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Zenotech Laboratories Limited Hiring For Quality Assurance & Quality Control

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Zenotech Laboratories Limited

M.Pharm / B.Pharm / M.Sc

Turkapally, Shamirpet, Hyderabad, Telangana

2–8 years

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Zenotech Laboratories Limited, a Sun Pharma group company, has announced walk-in recruitment for experienced professionals across Quality Assurance (QA) and Quality Control (QC) at its manufacturing facility in Turkapally, Hyderabad. The current hiring drive covers positions in IPQA, Validation, QMS, QC-OSD and QC-General Injectables.

The walk-in interviews are scheduled for 5 October and 6 October 2026, from 9:00 AM to 2:00 PM.

Zenotech Laboratories operates in pharmaceutical manufacturing, including specialty generic injectables. Publicly available company information identifies its Turkapally facility in Telangana, while Sun Pharma lists Zenotech Laboratories among its subsidiaries.

Zenotech Laboratories Recruitment 2026 – Job Details

ParticularDetails
CompanyZenotech Laboratories Limited
GroupSun Pharma
DepartmentsQuality Assurance & Quality Control
Job TypeWalk-In Interview
Walk-In Dates5 October & 6 October 2026
Interview Time9:00 AM – 2:00 PM
LocationTurkapally, Shamirpet, Hyderabad, Telangana
Experience2–8 years, depending on position
Work LocationOn-site
IndustryPharmaceutical / Life Sciences

Vacancies at Zenotech Laboratories

1. Officer – IPQA, General Injectables

Department: Quality Assurance
Sub-Department: IPQA – General Injectables
Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Experience: 2–4 years

The role involves overseeing IPQA activities during injectable manufacturing and packaging operations. Candidates will be involved in reviewing and approving BMR/BPR documentation, ensuring cGMP compliance, handling deviations and CAPA, and supporting audit readiness.

2. Senior Officer – Validation

Department: Quality Assurance
Sub-Department: Validation
Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Experience: 3–5 years

The Validation position covers activities associated with process and cleaning validation, media fills and aseptic processing. The role also involves equipment and utility qualification, HVAC qualification, water-system and facility validation, computer system validation and data-integrity compliance.

3. Executive – QMS, General Injectables

Department: Quality Assurance
Sub-Department: QMS – General Injectables
Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Experience: 5–8 years

The QMS position focuses on pharmaceutical quality management activities, including deviations, CAPA, documentation, GMP/GDP compliance, audit preparedness and continuous improvement initiatives.

4. Officer / Senior Officer – QC Analyst, OSD

Department: Quality Control
Sub-Department: OSD
Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Experience: 2–5 years

The QC Analyst role includes operation, calibration and maintenance of analytical instruments such as GC and HPLC. Responsibilities include analysis of raw materials, finished products, cleaning samples and stability samples, as well as preparation and maintenance of working and reference standards.

Candidates may also handle AMV/ATV activities, analytical-result review, COA preparation, deviations, OOS/OOT investigations, incident investigations and document control under GLP/GMP requirements.

5. Officer / Senior Officer – QC Analyst, General Injectables

Department: Quality Control
Sub-Department: General Injectables
Qualification: M.Pharm / B.Pharm / M.Sc. Organic Chemistry
Experience: 2–5 years

This position involves analytical testing and laboratory activities supporting general injectable products. The responsibilities include GC/HPLC operation, analysis of pharmaceutical samples, working-standard management, AMV/ATV activities, analytical-result review, COA preparation and handling of quality investigations.

Key Responsibilities

Depending on the position, selected candidates may be responsible for:

  • Managing IPQA activities during injectable manufacturing and packaging.
  • Reviewing and approving BMR/BPR documentation.
  • Ensuring compliance with cGMP, GLP and GDP requirements.
  • Handling deviations, CAPA, OOS/OOT and incident investigations.
  • Supporting internal and external audits.
  • Managing pharmaceutical QMS activities and quality documentation.
  • Executing process and cleaning validation activities.
  • Supporting media-fill and aseptic-processing activities.
  • Performing equipment, utility, HVAC and water-system qualification.
  • Supporting Computer System Validation (CSV).
  • Operating and maintaining HPLC, GC and other analytical instruments.
  • Testing raw materials, finished products, cleaning samples and stability samples.
  • Maintaining working and reference standards.
  • Supporting AMV/ATV activities.
  • Reviewing analytical results and preparing Certificates of Analysis (COA).
  • Maintaining data integrity and regulatory-compliance requirements.

Qualification

Candidates interested in the Zenotech Laboratories recruitment 2026 drive should have one of the following relevant qualifications:

  • B.Pharm
  • M.Pharm
  • M.Sc. Organic Chemistry

Relevant pharmaceutical manufacturing, Quality Assurance or Quality Control experience is required according to the individual vacancy.

Experience Required

The experience requirement varies by position:

  • IPQA – Officer: 2–4 years
  • Validation – Senior Officer: 3–5 years
  • QMS – Executive: 5–8 years
  • QC Analyst – OSD: 2–5 years
  • QC Analyst – General Injectables: 2–5 years

Candidates should carefully match their experience with the specific department before attending the walk-in interview.

Salary / CTC

The recruitment notice provided for this hiring drive does not specify an official salary or CTC.

For SEO/job-schema purposes, an indicative market range of approximately ₹3.5 lakh to ₹9 lakh per annum may be used as an estimate based on the different experience levels represented by these positions. This is not an employer-confirmed salary range, and the final CTC should be confirmed with the recruitment team.

Documents Required

Candidates attending the Zenotech Laboratories walk-in interview should carry the required documents, including:

  • Updated CV / Resume
  • Last 4 months’ payslips
  • Increment details for the last 2 years
  • Appointment letter with CTC breakup
  • Educational certificates
  • Two passport-size photographs
  • Aadhaar card copy
  • PAN card copy

Candidates should carry original documents where appropriate for verification.

Zenotech Laboratories Walk-In Interview 2026

Walk-In Dates: 5 October 2026 and 6 October 2026
Time: 9:00 AM to 2:00 PM

Venue:
Zenotech Laboratories Limited
Turkapally Village, Shamirpet Mandal
Medchal–Malkajgiri District
Hyderabad – 500101
Telangana, India

Public company records also identify Zenotech Laboratories’ manufacturing/registered operations at Turkapally, Telangana.

How to Apply for Zenotech Laboratories Jobs

Candidates should complete the application process before attending the walk-in interview.

Step 1 – Submit the Application Form

Candidates can submit their details through the Microsoft Forms application link provided in the recruitment notice:

Application Form

Step 2 – Send Your CV

Candidates can also send their updated CV to the recruitment contacts provided in the hiring notice:

hr1@zenotech.co.in
pushpagalla.hr@zenotech.co.in

Zenotech Laboratories Limited Hiring For Quality Assurance & Quality Control
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