Pharmaceutical Manufacturing Operator
for section headings. Use - for any list of duties/requirements/benefits. Use
for prose. Remove boilerplate (EEO, accommodation request, etc). Also remove duplicated lines. Keep all substantive info.
We need to decide sections: About the role (maybe overview), Responsibilities, Requirements (minimum), Preferences (additional preferences), Other Information (shift, schedule, etc), Benefits, Pay. Must only include sections if there is real content.
Let's extract content.
Company overview: "At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. For 140 years, Lilly has manufactured medicines that improve people’s lives around the world. We produce our medicines using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards, procedures and behaviors to develop medicines with safety first and quality always. Lilly is currently constructing a cutting-edge facility for the manufacture of new modalities including Gene Therapy in Lebanon, Indiana. This facility will be Lilly’s most technically advanced manufacturing site focused on the delivery of the next wave of innovative products at Lilly. It will include next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety, quality, and process performance. This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing site, and the successful candidate will help to start up the facility for both clinical and commercial supply. This is an exciting opportunity to help start up a state-of-the-art facility and build a manufacturing supply chain from ground-up."
That's a lot of prose; we can put under
About the role
maybe.
Responsibilities: list bullet points after "The Manufacturing Operator will be responsible for performing routine manufacturing activities across GMP manufacturing areas, including: Cell Culture, Downstream Purification, and Fill & Finish at the Lebanon Advanced Therapies, LP2 site. Initially, the Operator will be responsible for supporting execution of equipment qualification, developing site operations procedures and setting up production areas. During this initial project delivery/startup phase of the project, roles will be fluid and dynamic. Once the plant is operational, the Manufacturing Operator will be responsible for execution of production activities on their shift under the leadership of the shift supervisor. As a Manufacturing Operator, Your Responsibilities Will Include ..." Then bullet list:
- Work in a cleanroom environment to produce advanced therapies in a safe and quality manner.
- Coordinate production activities with Quality Control, Quality Assurance, and Plant Maintenance to facilitate on-time release of advanced therapies.
- Participate in equipment commissioning and qualification testing and process validation activities in collaboration with other departments.
- Safely work with BSL-2 materials, following site biologics safety program.
- Conduct and appropriately document production of advanced Therapies via strict adherence to digital manufacturing batch records and affiliated SOPs.
- Utilize and monitor manufacturing equipment to ensure performance and safety standards are met.
- Collaborate with maintenance technicians, equipment manufacturers, and quality assurance to ensure that all production equipment is in good working order and is validated for use.
- Provide verbal and written reports to supervisors and other teams in a clear and concise manner.
- Maintain accurate and complete electronic records and logbooks as per cGLP and/or cGMP, as appropriate.
- Adhere to all applicable procedures, cGLP, cGMPs, company policies, and any other quality or regulatory requirements.
- Compliance with cleanroom gowning requirements required for completing specific work in drug substance and drug product.
- Work well in a fast-paced team environment.
We'll put under Responsibilities
with .
Minimum Requirements: "Minimum Requirements High School diploma or equivalent Direct manufacturing experience with automatic, manual, and semi-automated equipment, following operational procedures. Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1."
We can put under Requirements
with maybe.
Additional Preferences: list bullet points:
- 3+ years pharmaceutical cleanroom experience or equivalent comparable manufacturing experience
- Drug Substance experience; hands-on expertise working with bioreactors, sums, TFFs, purification, and similar processes
- Technical problem-solving skills.
- Good communications skills (both oral and written).
- Requires learning and understanding Good Manufacturing Practices and strict adherence to GMP regulations.
- Will be expected to adhere to all safety and environmental guidelines and to promote safety and environmental compliance in all areas.
- Good organization skills.
- Ability to work with and learn new digital systems
- Ability to demonstrate attention to detail
We can put under Preferences
or Additional Preferences
. Use heading "Additional Preferences".
Other Information: includes shift info: "During the start-up phase of the project, the shift will be primarily day shift. As the site nears normal operation, shift work will be required. Anticipated to be 2-2-3 12 hour shift. Ability to maintain focus on a complex task for 4-6 hours at a time. Adaptable to work in a fast-paced and evolving environment. Maintain clear, consistent, and constant verbal communication with one or more team members during performance of duties. Some overtime required."
We can put under Shift and Schedule
maybe. But we need to only include Schedule section if posting actually states them. It does state shift info, so we can include Schedule. Could also include "Other Information" but better to use "Schedule". Use Schedule
with describing.
Benefits: "Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)." Also mention company bonus. We'll put under
Benefits
with .
Pay: "Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $17.30 - $34.38 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance)." So we have pay range and bonus. We'll put under Pay
with .
We must not include boilerplate: EEO, accommodation request, ERG lists, Lilly reserves right to amend compensation, hashtag, etc. Also remove duplicated lines (like repeated "At Lilly, we unite caring with discovery...").
We need to preserve all substantive information; do not invent or summarize away detail. Must not omit any substantive info. Let's ensure we keep all details from the posting that are substantive.
Let's list all substantive info chunks:
- Company overview (multiple sentences). We'll keep them but avoid duplication.
- Opportunity description: unique opportunity to be part of team for startup of greenfield manufacturing site, help start up facility for clinical and commercial supply, exciting opportunity to help start up state-of-the-art facility and build manufacturing supply chain from ground-up.
- Role: Manufacturing Operator responsibilities.
- Responsibilities bullet list (as above).
- Minimum Requirements: HS diploma or equivalent; direct manufacturing experience with automatic, manual, semi-automated equipment, following operational procedures; authorized to work in US full-time; Lilly will not sponsor work authorization/visas (list).
- Additional Preferences: 3+ years pharmaceutical cleanroom experience or equivalent; Drug Substance experience; hands-on expertise with bioreactors, sums, TFFs, purification, similar processes; technical problem-solving skills; good communication skills (oral/written); learning and understanding GMP and strict adherence; adhere to safety/environmental guidelines and promote compliance; good organization skills; ability to work with and learn new digital systems; ability to demonstrate attention to detail.
- Other Information: shift start-up primarily day shift; as site nears normal operation, shift work required; anticipated 2-2-3 12 hour shift; ability to maintain focus on complex task 4-6 hours; adaptable to fast-paced evolving environment; maintain clear consistent constant verbal communication with team members; some overtime required.
- Benefits: comprehensive benefit program including 401(k), pension, vacation, medical/dental/vision/prescription drug, flexible benefits (healthcare/dependent day care FSA), life insurance/death benefits, certain time off/leave of absence, well-being benefits (EAP, fitness, employee clubs/activities). Also company bonus eligibility.
- Pay: actual compensation depends on education, experience, skills, location; anticipated wage $17.30 - $34.38; full-time eligible for company bonus (depending on company/individual performance).
We must not include the accommodation request, EEO, ERG lists, Lilly reserves right to amend compensation, hashtag #WeAreLilly.
Now produce HTML.
Structure:
About the role
... (company overview + opportunity description)
Responsibilities
- ...
...
Requirements
- High school diploma or equivalent
- Direct manufacturing experience with automatic, manual, and semi-automated equipment, following operational procedures
- Applicants must be authorized to work in the United States on a full‑time basis
- Lilly will not provide support for or sponsor work authorization or visas for this role (including F‑1 CPT, F‑1 OPT, F‑1 STEM OPT, J‑1, H‑1B, TN, O‑1, E‑3, H‑1B1, or L‑1)
Additional Preferences
- 3+ years pharmaceutical cleanroom experience or equivalent comparable manufacturing experience
- Drug substance experience; hands‑on expertise working with bioreactors, sums, TFFs, purification, and similar processes
- Technical problem‑solving skills
- Good communication skills (both oral and written)
- Requires learning and understanding Good Manufacturing Practices and strict adherence to GMP regulations
- Will be expected to adhere to all safety and environmental guidelines and to promote safety and environmental compliance in all areas
- Good organization skills
- Ability to work with and
for prose. Remove boilerplate (EEO, accommodation request, etc). Also remove duplicated lines. Keep all substantive info. We need to decide sections: About the role (maybe overview), Responsibilities, Requirements (minimum), Preferences (additional preferences), Other Information (shift, schedule, etc), Benefits, Pay. Must only include sections if there is real content. Let's extract content. Company overview: "At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. For 140 years, Lilly has manufactured medicines that improve people’s lives around the world. We produce our medicines using some of the most sophisticated manufacturing technologies and rigorous quality standards. Lilly Manufacturing strives for excellence in its process, standards, procedures and behaviors to develop medicines with safety first and quality always. Lilly is currently constructing a cutting-edge facility for the manufacture of new modalities including Gene Therapy in Lebanon, Indiana. This facility will be Lilly’s most technically advanced manufacturing site focused on the delivery of the next wave of innovative products at Lilly. It will include next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety, quality, and process performance. This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing site, and the successful candidate will help to start up the facility for both clinical and commercial supply. This is an exciting opportunity to help start up a state-of-the-art facility and build a manufacturing supply chain from ground-up." That's a lot of prose; we can put under
About the role
maybe. Responsibilities: list bullet points after "The Manufacturing Operator will be responsible for performing routine manufacturing activities across GMP manufacturing areas, including: Cell Culture, Downstream Purification, and Fill & Finish at the Lebanon Advanced Therapies, LP2 site. Initially, the Operator will be responsible for supporting execution of equipment qualification, developing site operations procedures and setting up production areas. During this initial project delivery/startup phase of the project, roles will be fluid and dynamic. Once the plant is operational, the Manufacturing Operator will be responsible for execution of production activities on their shift under the leadership of the shift supervisor. As a Manufacturing Operator, Your Responsibilities Will Include ..." Then bullet list: - Work in a cleanroom environment to produce advanced therapies in a safe and quality manner. - Coordinate production activities with Quality Control, Quality Assurance, and Plant Maintenance to facilitate on-time release of advanced therapies. - Participate in equipment commissioning and qualification testing and process validation activities in collaboration with other departments. - Safely work with BSL-2 materials, following site biologics safety program. - Conduct and appropriately document production of advanced Therapies via strict adherence to digital manufacturing batch records and affiliated SOPs. - Utilize and monitor manufacturing equipment to ensure performance and safety standards are met. - Collaborate with maintenance technicians, equipment manufacturers, and quality assurance to ensure that all production equipment is in good working order and is validated for use. - Provide verbal and written reports to supervisors and other teams in a clear and concise manner. - Maintain accurate and complete electronic records and logbooks as per cGLP and/or cGMP, as appropriate. - Adhere to all applicable procedures, cGLP, cGMPs, company policies, and any other quality or regulatory requirements. - Compliance with cleanroom gowning requirements required for completing specific work in drug substance and drug product. - Work well in a fast-paced team environment. We'll put underResponsibilities
with- .
Minimum Requirements: "Minimum Requirements High School diploma or equivalent Direct manufacturing experience with automatic, manual, and semi-automated equipment, following operational procedures. Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1."
We can put under
- ... ...
- High school diploma or equivalent
- Direct manufacturing experience with automatic, manual, and semi-automated equipment, following operational procedures
- Applicants must be authorized to work in the United States on a full‑time basis
- Lilly will not provide support for or sponsor work authorization or visas for this role (including F‑1 CPT, F‑1 OPT, F‑1 STEM OPT, J‑1, H‑1B, TN, O‑1, E‑3, H‑1B1, or L‑1)
- 3+ years pharmaceutical cleanroom experience or equivalent comparable manufacturing experience
- Drug substance experience; hands‑on expertise working with bioreactors, sums, TFFs, purification, and similar processes
- Technical problem‑solving skills
- Good communication skills (both oral and written)
- Requires learning and understanding Good Manufacturing Practices and strict adherence to GMP regulations
- Will be expected to adhere to all safety and environmental guidelines and to promote safety and environmental compliance in all areas
- Good organization skills
- Ability to work with and
Requirements
with- maybe.
Additional Preferences: list bullet points:
- 3+ years pharmaceutical cleanroom experience or equivalent comparable manufacturing experience
- Drug Substance experience; hands-on expertise working with bioreactors, sums, TFFs, purification, and similar processes
- Technical problem-solving skills.
- Good communications skills (both oral and written).
- Requires learning and understanding Good Manufacturing Practices and strict adherence to GMP regulations.
- Will be expected to adhere to all safety and environmental guidelines and to promote safety and environmental compliance in all areas.
- Good organization skills.
- Ability to work with and learn new digital systems
- Ability to demonstrate attention to detail
We can put under
Preferences
orAdditional Preferences
. Use heading "Additional Preferences". Other Information: includes shift info: "During the start-up phase of the project, the shift will be primarily day shift. As the site nears normal operation, shift work will be required. Anticipated to be 2-2-3 12 hour shift. Ability to maintain focus on a complex task for 4-6 hours at a time. Adaptable to work in a fast-paced and evolving environment. Maintain clear, consistent, and constant verbal communication with one or more team members during performance of duties. Some overtime required." We can put underShift and Schedule
maybe. But we need to only include Schedule section if posting actually states them. It does state shift info, so we can include Schedule. Could also include "Other Information" but better to use "Schedule". UseSchedule
withdescribing. Benefits: "Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)." Also mention company bonus. We'll put under
Benefits
with- .
Pay: "Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $17.30 - $34.38 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance)." So we have pay range and bonus. We'll put under
Pay
with. We must not include boilerplate: EEO, accommodation request, ERG lists, Lilly reserves right to amend compensation, hashtag, etc. Also remove duplicated lines (like repeated "At Lilly, we unite caring with discovery..."). We need to preserve all substantive information; do not invent or summarize away detail. Must not omit any substantive info. Let's ensure we keep all details from the posting that are substantive. Let's list all substantive info chunks: - Company overview (multiple sentences). We'll keep them but avoid duplication. - Opportunity description: unique opportunity to be part of team for startup of greenfield manufacturing site, help start up facility for clinical and commercial supply, exciting opportunity to help start up state-of-the-art facility and build manufacturing supply chain from ground-up. - Role: Manufacturing Operator responsibilities. - Responsibilities bullet list (as above). - Minimum Requirements: HS diploma or equivalent; direct manufacturing experience with automatic, manual, semi-automated equipment, following operational procedures; authorized to work in US full-time; Lilly will not sponsor work authorization/visas (list). - Additional Preferences: 3+ years pharmaceutical cleanroom experience or equivalent; Drug Substance experience; hands-on expertise with bioreactors, sums, TFFs, purification, similar processes; technical problem-solving skills; good communication skills (oral/written); learning and understanding GMP and strict adherence; adhere to safety/environmental guidelines and promote compliance; good organization skills; ability to work with and learn new digital systems; ability to demonstrate attention to detail. - Other Information: shift start-up primarily day shift; as site nears normal operation, shift work required; anticipated 2-2-3 12 hour shift; ability to maintain focus on complex task 4-6 hours; adaptable to fast-paced evolving environment; maintain clear consistent constant verbal communication with team members; some overtime required. - Benefits: comprehensive benefit program including 401(k), pension, vacation, medical/dental/vision/prescription drug, flexible benefits (healthcare/dependent day care FSA), life insurance/death benefits, certain time off/leave of absence, well-being benefits (EAP, fitness, employee clubs/activities). Also company bonus eligibility. - Pay: actual compensation depends on education, experience, skills, location; anticipated wage $17.30 - $34.38; full-time eligible for company bonus (depending on company/individual performance). We must not include the accommodation request, EEO, ERG lists, Lilly reserves right to amend compensation, hashtag #WeAreLilly. Now produce HTML. Structure:
About the role
... (company overview + opportunity description)