Jobs · Research · Wisconsin

Supervisor, Cell and Gene Therapy (GMP Lab)

Thermo Fisher Scientific · Middleton, WI · 1 mo ago
On-siteResearchFull-time
We need to output HTML fragment with sections: Use

for section headings 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 job posting. Key info: - Work Schedule Standard (Mon-Fri) -> schedule info: Monday-Friday standard work schedule. So we can include Schedule section. - Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards -> maybe part of Work Environment. - Supervisor Department: Cell and Gene Therapy Location: Middleton, Wisconsin This is a fully onsite role based at our GMP Laboratory in Middleton, WI. We welcome applicants from all locations within the US. 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... (mission statement) - could be About the role? Actually "About the role" could be role overview. - Role Overview: The Supervisor provides line-level management coordination of resources and work schedules, oversees daily operations, assist in preparation and implementation of company policies, quality systems and training programs. Additionally, the Supervisor ensures that projects are completed in a timely manner so that company revenues are met and clients are satisfied with the quality and turnaround time of work being performed and that staff continue to be developed to keep pace with department goals and growth. - Key Responsibilities: list bullet points. - Key Qualifications: Education and Experience: ... Knowledge, Skills, Abilities: list. - Work Environment: list bullet points. - Benefits? Not mentioned. Pay? Not mentioned. So we should not include Benefits or Pay sections. - Schedule: we have Work Schedule Standard (Mon-Fri). So we can include Schedule section. - Possibly "About the role" could be the introductory paragraph about mission etc. But we need to decide. We need to preserve all substantive information, not invent or summarize away detail. So we need to include all details: location, onsite, relocation, work authorization, background check, mission statements, role overview, responsibilities, qualifications (education/experience, knowledge/skills/abilities), work environment, schedule. We must not repeat the job title as heading. The title is Supervisor? Actually job title is Supervisor (Cell and Gene Therapy). We should not repeat it as heading. We must not put Job ID/requisition numbers as headings (none present). We must remove boilerplate: cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, application instructions. So we need to strip out the EEO statement, accessibility line, "Apply today! http://jobs.thermofisher.com", etc. Also remove the mission statement duplication? The mission appears multiple times: "At Thermo Fisher Scientific, you’ll discover meaningful work..." and later "Our Mission is to enable our customers..." and also "#StartYourStory..." etc. Those are boilerplate? They are somewhat promotional but maybe considered part of "About the role"? The instruction says remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. The mission statements might be considered boilerplate but they are also substantive? They are generic corporate messaging. Might be considered boilerplate but not explicitly listed. Safer to keep them? The instruction: "Preserve ALL substantive information; do NOT invent or summarize away detail." The mission statements are not specific to the role; they are generic. Might be considered boilerplate but not explicitly listed. However they are duplicated. The instruction says remove duplicated lines. So we should remove duplicated mission statements. Keep only one instance? Might be better to keep a single concise "About the role" summarizing the role overview, not the generic mission. Thus we can create sections: - About the role: maybe combine role overview and location etc? But we have separate sections for Responsibilities, Qualifications, Skills, Work Environment, Schedule. We need to decide headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We have Responsibilities (Key Responsibilities). We have Qualifications (Education and Experience). We have Skills (Knowledge, Skills, Abilities). We have Work Environment (maybe could be under Requirements? But we have no specific heading for Work Environment; we could put under Requirements or maybe under About the role? But we have a heading for Requirements; we could put work environment there. However the instruction says use headings for those specific categories if content exists. There's no explicit "Work Environment" heading in list, but we could treat it as part of Requirements or About the role. Better to put under Requirements (since it's about job requirements). Or we could create a custom heading? Not allowed; only those headings. So we need to map content to those headings. Thus: - About the role: maybe a brief description: location, onsite, department, mission? Could include the role overview? But role overview is more about what supervisor does; could be under About the role. - Responsibilities: Key Responsibilities list. - Requirements: could include education/experience, work authorization, background check, relocation, location, schedule? Actually schedule is separate heading. - Qualifications: maybe education/experience? But we already used Requirements for education/experience? The distinction is fuzzy. Usually Qualifications = education/experience, Skills = knowledge/skills/abilities. Requirements could be other mandatory items like work authorization, background check, relocation, etc. Let's follow that. Thus: About the role: role overview paragraph. Responsibilities: list of responsibilities. Requirements: items like location (Middleton, WI, fully onsite), work authorization (legally authorized to work in US without sponsorship), background check/drug screening, relocation assistance not provided, must be able to pass background check, maybe also "Must be able to work upright and stationary..."? That's work environment; maybe under Requirements as well. Qualifications: Education and Experience: Bachelor's degree or equivalent preferred, 5+ years experience, 1+ year leadership. Skills: Knowledge, Skills, Abilities list. Schedule: Work Schedule Standard (Mon-Fri). We should not include Benefits or Pay. Now we need to format lists with
  • . For prose, use

    . We must not include any empty sections. Let's extract details precisely. About the role: We can use the Role Overview paragraph: "The Supervisor provides line-level management coordination of resources and work schedules, oversees daily operations, assist in preparation and implementation of company policies, quality systems and training programs. Additionally, the Supervisor ensures that projects are completed in a timely manner so that company revenues are met and clients are satisfied with the quality and turnaround time of work being performed and that staff continue to be developed to keep pace with department goals and growth." We might also include a brief statement about department and location? But that could be in Requirements. Better to keep About the role as the role overview only. Responsibilities: list each bullet: - Supervises the daily activities of staff, including interviewing, selection, hiring, professional development, performance management, and reviews and approves time records, requests for leave, and overtime. - Manages daily workflow, allocates resources, and tracks performance metrics. - Identifies and recommends process improvements and efficiency gains to optimize processes. - Monitors and ensures compliance with quality standards, investigates and resolves complex problems through root cause analysis, and implements corrective actions. - Responds to facility audit findings. - Assists management in their responsibilities. - Assists in preparation and implementation of PPD/client SOPs and company operational policies. - Ensures adherence to SOPs, safety standards and company policies. Note: The original had some run-on sentences without periods; we need to keep as is but ensure proper punctuation? We should preserve the text exactly; but we can keep as is. It's okay. Requirements: include: - Location: Middleton, Wisconsin (fully onsite role based at our GMP Laboratory in Middleton, WI). - Work authorization: Must be legally authorized to work in the United States without sponsorship. - Background check: Must be able to pass a comprehensive background check, which includes a drug screening. - Relocation: Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. - Work environment/physical requirements: 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, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. We could also include "Adherence to all Good Manufacturing Practices (GMP) Safety Standards" maybe as part of work environment. We should not duplicate lines. Qualifications: Education and Experience: - Bachelor's degree or equivalent preferred. - Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years) or equivalent and relevant combination of education, training, & experience. - 1+ year demonstrated leadership qualities. - In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. We could combine into a paragraph or list. Since it's a list, we can use

    • . Skills: Knowledge, Skills, Abilities list: - Demonstrated proficiency of good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging deadlines. - Proven leadership skills - Ability to train and mentor junior staff - Demonstrated ability to be project solution driven - Good written and oral communication skills as well as presentation skills - Can independently perform root cause analysis - Technical writing skills; ability to write quality documents (SOPs, investigation forms, etc.) - Demonstrated knowledge of QA metrics of program base; ability to write and recommend changes to PPD SOPs - Project and time management skills Schedule: - Work Schedule Standard (Mon-Fri) Now we need to output HTML fragment with

      headings and

      or

      • . We must not include any extra text like explanations. Let's craft:

        About the role

        The Supervisor provides line-level management coordination of resources and work schedules, oversees daily operations, assist in preparation and implementation of company policies, quality systems and training programs. Additionally, the Supervisor ensures that projects are completed in a timely manner so that company revenues are met and clients are satisfied with the quality and turnaround time of work being performed and that staff continue to be developed to keep pace with department goals and growth.

        Responsibilities

        • Supervises the daily activities of staff, including interviewing, selection, hiring, professional development, performance management, and reviews and approves time records, requests for leave, and overtime.
        • Manages daily workflow, allocates resources, and tracks performance metrics.
        • Identifies and recommends process improvements and efficiency gains to optimize processes.
        • Monitors and ensures compliance with quality standards, investigates and resolves complex problems through root cause analysis, and implements corrective actions.
        • Responds to facility audit findings.
        • Assists management in their responsibilities.
        • Assists in preparation and implementation of PPD/client SOPs and company operational policies.
        • Ensures adherence to SOPs, safety standards and company policies

        Requirements

        • Location: Middleton, Wisconsin (fully onsite role based at our GMP Laboratory in Middleton, WI).
        • 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.
        • Please note that relocation assistance is

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