Author: Sudheer vanguri

Micro Labs Limited – Goa Plant is looking for a motivated and detail-oriented professional to join its Quality Assurance team.
The opening is in QA – Sampling / Qualification, with responsibilities related to raw material and packing material sampling.
Candidates with a B.Sc. qualification and 0–5 years of experience can apply for this opportunity.
The position is based at the Goa Plant and involves GMP-compliant sampling, equipment verification and documentation activities.

Micro Labs Limited – QA Sampling / Qualification

Micro Labs Limited – Quality Assurance Department

Department: Quality Assurance – Sampling / Qualification
Designation: QA – Sampling / Qualification
Location: Goa
Experience: 0–5 Years
Qualification: B.Sc.

Micro Labs Limited – Key Responsibilities

• Perform sampling of Raw Materials and Packing Materials as per established procedures.
• Conduct Individual Container Identification Tests using a Raman Spectrometer.
• Perform daily verification and monthly calibration of balances.
• Ensure sampling and related activities are carried out in compliance with GMP and applicable quality standards.
• Maintain accurate documentation and records related to sampling and equipment verification.

Eligibility & Qualifications

Micro Labs Limited – Required Education

B.Sc.

Candidates with a B.Sc. qualification can apply for the QA Sampling / Qualification position.

Experience Requirements

0–5 Years

The opening is suitable for candidates with 0–5 years of relevant experience.

How to Apply

Interested candidates can share their updated CV at:

goahr@microlabs.in

Candidates should submit their updated CV with relevant qualification and experience details.

Job Summary

Centurion Group of Companies is expanding its pharmaceutical team and inviting applications from qualified professionals for multiple positions.
The recruitment includes opportunities across Production, Quality Control, Quality Assurance, IPQA, Formulation & Development, Packing and Maintenance.
Candidates with M.Pharm, B.Pharm, B.Sc, M.Sc and B.E. qualifications can apply for the available roles.
The openings are suitable for candidates with 0–3 years of experience looking to build their career in the pharmaceutical industry.

Centurion Group of Companies – Open Positions

Centurion Group – Production Department

Position: Production Officer
Experience: 0–3 Years

The role is part of the Production function and is suitable for candidates with relevant pharmaceutical qualifications.

Centurion Group – Quality Control Department

Position: QC HPLC Chemist
Experience: 0–3 Years

Candidates with relevant pharmaceutical or science qualifications and an interest in HPLC-based quality control activities can apply.

Centurion Group – Quality Assurance Department

Position: QA Documentation
Experience: 0–3 Years

The position focuses on documentation-related activities within the Quality Assurance function.

Centurion Group – IPQA Department

Position: IPQA Officer
Experience: 0–3 Years

Candidates can apply for the In-Process Quality Assurance position with relevant pharmaceutical qualifications.

Centurion Group – Formulation Department

Position: Ointment Chemist
Experience: 0–3 Years

The position is associated with pharmaceutical formulation activities involving ointment products.

Centurion Group – Packing Department

Position: Packing Chemist
Experience: 0–3 Years

Candidates interested in pharmaceutical packing operations can apply for this position.

Centurion Group – Maintenance Department

Position: Maintenance Officer
Experience: 0–3 Years

The position is available within the pharmaceutical maintenance function.

Centurion Group – Formulation & Development Department

Position: Formulation & Development
Experience: 0–3 Years

Candidates with relevant pharmaceutical or science qualifications can apply for opportunities in Formulation & Development.

Eligibility & Qualifications

Centurion Group – Required Education

M.Pharm | B.Pharm | B.Sc | M.Sc | B.E.

Candidates should possess a relevant qualification for the position they are applying for.

Experience Requirements

0–3 Years

The recruitment notice indicates opportunities for candidates with up to 3 years of experience.

Job Locations

Centurion Group – Manjusar

Opportunities are available at Manjusar, Gujarat.

Centurion Group – Gorwa

Opportunities are also available at Gorwa, Gujarat.

How to Apply

Interested candidates can send their updated resume to either of the following email addresses:

hr@centurionremedies.com
hr@centurionlaboratories.com

Contact

Phone: +91 99255 31580

Candidates should mention the position they are applying for while submitting their resume.

Job Summary

Cronus Pharma Specialities India Pvt. Ltd. is hiring professionals for its Analytical Research & Development (AR&D) department.
The opportunity is available for candidates with 1–3 years of experience in analytical research and development.
Candidates with hands-on experience in method development, method validation and stability studies can apply.
Experience with OSD, SSD, injectables, HPLC, UV-Visible Spectroscopy and IVRT will be relevant for this position.

Cronus Pharma – Analytical Research & Development

Analytical R&D – Executive / Research Professional

Location: Shamshabad, Hyderabad
Department: Analytical Research & Development (AR&D)
Experience: 1–3 Years
Qualification: M.Sc. / M.Pharm
Preference: Immediate Joiners Highly Preferred

Cronus Pharma – Method Development & Validation

Candidates should have hands-on experience in:

• Method Development
• Method Validation
• Stability Studies

Cronus Pharma – Formulation Experience

Experience with the following formulations is required:

• Oral Solid Dosage (OSD)
• Semi Solid Dosage (SSD)
• Injectables

Cronus Pharma – Analytical Instruments & Techniques

Proficiency in analytical instruments and techniques including:

• HPLC
• UV-Visible Spectroscopy
• IVRT
• Other relevant analytical techniques

Eligibility & Qualifications

Cronus Pharma – Analytical R&D Qualifications

M.Sc. | M.Pharm

Candidates should have relevant experience in Analytical Research & Development and practical exposure to analytical methods and pharmaceutical formulations.

Experience Requirements

• 1–3 years of relevant experience.
• Hands-on experience in method development.
• Experience in method validation.
• Experience in stability studies.
• Exposure to OSD, SSD or injectable formulations.
• Working knowledge of HPLC, UV-Visible Spectroscopy and IVRT.
• Immediate joiners are highly preferred.

How to Apply

Interested candidates can share their updated resume at:

eravi@cronuspharma.com

Application Preference

Immediate joiners are highly preferred.

Job Summary

Ipca Laboratories Limited is conducting a Walk-In Interview for experienced and dynamic candidates across multiple pharmaceutical departments.
The recruitment drive includes opportunities in Production, Packing, Quality Assurance, Quality Control, Engineering and Operations.
Candidates with qualifications such as B.Pharm, M.Pharm, B.Sc, B.E./B.Tech, ITI, HSC and SSC can apply for relevant positions.
The available roles require experience ranging from 2 to 8 years, with selected fresher opportunities in Plant Maintenance.

Ipca Laboratories – Production Department

Granulation – Operator

Qualification: ITI | HSC | SSC
Experience: 2–4 Years

Job Profile: Operation activity of granulation.

Compression – Officer

Qualification: B.Pharm
Experience: 2–4 Years

Job Profile: Supervision of the compression area.

Compression – Operator

Qualification: ITI | HSC | SSC
Experience: 2–4 Years

Job Profile: Operation activity of compression.

Coating – Officer

Qualification: B.Pharm
Experience: 2–4 Years

Job Profile: Supervision of the coating area.

Coating – Operator

Qualification: ITI | HSC | SSC
Experience: 2–4 Years

Job Profile: Operation activity of the coating area.

QMS – Senior Officer / Executive

Qualification: B.Pharm | M.Pharm
Experience: 2–4 Years

Job Profile:

• Review of BMR.
• Risk assessment for validation activity.
• CCP and CAPA activities.
• Work with software including LMS, EDMS and TrackWise.

Ipca Laboratories – Packing Department

Primary & Secondary Packing – Operator

Qualification: ITI | HSC | SSC
Experience: 2–4 Years

Job Profile: Operation of primary and secondary packing lines.

Ipca Laboratories – Quality Assurance Department

IPQA – Senior Officer

Qualification: B.Pharm
Experience: 4–7 Years

Job Profile: In-process activities related to manufacturing and packaging.

Equipment Qualification – Senior Officer

Qualification: B.Pharm
Experience: 4–7 Years

Job Profile: Equipment qualification and CSV activities.

Ipca Laboratories – Quality Control Department

Microbiology – Senior Officer

Qualification: B.Sc.
Experience: 4–7 Years

Job Profile: Supervision of microbiology activities.

Ipca Laboratories – Engineering Department

Utility – Executive / Senior Officer

Qualification: B.E. / B.Tech
Experience: 5–7 Years

Job Profile: Supervision of the utility area.

Utility – Operator

Qualification: ITI
Experience: 2–4 Years

Job Profile: Utility operator activities.

HVAC – Officer

Qualification: B.E. / B.Tech
Experience: 2–4 Years

Job Profile: Supervision of the HVAC area.

Plant Maintenance – Officer

Qualification: B.E. / B.Tech
Experience: 2–4 Years

Job Profile: Supervision of plant maintenance.

Plant Maintenance – Operator

Qualification: ITI
Experience: 2–4 Years

Job Profile: Plant maintenance operator activities.

Plant Maintenance – Fresher / Apprentice

Qualification: B.E. / B.Tech
Experience: Fresher

Job Profile: Apprentice – Plant Maintenance.

Ipca Laboratories – Operations Department

Production Planning – Senior Officer / Executive

Qualification: B.Pharm | M.Pharm
Experience: 5–8 Years

Job Profile: Production planning activities.

Eligibility & Qualifications

Ipca Laboratories – Eligible Qualifications

B.Pharm | M.Pharm | B.Sc. | B.E. | B.Tech | ITI | HSC | SSC

Candidates should meet the qualification and experience requirements specified for the respective department and position.

Experience Requirements

• Production: 2–4 Years
• Packing: 2–4 Years
• Quality Assurance: 4–7 Years
• Quality Control – Microbiology: 4–7 Years
• Engineering: 2–7 Years
• Operations – Production Planning: 5–8 Years
• Plant Maintenance Apprentice: Freshers

Walk-In Interview Details

Date: 4 October 2026 (Sunday)
Time: 10:00 AM to 4:00 PM

Interview Venue

Ipca Laboratories Limited
Plot No. 65, 99 & 126, Dan Udyog Industrial Estate,
Piparia, Silvassa.

How to Apply

Interested candidates can attend the walk-in interview with their updated resume and the required documents.

Documents Required

For experienced candidates, please carry:

• Updated resume
• Original certificates
• Passport-size photographs (02)
• Latest increment letter
• Last 03 months’ salary slips

Candidates should also carry copies of their educational certificates and previous companies’ experience letters.

Experienced candidates with regulatory exposure to USFDA / MHRA will be preferred.

Contact Details

Phone: 0260-3514400 / 406
Email: hrd.piparia@ipca.com

Job Summary

Bioagile Therapeutics Pvt. Ltd. is hiring a Clinical Research Associate (CRA) to join its clinical research team.
The company is looking for candidates with 1–2 years of experience in CRA, CRC or CTA roles.
This opportunity is suitable for professionals with relevant clinical research experience seeking to continue their career in clinical operations.
Interested candidates can share their updated CV directly with the company for consideration.

Bioagile Therapeutics – Clinical Research Department

Clinical Research Associate (CRA)

Experience: 1–2 Years
Relevant Experience: CRA / CRC / CTA

The selected candidate will be part of the clinical research function and support clinical trial activities according to the requirements of the role.

Eligibility & Qualifications

Bioagile Therapeutics – CRA Qualification

The provided recruitment notice does not specify an educational qualification. Candidates with relevant qualifications in Pharmacy, Life Sciences, Biotechnology, Medicine or related clinical research disciplines may be considered based on their experience.

B.Pharm | M.Pharm | Pharm.D | MBBS | B.Sc. Life Sciences | M.Sc. Life Sciences | Biotechnology | Clinical Research

Experience Requirements

• 1–2 years of professional experience in Clinical Research.
• Experience in CRA, CRC or CTA roles is required.
• Candidates should have relevant exposure to clinical research or clinical trial operations.

How to Apply

Interested candidates can send their CV to:

hr@bioagiletherapeutics.com

Candidates should include the Clinical Research Associate (CRA) position in the email subject line.

Job Summary

Virchow Biotech Private Limited is hiring a Senior Executive – Regulatory Affairs for its regulatory team.
The role focuses on National Regulatory Affairs, CDSCO and State FDA / DCA submissions.
Candidates with pharmaceutical regulatory affairs experience and prior r-DNA regulatory experience can apply.
The position requires 3–6+ years of experience, with M.Pharm in Regulatory Affairs preferred.

Virchow Biotech – Regulatory Affairs Department

Senior Executive – Regulatory Affairs

Department: Regulatory Affairs
Area: National Regulatory, CDSCO & State FDA / DCA
Experience: 3–6+ Years in Pharmaceutical Regulatory Affairs
Salary: As per present package
Location: Hyderabad, Telangana

Scope of Work – Regulatory Affairs

Scope 01: Regulatory Submissions

• Registrations & renewals
• Variations & amendments
• Licences & permissions
• NOC applications

Scope 02: Regulatory Compliance

• CDSCO & State FDA filings
• Deficiency responses
• Label & artwork review
• Audit & inspection support

Eligibility & Qualifications

Educational Qualifications

B.Pharm | M.Pharm | M.Pharm in Regulatory Affairs

M.Pharm in Regulatory Affairs is preferred for the position.

Experience Requirements

• 3–6+ years of experience in pharmaceutical Regulatory Affairs.
• Previous r-DNA regulatory experience is mandatory.
• Experience with ODLS, NSWS, CDSCO Sugam, CDSCO MD and ONDLS is required.
• Knowledge of Drugs & Cosmetics Rules, GMP and ICH requirements.

Required Regulatory Knowledge

Candidates should have relevant knowledge and experience in:

• r-DNA regulatory submissions
• CDSCO regulatory requirements
• State FDA / DCA requirements
• Regulatory registrations and renewals
• Variations and amendments
• Licences and permissions
• NOC applications
• Deficiency responses
• Label and artwork review
• Audit and inspection support
• Drugs & Cosmetics Rules
• GMP
• ICH requirements

Must-Have Requirement

Previous r-DNA regulatory experience is mandatory for this position.

Documents Required

Candidates are requested to bring the following documents:

• Updated CV
• One passport-size photograph
• Last three payslips
• Bank statement
• Increment letter
• Original educational and experience certificates
• Government photo identity proof

How to Apply

Interested candidates can send their updated CV to:

hr@virchowbiotech.com

Candidates should mention “Sr. Executive – Regulatory Affairs” in the subject line of the email.

Contact Details

Phone: +91 91001 25845
Email: hr@virchowbiotech.com

Walk-In / Interview Venue

Virchow Biotech Private Limited
Unit – I, Gagillapur,
Hyderabad – 500043, Telangana.

Only shortlisted candidates will be contacted.

Job Summary

Exemed Pharmaceuticals is hiring experienced professionals for multiple functions in its pharmaceutical API manufacturing operations.
The company has openings across R&D Documentation, QA, Quality Control, Microbiology, Electrical and Process Engineering departments.
Candidates with relevant pharmaceutical, chemistry, microbiology and engineering qualifications can apply for the available positions.
The openings require 2–9 years of experience, depending on the role and department.

Exemed Pharmaceuticals – R&D Department

Executive – R&D Documentation

Experience: 5–7 Years
Qualification: M.Sc. Organic Chemistry
Department: R&D

Key Responsibilities

• Prepare, review and maintain R&D documentation, including SOPs, STPs, protocols and reports.
• Ensure data integrity and compliance with cGMP / GLP.
• Support development reports, stability studies and regulatory submissions such as DMF/CTD.

Exemed Pharmaceuticals – Quality Assurance Department

Executive – AQA

Experience: 5–7 Years
Qualification: M.Sc.
Department: QA

Key Responsibilities

• Review and approve analytical documents, including SOPs, STPs and test methods.
• Ensure compliance with GMP, cGMP and regulatory requirements.
• Handle laboratory investigations, OOS/OOT and change controls.
• Support audits and regulatory inspections.

Exemed Pharmaceuticals – Quality Control Department

Officer – HPLC

Experience: 3–5 Years
Qualification: B.Sc. or M.Sc.
Department: Quality Control (QC)

Key Responsibilities

• Operate and analyze samples on HPLC, including method validation and routine analysis.
• Maintain HPLC instruments and Chromeleon / relevant software.
• Ensure data integrity and compliance with GMP requirements.
• Prepare analytical reports and support regulatory audits.

Exemed Pharmaceuticals – Microbiology Department

Officer – Microbiologist

Experience: 3–5 Years
Qualification: M.Sc.
Department: Microbiology (QC/QA)

Note: Male candidate required.

Key Responsibilities

• Conduct microbiological analysis of raw materials, intermediates and finished products.
• Perform microbial limits, bioburden and environmental monitoring.
• Maintain documentation as per GMP requirements.
• Support method validation and laboratory compliance.

Exemed Pharmaceuticals – Engineering / Maintenance Department

Electrician

Experience: 2–5 Years
Qualification: ITI (Electrician)
Department: Engineering / Maintenance

Key Responsibilities

• Troubleshoot and maintain electrical systems and equipment.
• Perform preventive and breakdown maintenance of plant utilities.
• Ensure safety and compliance with electrical standards.
• Support installation, testing and commissioning of electrical equipment.

Exemed Pharmaceuticals – Process Engineering Department

Senior Executive – Process Engineering

Experience: 7–9 Years
Qualification: B.E. Chemical
Department: Process Engineering

Note: Pharma API experience required.

Key Responsibilities

• Handle process engineering activities for API manufacturing.
• Manage process optimization, scale-up, troubleshooting and debottlenecking.
• Prepare and review process documents, PFD, P&ID and SOPs.
• Support technology transfer, new product commercialization and regulatory compliance.

Eligibility & Qualifications

Educational Qualifications

M.Sc. Organic Chemistry | M.Sc. | B.Sc. | ITI Electrician | B.E. Chemical

Candidates should have the relevant educational qualification and experience required for the respective position.

Experience Requirements

• Executive – R&D Documentation: 5–7 Years
• Executive – AQA: 5–7 Years
• Officer – HPLC: 3–5 Years
• Officer – Microbiologist: 3–5 Years
• Electrician: 2–5 Years
• Senior Executive – Process Engineering: 7–9 Years

How to Apply

Interested candidates can send their updated CV to:

recruitment@exemedpharma.com

Application Details

Candidates should mention the position and department they are applying for in the subject line of the email to help the recruitment team identify the application correctly.

Job Location

Exemed Pharmaceuticals
Block No. 628 A&B, ECP Canal Road,
At & Po – Luna, Ta – Padra,
Dist – Vadodara, Gujarat.

Job Summary

Pontika Aerotech is conducting a Walk-In Drive for experienced professionals across multiple pharmaceutical departments.
The company has openings in Packing, Production, Quality Control and Warehouse functions.
Candidates with relevant pharmaceutical, science, ITI, 10th, 12th and graduate qualifications can apply for the available positions.
The recruitment covers multiple dosage forms and manufacturing areas, including Aerosol, Nasal, Semisolid, Liquid, Cream, Tablet, Capsule and Injectable operations.

Pontika Aerotech – Packing Department

Officer / Executive – Packing

Experience: 1–8 Years
Qualification: B.Sc. / B.Pharma / D.Pharma / M.Pharma

The position is associated with packing operations across pharmaceutical dosage forms.

Pontika Aerotech – Packing / Production Department

Operators – Packing / Production

Experience: 1–8 Years
Qualification: ITI / 10th / 12th

Candidates can be considered for packing and production operations involving the listed dosage forms and manufacturing areas.

Pontika Aerotech – Production Department

Officer / Executive – Production

Experience: 1–6 Years
Qualification: B.Sc. / B.Pharma / M.Pharma

The production openings cover pharmaceutical manufacturing operations across multiple dosage forms.

Pontika Aerotech – Quality Control Department

Officer / Executive – Quality Control

Experience: 1–8 Years
Qualification: B.Sc. / M.Sc. / M.Pharma

The Quality Control positions cover all QC sections and include opportunities across the listed pharmaceutical dosage forms.

Pontika Aerotech – Warehouse Department

Officer / Executive – Warehouse

Experience: 1–8 Years
Qualification: Any Graduate

The Warehouse position involves RM dispensing and receiving activities.

Dosage Forms & Manufacturing Areas

Pontika Aerotech – Dosage Forms

The recruitment covers the following dosage forms:

• Aerosol
• Nasal
• Semisolid
• Liquid
• Cream
• Tablet
• Capsule
• Injectable

Pontika Aerotech – Production & Packing Areas

Relevant manufacturing areas include:

• Autoclave
• Filling
• Labelling
• Autocartoner
• Packing

Pontika Aerotech – Quality Control Areas

The Quality Control opportunity covers:

• Aerosol
• Nasal
• Semisolid
• Liquid
• Cream & Injectable
• All QC Sections

Eligibility & Qualifications

Educational Qualifications

B.Sc. | M.Sc. | B.Pharma | M.Pharma | D.Pharma | Any Graduate | ITI | 10th | 12th

Candidates should meet the qualification and experience requirements specified for the respective position.

Experience Requirements

• Packing – Officer / Executive: 1–8 Years
• Packing / Production – Operators: 1–8 Years
• Production – Officer / Executive: 1–6 Years
• Quality Control – Officer / Executive: 1–8 Years
• Warehouse – Officer / Executive: 1–8 Years

How to Apply

Interested candidates can apply via WhatsApp at:

8278729004

Walk-In Interview Details

Date: 27 September 2026
Time: 10:00 AM to 3:00 PM
Location: Paonta Sahib, Himachal Pradesh
Venue: Pontika Aerotech

Candidates should carry their updated resume and relevant educational and experience documents for the interview.

Job Summary

Marksans Pharma Ltd is hiring professionals for its Quality Assurance Department under the IPQA section.
The opening is for Officer / Sr. Officer positions for candidates with relevant pharmaceutical quality experience.
Candidates holding B.Pharm or M.Pharm qualifications and 2–5 years of experience can apply.
Immediate joiners are preferred for this Quality Assurance opportunity.

Marksans Pharma – Quality Assurance Hiring

Officer / Sr. Officer – Quality Assurance | Marksans Pharma

Department: Quality Assurance
Section: IPQA
Experience: 2–5 Years
Qualification: B.Pharm / M.Pharm
Preference: Immediate joiners preferred

The position is within the In-Process Quality Assurance (IPQA) function and is suitable for candidates with relevant pharmaceutical quality assurance experience.

Eligibility & Qualifications

Educational Qualification

B.Pharm | M.Pharm

Candidates with a relevant pharmaceutical qualification and experience in Quality Assurance / IPQA can apply.

Experience Required

2–5 Years

Relevant experience in pharmaceutical Quality Assurance and IPQA is applicable to the advertised position.

How to Apply

Interested candidates can share their updated resume with:

Email: muskan.shaikh@marksanspharma.com

Candidates should include their relevant qualification, experience and current availability in their resume.

Job Summary

Veedo Lifesciences is hiring freshers for its Bioanalytical Research team through a walk-in drive.
The available roles include Analyst, BQM and Custodian, offering opportunities for candidates with pharmaceutical and life sciences qualifications.
The roles involve sample analysis, analytical data review, laboratory documentation and proper handling of biological samples and laboratory materials.
Candidates with B.Pharm, M.Pharm or M.Sc. qualifications can attend the walk-in drive in Ahmedabad.

Veedo Lifesciences – Analyst, BQM & Custodian

Analyst – Bioanalytical Research | Veedo Lifesciences

The Analyst role involves sample collection, sample processing and analytical testing as part of bioanalytical research activities.

Role & Responsibilities

• Collect samples for analysis from the custodian.
• Process samples using various sample extraction techniques to determine the concentration of analyte.
• Perform analysis via LCMS.
• Follow GXP requirements during analytical activities.

BQM – Bioanalytical Research | Veedo Lifesciences

The BQM role involves reviewing analytical data and laboratory documentation to support compliance and accuracy.

Role & Responsibilities

• Review compiled data including MV, MD and study data.
• Review system and analytical laboratory equipment calibration records.
• Review equipment logbooks and preventive maintenance schedules.
• Verify documentation from the analyst/GL in accordance with respective SOPs.
• Review method SOPs, study plans and method validation protocols.
• Provide observation reports to the respective GL for correction purposes.

Custodian – Bioanalytical Research | Veedo Lifesciences

The Custodian role focuses on the appropriate handling, storage, documentation and disposal of laboratory materials.

Role & Responsibilities

• Ensure proper handling of biological samples, chemicals and laboratory materials.
• Maintain appropriate storage and documentation.
• Ensure proper disposal of biological samples, chemicals and laboratory materials.
• Follow GLP, GCP and applicable regulatory guidelines.

Eligibility & Qualifications

Veedo Lifesciences – Analyst, BQM & Custodian

B.Pharm | M.Pharm | M.Sc.

Candidates with relevant pharmaceutical, life sciences or analytical laboratory backgrounds can apply for the available Bioanalytical Research positions.

Experience Requirements

The recruitment is specifically mentioned for Freshers.

Experience: Freshers

Walk-In Interview Details

Date: 27 September 2026, Sunday
Time: 10:00 AM to 2:00 PM

Venue – Veedo Lifesciences

Satyamev Corporate
Opp. Prahlad Nagar Fire Station
Near Shalin Bungalows
Corporate Road, Prahlad Nagar
Ahmedabad, Gujarat – 380015

How to Apply

Interested and eligible candidates can attend the walk-in interview at the venue mentioned above.

Candidates should carry their updated CV and relevant educational documents for the interview.

Job Summary