Syngene Hiring Study Personnel (Senior Executive) – Bioanalytical Laboratory

Syngene Hiring Study Personnel (Senior Executive) – Bioanalytical Laboratory GLP Jobs in Bangalore

Syngene International Limited is hiring Study Personnel (Senior Executive) for its Bioanalytical Laboratory operating under GLP standards at its Bengaluru research facility. This opportunity is designed for professionals with strong academic backgrounds in MSc or MPharm who are interested in advancing their careers in bioanalytical research, pharmaceutical laboratory analysis, and regulated drug development environments.

The position is part of Syngene’s scientific services division and focuses on bioanalytical method development, method validation, and biological sample analysis in compliance with international regulatory standards. Professionals working in pharmaceutical research laboratories, CRO environments, or regulated bioanalytical testing labs will find this role aligned with long‑term growth in clinical research, drug development, and regulated laboratory science.

The role is based in Bangalore, India, and offers the opportunity to work with advanced analytical instruments and global pharmaceutical clients while contributing to high‑quality bioanalytical data generation for regulated studies.

Company Overview

Syngene International Limited is a leading contract research, development, and manufacturing organization (CRDMO) that provides integrated scientific services to global pharmaceutical, biotechnology, and healthcare companies. The organization supports partners across the entire drug development lifecycle, from early discovery research to clinical development and commercial manufacturing.

Headquartered in Bengaluru, Syngene collaborates with some of the world’s largest pharmaceutical companies and innovative biotech organizations. Its services span drug discovery, bioanalytical research, clinical development support, and manufacturing solutions, making it one of India’s most respected research organizations in the global CRO and CDMO industry.

Syngene places strong emphasis on quality, scientific excellence, and regulatory compliance, ensuring that all laboratory operations follow international regulatory guidelines such as USFDA, OECD, and ICH standards.

Safety is also a core value across the organization. Employees are expected to adhere to strict environment, health, and safety (EHS) practices, maintain laboratory integrity, and follow quality standards that ensure reliable scientific outcomes.

Job Role and Responsibilities

The Study Personnel (Senior Executive) will work within the GLP-compliant Bioanalytical Laboratory and support regulated studies involving analytical method development, validation, and biological sample testing.

The role requires hands-on experience with analytical instruments, laboratory documentation practices, and regulatory-compliant bioanalytical workflows used in pharmaceutical research and drug development programs.

Method Development and Validation

• Perform bioanalytical method development and method validation for biological matrices

• Conduct sample preparation and analysis for regulated bioanalytical studies

• Apply different extraction techniques used in bioanalytical testing

• Ensure accuracy, precision, and reproducibility of analytical methods

• Troubleshoot analytical challenges encountered during method development

Analytical Instrument Handling

• Operate and maintain advanced analytical instruments including GC, UPLC, HPLC, and LC‑MS systems

• Use laboratory equipment such as pH meters, micropipettes, and ancillary instruments

• Review calibration and maintenance records for analytical equipment

• Ensure instruments are used according to laboratory standard operating procedures

Data Integrity and Documentation

• Maintain accurate laboratory documentation including logbooks and raw data records

• Ensure compliance with data integrity standards and regulatory documentation practices

• Prepare reports related to bioanalytical studies and laboratory activities

• Maintain proper record keeping for audit readiness and regulatory compliance

Quality and Regulatory Compliance

• Follow GLP guidelines and regulatory standards such as USFDA, ICH, and OECD requirements

• Ensure laboratory operations comply with internal quality management systems

• Participate in continuous improvement initiatives within the laboratory

• Maintain strict adherence to laboratory quality standards and documentation protocols

Collaboration and Communication

• Work collaboratively with scientific teams and project leaders

• Coordinate with offshore clients and research stakeholders

• Participate in scientific discussions and provide technical inputs where required

• Contribute to project timelines and deliverables for regulated bioanalytical studies

Safety and Laboratory Practices

• Follow strict environment, health, and safety (EHS) guidelines in the laboratory

• Maintain safe laboratory practices for handling biological samples and chemicals

• Ensure completion of mandatory training related to laboratory safety and data integrity

• Promote a safety-first culture across laboratory teams

Through these responsibilities, the role contributes directly to high‑quality bioanalytical research that supports pharmaceutical drug development and regulatory submissions worldwide.

Eligibility and Qualifications

Candidates applying for the Study Personnel (Senior Executive) – Bioanalytical Laboratory role should have strong academic qualifications in pharmaceutical sciences and relevant laboratory research experience.

Educational Qualification

Master’s degree in pharmaceutical sciences or life sciences.

Relevant educational backgrounds include:

MSc Analytical Chemistry, MSc Biotechnology, MSc Biochemistry, MSc Microbiology, MSc Life Sciences, MSc Pharmaceutical Analysis, MPharmacy Pharmaceutical Analysis, MPharmacy Pharmaceutics, MPharmacy Pharmacology, MPharmacy Pharmaceutical Chemistry.

Experience

• Experience in bioanalytical method development, method validation, and biological sample analysis

• Hands-on experience working in GLP-compliant bioanalytical laboratories is preferred

Technical Skills

• Experience with analytical instruments including HPLC, UPLC, GC, and LC‑MS systems

• Knowledge of bioanalytical sample preparation and extraction techniques

• Familiarity with regulatory standards such as USFDA, OECD, and ICH guidelines

• Experience maintaining laboratory documentation and raw data records

• Understanding of analytical method validation protocols

Professional Skills

• Strong scientific problem‑solving abilities

• Ability to work under pressure and meet project deadlines

• Strong collaboration and teamwork skills

• Good written and verbal communication skills

• Ability to work in multidisciplinary research teams

Professionals with expertise in bioanalytical research, pharmaceutical laboratory testing, and regulated analytical method development will find this role highly suitable for long‑term growth in the CRO and pharmaceutical research industry.

Location and Salary

Location: Bangalore, Karnataka, India

Work Type: On‑site laboratory role

Salary: Competitive salary package aligned with pharmaceutical CRO industry standards and candidate experience.

Application Process

Candidates interested in applying for the Study Personnel (Senior Executive) – Bioanalytical Laboratory role can submit their application through the official Syngene careers portal.

Apply Here:

https://careers.syngeneintl.com/job/Bangalore-Study-Personnel-KA-560099/1358250766/

Applicants are encouraged to apply early as research roles in regulated bioanalytical laboratories often receive significant interest from qualified candidates.

Frequently Asked Questions

What does Study Personnel do in a bioanalytical laboratory?

Study Personnel support regulated laboratory studies by performing analytical method development, validation, and biological sample testing while ensuring compliance with GLP and regulatory guidelines.

Who can apply for this Syngene role?

Candidates with MSc or MPharm degrees in pharmaceutical sciences, biotechnology, biochemistry, or analytical chemistry with experience in bioanalytical research can apply.

What instruments are used in bioanalytical laboratories?

Common analytical instruments include HPLC, UPLC, LC‑MS, GC systems, and laboratory equipment used for pharmaceutical sample analysis.

Is regulatory knowledge important for this role?

Yes. Knowledge of regulatory guidelines such as USFDA, OECD, and ICH standards is essential for working in GLP‑compliant bioanalytical laboratories.

Where is the job located?

The role is based in Bangalore, India, at Syngene’s bioanalytical research facility.

Job Summary

Category	Details
Company	Syngene International Limited
Vacancies	Study Personnel (Senior Executive) – Bioanalytical Laboratory
Required Education	MSc Analytical Chemistry, MSc Biotechnology, MSc Biochemistry, MSc Microbiology, MSc Life Sciences, MSc Pharmaceutical Analysis, MPharmacy Pharmaceutical Analysis, MPharmacy Pharmaceutics, MPharmacy Pharmacology, MPharmacy Pharmaceutical Chemistry
Experience	Experience in Bioanalytical Method Development, Validation and Sample Analysis

Tagged as: Pharma Jobs in Bangalore