TitanPharmaplus Pvt Ltd, a leading pharmaceutical laboratory based in Mahad, is dedicated to delivering high-quality pharmaceutical products and services. With a focus on cutting-edge technology and precision, we are committed to maintaining the highest standards in the pharmaceutical industry. As part of our growth, we are looking for a Senior Research Associate/Executive to join our Quality Control (LCMS) team. This role offers an exciting opportunity to work with advanced analytical techniques in a dynamic and collaborative environment.

Key Responsibilities in the Job

As a Senior Research Associate/Executive in the Quality Control (LCMS) department at TitanPharmaplus, your primary responsibilities will include:

• Instrument Operation & Maintenance: Operating and maintaining a wide range of advanced analytical instruments such as HPLC, GC, GC-MS, ICP-MS, IC, LC-MS, and HR-MS.
• Analytical Testing: Performing routine and specialized analyses in strict compliance with GLP/GMP and regulatory standards.
• Method Development & Validation: Assisting in the development, optimization, and validation of analytical methods for various procedures.
• Sample Preparation: Accurately preparing samples, reagents, and standards to ensure reliable results.
• Data Interpretation: Collecting, processing, and interpreting data, and compiling detailed analytical reports.
• Laboratory Record Keeping: Maintaining comprehensive laboratory records and ensuring full documentation compliance.
• Calibration & Maintenance: Performing regular instrument calibration, maintenance, and performance checks to ensure optimal operation.
• Collaboration: Working closely with R&D, Quality Control, and other cross-functional teams to ensure project goals are met.

Qualifications for the Role

To be considered for the Senior Research Associate/Executive role, candidates must meet the following qualifications:

• Educational Background: A Master’s degree in Chemistry, Analytical Chemistry, Biochemistry, or a related field.
• Experience: A minimum of 2-6 years of hands-on experience with analytical instruments such as HPLC, GC, GC-MS, ICP-MS, IC, and LC-MS.
• Technical Expertise: Proficiency in analytical method development and validation is essential.
• Regulatory Knowledge: Familiarity with GLP, GMP, and other relevant regulatory standards is a must.
• Data Analysis Skills: Strong analytical and data interpretation skills, with a high level of accuracy and attention to detail.

Skills and Competencies Required

The ideal candidate will possess the following skills:

• Problem-Solving: Strong problem-solving abilities to troubleshoot and resolve issues quickly and efficiently.
• Time Management: Excellent time management skills to handle multiple tasks and meet deadlines in a fast-paced environment.
• Teamwork: Ability to collaborate effectively with cross-functional teams and work well in a team-oriented environment.
• Software Proficiency: Experience with laboratory software such as Chromeleon, Analyst, LabSolutions, or Empower (preferred).

How to Apply

If you meet the qualifications and are ready to contribute to the success of TitanPharmaplus Pvt Ltd, we encourage you to apply. To submit your application, send your updated resume and cover letter to shweta.m@titanpharma.com. Please include the subject line: “Application for Senior Research Associate/Executive – QC (LCMS).”