SENIOR SCIENTIST

StrainX Biotech; Bengaluru; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Syngene International Ltd. in Bangalore is seeking a Senior Scientist – EGMP in Analytical Development.

The role involves planning and allocating the team’s routine and non-routine activities, coordinating with QA, and ensuring compliance with QMS, TAT and TPA matrices. The candidate should have 3–6 years of experience and a strong background in analytical techniques (HPLC/GC, LC-MS, KF, IR/UV) with familiarity in Chromeleon and LIMS.

Qualifications

• MSc or MPharma with Analytical/General Chemistry focus.
• 3–6 years of relevant experience in analytical development.
• Strong knowledge of analytical techniques and QA practices.

Responsibilities

• Plan and allocate routine and non-routine activities for the team.
• Review in-process, cleaning, intermediate and finished product specs.
• Coordinate with QA for deviation investigations and change controls.
• Interact with production, R&D, and QA to ensure project progress.
• Review validation reports and method transfer protocols.

Skills

HPLC/GC

LC-MS

KF/KFC

IR/UV

LIMS proficiency

Education

MSc / MPharma (Analytical/General chemistry)

Tools

Chromeleon

LIMS

Job description

Job DescriptionDesignation: Senior Scientist – EGMP

Job role – Senior Scientist

Location:

Bangalore, KA, IN, 560099

Division: Development Services

Job Location: Bangalore

Department: EGMP – Analytical Development

About Syngene

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 worldwide. 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 dedicated 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 Description:

Planning and allocation of Routine and non-routine activities for the entire team member. Investigation of QMS Elements and Report Generation, Approval and co-ordination with QA and Maintaining a QMS/TAT/TPA matrix.

Key Responsibilities

• Responsible for taking any other job allocated by Head of the Department.
• Analysis of RM, PM, INT, IPFP, FP, Stability samples and validation activities.
• Planning and allocation of Routine and non-routine activities for the entire team member.
• Interaction with production, ADL, R&D, QA and other department for QC related functions.
• Interaction with client and Project team for the smooth functioning of project related activities.
• To review the In-process, cleaning, intermediate and finished product specification.
• Initiate the change control and taking approval from analytical QA.
• Planning and allocation of Documentation preparation.
• Review of routine/non-routine validation reports.
• Review of method verification and method validation protocol.
• Review of standard qualification protocol forced degradation protocol and method transfer protocol.
• Ensuring, verifying and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP.
• To maintain the sampling packing area
• Investigate and close for planned and unplanned deviations.
• Review of Certificate of analysis.
• Review and Approval of specification of non-technical batches.
• Responsible for Ensuring that the Good Laboratories Practices are followed while working in QC Laboratory.
• Responsible for Ensuring the Use of required safety apparels while sampling, analysis and working in Laboratory.
• Responsible for taking any other job allocated by Head of the Department.
• To ensure safety compliance as per Syngene policy and EHSS requirements.

Educational Qualification: M Sc / M Pharma (Analytical/General chemistry)

Technical/Functional Skills

• Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc…
• Being well-versed in the Chromeleon data management application and LIMS will be advantageous.

Experience: 3-6 years

Behavioural Skills

• Should be an adaptive learner.
• Should demonstrate effective Communication skills.
• Organization and ability to balance work and Life.
• Should possess good Time Management abilities.

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.

Seniority levelMid-Senior level

Employment typeFull-time

IndustriesPharmaceutical Manufacturing