MPharma Job Openings in QC at Syngene
Syngene International Ltd. is seeking a skilled and experienced Senior Executive – Analytical Analyst (ICP-MS/ICP-OES) to join its Analytical Department at the Bangalore-based Baxter Global Research Center (BGRC). This is an excellent opportunity for professionals with a background in M.Pharm or M.Sc and 3–5 years of experience to contribute to method validation, trace analysis, and stability operations using advanced instrumentation, such as ICP-MS and ICP-OES.
- Job Position: Senior Executive – Analytical Analyst (ICP-MS/ICP-OES)
- Location: Bangalore, Karnataka, India – 560099
About the Company:
Syngene International Ltd., incorporated in 1993, is a global contract research, development, and manufacturing organization. The company delivers integrated scientific services to pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors worldwide. Clients include top global players like Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. With a team of over 4,240 scientists, Syngene is committed to addressing scientific challenges, enhancing R&D productivity, and reducing time-to-market.
Job Description:
As a Senior Executive in the Analytical department, you will oversee method transfer, validation activities, and trace element analysis. This role requires a strong understanding of elemental impurities, regulatory guidelines, and hands-on experience with advanced instrumentation.
Key Responsibilities:
- Plan daily activities and review analytical documents.
- Execute stability analysis, validations, and method transfers using FES, AAS, ICP-OES, and ICP-MS.
- Review documentation for validation, method transfers, and calibration.
- Prepare and execute validation and stability protocols.
- Develop SOPs, EOPs, and IOPs and conduct training.
- Draft investigation reports for deviations, incidents, OOC, and OOS.
- Ensure instruments meet 21 CFR Part 11 compliance.
- Maintain quality and compliance in stability operations and LIMS.
- Follow and promote EHS standards in the workplace.
Qualifications:
- Educational Qualification: M. Pharm / M.Sc.
- Experience: 3–5 years in Quality Control or Analytical Development Lab.
- Technical Skills:
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- Expertise in ICP-MS, ICP-OES, AAS, and FES.
- Familiar with cGMP, ICH, and US/EU pharmacopoeias.
- Proficiency in stability testing per ICH guidelines.
- Exposure to USFDA audits and 21 CFR Part 11 compliance.
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Behavioral Skills:
- Strong communication and technical writing skills.
- Team-oriented with the ability to follow instructions.
- Professional email and report etiquette.
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