Fresher Regulatory Affairs Jobs

Position: Research And Development ApprenticeshipEligibility: LGBT Applicants Only + B.Pharm/M.Pharm (2022, 2023 or 2024 pass outs) + Bangalore City candidate***The above 3 parameters in Eligibility will be considered ONLY***Qualification: (2022, 2023 & 2024 Pass Outs) B. Pharm / M. PharmStipend: INR 25,000 per month (in hand)Duration: 12 monthsCTA: Depending on performance maybe be converted into full time resources at the end of the internship periodWork Timing, General Shift: 9AM to 5 PMLocation: Bengaluru OnlyWho Can Apply - LGBT+ (Lesbian, Gay, Bisexual, Transgender+) Pharma Job Seekers who are based in and around Bengaluru only Role Requirements-Good English language skills written and verbal particularly in scientific/medical terminologyAbility to evaluate data and draw conclusions with appropriate guidance from senior team members or managerGood attention to detailGood interpersonal, presentation and communication skillsService-oriented attitude and ability to be a team player and interact effectively with all levels of personnel in an interdisciplinary and matrix environmentComputer proficiency, IT skills, the expertise and ability to work with web-based applicationsGood level of flexibility and ability to prioritize workIf you belong from LGBT Community then please send CVs at pamela@thepridecircle.com

Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy. Timely compile materials for license renewals, updates and registrations. Maintain regulatory files/database and chronologies in good order. Establish and maintain system for tracking changes in documents submitted to agencies or partners. Review labeling and labels for compliance with regulatory requirements Review changes to existing products and SOPs to define the requirements for regulatory submissions Provide the regulatory reviews of customer complaints and define the regulatory re-portability Responsible for timely registration of the facility Maintain current knowledge of FDA and international regulation, guidance and standards applicable to company products Actively participate in evaluation of regulatory compliance of document / product /process /test methods changes Participate in research of regulatory issues and dissemination regulatory information to Production, QA, QC and R&D departments and senior management as required

After 45 days of free training (technical) followed by 15 days (non technical), candidates can be placed in pharma company. During training candidate need to take care of living expenses including food accomodation and local travel.

Studying Scientific and Legal Documentsmaintaining Familiarity with Company Product Rangesoutlining Requirements for Labelling, Storage and Packagingproviding Advice About Regulations to Manufacturers/scientistswriting Comprehensible, User-friendly, Clear Product Information Leaflets and Labelspreparing Documentationcandidate is Qualified with B.pharma & M.pharmaknowledge of Iso13485, Qms & Ce Marking is Must.

We have vacancy for 2 Drug regulatory affairs executive Jobs in Pune for Freshers Educational Qualification : B.Pharma, B.Sc, M.Pharma, M.Sc Skill Drug Regulatory Affairs,pharmacology,quality assurance,Formulations etc.

Hiring for 50 Production Executive Jobs in Chennai for Freshers,Required Educational Qualification is : Secondary School, Diploma with Good knowledge in Time Management,Regulatory etc.

M Pharm candidate Preferably done Internship in Regulatory Affairs Department with any Pharma Company / Chemical,/ Health Care Company.Experience: Minimum 6 months of work experience with Any Pharma Company in Regulatory Affairs Department.

Hiring B-tech( Electrical,Mechanical, Safety ) Fresher

Developing and implementing quality standards.Developing and implementing quality control systems.Monitoring and analyzing quality performance.Inspecting and testing materials, equipment, processes, and products to ensure quality specifications are met.Collaborating with operations managers to develop and implement controls and improvements.Ensuring that workflows, processes, and products comply with safety regulations.Investigating and troubleshooting product or production issues.Developing corrective actions, solutions, and improvements.Reviewing codes, specifications, and processes.

it is vacancy for quality in process engineer it would be able handle the inspector or handling a shift