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- ...Design concept and cycle time study. Preparing ROI calculations, manpower and process study for new automation developments. · Manage automation budgets, timelines, and vendor coordination. Define project budget and timeline Monitoring project budget and deadlines...SuggestedWorldwide
all time plastics limited
Daman5 days ago - ...Experience: Typically 8–15 years 1. Job Purpose The QC Manager is responsible for overseeing all quality control activities related to raw materials, in-process materials, and finished medical devices to ensure compliance with regulatory standards, GMP, and internal...SuggestedFull time
- ...regulatory records, licenses, registrations, and submission trackers in an organized manner. • Ensure compliance with internal quality management systems and applicable standards. Requirements • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology,...SuggestedFull time
- ...Job Title: Sr. Educational Manager – Medical & Clinical Education Department: Meril Academy Global – Medical Education Location: Vapi Reports To: GM – Meril Academy Global Job Purpose: To design, deliver, and manage scientifically robust, specialty...SuggestedLong term contract
MERIL
Vapi4 days ago - ...We are seeking a results-driven Sales Manager to lead, mentor, and scale our sales team. The ideal candidate has a proven track record of achieving revenue targets, building client relationships, and creating structured sales strategies. This role requires strong leadership...SuggestedFull time
- ...Information Technology Executive, located in vapi Gujrat. The responsibilities include providing technical support, troubleshooting IT issues, managing network systems, and overseeing daily IT operations. The Information Technology Executive will be tasked with maintaining...SuggestedFull time
DEVANG PAPER MILLS PRIVATE LIMITED
Vapi22 days ago - ...Job Summary: The Product Registration Specialist for Global Markets is responsible for overseeing and managing the regulatory submission and product registration process for medical devices in non-EU and non-US regions. This includes countries such as Canada, China, Japan...SuggestedLocal area
MERIL
Vapi4 days ago Rs 4 - 7 lakhs p.a.
...process wastage. Ensure product quality in coordination with QA/QC teams. Supervise production operators, technicians, and helpers; manage shift handovers and manpower allocation. Maintain production records, reports, and MIS. Support continuous improvement...SuggestedShift workPeople Alliance Workforce
Vapia month ago- ...new prevention measures Report on health and safety awareness, issues and statistics About You Proven experience as safety manager Should have completed at least 1-2 Projects of Solar Glass manufacturing/ Institutional/ Pharma/ power/chemical/ industrial end to...SuggestedFlexible hours
Cushman & Wakefield
Valsad4 days ago - ...Job Purpose: Managing timely commission of Green Field Project & manufacturing of Pharma Intermediates & API’s Products, its operations, production/ productivity ensuring quality & regulatory affairs. Key Responsibilities # Managing plant of operations of Pharma Intermediates...SuggestedFor contractors
jay finechem private limited
Vapi8 days ago - ...This is a full-time on-site role located in Valsad for a Senior Production Executive. The Senior Production Executive will oversee and manage production activities, including planning, monitoring, and ensuring efficient production processes. The role entails implementing...SuggestedFull time
Atul
Valsad5 days ago - Gelatin Production Executive Start Date Starts Immediately CTC (ANNUAL) Competitive salary Competitive salary Experience...SuggestedImmediate start
- ...under Geo-expansion ~Work on delivering critical business projects as assigned from time to time. ~Provide relevant data points for Management reporting Required Qualifications And Experience ~Graduate/ Post Graduate ~With relevant experience of 1-2 prior work...Suggested
Bajaj Finserv
Valsad4 days ago - ...and training. Coordinate with external testing facilities or CROs (Contract Research Organizations). 4. Data Integrity & Risk Management Monitor study execution to ensure accurate data collection and analysis. Evaluate biological responses, device performance,...SuggestedContract work
MERIL
Pardi4 days ago - ...Job Title: Clinical Executive Department: Meril Academy Global – Clinical Affairs Location: India Reports To: Manager / Senior Manager – Clinical Affairs / Meril Academy Global Job Purpose: To support and execute clinical studies, trials, and observational...Suggested
MERIL
Vapi4 days ago - ...regulatory records, licenses, registrations, and submission trackers in an organized manner. • Ensure compliance with internal quality management systems and applicable standards. Qualifications : Bachelor's or Master's degree in Pharmacy, Life Sciences, Biotechnology,...
MERIL
Vapi4 days ago - ...compliant sales culture across the channel to drive acquisitions, profitability and employee development. Duties And Responsibilities ~Managing and supporting the effective deployment of team of sales professionals with respect to that geographical area, exploring new markets...
Bajaj Finserv
Vapi4 days ago - ...Surgical Robotics. Department: Quality Assurance – Surgical Robotics Division. Location: Vapi, Gujarat. Reports To: Manager / Senior Manager – Quality Assurance. Job Purpose: To support the Quality Assurance system for surgical robotic products by...
Meril
Vapi4 days ago - ...Neonatal Medical Devices) Department: R&D / Quality Assurance Neonatal Division Location: Vapi, Gujarat Reports To: Manager / Senior Manager R&D / QA Neonatal Segment Job Purpose: To prepare, maintain, and control structured technical, regulatory,...Immediate start
- ...to adhere to industry standards and compliance requirements Bachelor's degree in Chemistry, Engineering, or a related field Knowledge of ISO quality management systems and standards is a plus Detail-oriented with excellent problem-solving and organizational skills...Full time
Megaplast India Pvt. Ltd.
Daman20 days ago - ...resources Report current expenditure and utilization of resources Implement contingency plan for fluctuations in demand Assist Manager for preparation of daily & monthly MIS. Prepare updated database on vendor, pricing, and manufacturer information....Flexible hours
DIAGEO India
Daman4 days ago - ...also for Manufacturing System software's like Archival / backup, restoration, validation & qualification etc. Responsibilities Manage and perform Quality Management System like Change Control/Deviation etc. To maintain software related data of Laboratory Instrument...
SUN PHARMA
Daman4 days ago - ...boost morale, culture, and belonging Onboarding & Induction – Deliver smooth and impactful new-joiner experiences Performance Management (PMS) – Enable a high-performance culture with structured systems HR Audits & Compliance – Ensure statutory and policy compliance...Full time
Unitile
Valsad5 days ago - ...Key Responsibilities 1. Shift Monitoring: ○ Oversee and manage the entire production process during the assigned shift. ○ Ensure smooth plant operations and coordinate with different teams (maintenance, quality, and logistics). 2. DCS Operation: ○ Operate and monitor...Shift work
jay finechem private limited
Vapi8 days ago - ...Systems (X-Ray / C-Arm / DR / CT) Department: Quality Assurance – Radiology Division Location: Vapi, Gujarat Reports To: Manager / Senior Manager – Quality Assurance Job Purpose: To ensure product and process compliance in the manufacturing of radiology...
Meril
Vapi4 days ago - ...Job Description :- Study Design & Management : Designing and executing pre clinical studies (animal models, bench testing) to evaluate performance and safety. Regulatory Compliance : Ensuring all studies follow GLP (Good Laboratory Practice) guidelines and generating documentation...Work at office
MERIL
Vapi4 days ago Rs 15.5 - 20 lakhs p.a.
• Manage SAP hypercare support activities post go-live using ServiceNow as the ticketing tool. • Coordinate issue intake, triage, and resolution across functional and technical teams. • Monitor and manage incidents, problems, and escalations to ensure timely resolution....Global Business Ser 4u
Daman29 days ago- ...Job Purpose To oversee and manage day-to-day production activities in the Oral Solid Dosage (OSD) manufacturing area, ensuring compliance with cGMP, USFDA, and other regulatory requirements while meeting production targets. Key Responsibilities Supervise and execute...
SUN PHARMA
Daman4 days ago - Job Description: QA – IPQA (In-Process Quality Assurance) Experience: 4–8 Years Qualification: B.Pharm / M.Pharm / M.Sc Key Responsibilities: Perform in-process checks during manufacturing activities. Line clearance for aseptic filling, compounding, filtration...
- Job Description: QC – Microbiology Experience: 4–8 Years Qualification: M.Sc (Microbiology / Biotechnology) Key Responsibilities: Perform microbiological testing of raw materials, finished products, and water samples. Conduct environmental monitoring (air, surface...
