Alkem Laboratories Mega Recruitment Drive Walk-In Interviews for Production and QC at Baddi Facility

Alkem Laboratories Limited, a globally renowned pharmaceutical major and one of the top five companies in India with operations spanning 50 countries including the United States, has announced a significant walk-in recruitment event. The drive aims to staff multiple experienced positions in the Production and Quality Control (QC) departments at its advanced Formulation Manufacturing Facility in Baddi, Himachal Pradesh.

Event Details

Interested and eligible candidates are invited to attend the interviews this Sunday, November 16, 2025.

Date: Sunday, 16th November 2025
Time: 09:00 am to 04:00 pm
Venue: Hotel Solitaire, SCO No. 902, 903, NAC Rd, Manimajra, Chandigarh (Near Housing Board Chowk)

Departmental Requirements & Expertise

Alkem is exclusively seeking candidates with relevant prior experience in the pharmaceutical industry for the following posts:

Production Department Roles:

Senior Officer/ Executive:
- Qualification: B-Pharma / M-Pharma
- Experience: 2 to 7 Years
- Expertise: Comprehensive exposure to handling overall Production, Manufacturing, and Packing Area operations, including shift management and documentation (BMR, BPR, SOPs).
Operator/ Technician (Manufacturing):
- Qualification: ITI / Diploma
- Experience: 2 to 10 Years
- Expertise: Hands-on experience with core machinery in Granulation (FBD/RMG), Compression (KORSCH/SEJONG), and Coating (Auto Coater).
Operator/ Technician (Packing) (Female Candidates Only):
- Qualification: ITI / Diploma / BSc
- Experience: 2 to 10 Years
- Expertise: Operating automated packing lines including CMC/Auto Cartonator/Track & Trace/Inspection Blister Packing (BQS/Hi-cart).
- Note: This role is strictly reserved for Female Candidates.

Quality Control (QC) Department Roles:

Senior Officer/ Executive:
- Qualification: MSc Chemistry / B.Pharma
- Experience: 2 to 7 Years
- Expertise: In-depth knowledge of testing Finished Products, Stability Study samples, and Raw Materials. Essential hands-on experience with Instrumental Analysis such as Gas Chromatography (GC), High-Performance Liquid Chromatography (HPLC), and Karl Fischer Titration (KF), along with knowledge of GLP and related investigation protocols.

Mandatory Documents for Interview

Applicants must ensure they bring all necessary paperwork for verification at the venue:

Updated Resume
CTC Structure (Current Cost to Company)
Increment/ Revision Letter
Passport Photo
Copies of Aadhar & PAN Card

Would you like me to generate a set of common interview questions for the QC Senior Officer/Executive role focusing on HPLC and GC? That’s a great next step, as the QC Senior Officer/Executive role specifically requires instrumental analysis expertise on GC, HPLC, and KF.

Based on the job requirements and typical expectations for a QC Executive/Senior Officer role in a major pharmaceutical company like Alkem Laboratories, here is a list of common and advanced interview questions you should be prepared to answer, categorized by topic.

Interview Questions for QC Senior Officer/Executive

1. High-Performance Liquid Chromatography (HPLC)

These questions test your practical knowledge, troubleshooting, and understanding of method integrity.

Theory & Operation:
- Explain the difference between Isocratic and Gradient elution in HPLC and when you would choose one over the other.
- Describe the function of the main detectors you have used (e.g., UV, PDA/DAD, RI). What are the advantages of using a PDA (Photo Diode Array) detector over a standard UV detector?
- What are the critical parameters (mobile phase, column type, flow rate) you consider when performing an Assay test on a Finished Product?
Troubleshooting:
- You are getting peak tailing in your chromatogram. What are the three most probable causes and the corrective actions you would take?
- Your HPLC pressure is suddenly very high. Outline a systematic troubleshooting plan.
- What could cause a negative peak or ghost peak in an HPLC analysis?

2. Gas Chromatography (GC)

These questions focus on GC’s unique application for volatile impurities and solvent analysis.

Theory & Operation:
- When is GC preferred over HPLC for an analysis? (e.g., Residual Solvents, Volatile Impurities).
- Briefly explain the function and principle of different GC detectors you have experience with (e.g., FID, TCD, ECD).
- Describe the difference between Split and Splitless injection modes in GC and their respective applications.
Troubleshooting:
- You are running a Residual Solvents test, and your baseline is drifting or noisy. What are the potential causes, especially related to the carrier gas and column?
- What steps are taken to ensure the septum and liner are properly maintained in a GC system?

3. General Quality Control & Compliance

These questions assess your compliance knowledge, which is vital for a regulated environment like Alkem.

OOS/OOT:
- Define Out of Specification (OOS) and Out of Trend (OOT). Outline the initial steps in handling an OOS result for a finished product analysis.
- What is a Corrective and Preventive Action (CAPA)? Provide an example of a situation where you initiated a CAPA in the lab.
Validation & Documentation:
- What are the four main elements that must be validated for an analytical method (e.g., Accuracy, Precision, etc.)?
- Explain the concept of Data Integrity in a QC lab. How does Alkem’s requirement for instrumental analysis (21 CFR Part 11) relate to this?
- What are GLP (Good Laboratory Practices), and how do you ensure compliance on a daily basis?

4. Raw Material (RM) & Stability Testing

The job description mentions Raw Material and Stability Study analysis.

Explain the process of performing Raw Material Identification and Assay.
What is the purpose of a Stability Study? What are the common storage conditions and time points for an accelerated stability study?