIBILITIES** The primary responsibilities of this role, Director of Software Architecture, Cevego, are to: + Support the overall development and delivery of the Cevego Software product including Device Software Solutions, Class I and II Software as a Medical Device Applications; + Provide technical advice to the Cevego Software Team Lead for the integration and implementation of combinations of hardware and software, software only components and Class II application development; + Define architecture and lead integration of common architecture across within the Cevego project team incorporating solutions such as the Common Software Platform, Interfaces with RDL and Silverlight, and User Experience common architecture and Look-and-Feel; + Optimize the use of development tools and processes across the Cevego device software and Class II application development teams; + Ensure agile development principles are applied as appropriate and continuously develop the team toward these principles; + Ensure that DevOps and Continuous Integration and Continuous Delivery practices are integrated into the architectural vision; + Contribute to a strategic software technology roadmap in alignment with the device development pipeline and the Radiology Software Technology Roadmap; + Anticipate future capability needs, create vision, and drive departmental strategies to anticipate clinical/market trends, enabling future growth consistent with corporate strategies; + Discover and develop strategic external partnerships to secure functional expertise and fill gaps; + Contribute to the setting of strategy with executive management, providing input, challenging, and ultimately directing and managing implementation; + Build high-performing teams within an agile and empowered culture, based on continuous adaptation to new ways of working within the framework of the necessary compliance and quality + The primary location for this role is Indianola, PA. **WHO YOU AR** **E** Bayer seeks an incumbent who possesses the following: **Required Qualifications:** + A tertiary qualification (Bachelor's Degree or Higher) in Software Engineering, Computer Science, or a related field; + Significant and long-term experience of relevant medical device and embedded software development in a regulated environment; + Excellent leadership and motivational skills; + Deep understanding of software development processes, software architecture, data structure and compliance as it relates to medical device software and software as a medical device; + Demonstrated experience in implementing consistent quality software development processes; + Demonstrated experience in building distributed software and platform-based solutions. **Preferred Qualifications:** + Master's degree in Computer Sciences or equivalent technology discipline; + Preferred skills include: Qt, C++, MongoDB, gRPC, YoctoOS, C, SafeRTOS; + Extensive knowledge of radiology workflows and the technology components and standards applicable to radiology, such as PACS, RIS, DICOM, FHIR. This posting will be available for application until at least 1/26/2026. Employees can expect to be paid a salary between $147,040.00 - $220,560.00. Additional compensation may include a bonus or commission (if relevant). Other benefits include health care, vision, dental, retirement, PTO, sick leave, etc. If selected for this role, the offer may vary based on market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. \#LI-US **YOUR APPLICATION** Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. **Location:** United States : Pennsylvania : Indianola **Division:** Pharmaceuticals **Reference Code:** 859387 **Contact Us** **Email:** hrop_*************

**At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where ,Health for all, Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.** **Primary Care & Specialty Sales Consultant - Norristown, PA** **Primary Care & Specialty Sales Consultant - Norristown, PA** **PURPOSE** The Primary Care & Specialty Sales Consultant (SC) is accountable for implementing the sales strategies for an approved Cardiorenal product. Responsibilities of the role include driving demand, clinical education and sales by developing, coordinating, and implementing a strategic business plan for Primary Care Physicians and Nephrologists, primarily in the Community settings. The position reports to the CVR Area General Manager (AGM) and will be an integral part of the Area Customer Squad, collaborating closely with Marketing, Market Access, Patient Services, and other internal partners, as appropriate, to drive the US Pharma outcomes. The span of coverage will be within the following metropolitan areas: Norristown, Northeast Philadelphia, Blue Bell, Pottstown, Quakertown areas. Travel up to 50% within the territory. The position is residence based, the candidate must be domiciled within the territory. **YOUR TASKS AND RESPONSIBILITIES** The primary responsibilities of this role are to: + Build and develop professional relationships with (but not limited to) primary care, nephrology, endocrinology, pharmacy staff, within assigned customers; + Drive appropriate utilization of approved cardiovascular and menopause products; incumbent works closely with the Customer Squad to generate pull-through within local payers, community HCPs; + Leverage expertise and knowledge of diabetes and menopause marketplace, applicable competitors, industry and cross-functional activities/plans to anticipate and effectively manage business opportunities and challenges; + Provide relevant, thoughtful input to other commercial colleagues (e.g. sales leadership, regional account managers) regarding strategic and tactical planning for territory, area, and region; + Develop and implements effective customer specific business plans; communicate insights to internal stakeholders; + Prioritize time and effort to ensure optimal coverage of appropriate physician specialists based on opportunity and potential; + Understand fully the assigned customers' product and business needs and works to meet those needs while adhering to all of Bayer company ethics and compliance standards; + Anticipate potential barriers to achievement of goals and proposes responsible solutions for success; + Handle customer objections effectively and exceed customer expectations with the value they bring to physicians. Occasionally will be called on to share your exemplary skills with others in the region in a training capacity; + Leverage and embrace emerging technologies to enhance performance, while continuously striving to improve your proficiency; + Understand and comply with pharmaceutical industry guidelines and regulations and apply high ethical standard in day-to-day work. **WHO YOU ARE** Bayer seeks an incumbent who possesses the following: **REQUIRED QUALIFICATIONS** + Bachelor's degree or 10 years of relevant sales experience in competitive landscapes in lieu of a Bachelor's degree; + Proven track record of consistent high performance in a sales or other relevant experience; + Proven track record in developing long-standing relationships with customers; + Outstanding written and oral communication skills; + Demonstrated leadership and foster an environment that promotes ethical behavior and compliance with company policies and applicable laws; + Ability to comply with any customer credentialing and safety requirements (e.g., up-to-date vaccinations, trainings); + Valid driver's license and clean driving record required. **PREFERRED QUALIFICATIONS** + An advanced degree is a plus; + 5+ years of experience in pharmaceutical sales, in primary care and specialty; + In depth knowledge in the cardiovascular and/or diabetes and/or menopause disease states; + Product launch experience; + Strong analytical and computer capabilities; + Virtual Sales Experience; + Strong local relationships with HCPs and understanding of local market. Employees can expect to be paid a salary between $120,974.00 to $181,462.00. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 1/23/26. \#LI \#LI-AMS **Location:** United States : Pennsylvania : Norristown || United States : Pennsylvania : Philadelphia **Division:** Pharmaceuticals **Reference Code:** 859053

For over 40 years, RJ Lee Group has been a trusted leader in scientific consulting, laboratory testing, and materials characterization. We deliver rigorous data, clear insights, and actionable solutions to clients ranging from industry innovators to government agencies. Our mission: combine scientific expertise with innovation to solve real-world challenges. Position Summary We're expanding our current BioPharm business line-and we're looking for a visionary BioPharm Study Director to lead the way. This is a unique opportunity to shape a new service offering, drive technical excellence, and build strong client relationships in the biotechnology, pharmaceutical, and biomedical sectors. Your expertise and entrepreneurial mindset will help us expand capabilities, exceed client expectations, and create measurable impact. If you thrive in a dynamic environment and want to make your mark, we want to hear from you. Lead and grow BioPharm analytical services through hands-on technical work and strategic planning. Represent RJ Lee Group to existing and prospective clients; serve as a trusted technical advisor. Drive business development by attending trade shows, networking, and identifying new opportunities. Design and direct studies that meet client needs and regulatory standards. Ensure compliance with cGMP standards, 21 CFR guidelines, and other regulatory requirements. Collaborate with QA teams to maintain quality assurance and accreditation standards. Mentor and train junior staff on cGMP workflows and best practices. Manage projects end-to-end-from planning through client delivery-with precision and accountability. What You Bring Master's or Ph.D. in Biomaterials, Organic Chemistry, Analytical Chemistry, Biochemistry, or related field. Minimum 2 years of experience in biopharmaceutical roles (lab, QA, or project management). Strong knowledge of analytical techniques: FTIR, DSC, GCMS, LCMS, SEM. Hands-on experience in cGMP-regulated environments. Understanding of GMP quality assurance requirements and regulatory frameworks (21 CFR, FDA, ISO 17025). Proven ability to manage projects and collaborate across teams. Excellent communication skills for technical and non-technical audiences. Preferred: Startup mindset-flexible, resourceful, and eager to build something new. Previous client-facing technical roles or business development experience. Familiarity with FDA regulations and accreditation processes. Willingness to travel and adapt to project demands. Why Join RJ Lee Group? Impactful Work: Support industries where precision and compliance matter. Career Growth: Mentorship, leadership opportunities, and continuous learning. Collaboration & Innovation: Join a passionate team solving complex challenges. Comprehensive Benefits: Competitive salary, PTO, medical/dental/vision, 401(k), life and disability insurance, flexible spending options. Inclusive Culture: We value diversity and believe every perspective strengthens our team. Equal Opportunity Employer RJ Lee Group celebrates diverse backgrounds and is committed to building an inclusive workplace for all.

The LCMS Analyst will support the analytical functions of the LCMS Group, ensuring high-quality data generation and method execution. This role combines hands-on laboratory work with technical leadership, supporting complex analyses using advanced instrumentation such as Tandem Mass Spectrometry, High-Resolution Mass Spectrometry, and HPLC systems. The position requires strong problem-solving skills, attention to detail, and the ability to collaborate across multiple teams to deliver accurate and timely results for diverse projects. Key Responsibilities: Support the analytical functions of the LCMS Group, ensuring accurate and timely results. Perform sample preparation and apply established LCMS methods for diverse projects. Conduct data quality review and prepare detailed reports. Maintain LCMS instruments to ensure optimal performance. Manage laboratory supplies and oversee day-to-day operations. Collaborate with internal experts and cross-functional teams, including Analytical Services and Technical Consulting Groups. Support method development and contribute to new project initiatives. Uphold compliance with national and state accreditation standards and safety protocols. Qualifications: Bachelor's degree in Chemistry or a related field with a minimum of 2 years of laboratory experience, including sample preparation and analysis. Knowledge of analytical methods such as EPA and ASTM protocols. Experience analyzing environmental samples. Experience working under national and state accreditation standards. Ability to work independently and collaboratively in a team environment. Strong attention to detail and commitment to quality standards. Eagerness to learn and take on diverse tasks. Preferred Experience: 3-5 years in a commercial laboratory setting with exposure to diverse characterization techniques, including LCMS analysis. Familiarity with EPA and ASTM analytical methods for environmental sample analysis. Background in PFAS extraction and analysis (EPA Methods 537.1, 533, 1633) and pesticide/PCB sample analysis is highly desirable. Skills and Competencies: Technical Expertise: Proficiency in LCMS techniques, including Tandem MS, HRMS, and HPLC systems with UV and fluorescence detection. Analytical Skills: Ability to interpret complex data sets, ensure data integrity, and troubleshoot analytical issues. Attention to Detail: Commitment to accuracy and quality in all aspects of laboratory work. Problem-Solving: Strong ability to identify issues and implement effective solutions quickly. Collaboration: Skilled at working with cross-functional teams and supporting internal experts. Time Management: Ability to prioritize tasks and manage multiple projects in a fast-paced environment. Communication: Clear and concise written and verbal communication for reporting and team interaction. Adaptability: Willingness to learn new techniques and take on diverse responsibilities.

**At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.** **Associate Director, Human Factors Engineering** **Associate Director, Human Factors/Usability Engineering** We are seeking a highly experienced Senior Human Factors / Usability Engineer to guide cross-functional device development teams in navigating the field of user-centric development. This pivotal role will be at the interface between patients/users, product leadership, commercial, medical/clinical, and engineering teams, ensuring that medical devices and drug-device combination products are designed with the user in mind to enhance safety, effectiveness, and the user experience. The Senior Human Factors/Usability Engineer will integrate Human Factors/Usability Engineering (HF/UE) principles into the design and development of products within Bayer's global Radiology and Pharma portfolios. This role will leverage user insights to optimize usability, ensure compliance with relevant standards and regulations, and maximize contributions to Bayer's business strategy. Success in this role requires a deep understanding of user-centric development principles, industry best practices, and regulatory expectations (including those of US FDA, EMA/NBs, UK MHRA, and China NMPA). Effective communication with stakeholders and a commitment to sharing knowledge for mutual growth are essential. You will join a global team of passionate Human Factors/Usability Engineers in a non-managerial role, located in Bayer Radiology R&D, Indianola (Pittsburgh, PA). **YOUR TASKS AND RESPONSIBILITIES:** + Develop and execute the HF/UE strategy for Bayer's Radiology and Pharma products, ensuring compliance with internal procedures and industry standards; + Align HF/UE strategy with regulatory strategies and marketing objectives; manage stakeholder interactions and represent HF/UE in consultations with regulatory bodies; + Plan and oversee usability evaluations across the development lifecycle (exploratory, formative, summative, and post-market), both conducted internally or with external HF/UE service providers; + Contribute to device development activities, including requirements engineering, risk management, user interface design, and verification & validation (V&V) planning and execution; + Document HF/UE results for design history files and submission dossiers, ensuring accuracy and thoroughness; + Stay ahead of industry trends and support continuous learning and improvement within the HF/UE team; + Advocate for a user-centric mindset across relevant areas of the Bayer organization. **WHO YOU ARE:** Bayer seeks an incumbent who possesses the following: **Required Qualifications:** + Minimum of a Master's degree in engineering sciences, ergonomics, psychology, or a related field; + Minimum of 7 years of experience in HF/UE for medical devices and/or drug-device combination products, in accordance with IEC 62366-1 and FDA HF/UE guidance; + Proven experience in HF/UE submissions as well as in successful interactions with regulatory bodies, especially with the US FDA; + Strong background in user-centric design, design controls (CFR 820.30, ISO 13485), risk management (ISO 14971), EU MDR, and requirements engineering; + Patient/user advocacy with a solution-oriented mindset; + Excellent lateral leadership and communication skills in English; + Ability to thrive in a dynamic global matrix environment, embracing change and decision-making. This posting will be available for application until at least 1/22/2026. Employees can expect to be paid a salary between $128,000 and $192,000. Additional compensation may include a bonus or commission (if relevant). Other benefits include health care, vision, dental, retirement, PTO, sick leave, etc. If selected for this role, the offer may vary based on market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. \#LI-US **YOUR APPLICATION** Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. **Location:** United States : Pennsylvania : Indianola **Division:** Pharmaceuticals **Reference Code:** 860123 **Contact Us** **Email:** hrop_*************

The Cement Chemist will play a key role in advancing RJ Lee Group's Concrete Materials Department by applying expertise in cement chemistry and materials science. This position involves method development, client support, and the expansion of our capabilities in natural pozzolans and supplementary cementitious materials (SCMs), along with collaboration across multidisciplinary teams to deliver innovative solutions for construction and infrastructure projects. Essential Duties and Responsibilities Perform hands-on technical work to support and expand the Concrete Materials Department. Develop and validate analytical methods for cement, SCMs, and concrete materials. Provide expert guidance on the use and evaluation of natural pozzolans and supplementary cementitious materials. Independently manage research projects from planning through client delivery. Collaborate with engineers and manufacturers to develop innovative solutions. Communicate technical findings clearly to diverse audiences. Assist with business development and client engagement activities. Promote scientific integrity, compliance, and continuous improvement. Qualifications Education and Experience: PhD (preferred) or MS in Cement Chemistry, Materials Science, Civil Engineering, or related field. Minimum 3 years of experience in cement, concrete, or construction materials laboratory settings. Technical Skills: Strong knowledge of cement chemistry, hydration mechanisms, SCMs, and pozzolans. Proficiency in analytical techniques: XRD, XRF, TGA, SEM/EDS, FTIR. Familiarity with ASTM, AASHTO standards; ISO 17025 experience preferred. Other Requirements: Proven ability to manage projects and work collaboratively. Excellent communication skills for technical and non-technical audiences. Willingness to travel and flexibility for project demands. Preferred Qualifications Experience with multi-year client programs or method validation studies. Previous client-facing technical roles or business development support. Why RJ Lee Group Impactful Work: Contribute to industries where materials science drives innovation. Career Growth: Access mentorship, leadership opportunities, and continuous learning. Collaborative Culture: Work in a supportive environment committed to excellence.

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Chief Architect As the Chief Architect within Bayer's Radiology Software Development organization, you will spearhead the design and implementation of innovative software architectures that drive our Software in a Medical Device (SiMD) products as well as our Software as a Medical Device (SaMD) features and associated Data and Connectivity platforms. You will also be responsible for setting the strategic software technology roadmap for Radiology and ensuring that all software development aligns with the architectural and technology roadmaps in addition to relevant regulatory standards. Your leadership will be pivotal in fostering a culture of excellence, collaboration, and continuous improvement within the software development teams. The role will lead a group of architects and cyber-security specialists and you will be a key member of the Software Development organization's Senior Leadership Team. YOUR TASKS AND RESPONSIBILITIES: * Develop a common Radiology software technology strategy, aligning technology initiatives with business strategy and organizational goals; * Empower the central architecture team and review boards to drive architecture harmonization and establish processes for managing scope changes; * Integrate AI tools into the technology strategy with a focus on compliance and ethical considerations; * Build, lead, and mentor a high-performing team of software architects, cyber-security engineers, and software specialists; * Ensure all software development activities comply with industry regulations and standards such as ISO 13485 and IEC 62304; * Represent the software architecture team in the Software Development Leadership Team, engaging with key stakeholders to gather insights and feedback. * This role can be based in either Whippany, NJ, or Indianola, PA, however, residence-based candidates based in the US may also be considered based upon the needs of the business. Relocation assistance will be available. * Visa sponsorship may be available for this role. WHO YOU ARE: Bayer seeks an incumbent who possesses the following: Required Qualifications: * Minimum of a Bachelor's Degree in Computer Science or a related technology discipline (or equivalent combination of education and experience); * Proven track record of building and scaling international, multi-site software development teams; * In-depth understanding of data governance, compliance, and regulations related to digital product development; * Extensive experience in implementing Agile methodologies and building cloud-based, regulated software solutions; * Strong knowledge of radiology workflows and technology standards, including PACS, RIS, DICOM, and FHIR. * A results-driven mindset with a commitment to innovation and experimentation to deliver customer value; * Ability to drive efficiency through accountability, lean practices, and empowering team members. Preferred Qualifications: * Masters or PhD in a relevant technical area; * At least 15 years of experience in SiMD and SaMD software product development and maintenance; * Visionary capabilities to set a framework and engage others to adopt/embrace defined approach; * Exceptional leadership and motivational skills, with the ability to cultivate and sustain internal and external networks; * Strength in being able to work in a matrix organization and effectively influence others. This posting will be available for application until at least 1/23/2026. Employees can expect to be paid a salary between $190,796.80 to $286,195.20. Additional compensation may include a bonus or commission (if relevant). Other benefits include health care, vision, dental, retirement, PTO, sick leave, etc. If selected for this role, the offer may vary based on market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location:United States : New Jersey : Whippany || United States : Pennsylvania : Indianola Division:Pharmaceuticals Reference Code:855428 Contact Us Email:hrop_*************

**At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.** **What You Will Do** The Field Research Scientist supports and manages the day-to-day operations of the research program in an assigned territory, by working with regional Site Leads and key stakeholders to plan, establish, maintain, collect accurate agronomic data from, and harvest corn soybean, wheat, and cotton trials. **Key Tasks and Responsibilities:** Responsibilities include, but are not limited to the following: + Must be located in or around one of the following areas: Southern New York, Pennsylvania, Maryland, or Virginia. + Ensure safe and efficient operation of the research program with respect to budgetary guidelines and expectations and support the site ESH program as it applies to North American Field Testing and Operations. + Selection, preparation, and maintenance of multiple field testing sites. This requires safe driving including frequent trailer use hauling loads in excess of 10,000 lbs; pre-trip inspections and use of log books. + Plays a vital role in trial preparation including seed processing, packaging, shipping, protocol review, trial placement, and mapping/field design. + Maintain field trial sites as week, insect, and disease free; + Having a confident ability in identifying key weeds, insect, and disease problems is critical, as is timely and accurate implementation of control measures; + With the use of handheld electronic equipment and Monsanto proprietary software, collect notes on various agronomic traits (e.g. emergence uniformity, flowering date, lodging, height, maturity, shattering resistance) in a timely manner throughout the growing season; + Harvest plots and collect samples for quality and statistical analysis; ensure harvest data is evaluated and relinquished in accordance with crop advancement deadlines to aid in product advancement decisions; + Develop, maintain, and implement the use of controlled SOP documents, QMS procedures, and investigative protocols; + Comply with all Monsanto regulatory compliance guidelines for Confined Release and Stewarded Trial material; + Collaborate with other Agronomic Research Specialists, Site Leads, and Principal Investigators in order to facilitate efficient trial planning and placement; + Sharing of ideas and techniques and quick response to issues that may arise (e.g. weather or pests affecting trials); + Works closely with Plant Breeders, Principal Investigators, and Agronomic Research Specialist to filly understand the multiple stages of crop development and the importance of each step involved and share experiences cross-functionally as needed; + Field selection, cooperator relations, and ability to learn research equipment operations and basic maintenance (all types), field maintenance, and data collection; + Basic Agronomic knowledge/Crop Management knowledge; + Technical savvy and ability to adhere to compliance and safety policies; + Utilization of IT tools, time management, prioritization skills; + Must be self motivated with good decision-making abilities; + Accountable for business unit or project results through leadership and coordination across site strategy; + Ability to prioritize and monitor projects to ensure completion within deadlines and budgets; + Build partnerships and share technical knowledge across sites; + Stay involved in industry working groups. **Required Qualifications:** + PhD with minimum years relevant experience, OR MS with minimum of 2 years relevant experience, OR BS with minimum of 5 years relevant experience; + Located in or around southern New York, Pennsylvania, Maryland, or Virginia; + Valid Driver's License; + Ability to lift up to 60lbs; + Ability to obtain pesticide applicator license; + Ability to work extended hours during peak operational seasons; + CDL license or ability to obtain one. **Preferred Qualifications:** + Ability to obtain UAV license for operating drones. This posting will expire on January 28th, 2026. _Employees can expect to be paid a salary of $76480.00 - 114720.00_ _per year. Additional compensation may include a bonus or commission (if relevant). Other benefits include health care, vision, dental, retirement, PTO, sick leave, etc. If selected for this role, the offer may vary based on market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors._ Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Job postings will remain open for a minimum of ten business days and are subject to immediate closure thereafter without additional notice. **Division:** Crop Science **Reference Code** 860475 **Functional Area:** Biological R&D **Location:** United States : New York : Albany || United States : Maryland : BALTIMORE || United States : Maryland : Baltimore || United States : Maryland : College Park || United States : Maryland : Columbia || United States : Maryland : Frederick || United States : Maryland : Gaithersburg || United States : Maryland : Galena || United States : Maryland : Glen Burnie || United States : Maryland : HYATTSVILLE || United States : Maryland : Laurel || United States : Maryland : Residence Based || United States : Maryland : SALISBURY || United States : Maryland : Silver Spring || United States : Maryland : Towson || United States : Maryland : Waldorf || United States : New York : BUFFALO S || United States : New York : Bronx || United States : New York : Brooklyn || United States : New York : Buffalo || United States : New York : Canandiagua || United States : New York : Commack || United States : New York : Garden City || United States : New York : HEMPSTEAD || United States : New York : JAMAICA || United States : New York : LIVERPOOL || United States : New York : Long Island || United States : New York : Manhattan || United States : New York : Newburgh || United States : New York : Poughkeepsie || United States : New York : Queens || United States : New York : Residence Based || United States : New York : Rochester || United States : New York : SARATOGA SPRINGS || United States : New York : SCHENECTADY || United States : New York : SPRING VALLEY || United States : New York : SYRACUSE S || United States : New York : Schenectady || United States : New York : Staten Island || United States : New York : Syracuse || United States : New York : Tarrytown || United States : New York : UTICA || United States : New York : WEBSTER || United States : New York : White Plains || United States : Pennsylvania : Allentown || United States : Pennsylvania : Bensalem || United States : Pennsylvania : Bethlehem || United States : Pennsylvania : Butler || United States : Pennsylvania : CARLISLE || United States : Pennsylvania : Drexel Hill || United States : Pennsylvania : ERIE || United States : Pennsylvania : Greensburg || United States : Pennsylvania : Harrisburg || United States : Pennsylvania : Indianola || United States : Pennsylvania : Johnstown || United States : Pennsylvania : LANCASTER || United States : Pennsylvania : Lancaster || United States : Pennsylvania : Lawrence || United States : Pennsylvania : Levittown PA || United States : Pennsylvania : Manchester || United States : Pennsylvania : Manheim || United States : Pennsylvania : Myerstown || United States : Pennsylvania : Norristown || United States : Pennsylvania : PHILADELPHIA E || United States : Pennsylvania : PITTSBURGH NE || United States : Pennsylvania : Philadelphia || United States : Pennsylvania : Pittsburgh || United States : Pennsylvania : Pittsburgh Heilman || United States : Pennsylvania : Pottstown || United States : Pennsylvania : Reading || United States : Pennsylvania : Residence Based || United States : Pennsylvania : Saxonburg || United States : Pennsylvania : Scranton || United States : Pennsylvania : State College , Williamsport || United States : Pennsylvania : WILKES BARRE || United States : Pennsylvania : Warrendale || United States : Pennsylvania : West Chester || United States : Pennsylvania : Wilkes Barre || United States : Pennsylvania : York || United States : Pennsylvania : Youngstown || United States : Residence Based : Residence Based || United States : Virginia : Arlington || United States : Virginia : CHARLOTTESVILLE || United States : Virginia : Chantilly || United States : Virginia : Charlottesville || United States : Virginia : Chesterfield || United States : Virginia : Fairfax || United States : Virginia : Fredericksburg || United States : Virginia : Hampton || United States : Virginia : Lynchburg || United States : Virginia : Norfolk || United States : Virginia : Residence Based || United States : Virginia : Richmond || United States : Virginia : Roanoke || United States : Virginia : Virginia Beach || United States : Virginia : WOODBRIDGE **Employment Type:** Regular **Position Grade:** M07 **Contact Us** AddressTelephone **Creve Coeur, MO** *****************, option #5** **63167** OR **Submit a ticket via** **the self-service option by visiting** go/askhr

RJ Lee Group, Inc. is currently seeking a Lab Technician for Our TEM Department to perform sample preparation tasks in support of our electron microscopy laboratory. Job Responsibilities: The Lab Technician - TEM conducts and observes standardized tests following test parameters and as required, obtains and records data or ensures capture of correct data. Operates requisite laboratory equipment and instruments. Troubleshoots problems encountered with test equipment and maintains and makes minor adjustments to equipment. Prepares samples for analysis by grinding, crushing, weighing, filtering, or digesting with acids. Engages in safe work practices and advises supervisor on improvements to test equipment fabrication, installation, and operation to ensure a safe laboratory operation. Qualifications and Requirements: Must possess manual dexterity adequate for handling small, delicate items. Experience with sample preparation is preferred but not required; Prior experience working in a laboratory environment is strongly desired. A high school or equivalent education or a combination of one to five years continuing education or trade school. An associate degree in a related Science is preferred. Ability to multitask in a fast-paced environment Familiarity with Microsoft Office products Strong motivation to learn and grow Excellent written and verbal communication skills Ability to work independently or with a team and to prioritize tasks effectively to meet deadlines Familiarity with microscopy and microanalytical techniques is desired Willingness to work a flexible, off-shift schedule RJ Lee Group offers full-time employees a total benefits package that includes: Competitive salaries Paid time off benefits, 9 company paid holidays Medical, dental, vision and medical/dependent care flexible and health savings account benefits Company paid group life insurance and disability insurance 401(k) Retirement Savings Plan About RJ Lee Group, Inc.: For more than 35 years, RJ Lee Group's scientific and investigative resources have provided the competitive edge by defining solutions. As the field of Industrial Forensics advanced and embraced more sophisticated and complex issues such as nanoparticles and electronic materials, RJ Lee Group determined that the need for in-depth resolution was essential and that a single solution was no longer acceptable. Today RJ Lee Group's expert scientists address these issues and can investigate the entire product life cycle including regulatory compliance in the workplace. The resolution RJ Lee Group brings to industry using precise scientifically sound techniques often provides the competitive edge needed to advance in the market and increase the bottom line. RJ Lee Group, Inc. is an Equal Opportunity Employer - EEO/AA/Veterans/Disabled/LGBTQ All qualified applicants will receive consideration for employment without regard to race, age, color, religion, sex (including pregnancy), national origin, disability, sexual orientation, gender identity, marital status, military status, protected veteran status, genetic information, or any other characteristic or status protected under applicable law or regulations. RJLG seeks diversity among its employees. Reasonable accommodation may be made to enable individuals to perform the essential job functions.

**At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice.** **Institutional & Specialty Sales Consultant, Cardiology - Main Line, PA** **Institutional & Specialty Sales Consultant, Cardiology - Main Line, PA** **PURPOSE** The Institutional and Specialty Sales (ISS) team is being established to lead and drive launch activities for indications within the CVR portfolio. Responsibilities include driving demand, clinical education and sales by developing, coordinating, and implementing a strategic business plan for top priority Institutions (i.e., Hospitals and Health Systems), Cardiologists and Nephrologists both in the Institutional and Community settings. The ISS reports to the CVR Area General Manager (AGM) and will be an integral part of the Area Customer Squad, collaborating closely with Marketing, Market Access, Patient Services, and other internal partners, as appropriate, to drive the US Pharma outcomes. The span of coverage will be within the Main Line area - Bryn Mawr, Paoli, Langhorne, Doylestown, & Abinton, PA. Travel up to 50% within the territory. The position is residence based. The candidate must be domiciled within the territory. **KEY TASKS AND RESPONSIBILITIES** The primary responsibilities of the Institutional and Specialty - Hospital Sales Consultant are to: + Drive clinical demand, education and sales, building deep understanding of disease state, unmet needs and treatment options to effectively educate healthcare professionals and business stakeholders on the unique benefits of assigned products while balancing both efficacy and safety through detailing of approved clinical information for community-based healthcare professionals and health systems; + Build institutional advocacy to drive formulary/pathway/protocol adoption of cardiovascular-renal brand(s) to drive appropriate pull-through of approved products; + Develop, co-create with external and internal stakeholders and implement strategic business plans for identified top strategic Institutions with an in-depth understanding of local market dynamics that influence product sales; + Demonstrate expertise and knowledge of disease state, the marketplace, competitors, industry, and cross-functional activities/plans as well as possess analytical rigor to anticipate and identify business opportunities and challenges; + Build key business relationships within prioritized customers in the community and including key stakeholders at the Institutions (i.e., C and D Suite and Head of Pharmacy, Head of Quality), Cardiologists and Nephrologists; + Manage the P&T committee processes at the priority Institutions; + Collaborate with the cross functional and Area Customer Squads to develop and pull through the strategic partnerships with key customers; + Provide support to Area General Managers in strategic projects, as needed; + Leverage and embrace emerging technologies to enhance performance, while continuously striving to improve your proficiency; + Understand and comply with pharmaceutical industry guidelines and regulations and apply high ethical standard in day-to-day work. **WHO YOU ARE** Bayer seeks an incumbent who possesses the following: **REQUIRED QUALIFICATIONS** + Bachelor's degree or 10 years of relevant sales experience in competitive landscapes in lieu of a Bachelor's degree; + Deep expertise and understanding of the cardiovascular and/or renal therapeutic area(s); + Experience launching new products and product indications; + Excellent facilitation and verbal/written communication skills; + Ability to work under pressure and meet short deadlines; + Ability to comply with any customer credentialing and safety requirements (e.g., up-to-date vaccinations, trainings); + Valid driver's license and clean driving record required. **PREFERRED QUALIFICATIONS** + Advanced degree (preferably in the Life Sciences, Pharmacy or business-related field;) + 5 years of successful pharmaceutical/biotech/medical sales experience in competitive landscapes; + Experience selling in Institutions and clinic settings and navigating the P&T committee process; + Experience in establishing and pulling-through in-patient to out-patient protocols . Employees can expect to be paid a salary between $120,960.00 to $181,440.00. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least 1/23/26. \#LI-US \#LI-AMS **YOUR APPLICATION** Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. **Location:** United States : Pennsylvania : Residence Based **Division:** Pharmaceuticals **Reference Code:** 858966 **Contact Us** **Email:** hrop_*************

Job Description The Software Solutions Architect will lead the design and architecture of complex, mission-critical, enterprise applications. This role involves working with a moderately sized team in a fast-paced environment and creating foundational architecture for multiple projects. The ideal candidate will also bring expertise in Artificial Intelligence (AI) and Machine Learning (ML) integration, ensuring modern, intelligent solutions are embedded into enterprise applications. Responsibilities & Accountabilities Design and document major aspects of product architecture, including user interface, middleware, infrastructure, and AI components. Establish and maintain uniform enterprise-wide application design standards. Collaborate with stakeholders to align architecture with business requirements and AI-driven strategies. Act as point of contact for technical product demonstrations, including AI-enabled features. Provide technical feasibility and proof of concepts, incorporating AI/ML models where applicable. Develop and present application/product architecture and approved changes to project leadership. Provide technical direction and leadership to development teams, including AI integration guidance. Ensure technical implementation aligns with system designs through design and code reviews. Align all RJLG software products for enterprise offerings, including AI capabilities. Perform software development tasks and defect fixing as needed. Recommend and lead areas for process improvements, including automation and AI-driven optimizations. Follow ISS and RJLG company standards, values, processes, and procedures. Mentor team members on emerging technologies, including AI/ML frameworks and best practices. Other miscellaneous tasks as an ISS team contributor. Minimum Qualifications Required Education: Bachelor's degree in Computer Science or relevant field. Advanced degree or certifications in AI/ML preferred. Experience: 8+ years of experience in R&D and implementing enterprise-wide, distributed, data-centric applications. 5+ years of experience in developing web applications in an agile environment using React, C#, JavaScript/TypeScript, Webservices, Python, SQL, NoSQL/Graph databases. 3-5 years building applications utilizing cloud-based AWS and/or MS Azure technologies and services. 2+ years of experience with AI/ML technologies, including model development, deployment, and integration into enterprise applications. Knowledge, Skills, & Abilities: High-level technical expertise with strong planning, coordination, leadership, and communication skills. Strong understanding of object-oriented design and AI/ML concepts (e.g., supervised/unsupervised learning, NLP, predictive analytics). Familiarity with AI frameworks such as TensorFlow, PyTorch, or Azure AI services. Knowledge of CI/CD processes and tools (Bitbucket, SVN, Puppet, Chef, Octopus). Strong problem-solving skills and ability to think creatively, including applying AI to business challenges. Ability to communicate technical concepts, including AI strategies, to diverse audiences. Team-oriented, positive attitude, and ability to mentor others in emerging technologies. Powered by JazzHR u6jU3oKeXz

The Instrument Technician is a role designed to train individuals in the fundamentals of instrumentation troubleshooting and repair. This position serves as a developmental pathway toward more advanced instrumentation responsibilities. The technician will receive hands-on training in equipment diagnostics, calibration procedures, and safe laboratory practices.Key Responsibilities · Perform standardized calibration checks and ensure accurate data capture via system software. · Identify and utilize appropriate laboratory equipment and instrument components. · Troubleshoot and resolve basic issues with company instrumentation. · Conduct routine maintenance and make necessary equipment adjustments. · Fill Dewars with liquid nitrogen daily and replace dry nitrogen tanks and other gases as needed. · Consistently adhere to and promote safe work practices in all laboratory activities.Qualifications Preferred: Minimum of 5 years of hands-on experience in instrumentation. Proficiency in using a multimeter. Ability to read and interpret schematics. Demonstrated willingness to learn and develop proficiency in troubleshooting and repairing instrumentation across applicable departments. Powered by JazzHR bKwyFbDFC3

Job DescriptionRJ Lee Group is hiring a Strategic Project Applications Manager to support our Industrial Hygiene/Environmental division. This full-time role, based in Monroeville, PA, involves 50% travel and offers a unique opportunity to work directly with our VP of Emerging Contaminants. The ideal candidate will combine technical expertise in air quality instrumentation with strong project management and business development skills. Responsibilities include operating advanced mobile platforms, supporting strategic initiatives, and managing client-facing projects. Candidates with a background in Materials Science, Chemistry, or related disciplines and experience in PTR-MS and AIM instrumentation are encouraged to apply.Key ResponsibilitiesBusiness Development & Strategic Planning Assist in identifying and qualifying new business opportunities Conduct market research and competitive analysis Help prepare proposals, presentations, and client communications Contribute to special initiatives and strategic planning efforts Technical Operations & Data Management Assist with data collection, instrument operation, method development, reporting, and quality control Track leads, opportunities, and client interactions in CRM systems Project Management & Coordination Support project planning, scheduling, and documentation Monitor project milestones and deliverables Coordinate meetings, take notes, and follow up on action items Process Improvement & Internal Support Help streamline workflows and improve internal process Qualifications Bachelor's degree in Materials Science, Chemistry, Geology, Physics, or a closely related scientific discipline is required; advanced degrees (Master's or Ph.D.) are preferred 5-7 years of professional experience in environmental science, industrial hygiene, or related technical fields Demonstrated expertise in volatile organic compound (VOC) and combustion analysis Hands-on experience with air quality monitoring systems and instrumentation Strong understanding of relevant analytical methods and industry standards Exceptional communication, organizational, and analytical problem-solving skills Preferred Skills Strong mass-spectrometry PTR MS, and AIM instrumentation Strong client relationship and technical writing abilities Join RJ Lee Group as a Strategic Project Applications Manager and help shape the future of environmental innovation! We're looking for a proactive leader with a passion for emerging contaminants, mobile platform instrumentation, and strategic growth. If you thrive in a fast-paced, collaborative environment and want to make a real impact, apply today! Powered by JazzHR 3oHsNEpQY5