Job Detail

Salary

Jobs Position Information
  • Job Vacancy:
    Assistant Quality Manage
  • Experience
  • Location
    Rudrapur Uttarakhand
  • Jobs Type
    Full Time

Jobs Description

 Job Opening: Assistant Quality Manager (Pharmaceutical)
Location: Sidcul, Pantnagar
Department: Quality Assurance
Experience Required: 8‑10 years in pharmaceutical
Salary Budget: ₹10,00,000 ‑ ₹12,00,000 per annum

Job Description
We are seeking a highly experienced and motivated Assistant Quality Manager to join our Quality Assurance team in our Sidcul, Pantnagar facility. The ideal candidate will take ownership of QA functions, ensure GMP compliance, drive quality improvements, and lead investigations & corrective actions to uphold the highest standards of pharmaceutical quality.

Key Responsibilities
Oversee and review batch manufacturing & packing records, release of finished goods, and in‑process controls to ensure compliance with internal standards and external regulations (cGMP, WHO, FDA etc.).
Manage and execute Deviation / OOS / OOT investigations and follow through with CAPA implementation and closure in a timely manner.
Lead development, review, and maintenance of Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs/BPRs), Master Batch Records, Validation / Qualification protocols and reports.
Coordinate internal & external audits, regulatory inspections, and ensure readiness of all quality systems & processes.
Monitor and support Change Controls, Risk Assessments, and Quality Management System (QMS) improvements.
Participate in personnel training on GMP, QA procedures, documentation best practices, quality culture, etc.
Support product stability studies, product complaint handling, and supplier / vendor quality assurance as needed.
Report to QA Manager / Head – QA, providing quality metrics & insights to guide process improvements and decision making.

Qualifications & Skills
Bachelor’s or Master’s degree in Pharmacy (B.Pharm / M.Pharm), Life Sciences, Chemistry, or related field.
Solid 8‑10 years of hands‑on experience in pharmaceutical manufacturing or QA department, with strong exposure to cGMP regulations.
Deep understanding of QA systems: Deviation, CAPA, Change Control, Audits, Validation & Qualification, SOP management.
Experience with regulatory standards (e.g., US FDA, WHO, EU, local regulatory body).
Strong analytical, documentation, and communication skills.
Leadership experience: able to lead teams, mentor juniors, coordinate with cross‑functional departments.
Proactive, detail‑oriented, good problem‑solving ability.

What We Offer
Competitive salary (₹10‑12 LPA)
Benefits as per company policy (PF, Medical, etc.)
Opportunity to work in a well‑equipped facility in an industrial growth zone (Sidcul, Pantnagar)
A dynamic team environment with scope for growth and professional development

Interested candidate share your resume at: 7830699111
Email: bdsjobconsultants@gmail.com

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