Dr.Reddy’s Laboratories Walk In Interview 2023.Dr. Reddy’s Laboratories Notification full details below. Interested and eligible candidates can attend interview on scheduled time and venue.Dr. Reddy€™s Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses – Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products .
Vacancy details:
- Post Name: Nasal Production/manufacturing/QC/Nasal -IPQA/AQA/Osd Production/Packing
- Qualification: M.Sc, B.Sc,Bpharm,Diploma,BE
- Experienced: 2 to 8 yrs
Job Description: Greeting from Dr. Reddy’s Laboratories !!!!
Important Details :
- Work Location: Pydibhimavaram-Vishakhapatnam
- Post of date:19/09/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Walk-in Interview details Below
Note: Candidates are supposed to carry government identity proof like Aadhar card/ Drivers license along with the CV
Interview Date & Day:24th September, 2023
Time: 9.30 Am to 3.00 PM
Venue: The Fern Kesarval Hotel Verna,Goa,Bus Stand,Kesarval Gardens,Edapally-Panvel Hwy,Quelossim,Goa
Manufacturing activities involved in the production of nasal drug delivery products typically include:
Formulation Development: Creating the drug formulation that is suitable for nasal administration, considering factors like drug solubility, stability, and dosage form (e.g., nasal spray, nasal drops, nasal gel).
Active Pharmaceutical Ingredient (API) Preparation: Synthesizing or sourcing the active drug compound in a suitable form for incorporation into the nasal product.
Excipient Selection: Choosing appropriate excipients (e.g., preservatives, stabilizers, pH adjusters) to optimize the formulation’s properties.
Mixing and Blending: Combining API and excipients to create a homogeneous mixture.
Sterilization: Ensuring the product is free from microbial contamination through sterilization processes like autoclaving or sterile filtration.
Filling and Packaging: Filling the nasal product into appropriate containers (e.g., nasal spray bottles) under sterile conditions and sealing them securely.
Quality Control and Testing: Conducting various tests to ensure product quality, including potency, purity, sterility, and stability testing.
Device Assembly: If the product requires a specific delivery device (e.g., nasal spray pump), assembling and testing these components.
Batch Documentation: Maintaining detailed records of the manufacturing process to ensure traceability and regulatory compliance.
Regulatory Compliance: Meeting regulatory requirements and obtaining necessary approvals for production.
Quality Assurance: Implementing quality control measures and processes throughout manufacturing to ensure consistent product quality.
Packaging and Labeling: Designing and labeling packaging for consumer information, branding, and regulatory compliance.
Batch Release: Authorizing the release of batches that meet quality standards for distribution.
Storage and Distribution: Properly storing and distributing the finished nasal drug delivery products to ensure they reach the end-users safely.
