Pharmaceutical Quality Assurance Unidos Technology
Unidos Technology
Office Location
Full Time
Experience: 3 - 3 years required
Pay:
Salary Information not included
Type: Full Time
Location: All India
Skills: Quality Assurance, Quality systems, Risk analysis, Conflict Management, Customer care, Interpersonal Skills, leadership skills, regulatory requirements, Auditing, HPCL, Quality Oversight, UV Spectrophotometry, KFR, Documentation Review, GMP Compliance
About Unidos Technology
Job Description
We are searching for a candidate to join our team in the Pharmaceutical Industry, specifically in Production or Quality Assurance. About the role: As a specialist in quality assurance, you will need to have a deep understanding of quality systems, risk analysis, conflict management, and customer care. Your problem-solving skills, interpersonal abilities, and demonstrated leadership qualities will be crucial in establishing effective relationships with both internal and external stakeholders. Responsibilities: - You will be responsible for ensuring that regulatory and quality requirements are met when outsourcing, with a focus on quality oversight and conducting audits. - Regular oversight checks will be required through audits or the review of key performance indicators. - Willingness to travel frequently within South India. - Experience in operating in-process quality control equipment. - Proficiency in preparing quality management SOPs. - Hands-on knowledge of quality control techniques such as UV Spectrophotometry, HPCL, KFR, etc. - Expertise in quality assurance aspects and reviewing documentation. - Strong understanding of regulatory requirements and staying updated on CDSCO and FSSAI regulations. - Serving as an internal/external point of contact for inquiries regarding product compliance and quality. - Contributing actively to the development of the Pharmaceutical Quality System (PQS) by identifying and addressing deficiencies. - Assisting in the compilation and review of Product Quality Reviews/Annual Product Reviews. - Monitoring and ensuring GMP compliance and the quality of contract-manufactured pharmaceutical products. - Additional responsibilities related to GMP compliance and quality assurance of manufactured pharmaceutical products may also be assigned. - This role may require occasional coverage beyond regular working hours and infrequent travel. Job Types: Full-time, Permanent Schedule: Day shift Education: Bachelor's (Preferred) Experience: Total work experience of 3 years (Preferred) Work Location: In person,