QA Officer

Position :- Sr. Officer / ExecutiveDepartment :- QA - Qualification & ValidationJob Location :- Ranu, VadodaraExperience:- 3-8 years, Regulated MARKET industry.Role & responsibilitiesPreparation of Validation Master Plan.Responsibility for initiation, review and co-ordination for QMS documents such as Change Control, Deviation, CAPA etc.Preparation and...

Job DescriptionLine clearance in dispensing and production area.To perform in-process sampling, testing and document the observations.To handle IPQA activity in warehouse and production area.Review of BMR, process documents etc.APR Preparation.To ensure timely validation of production equipment w.r.t. process, cleaning and to collect samples for cleaning...

About UsStar Plast Industries Pvt. Ltd.brings over 41 years of excellence and expertise in the field of plastic manufacturing. As a pioneer in producingDMF-grade primary packaging solutions for the pharmaceutical industry, the company is also a trusted manufacturer ofprecision plastic componentsserving diverse sectors such asElectronics, Automotive, Textile,...

Job Description:Key Responsibilities:Procurement of Raw Materials (APIs, excipients) and Packaging Materials (primary & secondary) as per production requirements.Vendor development, evaluation, and management to ensure quality and cost efficiency.Floating RFQs, price negotiations, and finalization of purchase orders.Coordination with QA, QC, production, and...

CTC 7.5LPANotice period daysthis is work from office - Vadodara• years of hands-on experience in quality assurance, with a strong focus on test automation (including back-end, front-end UI, and regression testing).• Minimum bachelor's degree in computer science or equivalent education/work experience.• Experience with performance and load testing tools...

URGENT OPENING FOR REGULATORY AFFAIRS OFFICER/ SR OFFICER LOCATION VADODARA Position:-Regulatory Affairs Officer/ Sr OfficerLocation:-VadodaraExperience:-1 to 3 Yrs (Formulation)Qualification :- B.Pharm/ M.Pharm Required Candidate profilePreparing dossiers as per country-specific guidelines.Compiling and reviewing documents.Coordinating with QA for...

Job Description:Job Description – Key Responsibilities: Support formulation development activities for regulated and semi-regulated markets, ensuring alignment with project timelines and quality standards Conduct pre-formulation, API-excipient compatibility studies, and stability testing to evaluate formulation feasibility Assist in scale-up and technology...

Job Description:Job Description:  Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations.? Preparation, Compilation & Review of Registration documents that include Administrative & Technical.? Reviewing the technical documents provided by QA, QC, Production providing them...

Job Description:Duties and Responsibilities :Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategyTimely compile materials for license renewals, updates and registrationsMaintain regulatory files/database and chronologies in good order....

Graduate Mechanical Engineer with 5 to 10 years of experience in, Quality Assurance & Control preferably in Super Critical Thermal Power projects.Familiarity with structural components, bought out items, pressure parts viz. pipes, tubes, fittings, forgings etc. Further, deep knowledge of various NDT methods, welding processes, RCA/why-why analysis is...