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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
- ...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...SuggestedFull time
- ...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....SuggestedFlexible hours
- ...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...Suggested
- ...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...Suggested
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....Suggested- ...compliance with USFDA, 21 CFR Part 11, EU‑GMP, and GAMP‑5 guidelines. The role ensures data integrity, regulatory compliance, and lifecycle management of computerized systems used in OSD manufacturing operations. Key Responsibilities Computer System Validation (CSV) Plan and...Suggested
- ...Position -: Manager Production Planning & Scheduling Job Accountabilities - Review production and consumption variance & identify improvement opportunities / actions Ensure model updation in APO based on the deviation between predicted vs. actual performance. Finalise...Suggested
- ...Job Title Manager 1 – Production Business Unit Sun Global Operations Job Grade G10 Location : Dadra At Sun Pharma, we commit to helping you 'Create your own sunshine'— by fostering an environment where you grow at every step, take charge of your journey...SuggestedShift work
- ...rotating equipment. Monitoring and ensuring equipment health through effective protective functions. Review and advice change management (alarms & trips) with proper risk analysis keeping business objectives in mind. Provide planning and scheduling estimate for rotating...Suggested
- ...Job Title - Associate Manager Production, PE City, Country - Daman, India At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work to not only benefit our People, Customers & Communities...Suggested
- ...Key Responsibilities Oversee accounting operations, bank reconciliations, and GOP transfers Manage cash flow planning and monitoring Support MIS preparation and financial reporting Handle TDS, GST (GSTR-1, GSTR-3B) and statutory compliance Coordinate with CA...Suggested
- Job Title: Showroom Sales Executive – Marble Division Location: Silvassa Job Summary: We are seeking a dynamic and result-oriented Showroom Sales Executive for our Marble Division in Silvassa. The ideal candidate should have prior experience in marble, granite, or...Suggested
- ...microbiology instruments. Investigation of OOT, OOS results. Ensure compliance with GLP and regulatory requirements. 4. QMS (Quality Management System) Experience: 4–8 Years Qualification: B.Pharm / M.Pharm / M.Sc Key Responsibilities: Handle deviation, CAPA, change...SuggestedFull time
- Job Description: Job Description: Regulatory & Compliance Manager 1. Position Description Job title Regulatory & Compliance Manager Department QA Reports to Vice President-R&D Direct Reports - Location Daman 2. Job Purpose Job Statement...SuggestedFull timeSide jobLocal area
Rs 80 per hour
...be based on the India 1 and India 2 markets and specific geographies assigned Responsibilities - Account & Partner Relationship Management . Onboard new accounts by explaining the requirements to the partners and coordinating with internal stakeholders . Meet the...Work at officeLocal areaFlexible hoursRs 4.5 - 8 lakhs p.a.
...JSA, risk assessments, and PSM practices. Promote continuous improvement culture using structured frameworks. Project & CAPEX Management Lead CAPEX projects to enhance productivity, quality, and cost efficiency. Manage installation, commissioning, and validation...- ...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...Full 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,...Full 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...Long term contract
- ...program (GROW Youth) and strive to make the center a model of excellence for the industry. S/he will seek support from the Regional Manager and other functions and take personal responsibility for achieving specific measurable outcomes and track results. Responsibilities...TraineeshipLocal areaShift work
- ...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...Immediate start
- ...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
- ...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
- ...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
- ...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...
- ...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...Full timeLocal area
- ...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,...Full timeContract work
- ...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
- ...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,...
