Pharma & Chemistry Executive Job Vacancy 2021 – Syngene

Pharma & Chemistry Executive Job Vacancy 2021 – Syngene

Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world.

Job Title: Senior Executive

Job Location: Bangalore

Department: Quality Control Common: Late phase Stability

Educational Qualification: M. Pharmacy or M.Sc. (Analytical Chemistry/Organic Chemistry)

Technical/Functional Skills:

• 3 to 6 years of working experience in Stability or Quality control.
• The candidate should have experience in the analysis of drug substances and drug products.
• Good analytical skill and shall perform analysis right the first time.
• Hand-on experience of HPLC, GC, KF coulometer, KF titrator, Dissolution tester, and IR. (experience in PXRD, DSC, Particle size analysis, LCMS is preferred.
• Experience in Chromeleon software, LIMS, Trackwise will be added advantage.
• Good understanding of GMP, GDP, and data integrity principles.
• Quick learner and early change adaptor.
• Experience in regulatory audits is a must.

Experience: 3-6 Years of working experience in Stability and Quality control. (Drug substances and drug products)

Behavioral Skills:

• Effective time Management.
• Reading Comprehension
• Communicating effectively: verbally and writing
• Team player.

Job Purpose:
To review and handle change control, deviation, and CAPA with

respect to Quality under GMP aspects and involve in the Document Management System.

Job Description: 

• Responsible for performing the physicochemical and instrumental analysis (HPLC, Dissolution, UPLC, GC, KF, pXRD, particle size, etc.)  and investigations (Drug Substance, Drug Product, Intermediate, and Excipient)
• Responsible for performing analytical method validation and analytical method transfer.
• Deliver results ‘Right First Time’ and within the established windows.
• Participation in internal, client, and regulatory audits.
• Compliance with quality systems in the laboratory.
• Ensure and comply with GMP, GDP, Data Integrity EHS policies laid down by the organization.
• Flexibility to work in any project/team as per the requirement.
• Preparation of documents like stability summary reports, stability protocols, SOP.
• Responsible for audit readiness.
• Performance of instrument calibration, qualification whenever required.
• Ensure and comply with EHSS and safety policies laid down by the organization.

Key Responsibilities:

• First, pass analysis of stability samples i.e. drug substances and drug products.
• Ontime escalation of laboratory issues.
• Initiation of QMS records on time.

Apply Online

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