VI
Quality Assurance Manager
virat infusions private limited · Ujjain · onsite · Posted 50d ago
Not disclosedFresherfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Company Description We are a pharmaceutical manufacturer specializing in both large-volume parenterals (LVPs) and small-volume parenterals (SVPs), including ophthalmic solutions. Our focus is on producing high-quality sterile injectable products that support patient care across a range of clinical settings. Candidates joining our organization will work in an environment that values regulatory compliance, product integrity, and continuous process improvement. Team members collaborate closely across functions to ensure safe, effective, and reliable products reach healthcare providers and patients.
Role Description The Quality Assurance Manager is a full-time, on-site role based in Ujjain. This position is responsible for overseeing day-to-day quality assurance activities, including reviewing and approving batch records, SOPs, and quality documentation, as well as ensuring adherence to GMP and regulatory requirements for LVPs, SVPs, and ophthalmic solutions. The role includes managing quality audits, deviations, CAPAs, change controls, and risk assessments, while collaborating with production, QC, and regulatory teams to resolve issues and improve processes. The Quality Assurance Manager will lead and mentor QA staff, support training on quality systems and standards, monitor key quality metrics, and drive initiatives that strengthen product quality, compliance, and operational efficiency.
Qualifications
Role Description The Quality Assurance Manager is a full-time, on-site role based in Ujjain. This position is responsible for overseeing day-to-day quality assurance activities, including reviewing and approving batch records, SOPs, and quality documentation, as well as ensuring adherence to GMP and regulatory requirements for LVPs, SVPs, and ophthalmic solutions. The role includes managing quality audits, deviations, CAPAs, change controls, and risk assessments, while collaborating with production, QC, and regulatory teams to resolve issues and improve processes. The Quality Assurance Manager will lead and mentor QA staff, support training on quality systems and standards, monitor key quality metrics, and drive initiatives that strengthen product quality, compliance, and operational efficiency.
Qualifications
- Strong knowledge of pharmaceutical quality systems, GMP guidelines, and regulatory requirements for sterile/ parenteral manufacturing.
- Experience managing QA operations, including batch record review, deviation handling, CAPA, change control, and internal/external audits.
- Ability to lead and develop teams, coordinate cross-functional activities, and communicate effectively with technical and non-technical stakeholders.
- Proficiency in documentation practices, quality risk assessment, and use of quality management software or electronic QMS tools.
- Bachelor's or master's degree in Pharmacy, Biotechnology, Chemistry, or a related scientific discipline.
- Prior experience in sterile injectables, parenterals, or ophthalmic solutions manufacturing is highly desirable.
- Strong analytical, problem-solving, and decision-making skills with attention to detail and a focus on continuous improvement.
- Ability to work on-site in Ujjain and collaborate in a structured, regulated manufacturing environment.
Sourced from foundit
Skills
electronic QMS toolsquality management softwareregulatory requirementsCAPAChange Controlexternal auditsdocumentation practicespharmaceutical quality systemsBatch record reviewGMP GuidelinesDeviation handlingQuality Risk Assessment