NATCO Pharma is a vertically integrated company dedicated to the development, manufacture, and supply of pharmaceutical and agrochemical products. Established with the mission to make specialty medicines accessible to all, we are rooted in integrity, respect, openness, collaboration, creativity, and quality. Founded in 1981, we now have a strong global presence in over 50 countries.
NATCO has emerged as an esteemed pharmaceutical company with a presence in Finished Dosage Formulations (FDF) and Active Pharmaceutical Ingredients (APIs) in both domestic and international markets. NATCO Pharma’s focused approach has led to expanded capabilities across diverse therapy segments, particularly in oncology.
We operate in two key segments: Pharmaceuticals and Agrochemicals. Our expertise excels in the FDF division, crafting intricate pharmaceutical solutions tailored to specific therapeutic needs. In the manufacturing of APIs, we maintain high quality and adhere to all regulatory standards with a focus on innovation. In the Crop Health Sciences (CHS) division, we produce high-value agricultural input products to meet farmers’ demands, including environmentally safer biocontrol products.
Operating globally, NATCO’s work contributes to its diverse market presence. NATCO believes in sustainable and balanced growth through the synergy of our talented workforce and an innovative culture. We are dedicated to maximizing shareholder value creation through innovation, employee engagement, process and system optimization.
DATE AND TIME:
- Date: Sunday, 01st March 2026
- Time: 9:00 AM to 2:00 PM
- Venue: Signature Hotels, Sheelanagar (Gajuwaka), Visakhapatnam, Andhra Pradesh – 530012
JOB DETAILS:
Work Location: Kothur – OSD Formulations (Production & Packing)
Qualification: ITI / Diploma / B. Pharmacy / M. Pharmacy
Skill Requirements:
- Operators – 5 to 8 years of experience in operating equipment in Granulation (Tapasya / ACG), Compression (GEA / Sejong), Coating (Neocota), Roll compaction (Alexander), Capsule Filling (Bosch / MG02), Spray Dryer (Labultima), Track-n-Trace (Optel), Bottle Packing (CVC), Blister Packing (CAM / IMA / ACG), Dry powder filling (Anchor), IPQC, Labelling (CVC / Maharshi), HAPA Printing.
- Executives – 4 to 8 years of experience in supervising Production (Granulation, Compression, Coating, Spray Dryer), Packing (Bottle / Blister) & HAPA Printing activities.
- Executive / Sr Executives – 4 to 8 years of Experience in QMS activities (Change Controls, Investigations, Incidents, & CAPA preparation)
Work Location: Nagarjuna Sagar – Sterile Injectables
Skill Requirements:
Production (Diploma / B.Sc. / B.Pharm. / M. Sc.)
- Asst. Manager – Handling end-to-end sterile injectable manufacturing lines, cGMP compliance, Production, and manpower (12+ yrs of exp)
- Filling Supervisors – Supervision of aseptic filling Ops (2 to 3 yrs of exp)
- Packing Supervisor – Supervision of production packaging (B. Pharm. Fresher)
- General Injectables Packing In-charge – (12+ yrs of exp)
- QMS Experience in Production QMS, cGMP, SOPs (3+ yrs of exp)
- Training Supervisor – Supervise Production trainings (B. Pharm. – Fresher)
- Operators – Filling, Compounding, Vial washing, Tunnel, Autoclave (2 to 3 yrs of exp)
Engineering (Diploma / B.Sc. / B. Tech.)
- Lyo In-charge – Hands-on experience on Lyophilization operations (8 to 10 yrs of exp)
- Expertise in Instrumentation activities (4 to 6 Yrs of exp)
Warehouse (B. Com./ B. Sc. / B.Pharm. / M.B.A.)
- Hands-on experience in the dispensing of raw materials & QMS activities (4 to 5 yrs of exp)
Microbiology ( M.Sc. – Microbiology / Biotechnology)
- Disinfectant preparation, Media Preparation, MLT, BET & Sterility Method Validations Executions & Documentation (2 to 6 yrs of exp)
Quality Assurance (B. Pharm. / M. Sc.)
- IPQA (3 to 5 yrs of exp)
- Documentation (3 to 5 yrs of exp)
- Documentation In-charge (10 to 12 yrs exp)
- Document review (5 to 8 yrs exp)
- QMS (3 to 5 yrs of exp)
- Vendor Management (3 to 5 yrs exp)
- Validation (6-to 8 yrs of exp)
- Assistant Manager – Handling end-to-end IPQA, Validation & QMS of Cyto block. (12 to 18 yrs of exp)
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