Quality Assurance Engineer Job Vacancies in Vapi

Designation:- Quality Assurance Engineer (ISO Documention)Qualification:- Degree/Diploma In Mechanical Engineering/B.Com/Any Graduate Experience:- 3 Years To 5 Year Experience In Production & Quality (ISO Documention)Salary:- As Per InterviewGender:- Male Vacancy:- 01Job Location:- Umbergaon, Gujarat Industry:- Manufacturing Company

Prepare, review, and maintain SOPs (Standard Operating Procedures), validation protocols, batch records, and other quality documents.Ensure compliance with cGMP, FDA, MHRA, WHO, and other regulatory guidelines.Conduct document control activities, including version control, issuance, retrieval, and archiving.Support internal and external audits by providing required documentation.Assist in equipment qualification (IQ, OQ, PQ) and validation processes.Coordinate with the QA/QC team to implement corrective and preventive actions (CAPA).Maintain training records for personnel involved in quality and compliance functions.Monitor and update quality documentation systems to enhance efficiency.

qa Engineer

Job Description:1) Closely communicate with the Inspection Coordinators to schedule the inspection assigned.2) Implement inspection according to operation guidelines, inspection guidelines, and any special instructions provided by the company.3) Complete the inspection report with photos and submit it to Technical Manager within the required time limit.4) Submit the inspectors job expense claim form and reimbursement documents monthly and meet financial requirements.5) Perform other duties and responsibilities as assigned by supervisor/management.Requirements:- College graduate or above.- Major in Engineering (Textile, Furniture, Mechanical, Electronic, etc.)- Having more than 1 year more working experience in the inspection field or quality control background of products of Softlinesor Hardlines.- Familiar with the AQL standard and good knowledge of safety and regulation standards.- Good command of written & oral English.- Ideal person is a well-organized team player, able to solve on-site problems independently, and with good interpersonal skills.- Integrity and honesty.- Willing to travel frequently.- Healthy body without color blindness and sight weakness.Job Types: Full-time, ContractContract length: 36 months

Qualification & Experience :-i) B.Tech / B.E. / M.Sc. / B. Pharm in Mechanical Engineering, Biotechnology, Pharmacy, or related field.ii) Experience: Minimum 5-6 years in a pharmaceutical equipment manufacturing company.iii) Strong knowledge of GMP, ISO 9001, 13485, and regulatory guidelines.Experience in QA, QC, and documentation control processes.iv) Proficiency in MS Office, ERP software, and document control systems.Excellent communication, analytical, and problem-solving skills.Gender:- Male Key Responsibilities:- i) Develop, implement, and maintain quality management systems (QMS).ii) Ensure GMP, ISO, and FDA compliance in all manufacturing processes.iii) Conduct internal audits and supplier audits for quality compliance.iv) Manage customer complaints and coordinate Corrective and Preventive Actions (CAPA).v) Work with cross-functional teams to improve quality standards and processes.

Qualification:- BSc Or M.Sc In Microbiology Experience:- 2Years To 3 Years Salary:- As Per Interview Job Responsibilities:- i) Day to day QC department activity - Micro and Chemical testing, physical inspection of products, records maintaining etcii) Preparing, Maintaining and taking care of QA / QC documents of all kinds including certificates, calibration, test results, inspection reports, non-compliance reports etc.iii) Document work on computer like SOPS, formats etc.iv) Handling and working on all instruments related QCv) Cary out inspection and checking for all quality related procedures---------------------------------------------Job Location:- Umbergaon, Gujarat