Jobs · Research · California

Scientist, Medicinal Chemistry

Bristol Myers Squibb EU Policy · San Diego, CA · 1 mo ago
Research$118k–$143k/yrFull-time
We need to output HTML fragment with sections for headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. We must not repeat job title as heading. Must not include Job ID/requisition numbers as headings; can fold minor metadata into short p or drop it. Must preserve all substantive info, not invent or summarize away detail. Remove boilerplate, navigation, legal, EEO, equal-opportunity, scam-warning, duplicated lines, application instructions. We need to parse the posting. Key content: - Intro: "Life at BMS At RayzeBio, every day is an opportunity to ignite meaningful change..." This is about the company, maybe "About the role"? Actually "About the role" could be description of role and company. We'll put that in

About the role

with paragraphs. - Job Description: "The Scientist will design and synthesize novel chemical constructs as potential new RPT therapies for cancer treatments. The Scientist I/II will be a highly motivated and technically skilled synthetic organic, peptide or medicinal chemist with excellent interpersonal and communication skills. Candidates will work as part of a team of scientists to synthesize and design both small molecules and peptide analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. The role is highly technical and will need a person who enjoys working at the bench with high productivity and data analysis skills and a comfort level in working under tight timelines." That's also about role. - Responsibilities: list bullet points after "Job Responsibilities Essential duties and responsibilities include the following. Other duties may be assigned." Then a long list of duties separated by periods. We need to extract each duty as list items. Let's list them: - Design and synthesize small molecule/novel peptide compounds in support of SAR campaigns for pipeline projects. - Contribute towards developing SAR on assigned projects, design and synthesize key target molecules to assess chemical/biological hypothesis. - Independently plan and execute organic synthesis routes for complex molecules. - Utilize modern purification and analytical tools to support synthesis and characterization of target compounds. - Work in close collaboration with interdisciplinary team members to provide needed chemistry support to guide programs through lead identification/optimization phases. - Work closely with chemists, DMPK, imaging and in vitro/vivo teams to ensure that target compounds are generated in a timely manner to support the screening funnel. - Contribute experimental efforts in support of target selection and initiation of new RPT projects. - Keep abreast of the literature in the field of RPTs, identify novel concepts and ideas to help advance the state of art in RPT field. - Contribute towards IP filings and drafting of publications, presentations. - Routinely present research findings, project updates in interdisciplinary team settings. - Adhere rigorously to safety guidelines, regulatory standards and company policies and ensure a safe working environment. - Uses AI tools to enhance individual productivity and quality of work That's responsibilities. - Education And Experience: "BS 5+ years or MS 3+ years or PhD 0 years". That's a requirement. Also "Preferred Qualifications PhD in synthetic organic, medicinal, or peptide chemistry with 0-4+ years of post-PhD/postdoc experience in Pharmaceutical/Biotech R&D environments demonstrating successful accomplishments and productivity. Experience in working on targeted cancer therapy modalities such as RPTs, ADCs, PDCs is highly desirable." - Skills And Qualifications: list bullet-like sentences: "Well versed in modern synthetic organic/peptide/med chem principles and demonstrated track record of high productivity and achievements in the lab. Multi-step organic synthesis, structure-based drug design, and operation of analytical tools like NMR and HPLC/LC-MS. High scientific curiosity and a learning mindset coupled with strong technical problem-solving skills and strong understanding of the concepts of drug design, SAR analysis, ADME/PK is important. The ability to share data and collaborate with cross functional team members is critical as is the ability to effectively interpret data and plan experiments without supervision. Excellent written and oral communication and presentation skills and ability to work in a fast-paced, dynamic, and collaborative environment." - Physical Demands: "While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision and distance vision. This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment." - Work Environment: "The noise level in the work environment is usually moderate. We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway." - Compensation Overview: "San Diego - CA - US: $118,259 - $143,302 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance." - Benefits: long paragraph about benefits. - Additional sections: "RayzeBio and Bristol Myers Squibb", "Supporting People With Disabilities", "Candidate Rights", "Data Protection". Those are boilerplate/legal; we should remove them per instruction: remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate. So we should omit those sections. Also we should not include "Job ID / requisition numbers as headings". There's a line "R1605076 : Scientist, Medicinal Chemistry". That's metadata; we can drop it or put in short p. Probably drop. We need to decide which sections to include: About the role (intro + job description), Responsibilities, Requirements (Education And Experience), Qualifications (maybe combine with Skills?), Skills, Benefits, Pay, Schedule? Schedule not mentioned; we should not create Schedule section unless posting actually states it. No schedule info. So omit Schedule. We need to decide if we need separate Qualifications and Skills sections. The posting has "Education And Experience", "Preferred Qualifications", "Skills And Qualifications". We could combine Education And Experience and Preferred Qualifications into a "Requirements" section (or "Qualifications") and Skills And Qualifications into a "Skills" section. The instruction: use headings for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we can have Requirements (education/experience), Qualifications (maybe preferred qualifications), Skills (skills). But we must not create sections with filler. We have content for each. Thus: - About the role: intro paragraph(s) about company and role description. - Responsibilities: ul list of duties. - Requirements: education/experience (BS 5+ years or MS 3+ years or PhD 0 years). Could also include "Preferred Qualifications" as part of Requirements? Might be better to have Requirements for mandatory, Qualifications for preferred. But we have both. Let's do:

Requirements

BS with 5+ years of experience, MS with 3+ years, or PhD (0 years).

Qualifications

Preferred: PhD in synthetic organic, medicinal, or peptide chemistry with 0-4+ years post-PhD/postdoc experience in Pharmaceutical/Biotech R&D environments demonstrating successful accomplishments and productivity. Experience in working on targeted cancer therapy modalities such as RPTs, ADCs, PDCs is highly desirable.

- Skills: list of skills. - Benefits: paragraph(s) about benefits. - Pay: paragraph(s) about compensation. We must not include Schedule. We need to preserve all substantive info; not invent or summarize away detail. So we need to keep details like "San Diego - CA - US: $118,259 - $143,302". Also mention discretionary incentive cash and stock opportunities, pay equity, etc. Benefits: need to keep details: wellbeing support, retirement, financial protection, insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees eligible for Flexible Time Off (FTO) with paid time off without set accrual limit, manager approval, plus 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits We must keep that. Now we need to strip boilerplate: The intro includes "Learn more about RayzeBio: https://careers.bms.com/rayzebio/" That's a link; we can keep as part of paragraph? It's not boilerplate; it's a link to learn more. Probably okay to keep. Also "RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals". That's substantive about company; keep. Now we need to ensure we don't duplicate content. The intro includes some repeated sentences maybe; we can combine. Now produce HTML fragment:

About the role

Life at BMS At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/ RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. The Scientist will design and synthesize novel chemical constructs as potential new RPT therapies for cancer treatments. The Scientist I/II will be a highly motivated and technically skilled synthetic organic, peptide or medicinal chemist with excellent interpersonal and communication skills. Candidates will work as part of a team of scientists to synthesize and design both small molecules and peptide analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. The role is highly technical and will need a person who enjoys working at the bench with high productivity and data analysis skills and a comfort level in working under tight timelines.

Then Responsibilities ul. Then Requirements p. Then Qualifications p. Then Skills: maybe ul list? The skills are sentences; we could make ul with each

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