"Exclusive Opportunity to Join Syngene as a Senior Executive - Apply Now!"

Syngene MPharma Executive Opportunity – Apply Online

Designation: Senior Executive

Job ID: 55379

Job Location: Bangalore

Department: Early Phase Stability

Incorporated in 1993, 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. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240-strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.

Job Purpose:

This role involves in the analysis of Drug Substance/ Drug Product.

Key Responsibilities:

  • Responsible for performing the physicochemical and instrumental analysis and investigations of samples (Drug substance, Drug Product, Intermediate, Excipient & Inactive) received at Early phase stability.
  • Preparation of protocols, ODS and Annexure as per client requirement.
  • Responsible for handling stability for multiple Client projects.
  • Preparing stability summary reports and review of final documents.
  • Actively participate in Client Audits and regulatory Audits.
  • Ensure to follow cGMP and GDP.
  • Deliver analytical results within the established windows and as per applicable guidelines.
  • Responsible for performing Validation activities and method transfers for multiple Client projects.
  • Preparing the Calculation excel sheets, certificate of Analysis for standards and impurities and Reports for Analytical Method Validation and Analytical Method Transfer.
  • Responsible for Performing Qualification and Calibration of assigned Instrument’s and Equipment’s.
  • Preparation of Instrument URS, DQ and IOP.
  • Preparing the Standard Operating Procedure.
  • Responsible for timely intimation/ investigation of any events, deviations to the Dept. Head, QA function and supporting the related investigations to the clients and its effective timely closure.
  • Responsible for Timely deliverables of projects.
  • Compliance & implementation of quality systems.
  • Ensure optimal utilization of Work hours & prioritization of activities to meet departmental commitments.
  • Flexibility to work in any project/team as per the requirement.
  • Responsible for the activities assigned within the team.
  • Escalation of issues / non conformity with applicable procedures/policies.
  • Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety.
  • Attend training on environment, health, and safety (EHS) measures imparted company.

Educational Qualification: M.Sc./ M. Pharm

Technical/Functional Skills:

  • Should have a Quality Control background.
  • Should know Analytical Techniques.

Experience: 3–6 Years

Behavioural Skills:

  • Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team.
  • Good speaking-listening-writing skills, attention to details, proactive self-starter
  • Ability to work successfully in a dynamic, ambiguous environment.
  • Ability to meet tight deadlines and prioritize workloads.
  • Ability to develop new ideas and creative solutions.
  • Should be strong in Data Integrity.
  • Should able to work in team and flexible for working in shifts
  • Should be a focused employee.

Link to Original Notification to apply: Apply Here

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