Quality Control Specialist

About Bal Pharma Limited

Bal Pharma Limited is a pharmaceutical company based in Bangalore, specializing in active pharmaceutical ingredients (APIs), intermediates, and finished formulations distributed to over 60 countries worldwide. The company operates six advanced manufacturing plants that have received approvals from multiple international regulatory bodies. It is a leading global producer of Gliclazide API and is pursuing US FDA approval for its Bepotastine API along with several other filings in regulated markets. Their product offering exceeds 200 finished formulations covering tablets, capsules, syrups, suspensions, IV infusions, creams, and ointments. The formulation facility holds EU GMP certification, emphasizing compliance and quality in production.

Role Overview

We are seeking a full-time Quality Control professional to join our Udaipur facility. The role focuses on performing both routine and specialized analyses of raw materials, intermediates, and finished pharmaceutical products to confirm adherence to internal quality benchmarks and regulatory requirements. Responsibilities include operating analytical instruments for laboratory testing, accurately documenting and reviewing test outcomes, and keeping comprehensive quality records. The candidate will work closely with production, quality assurance, and regulatory teams to investigate deviations, aid corrective and preventive measures, and foster ongoing quality enhancements. Compliance with GMP and quality guidelines is essential, along with participation in internal audits and support during external inspections and certification processes.

Qualifications and Skills

• Demonstrated expertise in pharmaceutical Quality Control and Quality Assurance procedures, including testing and documentation.
• Strong background in implementing and maintaining Quality Management Systems and procedures.
• Thorough understanding of Good Manufacturing Practice (GMP) standards and their application in daily operations.
• Experience supporting internal quality audits and preparing for regulatory inspections.
• Educational qualification in Pharmacy, Chemistry, or related scientific field.
• Previous work experience in pharmaceutical manufacturing or QC laboratory settings, preferably servicing regulated markets.
• Proficiency with analytical instrumentation and laboratory data management software, along with strong data interpretation skills.
• Excellent attention to detail, problem-solving capability, and effective communication skills to enable collaboration across teams.