Jaidev Pharma Placement
Website:
jaidevpharmaplacement.com
Job details:
Company Description Jaidev Pharma Placement is India’s leading pharma hiring partner, specializing in building high-performing teams across the pharmaceutical and healthcare sectors. In just five years, the firm has partnered with over 75 organizations nationwide, supported by a network of more than 350,000 pharma professionals. Led by experts with over 20 years of industry experience and 5+ years in recruitment, Jaidev Pharma Placement focuses on long-term talent alignment rather than transactional hiring. With offices in Gurgaon, Mumbai, and Hyderabad, and a dedicated nine-member team, the company delivers agile, results-driven hiring solutions. Its core expertise spans leadership, sales and marketing, technical and plant roles, and healthcare staffing, complemented by training and performance enhancement services.
Role Description This is a full-time, on-site role based in Meerut for Pharmaceutical QA positions at the Assistant Manager and Executive levels. The role involves managing and implementing Quality Management System (QMS) activities, including handling OOS (Out of Specification), OOT (Out of Trend), CAPA (Corrective and Preventive Actions), change control, and ensuring adherence to QMS requirements. Daily responsibilities include overseeing APQR (Annual Product Quality Review), BMR (Batch Manufacturing Record) compliance, process validation, and vendor qualification in line with regulatory and company standards. The position requires close coordination with cross-functional teams to investigate quality issues, document findings, and drive continuous improvement in manufacturing and quality processes. The CTC range for this role is 6–12 LPA, depending on experience and suitability.
Qualifications
- Candidates should possess strong Quality Assurance and Quality Management skills, with hands-on experience in QMS, CAPA, change control, APQR, and BMR compliance.
- Candidates should possess solid Quality Control skills, including familiarity with OOS/OOT investigations, process validation, and vendor qualification practices.
- Candidates should possess strong Analytical Skills to interpret data, identify trends, support root cause analysis, and recommend effective corrective and preventive actions.
- Candidates should possess clear and professional Communication skills to collaborate with cross-functional teams, prepare documentation, and support regulatory and internal audits.
- Candidates should ideally have a degree in Pharmacy, Chemistry, or a related life science field, with prior experience in pharmaceutical QA/QC operations.
- Candidates should be knowledgeable about GMP, regulatory guidelines (e.g., WHO, USFDA, EU), and quality documentation practices, with a focus on continuous improvement.
- Candidates should demonstrate attention to detail, ability to work in a structured environment, strong organizational skills, and readiness to take ownership of quality initiatives.
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