Business Partner - SFE

Roles & Responsibilities

• You will be responsible for validation and analytical method transfers of IP (In-Process) FP (Finished Product) API (Active Pharmaceutical Ingredient) Excipients and Packing materials.
• You will initiate and investigate CRN (Change Request Notice) Incidents OOT (Out of Trend) and OOS (Out of Specification).
• You will be responsible for approval of STPs (Standard Testing Procedures) Specifications SOPs (Standard Operating Procedures) Protocols and Analytical test reports.
• You will ensure Good laboratory practices Safety practices Good documentation practices and ensure the cleanliness of the laboratory.
• Your role involves ensuring the maintenance preparation procurement of laboratory standards and chemicals/solvents as per the laid down procedures.
• You will participate and organize equipment/instrument Qualifications & change control mechanism and procurement of laboratory requirements.
• You will ensure calibration/performance verification of analytical instruments and equipment as per master schedule.
• You will be responsible for preparation of response for Internal and external audits and other QMS (Quality Management System) related activities.
• Your responsibilities will include ensuring compliance in LIMS (Laboratory Information Management System) related activities and ensuring that all the QMS documents are investigated timely reviewed and appropriate CAPAs (Corrective and Preventive Actions) are taken and implemented.

Qualifications :

Educational qualification:

An . degree in Chemistry Analytical Chemistry or a related field

Minimum work experience:

10 to 12 years of experience

Skills & attributes: Technical Skills

• Expertise in method validation and analytical method transfers for IP FP API Excipients and Packing materials.
• Knowledge of calibration and performance verification of analytical instruments and equipment as per the master schedule.
• Experience in ensuring the maintenance preparation and procurement of laboratory standards chemicals and solvents according to established procedures.
• Participation and organization of equipment/instrument qualifications and change control mechanisms.
• Procurement expertise for laboratory requirements.

Behavioural Skills

• Attention to detail and commitment to ensuring compliance with QMS documents including OOS OOT and Incident investigations.
• Ability to respond to internal and external audits and participate in other QMS-related activities.
• Strong organizational skills for LIMS related activities.
• Effective communication and collaboration skills for coordinating and implementing CAPAs.

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 state-of-the-art 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 Cardio-vascular Central Nervous System and Anti-Diabetes. The 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 catalyze 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...

For more details please visit our career website at Work :

No

Employment Type :

Full-time