Walk-in | Senior scientist

Syngene; Bengaluru; On-site; INR 700,000 - 1,100,000; Full time

Job summary

Syngene in Bangalore is seeking a Senior Analyst for the Early Phase GMP (Analytical Development) team. This role involves performing analytical reference standard qualifications, method validations, and analysis of raw materials, intermediates, APIs, and finished products, while adhering to GLP and EHSS.

You will operate instruments (HPLC, GC, KF/KFC, IR, UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS) and utilize Chromeleon and LIMS, with responsibilities including documentation, reporting, and safety

Qualifications

• PG degree in analytical chemistry or related field.
• 1 to 6 years of relevant experience.

Responsibilities

• Follow GLP while working in the QC laboratory.
• Maintain and clean laboratory instruments.
• Use required safety apparel while sampling and analyzing.
• Carry out analysis of validation samples per approved protocols.
• Initiate laboratory incidents and deviations as required.
• Prepare calculation sheets and draft reports.
• Ensure proper disposal of samples after analysis.
• Perform additional duties as directed by HOD or Section Head.
• Analyze intermediates, finished products, and working standard qualifications.
• Verify and review instrument usage logs and labeling per SOPs.
• Prepare protocols and observation data sheets.
• Work with analytical techniques including HPLC, GC, KF/KFC, IR, UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS.
• Utilize Chromeleon data management software and LIMS effectively.
• Ensure compliance with Syngene safety policies and EHSS requirements.

Skills

GLP compliance

Lab safety practices

Documentation skills

Analytical method validation

Education

M.Sc. / M.Pharmacy (Analytical Chemistry / General Chemistry)

Tools

HPLC

GC

KF/KFC

IR

UV

LC-MS

GC-MS

IC

ICP-OES/ICP-MS

DSC

TGA

Chromeleon

LIMS

Job description

Designation: Senior Analyst
Department: Early Phase GMP (Analytical Development)
Job Location: Bangalore

About Syngene

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 Expectations for All Roles as per Syngene Safety Guidelines

• Overall adherence to safe practices and procedures for self and aligned teams.
• Contribute to the development of procedures, practices, and systems that ensure safe operations and compliance with company integrity and quality standards.
• Drive a corporate culture that promotes an Environment, Health and Safety (EHS) mindset and operational discipline at all times.
• Ensure safety of self, team members, and laboratory/plant by adhering to safety protocols and EHS requirements.
• Ensure completion of all mandatory trainings related to data integrity, health, and safety by self and team members within stipulated timelines.
• Ensure compliance with Syngene quality standards at all times.
• Hold self and team accountable for achieving safety goals.
• Govern and review safety metrics periodically.

Job Role

Perform analytical reference standard qualifications/characterizations, method validations/verifications and related documentation, as well as analysis of raw materials (RM), packing materials (PM), intermediates, APIs, and finished products.

Key Responsibilities

• Follow Good Laboratory Practices (GLP) while working in the QC laboratory.
• Maintain and clean assigned laboratory instruments.
• Use required safety apparel while sampling, analyzing, and working in the laboratory.
• Carry out analysis of validation samples as per approved protocols.
• Initiate laboratory incidents and deviations as required.
• Prepare calculation sheets and draft reports.
• Ensure proper disposal of samples after analysis.
• Perform any additional duties assigned by the HOD or Section Head.
• Analyze intermediates, finished products, and working standard qualifications as per specifications.
• Verify and review instrument usage logs periodically and ensure labeling compliance as per SOPs.
• Prepare protocols and observation data sheets.
• Work with analytical techniques including HPLC, GC, KF/KFC, IR, UV, LC-MS, GC-MS, IC, and ICP-OES/ICP-MS.
• Utilize Chromeleon data management software and LIMS effectively.
• Ensure compliance with Syngene safety policies and EHSS requirements.

Technical / Functional Skills

• Hands-on experience with analytical techniques such as HPLC, GC, KF/KFC, IR, UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, and TGA.
• Knowledge of Chromeleon data management application and LIMS will be an added advantage.

Education & Experience

Qualification: M.Sc. / M.Pharmacy (Analytical Chemistry / General Chemistry)
Experience: 1 to 6 years

Equal Opportunity Employer

Syngene is committed to providing equal employment opportunity (EEO) to all applicants and employees regardless of age, colour, national origin, citizenship status, disability, race, religion, creed, gender, sex, sexual orientation, gender identity or expression, genetic information, marital status, veteran status, or any other characteristic protected by applicable law. Reasonable accommodations will be provided for qualified individuals with disabilities.