India's DMPLOI - Jobs & Networking AppPontika Aerotech Ltd., a leading Contract Development and Manufacturing Organization (CDMO), has announced a recurring walk-in interview drive for experienced professionals in Quality Control (QC), Production, and Warehouse departments. The company specializes in topical pharmaceuticals, beauty and personal care products, ayurveda, hygiene products, cosmeceuticals, veterinary products, and other niche manufacturing segments.
This hiring initiative offers excellent career opportunities for candidates looking to work in a growing pharmaceutical and cosmetic manufacturing environment.
Walk-In Interview Details
Interview Schedule: Every Wednesday & Saturday
Time: 10:00 AM to 04:00 PM
Venue:
Pontika Aerotech Ltd.
Vill. Johron, P.O. Puruwala, Nahan Road,
Paonta Sahib, District Sirmaur,
Himachal Pradesh – 173001
Open Positions
1. Quality Control (QC)
Areas:
Document Reviewer
HPLC
GLP
GC
RM/FG/PM Analysis
Designation:
Officer
Senior Officer
Executive
Qualification:
D.Pharm
B.Pharm
M.Pharm
B.Sc
M.Sc
Experience:
1–6 Years
2. Production Department
Packing Section
Areas:
Labelling
Filling
Auto Cartonator
Aerosol Operations
Manufacturing Section
Areas:
Semi-Solid Manufacturing
Designation:
Officer
Senior Officer
Operator
Qualification:
10th / 12th
ITI
D.Pharm
B.Pharm
M.Pharm
B.Sc
M.Sc
Experience:
1–6 Years
3. Warehouse Department
Areas:
RM (Raw Material)
PM (Packing Material)
FG (Finished Goods)
WMS Operations
Designation:
Officer
Senior Officer
Executive
Qualification:
Any Graduate
Experience:
1–6 Years
Preferred Candidates
Candidates having experience in pharmaceutical and cosmetic external preparation manufacturing environments will be preferred.
Contact Information
Email:
careers@pontikaaerotech.com
admin.support@pontikaaerotech.com
Contact Numbers:
9805514664
7807888653
Technical Interview FAQs
1. What is the difference between HPLC and GC in Quality Control?
Answer:
HPLC (High Performance Liquid Chromatography) is used for analyzing non-volatile and thermally unstable compounds, while GC (Gas Chromatography) is used for volatile and thermally stable substances. Both techniques are widely used for assay, impurity profiling, and stability studies.
2. What is the purpose of GLP in a pharmaceutical laboratory?
Answer:
Good Laboratory Practices (GLP) ensure data integrity, traceability, accuracy, and compliance with regulatory requirements. GLP covers documentation, calibration, training, sample handling, and laboratory operations.
3. What are the key checks performed during line clearance in production?
Answer:
Line clearance includes verification of cleanliness, removal of previous product materials, status labeling, equipment readiness, document availability, and ensuring no mix-up or contamination risks exist before production starts.
4. What is FEFO and why is it important in warehouse operations?
Answer:
FEFO (First Expiry First Out) ensures materials with the nearest expiry date are issued first. This minimizes wastage, prevents expired material usage, and maintains inventory compliance.
5. What parameters are monitored during semi-solid manufacturing?
Answer:
Critical parameters include temperature, mixing speed, homogenization time, viscosity, pH, appearance, and batch yield. Monitoring these parameters ensures consistent product quality and process reproducibility.
Pontika Aerotech’s walk-in drive presents an excellent opportunity for professionals seeking growth in Quality Control, Production, and Warehouse functions within a rapidly expanding CDMO environment. Interested candidates meeting the eligibility criteria can attend the walk-in interviews every Wednesday and Saturday with updated resumes and relevant documents.
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