Scientist - LC-MS Bioanalytical

We need to output HTML fragment with sections: About the role? Actually the posting includes "Join Amgen’s Mission of Serving Patients" intro, then "Scientist - LC-MS Bioanalytical" title (should not repeat as heading). Then sections: "What You Will Do" (responsibilities), "What We Expect Of You" (qualifications/requirements), "What You Can Expect From Us" (benefits). Also there is mention of salary range: "The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted." No actual numbers given, so we cannot create Pay section because no specific numbers. So we should not include Pay section. Benefits: they list benefits in that paragraph; we can create Benefits section with list. Also maybe "Schedule" not present. So we will have sections: About the role? The intro paragraph could be considered "About the role" or maybe "About Amgen". The instruction: use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). We need to include a section only when posting has real specific content. The intro about mission could be "About the role" or maybe we can treat as "About the role". It's substantive. We'll include

About the role

with

containing the mission paragraph. Then Responsibilities: from "What You Will Do" bullet list (key responsibilities). We'll output

Responsibilities

• ... each bullet. Then Requirements/Qualifications: from "What We Expect Of You" includes Basic Qualifications, Preferred Qualifications. We'll combine into Requirements section maybe with subheadings? But we only allowed headings from list; we could use

  Requirements

  and then list items. Could separate Basic and Preferred as separate
  but still under same heading. That's fine. Then Benefits: from "What You Can Expect From Us" includes benefits list. We'll output

  Benefits

  with each benefit. We must not include Pay or Schedule because no specifics. We must remove boilerplate: EEO, sponsorship, etc. Also remove "Apply now..." etc. Also remove "Refer to the Work Location Type..." etc. Also remove "In any materials you submit..." etc. Also remove "Sponsorship Sponsorship for this role is not guaranteed." etc. Also remove repeated EEO statements. We need to preserve all substantive information: mission paragraph, responsibilities list, qualifications (basic and preferred), benefits list. Let's extract mission paragraph: "Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier live. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career." We need to correct grammar? Not needed; preserve as is. Now responsibilities list: The bullet points after "Key responsibilities include:" each line starts with a verb. We'll capture each. List: - Plan, execute, and document quantitative LC–MS/MS bioanalytical experiments. - Develop and implement fit-for-purpose bioanalytical methods with rapid turnaround. - Perform small- and large-molecule bioanalysis in nonclinical and clinical matrices, including plasma, urine, CSF, and tissues. - Prepare biological samples using protein precipitation, solid-phase extraction, liquid–liquid extraction, affinity capture, and related techniques. - Organize, analyze, interpret, and present bioanalytical data with strong attention to data integrity and fidelity. - Maintain complete, accurate, and concise documentation in electronic laboratory notebooks and other laboratory systems. - Ensure data and records meet applicable regulatory expectations for global submissions and remain current with relevant industry guidance. - Author and review study reports, analytical methods, SOPs, technical memos, and other regulatory-compliant documents. - Communicate bioanalytical results to discovery and development teams; contribute to publications and present findings at scientific meetings. - Support report quality control, effective time management, and clear cross-functional communication. - Follow all safety, training, documentation, and site-specific procedural requirements. - Perform routine laboratory housekeeping and operational support activities as needed. Now qualifications: Basic Qualifications: Doctorate degree Or Master’s degree and 2 years of relevant industrial/technical experience Or Bachelor’s degree and 4 years of relevant industrial/technical experience Preferred Qualifications: list: - Prefer Bachelor's or Master's experience (maybe ambiguous) Actually text: "Prefer Bachelor's or Master's experience" maybe means prefer Bachelor's or Master's degree? We'll keep as is. - Prior experience in CRO or pharma/biotech strongly desired - Strong technical expertise in quantitative mass spectrometry on triple quadrupole (QQQ) platforms as well as HRMS - Experience with an array of analytical technologies that can accelerate bioanalysis inclusive of automation and/or micro-sampling - Prior GLP and GCP experience. - Demonstrated expertise in working with a variety of sample types (e.g., blood, plasma, serum, tissues, cerebrospinal fluid). - Hands-on experience with automated or semi-automated sample preparation for LC-MS bioanalysis, including protein precipitation, SPE, affinity capture, and other high-throughput workflows, using platforms such as KingFisher APEX/FLEX, automated SPE systems, and robotic liquid handlers. - Prior experience in bioanalytical (regulated) assay execution and transfer to CROs - Must be willing to work in a fast-paced, multi-project environment with high workload demands, and consistently deliver high-quality results within established timelines. - Demonstrated ability to resolve scientific challenges efficiently and prioritize effectively - Excellent scientific problem-solving skills - Excellent project and time management abilities - Ability to work collaboratively with internal and external stakeholders - Supervisory and mentoring experience in a lab-based setting Now benefits: from "What You Can Expect From Us" paragraph: "From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accountsA discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plansFlexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies." We need to extract benefits list items: - Retirement and Savings Plan with generous company contributions - group medical, dental and vision coverage - life and disability insurance - flexible spending accounts - discretionary annual bonus program (or for field sales representatives, a sales-based incentive plan) - Stock-based long-term incentives - Award-winning time-off plans - Flexible work models where possible Also mention health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, career development opportunities. Could incorporate as separate items. We'll list them as bullet points. Now we need to output HTML fragment only, no markdown. We'll wrap sections in

  and

  or

  . Make sure not to include any extra text. Let's craft:

  About the role

  Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier live. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

  Responsibilities

  • Plan, execute, and document quantitative LC–MS/MS bioanalytical experiments.
  • Develop and implement fit-for-purpose bioanalytical methods with rapid turnaround.
  • Perform small- and large-molecule bioanalysis in nonclinical and clinical matrices, including plasma, urine, CSF, and tissues.
  • Prepare biological samples using protein precipitation, solid-phase extraction, liquid–liquid extraction, affinity capture, and related techniques.
  • Organize, analyze, interpret, and present bioanalytical data with strong attention to data integrity and fidelity.
  • Maintain complete, accurate, and concise documentation in electronic laboratory notebooks and other laboratory systems.
  • Ensure data and records meet applicable regulatory expectations for global submissions and remain current with relevant industry guidance.
  • Author and review study reports, analytical methods, SOPs, technical memos, and other regulatory-compliant documents.
  • Communicate bioanalytical results to discovery and development teams; contribute to publications and present findings at scientific meetings.
  • Support report quality control, effective time management, and clear cross-functional communication.
  • Follow all safety, training, documentation, and site-specific procedural requirements.
  • Perform routine laboratory housekeeping and operational support activities as needed.

  Requirements

  • Doctorate degree
  • Or Master’s degree and 2 years of relevant industrial/technical experience
  • Or Bachelor’s degree and 4 years of relevant industrial/technical experience
  • Prefer Bachelor's or Master's experience
  • Prior experience in CRO or pharma/biotech strongly desired
  • Strong technical expertise in quantitative mass spectrometry on triple quadrupole (QQQ) platforms as well as HRMS
  • Experience with an array of analytical technologies that can accelerate bioanalysis inclusive of automation and/or micro-sampling
  • Prior GLP and GCP experience.
  • Demonstrated expertise in working with a variety of sample types (e.g., blood, plasma, serum, tissues, cerebrospinal fluid).
  • Hands-on experience with automated or semi-automated sample preparation for LC-MS bioanalysis, including protein precipitation, SPE, affinity capture, and other high-throughput workflows, using platforms such as KingFisher APEX/FLEX, automated SPE systems, and robotic liquid handlers.
  • Prior experience in bioanalytical (regulated) assay execution and transfer to CROs
  • Must be willing to work in a fast-paced, multi-project environment with high workload demands, and consistently deliver high-quality results within established timelines.
  • Demon