QC Trainee -Fresher (B.Pharm /M.Sc)

About Strides Pharma: Established in 1990, Strides Pharma is today a global pharmaceutical company that mainly operates in the regulated markets of US, Europe, Canada, Australia and South Africa with an In-Market business in Africa, for Market branded generics strategy in Africa. We also operate an emerging market CIS, and SEA and are partnered with leading donor-funded agencies for the global tenders/procurement primarily in the Anti-retroviral (ARV) and Anti malaria (MAL) treatments.

As a fundamental strategy, we focus on niche domains, and our core competence is in the development and manufacture of a wide range of technically complex pharmaceutical products. This apart, we thrive on a consistent commitment to quality and compliance in a rapidly evolving pharmaceutical landscape.

Today, we have built scale, scope, knowledge, and capabilities to focus on innovation-led growth and to excel in the markets we operate. Our business is supported by a team of 3000 people across our 8 (5 of which are USFDA approved) global manufacturing sites based in India (Bengaluru, Pondicherry, Chennai), Singapore, Europe (Italy-Milan), Africa (Kenya & Nairobi) and United States (West Palm Beach-Florida).

We also have a dedicated R&D Centre in Bengaluru with 250+ scientists to file over 25 ANDAs per year. Our Corporate Office is based in Bangalore.

Role : Trainee

Department : Quality Control

Location : Bangalore, Alathur, Pondicherry

Education : M.Sc. (Chemistry), B-Pharm - 2024 Pass out

Candidate will work for 1 year as Trainee under Probation period which will be confirmed later based on performance.

Key Responsibilities / Outcomes:

1. Analysis of raw material, in-process, finished products & stability samples of various formulation products: oral solids, injectable & ophthalmic products.

2. Handling of QC Instruments like HPLC, GC, UV, FTIR, pH Meter, etc.

3. Working on software like Empowers, Labware LIMS.

4. Knowledge on the GLP & GDP practices.

5. Execution of validation, qualification and calibration activities in QC laboratory.

6. Preparation of SOP, GTP, STP, specification, protocol, IOCP, record of analysis and analysis reports.

7. Handling, issuance and maintenance of consumables, glassware's, chemicals, reference standards, working standards and chromatographic columns etc.

8. Exposure to regulatory audits like USFDA.

9. Investigation of OOS test results and laboratory incidences.

10. Ensure the compliance, Safety and 100% Good laboratory Practices.