Syngene Pharma Specialist Job Opening – Apply Online Now

Syngene Pharma Specialist Job Opening – Apply Online Now

Title: Specialist Development QA_Development Biology

Date: 11 Jun 2024

Job Location: Bangalore

Pay Grade: 8-I

Year of Experience: 6 – 9 Years

Job Title: Specialist Development QA_Development Biology

Department: Discovery and Development QA

Job Location: Bengaluru, India

About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply.

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit.

Mandatory expectation for all roles as per Syngene safety guidelines:

• Overall adherence to safe practices and procedures of oneself and the teams aligned.
• Contributing to the development of procedures, practices, and systems that ensure safe operations and compliance with the company’s integrity & quality standards.
• Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
• Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
• Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self.
• Compliance to Syngene’s quality standards at all times.
• Hold self and their teams accountable for the achievement of safety goals.
• Govern and Review safety metrics from time to time.

Core Purpose of the Role: Responsible for Quality Systems of Biopharmaceutical development Functions and relevant QA activities.

Role Accountabilities:

• Review and approval of laboratory Change control, deviations, investigations, and CAPA in Trackwise.
• Tracking CCF, deviation, and incident closure status on a weekly basis to achieve quality KPIs.
• Review and approval of SOP, IOP, OCP, and EOP.
• Handling customer projects and ensuring that the documents are reviewed and approved.
• Having experience in Biopharmaceutical process, handling QMS, and analytical knowledge.
• Perform self-inspection of BUs as per schedule.
• Review of Audit trials of application software instruments and electronic lab notebook (eLN).
• Review and approval of Instrument qualification and scheduled calibration documents.
• Coordinating with the laboratory personnel in handling customer queries.
• Issuance of workbooks and logbooks.
• Review of regulatory submission documents if any.
• Ensuring training compliance in line with training procedure and role-based curricula.
• Ensure lab compliance with respect to the laid-down quality systems.
• Review and approval of analytical documents, comprising chromatographic data files, Lab Notebooks, eLN.
• Review and approval of computerized system validation documents.
• Review and approval of Instrument qualification and scheduled calibration documents.
• Coordinating with the laboratory personnel in handling customer queries.
• Approval of validation/qualification documents as required.
• Other responsibilities as assigned by the reporting manager.

Syngene Values:

All employees will consistently demonstrate alignment with our core values:

• Excellence
• Integrity
• Professionalism

Experience: 06-10 years of relevant experience.

Skills and Capabilities: Team player, Result-oriented, and focused.

Education: Bachelor pharmacy / Master’s degree in pharmacy / Science