{"schemaVersion":"jobsearcher.job.v1","id":"fd5cb2aabbf4d3aafaf3cc64","url":"https://jobsearcher.com/jobs/fd5cb2aabbf4d3aafaf3cc64","canonicalUrl":"https://jobsearcher.com/jobs/fd5cb2aabbf4d3aafaf3cc64","title":"Mechanical Supervisor","description":"NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.\n\nJob Title : Project Lead - Mechanical (Supervisor)\n\nFLSA Classification : Professional, Exempt\n\nWork Location : Fall River, MA\n\nWork Hours : General: 8:30am - 5:00pm (may vary based on business needs)\n\nReports To : Site Engineering Manager\n\nSalary Range : $76,000- $103,000\n\nDuties and Responsibilities\n\nDesign, review and approve protocols for equipment and processes to produce pharmaceutical drug products meeting internal, external and regulatory guidelines.\n\nMaintain facility as per cGMP and regulatory requirement. Introduce new SOP's, equipment and instruments to improve the work environment by safety and quality point of view by working closely with Quality Assurance team.\n\nCompile and maintain records of validation documentation and electrical schematics, installed equipment, installation or operational problems, corrective, and preventive actions.\n\nReview the Design, Installation, Operational and Product qualification of operations machinery.\n\nProject planning, design, monitoring and project execution. Co‑ordination with project contractor for procurement and installation for projects work.\n\nPreparation of revised Layouts whenever modification system is done for plant or facility.\n\nModification / Changes of machine/process of facility as per requirement.\n\nTo raise the change controls, whenever required changes are to be made to facilities and equipment.\n\nCo‑ordinate with other departments such as Mechanical, Site Services, Quality Assurance, Production etc. for various day‑to‑day activities.\n\nLead mechanical engineering projects from concept through completion, including planning, execution, and close‑out.\n\nDevelop and manage detailed project plans, schedules, budgets, and resource allocations.\n\nTrack project milestones and deliverables, ensuring timely and cost‑effective execution.\n\nProvide technical expertise for mechanical equipment selection, installation, and optimization.\n\nOversee HVAC, cleanroom systems, compressed air, chilled water, steam, and other utility systems.\n\nEnsure mechanical designs and installations comply with cGMP, FDA, and other regulatory standards.\n\nCoordinate validation activities for mechanical systems including IQ/OQ/PQ documentation and execution.\n\nCollaborate with Validation and Quality teams to ensure mechanical systems meet performance and compliance requirements.\n\nSupport change control and risk assessments related to mechanical installations.\n\nPrepare and maintain documentation to support internal and external audits.\n\nEnsure mechanical engineering activities align with quality and regulatory requirements.\n\nCollaborate with Quality teams to address audit findings and implement corrective actions.\n\nWork with Finance and Procurement teams to manage project budgets and capital expenditures.\n\nReview and approve vendor quotes, purchase orders, and invoices.\n\nMonitor financial performance and report variances to management.\n\nPrepare and submit Capital Expenditure (CapEx) requests with detailed scope, and justification.\n\nTrack approval status and ensure alignment with corporate financial planning.\n\nSupport CapEx forecasting and reporting for mechanical engineering initiatives.\n\nEnsure accurate and timely data entry and reporting within SAP modules relevant to mechanical engineering and finance.\n\nPartner with Manufacturing, Quality Assurance, Validation, Regulatory Affairs, and external vendors.\n\nFacilitate effective communication and coordination across departments.\n\nIdentify potential risks and implement mitigation strategies.\n\nEnsure mechanical projects meet quality, safety, and environmental standards.\n\nImplementation of various projects pre‑requirement.\n\nTo maintain the safety norms as per the Health Safety & Environment guidelines.\n\nTo monitor project activity for the in Unit IV, Scheduling, monitoring and keeping track on CAPEX project activities. Detailing with respect to design, manufacture of tooling and methods, supervision of large onsite project.\n\nWork closely with external electrical/instrumentation service agencies on upgrading existing systems and troubleshoot errors and breakdowns.\n\nEnsure all process improvement projects are completed on time and within budget. Diagnose, test and analyze the performance of electrical components, assemblies, or systems.\n\nTroubleshoot the existing systems for any issues which hampers the operations in any manner.\n\nEnsure that the plant is maintained at all Time for audit readiness.\n\nPerform any other Job or responsibilities assigned by the reporting manager.\n\nAny other job allocated by Department Head.\n\nEducation and Experience\n\nBachelor's degree in Engineering (Mechanical, Electrical, or related field); Master's preferred.\n\nMinimum 5 years of experience in pharmaceutical or biotech engineering and validation project management.\n\nStrong knowledge of sterile manufacturing processes (vials, PFS, IV bags).\n\nExperience with validation lifecycle documentation and execution.\n\nFamiliarity with project management tools (e.g., MS Project, Primavera).\n\nExperience with SAP systems for engineering and financial operations.\n\nPMP certification is a plus.\n\nExperience with audit preparation, financial oversight, and CapEx processes.\n\nExcellent communication, leadership, and problem‑solving skills.\n\nWorking Conditions\nThis role works in a cGMP office environment. However, this role will frequently be present in a laboratory and manufacturing environment, where personal protective equipment may be required, which may include uniforms, lab coats, safety glasses, respiratory protection, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility may be required.\n\nPhysical Requirements\n\nUnassisted lifting up-to 10 kg, may be required\n\nStanding/walking for 80% or greater than an 8‑hour period.\n\nUsage of appropriate personal protective equipment when required\n\nEEO Statement\nCipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.\n\n#J-18808-Ljbffr","company":"Merck","rawCompany":"merck","city":"Fall River","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-06-20T05:07:06.400Z","occupations":[{"code":"17-2141.00","title":"Mechanical Engineers","slug":"mechanical-engineers"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"},{"code":"17-3027.00","title":"Mechanical Engineering Technologists and Technicians","slug":"mechanical-engineering-technologists-and-technicians"}],"industries":[{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"},{"code":"333993","title":"Packaging Machinery Manufacturing","slug":"packaging-machinery-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Mechanical Supervisor","description":"NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.\n\nJob Title : Project Lead - Mechanical (Supervisor)\n\nFLSA Classification : Professional, Exempt\n\nWork Location : Fall River, MA\n\nWork Hours : General: 8:30am - 5:00pm (may vary based on business needs)\n\nReports To : Site Engineering Manager\n\nSalary Range : $76,000- $103,000\n\nDuties and Responsibilities\n\nDesign, review and approve protocols for equipment and processes to produce pharmaceutical drug products meeting internal, external and regulatory guidelines.\n\nMaintain facility as per cGMP and regulatory requirement. Introduce new SOP's, equipment and instruments to improve the work environment by safety and quality point of view by working closely with Quality Assurance team.\n\nCompile and maintain records of validation documentation and electrical schematics, installed equipment, installation or operational problems, corrective, and preventive actions.\n\nReview the Design, Installation, Operational and Product qualification of operations machinery.\n\nProject planning, design, monitoring and project execution. Co‑ordination with project contractor for procurement and installation for projects work.\n\nPreparation of revised Layouts whenever modification system is done for plant or facility.\n\nModification / Changes of machine/process of facility as per requirement.\n\nTo raise the change controls, whenever required changes are to be made to facilities and equipment.\n\nCo‑ordinate with other departments such as Mechanical, Site Services, Quality Assurance, Production etc. for various day‑to‑day activities.\n\nLead mechanical engineering projects from concept through completion, including planning, execution, and close‑out.\n\nDevelop and manage detailed project plans, schedules, budgets, and resource allocations.\n\nTrack project milestones and deliverables, ensuring timely and cost‑effective execution.\n\nProvide technical expertise for mechanical equipment selection, installation, and optimization.\n\nOversee HVAC, cleanroom systems, compressed air, chilled water, steam, and other utility systems.\n\nEnsure mechanical designs and installations comply with cGMP, FDA, and other regulatory standards.\n\nCoordinate validation activities for mechanical systems including IQ/OQ/PQ documentation and execution.\n\nCollaborate with Validation and Quality teams to ensure mechanical systems meet performance and compliance requirements.\n\nSupport change control and risk assessments related to mechanical installations.\n\nPrepare and maintain documentation to support internal and external audits.\n\nEnsure mechanical engineering activities align with quality and regulatory requirements.\n\nCollaborate with Quality teams to address audit findings and implement corrective actions.\n\nWork with Finance and Procurement teams to manage project budgets and capital expenditures.\n\nReview and approve vendor quotes, purchase orders, and invoices.\n\nMonitor financial performance and report variances to management.\n\nPrepare and submit Capital Expenditure (CapEx) requests with detailed scope, and justification.\n\nTrack approval status and ensure alignment with corporate financial planning.\n\nSupport CapEx forecasting and reporting for mechanical engineering initiatives.\n\nEnsure accurate and timely data entry and reporting within SAP modules relevant to mechanical engineering and finance.\n\nPartner with Manufacturing, Quality Assurance, Validation, Regulatory Affairs, and external vendors.\n\nFacilitate effective communication and coordination across departments.\n\nIdentify potential risks and implement mitigation strategies.\n\nEnsure mechanical projects meet quality, safety, and environmental standards.\n\nImplementation of various projects pre‑requirement.\n\nTo maintain the safety norms as per the Health Safety & Environment guidelines.\n\nTo monitor project activity for the in Unit IV, Scheduling, monitoring and keeping track on CAPEX project activities. Detailing with respect to design, manufacture of tooling and methods, supervision of large onsite project.\n\nWork closely with external electrical/instrumentation service agencies on upgrading existing systems and troubleshoot errors and breakdowns.\n\nEnsure all process improvement projects are completed on time and within budget. Diagnose, test and analyze the performance of electrical components, assemblies, or systems.\n\nTroubleshoot the existing systems for any issues which hampers the operations in any manner.\n\nEnsure that the plant is maintained at all Time for audit readiness.\n\nPerform any other Job or responsibilities assigned by the reporting manager.\n\nAny other job allocated by Department Head.\n\nEducation and Experience\n\nBachelor's degree in Engineering (Mechanical, Electrical, or related field); Master's preferred.\n\nMinimum 5 years of experience in pharmaceutical or biotech engineering and validation project management.\n\nStrong knowledge of sterile manufacturing processes (vials, PFS, IV bags).\n\nExperience with validation lifecycle documentation and execution.\n\nFamiliarity with project management tools (e.g., MS Project, Primavera).\n\nExperience with SAP systems for engineering and financial operations.\n\nPMP certification is a plus.\n\nExperience with audit preparation, financial oversight, and CapEx processes.\n\nExcellent communication, leadership, and problem‑solving skills.\n\nWorking Conditions\nThis role works in a cGMP office environment. However, this role will frequently be present in a laboratory and manufacturing environment, where personal protective equipment may be required, which may include uniforms, lab coats, safety glasses, respiratory protection, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility may be required.\n\nPhysical Requirements\n\nUnassisted lifting up-to 10 kg, may be required\n\nStanding/walking for 80% or greater than an 8‑hour period.\n\nUsage of appropriate personal protective equipment when required\n\nEEO Statement\nCipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.\n\n#J-18808-Ljbffr","datePosted":"2026-06-20T05:07:06.400Z","dateModified":"2026-06-20T05:07:06.400Z","hiringOrganization":{"@type":"Organization","name":"Merck","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Fall River","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"fd5cb2aabbf4d3aafaf3cc64"},"url":"https://jobsearcher.com/jobs/fd5cb2aabbf4d3aafaf3cc64"}}