Job Summary
We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines processes and procedures. The primary objective is to ensure accuracy in results provided within timelines.
Roles & Responsibilities
- Your responsibilities encompass testing assigned samples and releasing data within defined timelines ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis.
- Your role involves documenting activities contemporaneously adhering to Good Documentation Practices and compliance expectations and conducting self-checks post-analysis to ensure accuracy.
- You will promptly inform the supervisor about risk actions providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines actively participate in laboratory investigations and discrepancy closures fulfilling defined roles in audits.
- Your responsibilities also include ensuring lab cleanliness proper sample storage chemical labeling removal of expired material usage of calibrated equipment equipment calibration maintenance and qualification.
- You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems and play a crucial role in training new team members on analytical techniques.
Qualifications :
Educational Qualification
An . . or . in Microbiology Biochemistry or Biotechnology
Minimum Work Experience
2 years
Skills & Attributes Technical Skills:
- Basic understanding of the Biologics/Biosimilar industry including processes regulations and trends.
- Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques including Size Exclusion Reverse Phase Ion Exchange chromatography and Peptide mapping analysis especially within the context of Analytics.
- Hands-on experience in Biochemical analysis techniques specifically Electrophoresis Enzyme-Linked Immunosorbent Assay (ELISA) and Polymerase Chain Reaction (PCR) with a focus on Analytics.
- Working experience in a cGMP (Current Good Manufacturing Practice) environment with a special emphasis on Good Documentation Practices (GDP).
- Basic knowledge in protein chemistry including an understanding of protein structure function and relevant analytical techniques.
- Basic knowledge and hands-on exposure to Microbiology techniques particularly relevant for individuals working in Microbiology Labs.
- Basic knowledge and hands-on exposure to cell culture techniques specifically for working in Bioassay (BA) Labs.
Behavioural Skills:
- Prioritizes effective communication and demonstrates a performance-oriented mind-set.
- Effective verbal and written communication skills.
- Performance-oriented approach consistently striving for high standards.
- Demonstrates flexibility in working shifts and a clear understanding of team dynamics.
Additional Information :
About the Department
Biologics
Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 1015-year time horizon...
Benefits Offered
At Dr. Reddys we actively help to catalyze your career growth and professional development through personalized learning programs. The benefits you will enjoy at Dr. Reddys are on par with the best industry standards...
Our Work Culture
Ask any employee at Dr. Reddys why they come to work every day and theyll say because Good Health Cant Wait. This is our credo as well as the guiding principle behind all our actions...
For more details please visit our career website at Work :
No
Employment Type :
Full-time