Jobs · Marketing · Virginia

Senior Operations Engineer - Drug Product

Merck · Elkton, VA · 3 wk ago
Marketing$96k–$151k/yrFull-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 job description. First, there is a job title: Senior Operations Engineer - Drug Product. Not to repeat as heading. We need sections: - About the role: maybe from "Job Profile" paragraph: "At our company, we aspire...". That's description. Could be About the role. - Responsibilities: list of primary responsibilities bullet points. - Requirements: Minimum Required Education, Experience bullet list. - Qualifications: Preferred Qualifications bullet list. - Skills: Required Skills list (maybe also Preferred Skills? but they gave Required Skills list). Also maybe include "Preferred Skills" but they gave "Current Employees apply HERE" etc not relevant. We'll include Skills section for Required Skills. - Benefits: they mention "We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days." Also mention annual bonus and long-term incentive. So Benefits section. - Pay: they have salary range: $96,200.00 - $151,400.00. Also mention annual bonus and long-term incentive. So Pay section. - Schedule: they mention Shift 1st - Day, Travel Requirements 10%, Flexible Work Arrangements Not Applicable, Relocation: Domestic VISA Sponsorship No, etc. So we can include Schedule section with shift, travel, flexible work, relocation, etc. We need to remove boilerplate: cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, application instructions. So we should omit EEO statements, accommodation link, application instructions, job posting end date, requisition ID, etc. Also remove "Search Firm Representatives", etc. We need to preserve all substantive information. Let's extract content. About the role: The "Job Profile" paragraph: "At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the power of leading-edge science to save and improve lives around the world. We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best work. We are building deep small molecule expertise in the U.S., and we want team members who are excited to grow their skills, help improve how we operate, and contribute to a site positioned for future growth." That's good. Responsibilities: list from "Primary Responsibilities". They are sentences separated by periods. We'll convert each to
  • . List: - Support commissioning, qualification, start-up, and operational readiness activities for the new DP Small Molecule facility in Elkton, VA. - Partner with Operations, Engineering, Quality, Technical Operations, Supply Chain, and other stakeholders to support safe, compliant, and effective plant start-up. - Provide technical and operational support during equipment and process start-up, troubleshooting, and optimization activities. - Support technology transfer and implementation of commercial manufacturing processes into the new facility. - Help define, implement, and improve operating practices, standard work, procedures, and routines that support reliable and compliant operations. - Coordinate and prioritize improvement activities and key areas of focus within the IPT in alignment with business objectives and operational performance goals. - Use our company Production System (MPS) tools and lean principles, including Kaizen, 5S, visual management, and Standard Work, to identify and support improvement opportunities. - Help embed best practices across shifts, functions, and workstreams to promote consistency, efficiency, and strong operational execution. - Support a culture of safety, quality, compliance, accountability, and continuous improvement. - Act as a delegate for the Production Lead when needed, supporting continuity of leadership and cross-functional coordination. - Contribute to an inclusive, collaborative, and performance-driven work environment. Also there is a later paragraph: "This is a unique opportunity to help shape the future of a growing Small Molecule site as it is established from the ground up. In this role, you will support the startup and operational readiness of the new facility, help establish effective ways of working, and contribute to continuous improvement efforts that enable safe, reliable, and high-quality medicine production for patients around the world. If you are a collaborative operations professional with strong technical acumen, a commitment to quality, and a passion for operational excellence, we encourage you to apply." This could be part of About the role or maybe a concluding statement. We'll incorporate into About the role maybe as additional paragraph. But we must not duplicate. We'll keep About the role as two paragraphs: first the Job Profile paragraph, second the unique opportunity paragraph. Now Requirements: Minimum Required Education, Experience bullet list. Extract: - Bachelor’s degree required. - Chemical Engineering, Pharmaceutical Engineering, Biochemical Engineering, Chemistry, or a related technical discipline preferred. - Minimum 5 years of experience in Drug Product/SDI manufacturing, to include operations, technical operations - Experience working in a cross-functional manufacturing, technical, or operational setting. - Experience contributing to operational improvement, troubleshooting, process support, or start-up-related activities. - Working knowledge of GMP, quality, and compliance expectations in pharmaceutical manufacturing. - Strong problem-solving, communication, collaboration, and organizational skills. - Ability to work effectively across Operations, Engineering, Quality, and Technical teams. - Ability to prioritize work in a dynamic, fast-paced environment. - Demonstrated commitment to safety, operational excellence, and continuous improvement. We'll list each as
  • . Qualifications: Preferred Qualifications bullet list. Extract: - Experience supporting commissioning, qualification, start-up, or validation activities. - Experience in a greenfield or new facility start-up environment. - Experience with technology transfer and implementation of commercial manufacturing processes. - Experience applying lean tools and methodologies, including Kaizen, 5S, and Standard Work. - Experience coordinating activities across shifts, teams, or functions. - Experience serving in a lead, coordinator, or delegate role supporting leadership continuity. - Experience identifying improvement opportunities and helping implement practical solutions in a manufacturing environment. Also maybe "This is a unique opportunity..." but that's not qualification. Now Skills: Required Skills list: they gave a long list: "Adaptability, Adaptability, Analytical Problem Solving, cGMP Compliance, Chemical Engineering, Cross-Functional Project Management, Data Analysis, Decision Making, Engineering Support, Focused Improvement, Inventory Management, Leadership Theories, Lean Six Sigma Continuous Improvement, Manufacturing, Manufacturing Processes, Manufacturing Strategies, Manufacturing Systems, Manufacturing Technologies, Operational Quality, Operations Engineering, Personal Initiative, Pharmaceutical Process Development, Pharmaceutical Process Engineering, Process Improvements, Process Optimization {+ 8 more}". We need to preserve all substantive information; we should list them as items. There's duplication of Adaptability twice; we can keep as is or deduplicate? Probably keep as given but we could deduplicate to avoid redundancy. The instruction: preserve ALL substantive information; do NOT invent or summarize away detail. Duplication is part of the original; we could keep both but it's redundant. I'd keep as given but maybe we can list unique items; but that would be summarizing away detail (removing duplicate). Safer to keep as given but we could note duplicate. I'd keep as given but maybe remove duplicate to avoid weirdness. However "preserve ALL substantive information" - duplicate is not substantive new info; removing duplicate is not losing substantive info. I'd deduplicate. Thus list skills: - Adaptability - Analytical Problem Solving - cGMP Compliance - Chemical Engineering - Cross-Functional Project Management - Data Analysis - Decision Making - Engineering Support - Focused Improvement - Inventory Management - Leadership Theories - Lean Six Sigma Continuous Improvement - Manufacturing - Manufacturing Processes - Manufacturing Strategies - Manufacturing Systems - Manufacturing Technologies - Operational Quality - Operations Engineering - Personal Initiative - Pharmaceutical Process Development - Pharmaceutical Process Engineering - Process Improvements - Process Optimization Plus "{+ 8 more}" indicates there are 8 more unspecified skills. We should preserve that note: maybe as a line "+ 8 more". We'll include as a list item: "+ 8 more". Now Benefits: we have: - Annual bonus and long-term incentive (if applicable) - Comprehensive package of benefits: medical, dental, vision healthcare and other insurance benefits (for employee and family) - Retirement benefits, including 401(k) - Paid holidays - Vacation - Compassionate and sick days - More information at link (we can omit link as it's application instruction? It's not exactly instruction but it's a link for more info; could be considered boilerplate? It's not navigation/legal/EEO; it's a benefits link. Might be okay to keep but it's a URL; maybe we keep as plain text? The instruction: remove application instructions. This is not exactly application instruction but it's a reference. I'd keep the description but not the URL. Could keep "More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits." That's a link; might be considered boilerplate? It's not navigation but it's a reference. Safer to omit the URL but keep the sentence "More information about benefits is available." However that loses detail. I'd keep the URL as it's substantive info about where to find more. The instruction says remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. This is not exactly those. I'd keep it. Thus Benefits section items: - Annual bonus and long-term incentive (if applicable) - Comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits (for employee and family) - Retirement benefits, including 401(k) - Paid holidays - Vacation - Compassionate and sick days - More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits. Now Pay: Salary range $96,200.00 - $151,400.00. Also mention annual bonus and long-term incentive (already in benefits). Could mention that salary range is lowest to highest we would pay. Also mention that employee’s position within the salary range will be based on factors. We'll include that as prose. Thus Pay section:

    The salary range for this role is $96,200.00 - $151,400.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

    Now Schedule: we have: - Shift 1st - Day - Travel Requirements 10% - Flexible Work Arrangements Not Applicable - Relocation: Domestic VISA Sponsorship No - Hazardous Material(s) NA - Job Posting End Date (but we remove as application instruction? It's a date; maybe we remove as it's not substantive for role? It's metadata; we could drop. The instruction: do NOT put Job ID / requisition numbers as headings — fold minor metadata into a short

    or drop it. So we could fold minor metadata like Job Posting End Date into a short p or drop it. Probably drop it as it's not needed for role. Also "Employee Status Regular". Could be minor metadata. We'll include shift, travel, flexible work, relocation, hazardous material. Thus Schedule section: maybe a

      with items:
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