Jobs · OTHR · Ohio

GMP Scientist II (Suspension)

Actalent · Westerville, OH · 1 mo ago
On-siteOTHR$28/hrContract
We need to output HTML fragment with sections: About the role (maybe from description), Responsibilities, Requirements (maybe Skills), Benefits, Pay, Schedule, etc. Must only include sections that have real specific content. Must not repeat job title as heading. Must not include Job ID etc. Must remove boilerplate like EEO, legal, etc. Must preserve all substantive info. We need to parse the job description. Content: Job Description paragraph: "The GMP Operations Scientist II is tasked with guiding all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). The role involves hands-on support and leadership for day-to-day GMP production operations, ensuring timely, compliant, and fiscally responsible delivery of products." That's about the role. Responsibilities: list bullet points after "Responsibilities". Let's extract them: - Solve, correct, and prevent problems while assigning tasks to junior staff. - Work towards specific measurable objectives with minimal supervision. - Lead and support a diverse and collaborative team, ensuring clear communication to achieve high productivity. - Provide leadership in daily operational activities related to GMP manufacturing of biological products. - Ensure availability of materials and proper documentation of GMP activities and product quality. - Set and maintain professional standards within the GMP area. - Support GMP resources and the supply chain, including ordering and maintaining materials inventory. - Maintain accurate documentation on all GMP operations. - Train and supervise junior staff to ensure proper operation of facility equipment and adherence to documentation standards. - Guide operations staff in deviation investigations, OOS results, and process troubleshooting. - Collaborate with GMP Management to identify and meet continuous improvement objectives. - Incorporate new projects and technologies into the GMP area. - Respond to alarm notifications from monitoring systems for laboratory temperature-controlled storage units. - Operate within the Quality Management System and maintain compliance with regulatory requirements for cellular and gene therapy products. - Demonstrate a high level of integrity and maintain a positive attitude. Essential Skills: list: - Relevant four-year Life Science degree or Master's degree. - Three years of relevant experience with a four-year degree or one year with a Master's degree. - Bg in life sciences, biotechnology, or gene therapy industries is ideal. (Probably "Background"? but keep as is) - Experience in a GMP or GLP setting. - Excellent communication, organization, and project management skills. - Proficiency in Microsoft Office (PowerPoint, Excel, Word), including data interpretation and reporting. - Ability to work independently and collaboratively in a diverse work environment. Additional Skills & Qualifications: - Technical writing/SOP writing experience. - Knowledge of GMP or bioprocessing. - Experience in Suspension or Bioreactors. - Experience in downstream processing, TFF, clarification, or large-scale cell culture. Work Environment: paragraph about team-oriented, collaborative, team expanding, dress code business casual with lab attire, shift flexible 7-8 AM to 5:30-6:30 PM, adjustments as necessary to balance hour (maybe incomplete). We'll keep as is. Job Type & Location: Contract position based out of Columbus, OH. Pay And Benefits: pay range $28.00 - $28.00/hr (so fixed $28/hr). Then description about compensation factors. Benefits list: Medical, dental & vision; Critical Illness, Accident, and Hospital; 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available; Life Insurance (Voluntary Life & AD&D for the employee and dependents); Short and long-term disability; Health Spending Account (HSA); Transportation benefits; Employee Assistance Program; Time Off/Leave (PTO, Vacation or Sick Leave). Workplace Type: fully onsite position in Columbus,OH. Application Deadline: anticipated to close on Sep 30, 2026. About Actalent: boilerplate about company, EEO, etc. We must remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. So we should drop the About Actalent paragraph and all the EEO statements, accommodation, San Francisco Fair Chance, Massachusetts Lie Detector, Use of AI, etc. Also drop "Application Deadline"? That's substantive info (deadline). Should we keep? It's not a standard heading but could be included as a paragraph maybe under a heading like "Application Deadline"? The instruction: include a section ONLY when the posting has real, specific content for it — never emit a heading followed by filler/placeholder text. The deadline is specific. Could we put it under a heading like "Application Deadline"? Not listed in allowed headings but we could use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). They gave examples but not exclusive; they said use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we should stick to those headings. Deadline could be placed under a paragraph maybe under "About the role" or separate? Probably better to include as a short paragraph under a heading like "Details" but not allowed. Could we embed it in a

after the sections? The instruction: Output ONLY the HTML fragment — no /, no markdown code fences. It didn't forbid extra paragraphs not under headings. But they said use

for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). Use
  • for any list of duties/requirements/benefits, and

    for prose. So we can have headings for those sections, and any other prose can be in

    without heading. So we can include deadline as a

    after sections. We must not include boilerplate like About Actalent etc. So we will omit that. Now decide which sections to include: - About the role: we have the introductory paragraph. Use

    About the role

    then

    ...

    - Responsibilities:

    Responsibilities

    then
    • ... each bullet. - Requirements / Skills: Could combine Essential Skills and Additional Skills & Qualifications under a heading like "Skills" or "Requirements". The instruction list includes Requirements, Qualifications, Skills. We could have

      Skills

      and list both essential and additional as
        . Or separate:

        Requirements

        for essential skills (education/experience) and

        Additional Skills & Qualifications

        but that's not in list but could be okay? They said use

        for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). So we can use Requirements, Qualifications, Skills. Probably best to put essential skills under Requirements, and additional skills under Skills or Qualifications. Let's do:

        Requirements

          for essential skills (education, experience, etc.)

          Skills

            for additional skills (technical writing, GMP knowledge, etc.) Alternatively combine but better to separate. - Benefits:

            Benefits

              list benefits. - Pay:

              Pay

              Pay range: $28.00 - $28.00/hr (fixed $28.00 per hour). Individual compensation offered ... etc. We need to preserve all substantive info. So include that paragraph. - Schedule:

              Schedule

              Shift is flexible, running from 7-8 AM to 5:30-6:30 PM, with adjustments as necessary to balance hour.

              (maybe also mention flexible). We'll keep. - Work Environment: Could be under a heading like "Work Environment" but not in list. Could be a

              without heading. But we could also treat as part of About the role? Probably better to add a

              Work Environment

              though not in examples but allowed? The instruction says use

              for section headings (e.g. About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule). It doesn't forbid other headings, but says "use

              for section headings (e.g ...)". It implies we should use those headings for sections. Safer to stick to those headings only. So we can put work environment info in a

              after sections without a heading. - Job Type & Location: Could be a

              without heading. - Workplace Type: Could be a

              . - Application Deadline: Could be a

              . We must not repeat job title as heading. Already not. We must not include boilerplate like About Actalent etc. Now produce HTML. Let's craft. First, About the role paragraph: "The GMP Operations Scientist II is tasked with guiding all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility (CMF). The role involves hands-on support and leadership for day-to-day GMP production operations, ensuring timely, compliant, and fiscally responsible delivery of products." Responsibilities list: copy bullet points. Requirements list (essential skills): - Relevant four-year Life Science degree or Master's degree. - Three years of relevant experience with a four-year degree or one year with a Master's degree. - Background in life sciences, biotechnology, or gene therapy industries is ideal. (We'll keep "Bg" as is? It says "Bg in life sciences, biotechnology, or gene therapy industries is ideal." Likely a typo for "Background". We'll preserve exactly as given: "Bg in life sciences, biotechnology, or gene therapy industries is ideal." - Experience in a GMP or GLP setting. - Excellent communication, organization, and project management skills. - Proficiency in Microsoft Office (PowerPoint, Excel, Word), including data interpretation and reporting. - Ability to work independently and collaboratively in a diverse work environment. Skills list (additional): - Technical writing/SOP writing experience. - Knowledge of GMP or bioprocessing. - Experience in Suspension or Bioreactors. - Experience in downstream processing, TFF, clarification, or large-scale cell culture. Benefits list: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Pay paragraph: "The pay range for this position is $28.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms." Schedule paragraph: "The shift is flexible, running from 7-8 AM to 5:30-6:30 PM, with adjustments as necessary to balance hour." Work Environment paragraph: "The work culture is team-oriented, with a diverse and growing group. Collaboration is essential as tasks cannot be completed alone. The team is expanding from four members and aims to grow significantly by the end of the year. The dress code is business casual with appropriate lab attire." Job Type & Location paragraph: "This is a Contract position based out of Columbus, OH." Workplace Type paragraph: "This is a fully onsite position in Columbus,OH." Application Deadline paragraph: "This position is anticipated to close on Sep 3

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