Analytical Chemistry Jobs at Syngene | Apply now for Executive – QC Position
Are you seeking a fulfilling career in pharmaceutical sciences and bioanalysis? Syngene International Ltd., a leading global discovery, development, and manufacturing organization, is hiring an Executive – QC for its Small Molecule Bioanalytical Research Laboratory in Bangalore. This role offers an opportunity to contribute to high-quality research, ensure compliance with global regulatory standards, and advance your expertise in bioanalytical research.
About Syngene
Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022) is an integrated research, development, and manufacturing solutions company serving global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. With over 4,500 scientists and 1.9 million sq. ft. of discovery, development, and manufacturing facilities, Syngene partners with world leaders such as Amgen, Baxter, Bristol-Myers Squibb, Herbalife, GSK, and Merck KGaA. Syngene’s mission is to deliver great science, robust data management, IP security, and quality manufacturing to improve time-to-market and lower the cost of innovation.
Job Details
- Job Position: Executive – QC (Small Molecule Bioanalytical Laboratory)
- Education: M.Sc. in Analytical Chemistry
- Experience: Minimum 3 years in regulated small molecule bioanalysis; hands-on experience in bioanalytical experiments is required. Experience with Bioanalytical CRO labs will be an advantage
About the Position
The Executive – QC is responsible for reviewing and ensuring the accuracy of bioanalytical data related to BA/BE studies. This role involves method development, validation checks, and study sample analysis reviews to maintain compliance with regulatory requirements. The position reports to the Head/Group Leader of the Small Molecule Bioanalytical Laboratory in Bangalore.
Key Responsibilities
- Perform QC checks for method development, validation, and sample analysis data
- Review STPs, protocols, validation, and bioanalytical reports
- Maintain documentation for audits (Sponsor/Regulatory)
- Handle Change Management and initiate change requests as required
- Conduct daily and monthly inspections in the laboratory
- Ensure studies adhere to GCP/GLP and regulatory guidelines
- Collaborate with leaders on corrective actions for QC observations
- Prepare QC observation trend analyses for management reviews
Core Competencies
- Strong scientific thinking with problem-solving ability
- Technical expertise in ICH, FDA, EMA, and ANVISA method validation guidelines
- Excellent data analysis, documentation, and reporting skills (ALCOA++ compliance)
- Effective communication and project management capabilities
- Attention to detail with minimal audit findings
Equal Opportunity Employer
Syngene is an equal opportunity employer, committed to providing equal employment opportunities regardless of age, gender, race, disability, sexual orientation, or any protected characteristic. The company also ensures reasonable accommodations for qualified individuals with disabilities.
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