Natco Pharma Mega Walk-In Drive Production, QA, Micro & Engineering | Vizag

Natco Pharma Mega Walk-In Drive 2026 | Production, QA, Micro & Engineering | Vizag

Natco Pharma is conducting a Mega Walk-In Interview on 1st March 2026 (Sunday) in Visakhapatnam for multiple vacancies across Production, Packing, Quality Assurance, Microbiology, Engineering, Warehouse, and QMS departments. Opportunities are available at two major manufacturing locations – Kothur (Formulation – OSD Division) and Nagarjuna Sagar (Parenteral – Sterile Injectables Division).

This recruitment drive includes positions for Operators, Supervisors, Executives, Assistant Managers, QA professionals, Microbiologists, and Engineering specialists. Freshers are eligible for select roles, including Packing Supervisor and Training Supervisor (B.Pharm), while experienced candidates with regulatory exposure and formulation manufacturing experience are strongly preferred for senior positions.

If you are looking for pharmaceutical manufacturing jobs in Hyderabad or sterile injectable plant careers in Telangana/Andhra Pradesh, this walk-in drive offers direct hiring opportunities in regulated manufacturing facilities.

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Company Overview

entity[“organization”,”Natco Pharma”,”pharmaceutical company india”] is a leading Indian pharmaceutical company known for its strong presence in oncology, specialty pharmaceuticals, and complex generics. With state-of-the-art manufacturing facilities and a strong global regulatory footprint, Natco supplies high-quality formulations and APIs to regulated markets including the US, Europe, and other international regions.

The company operates advanced formulation plants for Oral Solid Dosage (OSD) and sterile injectables, adhering to global regulatory standards such as USFDA, EU-GMP, and other international guidelines. Natco’s manufacturing excellence, quality systems, and regulatory compliance framework make it a preferred employer for professionals seeking growth in pharma production, quality assurance, and sterile manufacturing environments.

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Work Locations & Departments

1. Kothur (Hyderabad) – Formulation Division (OSD)

Department: Production & Packing

2. Nagarjuna Sagar (Nalgonda) – Parenteral Division

Departments: Production, Engineering, Warehouse, Microbiology & Quality Assurance

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Job Roles & Responsibilities

Kothur – OSD Production & Packing

Operators (5–8 Years Experience)

Experience in operating equipment such as:

• Granulation (Tapasya / ACG)
• Compression (GEA / Sejong)
• Coating (Neocota)
• Roll Compaction (Alexander)
• Capsule Filling (Bosch / MGO2)
• 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 / Supervisors (4–8 Years Experience)

• Supervision of granulation, compression, coating, and spray drying operations.
• Oversight of bottle and blister packing lines.
• Handling HAPA printing and packaging compliance activities.

Executive / Senior Executive – QMS (4–8 Years Experience)

• Change control management.
• Investigation handling.
• Incident reporting.
• CAPA preparation.
• Regulatory documentation support.

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Nagarjuna Sagar – Parenteral (Sterile Injectables)

Production

Assistant Manager (12+ Years Experience)

• End-to-end management of sterile injectable manufacturing lines.
• cGMP compliance oversight.
• Production planning and manpower management.

Filling Supervisors (2–3 Years Experience)

• Supervision of aseptic filling operations.

Packing Supervisor (B.Pharm – Fresher Eligible)

• Supervision of sterile production packaging activities.

Training Supervisor (B.Pharm – Fresher Eligible)

• Oversee production training programs and SOP compliance.

Operators (2–3 Years Experience)

• Filling
• Compounding
• Vial Washing
• Tunnel Operations
• Autoclave Handling

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Engineering (Diploma / B.Tech / B.Sc.)

Lyophilization In-Charge (8–10 Years Experience)

• Hands-on expertise in lyophilizer operations.

Instrumentation Specialist (4–6 Years Experience)

• Instrumentation maintenance and regulatory compliance activities.

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Microbiology (M.Sc. – Microbiology / Biotechnology)

• Disinfectant preparation
• Media preparation
• Microbial Limit Test (MLT)
• Bacterial Endotoxin Test (BET)
• Sterility method validation execution and documentation
  (2–6 Years Experience)

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Quality Assurance (B.Pharm / M.Sc.)

• IPQA (3–5 Years Experience)
• Documentation (3–5 Years Experience)
• Documentation In-Charge (10–12 Years Experience)
• Document Review (5–8 Years Experience)
• QMS (3–5 Years Experience)
• Vendor Management (3–5 Years Experience)
• Validation (6–8 Years Experience)
• Assistant Manager – Handling IPQA, Validation & QMS of Cyto Block (12–18 Years Experience)

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Eligibility & Qualifications

Accepted Qualifications:
I.T.I, Diploma, B.Sc., M.Sc., B.Pharm, M.Pharm, B.Tech (Engineering), Microbiology, Biotechnology, Pharmaceutical Sciences.

Only candidates with relevant formulation manufacturing experience and regulatory exposure will be considered for experienced roles.

Candidates must:

• Be willing to work in rotational shifts, including night shifts.
• Have strong understanding of cGMP guidelines.
• Possess regulatory audit exposure (USFDA/EU-GMP preferred).
• Demonstrate strong documentation and compliance practices.

Note: Preference may be given to male candidates for production-area roles due to shift and operational requirements.

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Interview Details

Date: 1st March 2026 (Sunday)
Time: 9:00 AM – 2:00 PM
Venue: Signature Hotel, Sheela Nagar (Gajuwaka), Visakhapatnam, Andhra Pradesh – 530012

Candidates should carry:

• Updated Resume
• Government ID Proof
• Relevant experience documents (if applicable)

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Frequently Asked Questions (FAQs)

1. Are freshers eligible for this walk-in drive?

Yes. B.Pharm freshers are eligible for Packing Supervisor and Training Supervisor roles in the Parenteral division.

2. Is prior regulatory exposure mandatory?

Yes. For experienced roles, only candidates with formulation and regulatory exposure will be considered.

3. Are night shifts compulsory?

Yes. Production roles require rotational shift flexibility, including night shifts.

4. Which divisions are hiring?

Oral Solid Dosage (OSD) and Sterile Injectables divisions.

5. Is prior sterile manufacturing experience required for parenteral roles?

Yes. For experienced sterile roles, aseptic and injectable manufacturing exposure is required.

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Summary Table

Company	Natco Pharma
Vacancies	Operators, Supervisors, Executives, QA, Microbiology, Engineering, Assistant Managers
Required Education	ITI, Diploma, BSc, MSc, BPharm, MPharm, BTech
Experience	Fresher (limited roles) to 18+ years depending on position