Quality Assistant

Role & responsibilitiesTo ensure that all incoming, in-process, and finished products meet quality standards and specifications through regular inspection, testing, and documentation.Preferred candidate profile* Conduct visual and dimensional inspection of raw materials, in- process, and finished goods.Verify product quality against drawings, specifications,...

Interested candidates can share their CV on with subject line- "Applying for Assistant Manager HR & Admin - Manufacturing".Role & responsibilitiesA. Contractual ManpowerManpower Supply and OnboardingResponsible to ensure labour supply to all divisions as per BOM without any deviation.Ensures induction in job role, safety, policies etc. of all before they...

 Researching and comparing: Researching and comparing suppliers, goods, andservices to select the most suitable ones Requesting cost proposals: Requesting cost proposals and negotiating contractsand prices Building relationships: Building and maintaining professional relationships withsuppliers Negotiating: Negotiating pricing, terms, and...

Job Description:  Job Role & Duties: 30/04/24 HPS/2024/271Fabrication ManagerMale110 to 15Any GraduationManaging production / project execution activities efficiently.Assigning work to subordinates (workers) and reporting daily output to MDMaintaining & improving quality of production.Tracking & continuous improvement in process time, suggesting ideas for...

Title: Senior Officer - Quality ControlDate: Sep 25, 2025Location: Dadra - Quality ControlCompany: Sun Pharmaceutical Industries LtdJob Summary:The QC Analyst is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with USFDA regulations, cGMP standards, and internal...

**Job Purpose**:Quality assistants are responsible for ensuring that products in production meet the safety and specification standards necessary for them to be forwarded to the last production stage. **Role**: Quality Assistants complete duties assigned by quality managers, such as handling customer complaints, training new staff, implementing quality...

Job SummaryThe QC Analyst is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with USFDA regulations, cGMP standards, and internal specifications. This role is critical in maintaining product quality, safety, and efficacy.Key ResponsibilitiesAnalytical...

Title: Executive - Engineering ProjectsDate: Oct 28, 2025Location: Dadra 1 - Engineering Block ACompany: Sun Pharmaceutical Industries LtdTo execute engineering projects related to facility upgrades, equipment installation, and compliance enhancements in alignment with cGMP and USFDA standards.Key Responsibilities:Project Execution & Management:Assist in...

Period of engagementEngagement shall be for 5 years from the date of appointment which may extend up to 7 yearsEducational qualificationsi. Graduate in any disciplineii. Retired Officers, Junior Commissioned Officers, or equivalent from Indian Army/ Indian Airforce/ Indian Navy/ Central Armed Police Forces (CAPF)/ Law Enforcement Agencies equivalent to Level...

Job Description:The job role of an environmental engineer involves the following duties:Carrying out site assessmentsConducting technical auditsEvaluating environmental impactMaking recommendations on clean-up, reclamation and waste management activitiesAssessing how a site complies with environmental regulationsUsing mathematical techniques and computer...