Study Personnel – Bioanalytical Laboratory (GLP)
Location: Bangalore, Karnataka, India
Experience Level: Experienced
Division: Essential Functions
Company: Syngene International Limited
About Syngene:
Syngene International Limited is a leading innovation-driven Contract Research, Development, and Manufacturing Organization (CRDMO) providing integrated scientific services from early discovery through commercial supply. The company is committed to scientific excellence, regulatory compliance, and operational safety, fostering a culture of integrity, professionalism, and innovation.
Position Overview:
Syngene invites experienced candidates to join its GLP-compliant Bioanalytical Laboratory as Study Personnel. This role is ideal for professionals skilled in bioanalytical method development, validation, and sample analysis across biological matrices. The primary focus is to ensure generation of high-quality, regulatory-compliant bioanalytical data while collaborating with global clients and internal cross-functional teams.
Key Responsibilities:
Perform bioanalytical method development, validation, and sample analysis in accordance with GLP standards.
Ensure data integrity, accuracy, and precise documentation of laboratory activities and results.
Maintain compliance with quality standards, regulatory guidelines (OECD, USFDA, ICH), and internal SOPs.
Operate and maintain analytical and ancillary instruments, including HPLC/UPLC, LCMS, GC, and pH meters.
Conduct calibration and maintenance of laboratory equipment, including micropipettes, and maintain records.
Collaborate with internal teams and offshore clients to support analytical objectives and study deliverables.
Promote laboratory safety, EHS compliance, and best practices at all times.
Required Qualifications & Experience:
M.Sc. or M. Pharm in a relevant discipline.
Proven experience in bioanalytical studies, including method development, method validation, and sample analysis in biological matrices.
Hands-on knowledge of extraction techniques and handling of analytical instruments (HPLC/UPLC, LCMS, GC).
Strong understanding of regulatory requirements (OECD, USFDA, ICH) and GLP compliance.
Demonstrated ability to work under pressure, troubleshoot complex problems, and develop scientific solutions.
Excellent documentation, communication, and collaborative skills.
Core Competencies & Skills:
Scientific rigor and attention to detail in all laboratory activities.
Ability to analyze complex data and ensure regulatory-compliant results.
Collaborative mindset with the ability to work effectively in a cross-functional global team.
Commitment to safety, quality, and continuous improvement in laboratory operations.
Why Join Syngene:
Opportunity to work in a GLP-compliant bioanalytical lab with exposure to global clients.
Develop hands-on expertise in bioanalytical method development and validation.
Collaborative environment fostering innovation, scientific growth, and regulatory excellence.
Core Values:
Excellence – Striving for the highest standards in scientific work.
Integrity – Upholding honesty, transparency, and ethics.
Professionalism – Maintaining quality, accountability, and collaboration in all activities.
Equal Opportunity Employer:
Syngene provides equal employment opportunities and reasonable accommodations to individuals with disabilities, ensuring a diverse and inclusive workplace.
Apply Now to join Syngene’s Bioanalytical team and contribute to cutting-edge research and development in the pharmaceutical and biotechnology industry.
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