Team Member - Quality Control Micro

Job Summary
We are seeking an associate for the Quality team responsible for conducting sampling and analysis of packaging and raw material samples. The role involves ensuring accuracy in documentation adherence to safety procedures reporting discrepancies and maintaining lab safety.

Roles & Responsibilities
You will be responsible for conducting sampling and analysis of packaging and raw material samples as allotted by the group leader.
You will be responsible for SAP activities ROA (Record of Analysis) preparation and reviewing analytical records and raw data against Specification and STP (Standard Testing Protocol).
You will ensure accuracy of the documentation before submitting it for the Group Leaders review or uploading online.
You will also be responsible for the proper use and care of instruments or equipment as instructed in relevant SOPs (Standard Operating Procedure) including cleaning before and after analysis.
You will adhere to safety precautions and procedures during analysis.
Your responsibilities include placing SOP/STP/reference standards at their designated locations after analysis and reporting discrepancies or incidents promptly to the Group Leader.
Lab safety following JSA (Job Safety Analysis) and using proper PPE (Personal Protection Equipment) at the workplace are emphasized.
You will oversee the handling and upkeep of the chemical and solvent store preparation of Speccheck catalog and result entries as well as maintaining volumetric solutions and reagents.
Your role also includes preparation of out lab testing samples (as required) timely destruction of samples as per SOP printing COA (Certificate of Analysis) completing assigned training and any additional responsibilities assigned by the Group Leader.

Qualifications :

Educational qualification: A Bachelors degree in Chemistry Analytical Chemistry or a related field

Minimum work experience: 2 to 5 years of experience in a laboratory setting preferably in the pharmaceutical or related industry

Skills & attributes:

Technical Skills
Proficient in various analytical techniques including sampling and analysis of packaging and raw material samples.
Experience with the operation and maintenance of analytical instruments ensuring proper use and care as per SOPs.
Competent in SAP activities related to sample tracking documentation and data entry.
Knowledgeable about cGMP SOPs and STPs ensuring accurate documentation and adherence to specifications.
Adheres to safety precautions and procedures during analysis emphasizing the importance of lab safety JSA (Job Safety Analysis) and proper use of PPE (Personal Protective Equipment).
Expertise in handling and upkeep of the chemical and solvent store including the preparation and maintenance of volumetric solutions and reagents.

Behavioural Skills
Keen attention to detail in analysis and documentation ensuring accuracy in all tasks.
Effective communication and collaboration skills for communicating with the Group Leader reporting discrepancies incidents and providing timely updates.
Takes initiative in ensuring the proper use and care of instruments timely destruction of samples and other assigned responsibilities.
Demonstrates problemsolving skills in addressing discrepancies incidents and ensuring smooth laboratory operations.
Upholds ethical standards compliance with SOPs and follows regulatory requirements in all activities.

Additional Information :

About the Department
Global Manufacturing Organisation (GMO)
At Dr. Reddys Laboratories we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence we are a leading force in the pharmaceutical industry.
We operate 19 stateoftheart manufacturing plants across Hyderabad Vizag Baddi Mexico Shreveport and Mirfield comprising 8 OSD facilities 3 Injectables facilities and 8 API facilities.
Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1150 drug master files across key therapy areas such as Oncology Cardiovascular Central Nervous System and AntiDiabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally Hyderabad as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive meeting business imperatives and meeting our ambitious ESG goals. Building such factories of the future is integral to innovation and to build healthcare of the future.


Benefits Offered
At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddys are on par with the best industry standards. They include among other things and other essential equipment joining & relocation support family support (Maternity & Paternity benefits) learning and development opportunities medical coverage for yourself and your family life coverage for yourself.

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. We see healthcare solutions not only as scientific formulations but as a means to help patients lead healthier lives and were always attuned to the new and the next to empower people to stay fit. And to do this we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system they can make magic.
For more details please visit our career website at !/ 

Remote Work :

No

Employment Type :

Fulltime