Jobs · Research · Wisconsin

Scientist II - Small Molecule

Thermo Fisher Scientific · Middleton, WI · 4 wk ago
On-siteResearchFull-time
We need to output HTML fragment with sections: headings

for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections if posting has real specific content. We need to parse the posting. First, remove boilerplate: cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, application instructions. Also remove "Apply today! http://jobs.thermofisher.com" and EEO statement, accessibility details. We need to preserve substantive info: Work Schedule First Shift (Days) Environmental Conditions Laboratory Setting This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the U.S. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. Then mission statements etc. Then "Division Specific Information As a Scientist you will work in a multi-functional environment supporting drug development and will collaborate in cross-functional teams. You will accomplish our mission through innovation and partnership, creative problem-solving, and use of state-of-the-art technology. A day in the Life: ..." This is responsibilities. Then Education, Experience, Knowledge, Skills, Abilities. Then Work Environment details. We need to decide sections: About the role (maybe overview), Responsibilities (the day in the life bullet list), Requirements (maybe education + experience?), Qualifications (maybe knowledge, skills, abilities?), Skills (maybe separate?), Benefits (none given), Pay (none), Schedule (we have Work Schedule First Shift (Days) - that is schedule info). So we can include Schedule section. We must not create sections with placeholder text. So only include sections where we have content. Let's extract content. First, heading: About the role: could be introductory paragraph: "This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the U.S. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening." Also maybe include mission statements? But those are generic; could be part of About the role. Responsibilities: The "A day in the Life:" list: multiple sentences describing duties. We can turn each sentence into
  • . Let's list: - Trains on routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines. - Performs a variety of routine to complex sample preparation and analysis procedures with minimal supervision/guidance to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. - Completes all laboratory documentation in clear and accurate language and according to SOP and GLPs. - Independently troubleshoots equipment & instruments. - Mentors others in troubleshooting when applicable. - Reviews and complies results from assignments and makes initial determination on acceptability per SOP acceptance criteria. - Performs work assignments accurately, and in a timely and safe manner. - Independently manages QC responsibilities. - Communicates project status to project leader and helps to identify gaps and anticipates roadblocks in project team workflow. - Completes QA facing tasks with minimal supervisor/QA input. - Authors low complexity quality records and participates in the OOS/OOT/Atypical investigation process. We need to ensure we keep the apostrophe correct: "Mentors' others" likely a typo; we can keep as "Mentors others". We'll keep as given but maybe fix? The instruction: preserve ALL substantive information; do not invent or summarize away detail. Changing wording could be considered altering. Safer to keep exactly as in text, but we can correct obvious typo? Might be considered altering. I'd keep as is: "Mentors' others in troubleshooting when applicable." Keep the apostrophe. Similarly "Communicates' project status" -> keep as is. Now Education: "Bachelor's degree in lab sciences such as chemistry, biochemistry, or similar" Experience: "Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’) Years of experience refer to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions." We could combine Education and Experience into Requirements or Qualifications. 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) and Qualifications (knowledge, skills, abilities). Or we could have Requirements and Skills separate. Let's decide. We have Knowledge, Skills, Abilities list: many bullet-like sentences. We can put them under Skills heading. But we also have "Knowledge, Skills, Abilities" heading in the posting. So we could make a Qualifications section with that list. Better: Requirements: Education + Experience. Qualifications: Knowledge, Skills, Abilities list. Skills: maybe not needed separately if we already have Qualifications. But we could still have Skills section with same list? Might be duplicate. The instruction: prefer a few substantive sections over many thin ones. So we can combine Knowledge, Skills, Abilities into Qualifications. Thus sections: About the role, Responsibilities, Requirements, Qualifications, Schedule, Work Environment? Work Environment is a section but not in the allowed headings list? The allowed headings list includes Benefits, Pay, Schedule. Work Environment not listed but we could still include as a section? The instruction: use

    for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). It says e.g., implying those are examples, not exclusive. But we should probably stick to those. However Work Environment is substantive; we could incorporate into About the role or Responsibilities? Might be better to have a Work Environment section even if not in examples; but instruction says use those headings for section headings (e.g...). It doesn't forbid other headings, but to be safe we could incorporate Work Environment details into About the role or Responsibilities. However it's a distinct set of requirements (physical demands). Could be part of Requirements. We'll include under Requirements maybe as a sub-list? But we need to use
    • for any list of duties/requirements/benefits. So we can have a list under Requirements for work environment. Thus Requirements section will contain Education, Experience, and Work Environment items as list items. Qualifications section will contain Knowledge, Skills, Abilities items as list. Schedule section: "Work Schedule First Shift (Days)". That's the schedule. We'll put as

      maybe. Now we need to strip boilerplate: remove EEO statement, accessibility details, "Apply today! http://jobs.thermofisher.com", "Watch as our colleagues explain 5 reasons to work with us." etc. Also remove "Our Mission is to enable our customers to make the world healthier, cleaner and safer." repeated maybe. Keep mission statements? Might be considered boilerplate? It's part of company description; could be kept in About the role. But it's generic; still substantive? Might be okay. We need to preserve ALL substantive information; do not invent or summarize away detail. So we should keep mission statements if they appear in the posting. They appear: "At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations." That's a lot of generic fluff but it's in the posting. We should keep it as part of About the role. Now we need to output only HTML fragment, no /, no markdown fences. Let's craft:

      About the role

      This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the U.S. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.

      Responsibilities

      • Trains on routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines.
      • Performs a variety of routine to complex sample preparation and analysis procedures with minimal supervision/guidance to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing.
      • Completes all laboratory documentation in clear and accurate language and according to SOP and GLPs.
      • Independently troubleshoots equipment & instruments.
      • Mentors' others in troubleshooting when applicable.
      • Reviews and complies results from assignments and makes initial determination on acceptability per SOP acceptance criteria.
      • Performs work assignments accurately, and in a timely and safe manner.
      • Independently manages QC responsibilities.
      • Communicates' project status to project leader and helps to identify gaps and anticipates roadblocks in project team workflow.
      • Completes QA facing tasks with minimal supervisor/QA input.
      • Authors low complexity quality records and participates in the OOS/OOT/Atypical investigation process.

      Requirements

      • Bachelor's degree in lab sciences such as chemistry, biochemistry, or similar
      • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’)
      • Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
      • Able to work upright and stationary and/or standing for typical working hours.
      • Able to lift and move objects up to 25 pounds.
      • Able to work in non-traditional work environments.
      • Able to use and learn standard office equipment and technology with proficiency.
      • May have exposure to potentially hazardous elements, including infectious agents,

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