Technician, Manufacturing Shared Services (onsite)

We need to output HTML fragment with sections for headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content. Remove boilerplate, navigation, EEO, etc. Must preserve all substantive info. We need to parse the job description. Key parts: - Title: POCS – Rahway: Technician, Operations Level: O2 Job Family: Manuf/Operations Technician, Operations Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. Positions will support development and clinical manufacturing and supply, as part of the FLEx-Sterile team, specifically in Manufacturing Shared Services which supports sterile supply, aseptic formulation and visual inspection. This position will be responsible for hands-on processing activities that include equipment assembly and disassembly, sterile processing, inventory management, open aseptic formulation in an isolator and closed formulation activities in a Grade C environment, and manual visual inspection of filled units (i.e. vials or syringes). These individuals are expected to partner with and support formulation development colleagues in further understanding and knowledge capture of processes, which could include providing feedback on product and process development. These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects. Positions may also support commissioning, qualification, and demonstration of new equipment and technologies. Successful candidates will collaborate closely with team members and partner groups including formulators, engineers, Quality, Safety, and Facilities management to drive overall success and performance of the area and clinical pipeline. That's about the role. Then "Key Responsibilities" list bullet points. Then "Education Minimum Requirements: High School Diploma/GED or higher" Then "Required Experience And Skills Minimum of 2 years of relevant GMP Pharmaceutical experience. Demonstrated written and verbal communication skills. Proficiency in computer systems and applications including but not limited to: Microsoft Office (Word, Excel and Outlook), Equipment HMI use, SAP, Calibration/Maintenance Database Systems. Must be willing and able to lift 50 lbs, bend, stoop, squat, crawl, twist, climb ladders, and don & wear cleanroom protective gowning including respirators. Demonstrated ability to work and communicate both independently and as part of a team. Flexibility working overtime is a requirement in manufacturing." Then "Preferred Experience And Skills At least 2 years GMP manufacturing/processing experience. Familiarity with regulatory requirements and Good Documentation Practices (GDP). Experience with some of the following: highly complex and state of the art equipment, isolators, containment technology, aseptic filling using automated machinery, sterile manufacturing, visual inspection of product in glass vials, SAP or other ERP systems. Associates Degree in science or related field. BioWork Certificate (working in an FDA or similar regulated industry). Experience with automated systems (MES, SAP, or similar). Demonstrated troubleshooting / problem-solving skills." Then "#MSJR #eligibleforERP VETJOBS FLEx2026 Sterile2026 #PSCS" (ignore as metadata maybe not needed) Then "The salary range for this role is: $55,900 - $88,100 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. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. 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." Then "Required Skills Corrective Action Management, Equipment Maintenance, Good Manufacturing Practices (GMP), Manufacturing Operations, Procedure Adherence, Process Improvements, Regulatory Compliance, Safety Practices, Standards Compliance, Sterilizing Equipment Preferred Skills Aseptics, Cleaning, GMP Guidelines" Then "Current Employees apply HERE Current Contingent Workers apply HERE US And Puerto Rico Residents Only Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process." Then "Requirements As an Equal Employment Opportunity Employer..." (EEO boilerplate, remove) Then many more boilerplate lines: "As a federal contractor..." etc. Remove. Then "Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities...." Remove. Then "Employee Status Regular Relocation: Domestic VISA Sponsorship No Travel Requirements 10% Flexible Work Arrangements Not Applicable Shift 1st - Day Valid Driving License No Hazardous Material(s) n/a Job Posting End Date 10/12/2026 A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R419669" Remove. Thus we need sections: - About the role: combine the introductory paragraph(s) before "Key Responsibilities". Possibly also include the sentence about positions based in Rahway, NJ and 100% on-site. - Responsibilities: list from "Key Responsibilities" bullet points. - Requirements: maybe combine Education Minimum Requirements and Required Experience And Skills? The spec says use headings: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide what goes where. We have Education Minimum Requirements (High School Diploma/GED or higher) - could go under Requirements or Qualifications. Usually Requirements = mandatory qualifications. Qualifications = preferred? But we can follow typical: Requirements = mandatory (education, experience). Qualifications = preferred (associates degree, BioWork, etc). Skills = required skills list and preferred skills list. We have Required Experience And Skills (mandatory) and Preferred Experience And Skills (preferred). Also there is a separate "Required Skills" and "Preferred Skills" list later. We need to avoid duplication. We should consolidate. Let's extract: Mandatory: - Education: High School Diploma/GED or higher. - Experience: Minimum of 2 years of relevant GMP Pharmaceutical experience. - Skills: Demonstrated written and verbal communication skills. - Proficiency in computer systems and applications including but not limited to: Microsoft Office (Word, Excel and Outlook), Equipment HMI use, SAP, Calibration/Maintenance Database Systems. - Must be willing and able to lift 50 lbs, bend, stoop, squat, crawl, twist, climb ladders, and don & wear cleanroom protective gowning including respirators. - Demonstrated ability to work and communicate both independently and as part of a team. - Flexibility working overtime is a requirement in manufacturing. Preferred: - At least 2 years GMP manufacturing/processing experience (similar to mandatory? maybe redundant) - Familiarity with regulatory requirements and Good Documentation Practices (GDP). - Experience with some of the following: highly complex and state of the art equipment, isolators, containment technology, aseptic filling using automated machinery, sterile manufacturing, visual inspection of product in glass vials, SAP or other ERP systems. - Associates Degree in science or related field. - BioWork Certificate (working in an FDA or similar regulated industry). - Experience with automated systems (MES, SAP, or similar). - Demonstrated troubleshooting / problem-solving skills. Also there is a separate "Required Skills" list: Corrective Action Management, Equipment Maintenance, Good Manufacturing Practices (GMP), Manufacturing Operations, Procedure Adherence, Process Improvements, Regulatory Compliance, Safety Practices, Standards Compliance, Sterilizing Equipment And "Preferred Skills": Aseptics, Cleaning, GMP Guidelines We need to include Skills section: maybe combine required skills and preferred skills. We also have Benefits: 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. Pay: salary range $55,900 - $88,100, plus eligibility for annual bonus and long-term incentive. Schedule: Positions are based in Rahway, NJ and 100% on-site. Also maybe shift: Shift 1st - Day (but that's in boilerplate; we might include if it's substantive). The posting says "Positions are based in Rahway, NJ and 100% on-site." Also earlier: "Shift 1st - Day" appears in the metadata at end; we could include schedule: Day shift, 100% on-site. We should not include boilerplate like "Relocation: Domestic VISA Sponsorship No Travel Requirements 10% Flexible Work Arrangements Not Applicable". We'll keep only substantive schedule info: based in Rahway, NJ, 100% on-site, day shift. Now construct HTML. We need headings

for each section. Inside sections, use

for prose,

• for lists. We must not repeat job title as heading. We must not include Job ID etc. We must preserve all substantive info; do not invent or summarize away detail. We need to ensure we don't omit any substantive info. Let's list all substantive info we identified: About the role: - POCS – Rahway: Technician, Operations Level: O2 Job Family: Manuf/Operations Technician, Operations Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. - Positions will support development and clinical manufacturing and supply, as part of the FLEx-Sterile team, specifically in Manufacturing Shared Services which supports sterile supply, aseptic formulation and visual inspection. - This position will be responsible for hands-on processing activities that include equipment assembly and disassembly, sterile processing, inventory management, open aseptic formulation in an isolator and closed formulation activities in a Grade C environment, and manual visual inspection of filled units (i.e. vials or syringes). - These individuals are expected to partner with and support formulation development colleagues in further understanding and knowledge capture of processes, which could include providing feedback on product and process development. - These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation, proficiency in electronic systems, and participation in continuous improvement projects. - Positions may also support commissioning, qualification, and demonstration of new equipment and technologies. - Successful candidates will collaborate closely with team members and partner groups including formulators, engineers, Quality, Safety, and Facilities management to drive overall success and performance of the area and clinical pipeline. - Positions are based in Rahway, NJ and 100% on-site. (maybe include here or schedule) Responsibilities (Key Responsibilities): - Assembly: Able to read, understand, and follow drawings to assemble sterile equipment to utilize in clinical development and manufacturing processes. - Sterilization Processes: Operate and maintain cleaning and sterilization equipment, including parts washers, dry heat ovens, and autoclaves. - Supply Management: Receive, inspect, and store sterile supplies and equipment, ensuring proper inventory levels and organization within the sterile supply area. - Sterile Formulation: Prepare and formulate sterile products according to established protocols and batch records, ensuring accuracy and compliance with GMP standards. Able to perform closed formulation activities as well as open aseptic activities inside a Grade A isolator. Experience with operating isolator machines and/or Grade A aseptic experience is required. - Visual Inspection: Perform visual inspections of products and components to identify defects