Author and Document Reviewer

Date : 21 Aug 2025

Location :

Bangalore, KA, IN, 560099

Custom Field 1 : Essential Functions

Job Description

Job Title : Author and Document Reviewer

Job Location : Syngene International Limited, Bengaluru

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 development of procedures, practices and systems that ensures safe operations and compliance to 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

This is an exciting opportunity to play a role in Quality control department of Syngene. The role will provide several responsibilities of Preparation of Product Specification, Standard Operating Procedure, Instrument Operating Procedures, General procedures. Observation data sheets, calibration data sheets, protocols and reports etc. Handling of LMS, LIMS, ELN, TrackWise and EDMS Softwares for routine activities as applicable. Lab safety requirements and Compliance as per Syngene policy and EHSS requirement.

Role Accountabilities

surveillance on introduction / revision of new / revised monograph and general chapters / guidelines.

Syngene Values

All employees will consistently demonstrate alignment with our core values

Specific requirements for this role

Experience : 6 to 9 years

Skills And Capabilities

Expertise in handling multiple activities in Pharmaceutical Industry.

Capable of thinking scientifically to address complex problems and develop solutions.

Work as a team and have a collaborative mindset.

Good communication skills.

Education : MSC / B. Pharma

Equal Opportunity Employer

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and / or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

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Skills Required

Lms, trackwise , Edms, Lims, eln