PHARMA STUFF

Author: Sudheer vanguri

  • Pharma & Life Sciences Jobs in India | PharmaBharat

  • Zydus Lifesciences Manufacturing Apprentices ITI, Diploma, BSc

    Zydus Lifesciences Limited is conducting a walk-in interview for Manufacturing Apprentice positions at its SEZ-1 Manufacturing Unit, OSD Plant, in Ahmedabad, Gujarat. This opportunity is open to freshers with ITI, Diploma, or B.Sc. qualifications who have no prior work experience. Interested candidates should attend the walk-in interview on 25 October 2026, carrying their educational documents, all semester mark sheets, and passport-size photographs.

    Company Overview

    Zydus Lifesciences Limited is a pharmaceutical company operating across healthcare and life sciences. This recruitment drive is for its SEZ-1 Manufacturing Unit, OSD Plant, in Ahmedabad.

    Job Role & Responsibilities

    Designation: Manufacturing Apprentice
    Department: Manufacturing / Production
    Experience: Freshers
    Job Location: Ahmedabad, Gujarat
    Plant: SEZ-1 Manufacturing Unit, OSD Plant

    The recruitment announcement does not provide detailed job responsibilities for this position.

    Eligibility / Qualifications

    Candidates must meet the following requirements:

    • ITI

    • Diploma

    • B.Sc.

    Experience: Freshers with no prior work experience.

    Candidates should carry their educational details and mark sheets for all semesters when attending the interview.

    Location & Salary

    Location: Ahmedabad, Gujarat

    Walk-in Interview Venue:

    House No. 6 & 7, Sigma Commerce Zone, Near Iskcon Temple, Opposite BRTS, Ambli Bopal Road, Sarkhej Gandhinagar Highway, Satellite Road, Ahmedabad – 380015.

     

    Application Process

    Eligible candidates can attend the walk-in interview directly at the specified venue.

    • Date: 25 October 2026 (Sunday)

    • Time: 9:00 AM to 5:00 PM

    • Position: Manufacturing Apprentice

    Documents Required

    Candidates are specifically requested to bring:

    • Educational qualification details.

    • All semester mark sheets.

    • Passport-size photographs.

    Summary Table

    Company Zydus Lifesciences Limited
    Department Vacancies Manufacturing Apprentice
    Qualification ITI, Diploma, B.Sc.
    Experience Freshers, no prior experience
    Location Ahmedabad, Gujarat

  • Genomiki Solutions Genome Analyst Intern Jobs

    Genomiki Solutions is hiring for the position of Genome Analyst Intern in Delhi NCR. Candidates with 0–1 years of experience and a degree in Genetics, Genomics, Bioinformatics, Biotechnology, Life Sciences, or a related field can apply. The role focuses on next-generation sequencing (NGS) data analysis, genetic variant interpretation, genomic databases, and clinical genetics reporting.

    Company Overview

    Genomiki Solutions works in the genomics and bioinformatics space, with a focus on genomic data analysis and clinical genomics applications.

    Job Role & Responsibilities

    Designation: Genome Analyst Intern
    Location: Delhi NCR
    Experience: 0–1 years

    Key Responsibilities

    • Analyze germline and somatic next-generation sequencing (NGS) data.

    • Perform variant annotation, filtering, prioritization, and interpretation.

    • Support variant curation using databases such as ClinVar, OMIM, gnomAD, and COSMIC.

    • Assist with clinical genetic reports, genotype–phenotype correlation, and literature reviews.

    • Support quality control activities and workflow documentation.

    • Stay updated with current genomics guidelines and practices.

    Eligibility / Qualifications

    Candidates should meet the following requirements:

    Educational Background:

    • Genetics

    • Genomics

    • Bioinformatics

    • Biotechnology

    • Life Sciences

    • Related fields

    Experience: 0–1 years in clinical genomics or a related area.

    Required Knowledge and Skills:

    • Basic understanding of NGS data and genetic variants, including SNVs, InDels, and CNVs.

    • Familiarity with genomic databases such as ClinVar, OMIM, and gnomAD.

    • Knowledge of ACMG/AMP guidelines.

    • Basic familiarity with Linux and command-line tools.

    • Strong analytical skills and attention to detail.

    Location & Salary

    Location: Delhi NCR

    Application Process

    Interested and eligible candidates should apply through the official application form. Applications sent through personal email will not be accepted.

    Apply Online: https://docs.google.com/forms/d/e/1FAIpQLSctMWNBtL0oVgb5Nxqfys-6vSranMCpmNAOpha4s8Hmztp3yg/viewform

    Candidates should review the eligibility criteria before submitting their application.

    Summary Table

    Company Genomiki Solutions
    Department Vacancies Genomics / Bioinformatics – Genome Analyst Intern
    Qualification Genetics, Genomics, Bioinformatics, Biotechnology, Life Sciences, or a related field
    Experience 0–1 years
    Location Delhi NCR

  • Simson Pharma Synthesis and Analytical R&D Jobs

    Simson Pharma Limited is conducting a Mega Walk-In Drive for Synthesis R&D and Analytical R&D positions in Hyderabad, Telangana.
    Candidates with an M.Sc. or M.Pharm qualification in relevant Chemistry specializations and 0–3 years of experience are eligible to apply.
    This recruitment drive offers an opportunity for freshers and early-career professionals to explore research and development careers in the pharmaceutical industry.
    The walk-in interview is scheduled for 24 October 2026, from 10:00 AM to 2:00 PM, at Simson Pharma Limited, IDA, Kukatpally, Hyderabad.

    Simson Pharma Limited Walk-In Drive for R&D Jobs

    Simson Pharma Limited is inviting candidates to attend its Mega Walk-In Drive for Synthesis Research and Development and Analytical Research and Development positions. Candidates with relevant postgraduate qualifications and up to three years of experience can attend the interview at the company’s Hyderabad facility.

    Company Overview

    Simson Pharma Limited operates in the pharmaceutical sector, with opportunities in research and development for candidates interested in synthesis chemistry and analytical testing. This walk-in drive is intended for qualified candidates seeking early-career opportunities in pharmaceutical R&D.

    Job Role & Departments

    1. Synthesis R&D

    The Synthesis Research and Development department is one of the functional areas included in this recruitment drive. Candidates with relevant Chemistry specializations may apply.

    2. Analytical R&D

    The Analytical Research and Development department is also hiring through this walk-in drive. Candidates with suitable postgraduate qualifications in Chemistry-related disciplines may attend.

    Eligibility & Qualifications

    Educational Qualifications

    Eligible candidates should have one of the following qualifications in relevant Chemistry specializations:

    • M.Sc.

    • M.Pharm.

    Experience Required

    • Experience: 0–3 years.

    • Freshers and early-career candidates may apply, subject to the relevant qualification requirements.

    Candidates should have an educational background relevant to Synthesis R&D or Analytical R&D.

    Simson Pharma Walk-In Interview Details

    • Company: Simson Pharma Limited

    • Departments: Synthesis R&D and Analytical R&D

    • Interview Date: Saturday, 24 October 2026

    • Interview Time: 10:00 AM to 2:00 PM

    • Venue: Simson Pharma Limited, Shed No. 6A, Type-III, Prashanthi Nagar, IDA, Kukatpally, Hyderabad, Telangana – 500037.

    Documents Required

    Candidates should carry the following documents for the interview:

    • Updated resume

    • Educational certificates

    • Relevant experience documents, if applicable

    • Valid identification document

    How to Apply

    Interested and eligible candidates can attend the walk-in interview directly at the venue on 24 October 2026, between 10:00 AM and 2:00 PM.

    Candidates should carry their updated resumes and educational documents for verification during the interview.

    The recruitment announcement does not provide an application email address or online application link.

    Frequently Asked Questions

    1. Which company is conducting the walk-in drive?

    Simson Pharma Limited is conducting the Mega Walk-In Drive for R&D positions.

    2. Which departments have vacancies?

    The recruitment drive covers Synthesis R&D and Analytical R&D.

    3. What qualifications are required?

    Candidates with an M.Sc. or M.Pharm qualification in relevant Chemistry specializations are eligible to apply.

    4. Can freshers apply?

    The advertised experience range is 0–3 years, so freshers and candidates with relevant early-career experience may apply.

    5. When is the walk-in interview?

    The interview is scheduled for 24 October 2026, from 10:00 AM to 2:00 PM.

    6. Where is the interview venue?

    The interview will take place at Simson Pharma Limited, Shed No. 6A, Type-III, Prashanthi Nagar, IDA, Kukatpally, Hyderabad, Telangana – 500037.

    Job Summary

    Category Details
    Company Simson Pharma Limited
    Vacancies Synthesis R&D; Analytical R&D
    Required Education M.Sc. / M.Pharm in relevant Chemistry specializations
    Experience 0–3 years

     

  • Intas Pharmaceuticals Regulatory Affairs Recruitment

    Intas Pharmaceuticals Ltd. is inviting applications for the position of Regulatory Affairs Specialist / Senior Executive (ANZ – Injectables) at its Corporate Head Office in Ahmedabad, Gujarat.
    Candidates with B.Pharm, M.Pharm, or a relevant Life Sciences qualification and 3–5 years of experience are eligible to apply.
    The role focuses on regulatory affairs for injectable products, including dossier preparation, regulatory submissions, variations, renewals, and artwork management.
    Professionals with experience in Australia’s TGA regulatory requirements, New Zealand markets, and CTD/eCTD documentation can apply for this work-from-office opportunity.

    Intas Pharmaceuticals Regulatory Affairs Recruitment

    Intas Pharmaceuticals Ltd. is expanding its Regulatory Affairs team for the ANZ (Australia and New Zealand) Injectables business. The company is seeking experienced professionals with knowledge of pharmaceutical regulatory compliance, injectable product documentation, and international regulatory requirements.

    This opportunity is based at the company’s Corporate Head Office in Ahmedabad, Gujarat, and is suitable for candidates with relevant regulatory affairs experience.

    Company Overview

    Intas Pharmaceuticals Ltd. is a pharmaceutical company with global operations. Its Regulatory Affairs department supports regulatory compliance, product registrations, and submissions across international markets.

    Job Role & Responsibilities

    Regulatory Affairs Specialist / Senior Executive (ANZ – Injectables)

    The selected candidate will support regulatory activities related to injectable pharmaceutical products for Australia and New Zealand markets.

    Key responsibilities and areas of expertise include:

    • Preparing and compiling regulatory dossiers for injectable products.

    • Managing regulatory submissions, variations, and renewals.

    • Responding to regulatory queries and supporting approval-related activities.

    • Working with CTD and eCTD documentation.

    • Supporting pharmaceutical regulatory compliance and artwork management.

    • Applying knowledge of international regulatory guidelines.

    • Coordinating regulatory documentation for Australia and New Zealand markets.

    Eligibility & Qualifications

    Educational Qualification

    Candidates with the following qualifications may apply:

    • B.Pharm

    • M.Pharm

    • Relevant Life Sciences qualifications

    Experience Required

    • Experience: 3–5 years, as applicable to the position.

    • Hands-on experience working with injectable pharmaceutical products.

    • Experience in regulatory affairs and pharmaceutical regulatory compliance.

    • Exposure to semi-regulated markets, particularly Australia and New Zealand.

    Required Technical Skills

    • Knowledge of Australia’s Therapeutic Goods Administration (TGA) requirements.

    • Experience in regulatory dossier compilation and submissions.

    • Understanding of variations, renewals, and regulatory query responses.

    • Knowledge of CTD/eCTD formats and international regulatory guidelines.

    • Experience with pharmaceutical artwork management.

    Location & Work Mode

    • Location: Intas Pharmaceuticals Ltd., Corporate Head Office, Ahmedabad, Gujarat.

    • Work Mode: Work from office.

    • Department: Regulatory Affairs.

    • Business Area: ANZ – Injectables.

    Salary Details

    The salary has not been specified in the recruitment announcement. Compensation may depend on the candidate’s experience, qualifications, and the company’s internal salary structure.

    How to Apply

    Interested and eligible candidates can share their updated resume directly with the recruitment contact.

    Candidates should include their relevant regulatory affairs experience, injectable product expertise, and Australia/New Zealand market exposure in their resumes.

    Applicants may also contact the recruitment team through the professional networking channel where the vacancy was shared.

    Important Recruitment Notice

    Intas Pharmaceuticals does not charge candidates any fee for job applications, processing, training, testing, or any other stage of recruitment.

    Candidates should avoid recruitment invitations requesting payment or monetary consideration.

    Frequently Asked Questions

    1. Which company is hiring for the Regulatory Affairs position?

    Intas Pharmaceuticals Ltd. is recruiting for its Regulatory Affairs department.

    2. What positions are available?

    The openings are for Regulatory Affairs Specialist / Senior Executive in the ANZ – Injectables team.

    3. What qualifications are required?

    Candidates with B.Pharm, M.Pharm, or a relevant Life Sciences qualification may apply.

    4. How much experience is required?

    The recruitment announcement specifies 3–5 years of experience, as applicable to the position.

    5. Is experience with injectable products required?

    Yes. Hands-on experience with injectable products is listed as a key requirement.

    6. How can candidates apply?

    Candidates can send their updated resumes to sdwivedi@intaspharma.com with the specified subject line.

    Job Summary

    Category Details
    Company Intas Pharmaceuticals Ltd.
    Vacancies Regulatory Affairs Specialist / Senior Executive (ANZ – Injectables)
    Required Education B.Pharm / M.Pharm / Relevant Life Sciences qualification
    Experience 3–5 years, as applicable

  • Evolet Pharmaceuticals DRA Executive Recruitment

    Evolet Pharmaceuticals Pvt. Ltd. is inviting applications for the position of Drug Regulatory Affairs (DRA) Executive at its facility in Roorkee, Uttarakhand.
    Candidates with a B.Pharm or M.Pharm qualification and relevant experience in pharmaceutical regulatory affairs are eligible to apply.
    The role involves product permissions, drug registrations, regulatory approvals, documentation, and coordination with the FDA and other regulatory authorities.
    Interested candidates with knowledge of drug licensing and pharmaceutical regulatory requirements can send their updated CV to the recruitment email address provided below.

    Evolet Pharmaceuticals DRA Executive Recruitment

    Evolet Pharmaceuticals Pvt. Ltd. is looking for an experienced professional to join its Drug Regulatory Affairs team in Roorkee, Uttarakhand. This opportunity is suitable for pharmacy graduates and postgraduates with relevant experience in regulatory documentation, product permissions, and liaisoning with regulatory authorities.

    Company Overview

    Evolet Pharmaceuticals Pvt. Ltd. is recruiting for its Drug Regulatory Affairs function. The selected candidate will support regulatory submissions, product approvals, licensing activities, and compliance with applicable pharmaceutical regulations.

    Job Role & Responsibilities

    Drug Regulatory Affairs (DRA) Executive

    The selected candidate will be responsible for managing regulatory activities and supporting the approval and registration of pharmaceutical products.

    Key responsibilities include:

    • Handling product permissions, registrations, and regulatory approvals.

    • Liaising with the FDA and other regulatory authorities.

    • Managing regulatory documentation, applications, renewals, and compliance.

    • Coordinating with regulatory authorities regarding approvals and regulatory queries.

    • Ensuring compliance with applicable pharmaceutical regulations.

    • Supporting drug licensing and regulatory documentation activities.

    Eligibility & Qualifications

    Educational Qualification

    Candidates must hold one of the following qualifications:

    • B.Pharm

    • M.Pharm

    Experience Required

    • Relevant experience in pharmaceutical regulatory affairs.

    • Strong experience in product permissions and FDA-related liaisoning.

    • Good knowledge of drug licensing and regulatory requirements.

    Candidates with practical experience in regulatory documentation, product registrations, and regulatory approvals are suited to this role.

    Location & Salary

    Job Location: Roorkee, Uttarakhand.

    Salary details have not been provided in the recruitment announcement. Compensation may depend on the candidate’s experience, qualifications, and the company’s salary structure.

    How to Apply

    Interested and eligible candidates can apply by emailing their updated CV to the recruitment team.

    • Email: am.hr2@evolet.in

    • Application Process: Send your updated CV to the email address above.

    • Subject Line: Drug Regulatory Affairs Executive Application

    Candidates should ensure their resumes clearly mention their pharmaceutical regulatory affairs experience, product registration activities, and regulatory documentation skills.

    Documents Required

    Candidates should prepare the following documents for the application and subsequent recruitment stages:

    • Updated CV or resume

    • Educational qualification details

    • Relevant work experience details

    • Supporting documents related to regulatory affairs experience, if applicable

    Frequently Asked Questions

    1. Which company is hiring for the DRA Executive position?

    Evolet Pharmaceuticals Pvt. Ltd. is hiring for the Drug Regulatory Affairs Executive position.

    2. What qualifications are required?

    Candidates with B.Pharm or M.Pharm qualifications are eligible to apply.

    3. Is experience required for this position?

    Yes. Relevant experience in pharmaceutical regulatory affairs is required.

    4. What are the key responsibilities of the DRA Executive?

    The role involves product permissions, registrations, regulatory approvals, documentation, renewals, drug licensing, and coordination with regulatory authorities.

    5. How can candidates apply?

    Candidates can send their updated CV to am.hr2@evolet.in.

    6. Where is the job located?

    The position is based in Roorkee, Uttarakhand.

    Job Summary

    Category Details
    Company Evolet Pharmaceuticals Pvt. Ltd.
    Vacancies Drug Regulatory Affairs (DRA) Executive
    Required Education B.Pharm / M.Pharm
    Experience Relevant experience in pharmaceutical regulatory affairs

  • Themis Medicare QA, QC and Store Operations Jobs

    Themis Medicare is hiring experienced pharmaceutical professionals for its Haridwar facility across Quality Assurance (QA), Quality Control (QC), and Store Operations.
    Candidates with 2–7 years of experience in the pharmaceutical industry and relevant qualifications in Pharmacy, Science, or related disciplines are eligible to apply.
    The openings include QA Officer/Executive, QC Officer/Executive/Senior Officer (HPLC), and Store Officer/Executive for Raw Material and Packing Material operations.
    Interested candidates can send their updated resumes to the recruitment email address provided below or contact the hiring team for further details.

    Themis Medicare Recruitment 2026: Pharmaceutical Jobs in Haridwar

    Themis Medicare is inviting applications from experienced candidates for pharmaceutical jobs at its Haridwar facility. The current openings are in Quality Assurance, Quality Control (HPLC), and Store Operations (RM/PM). Candidates with relevant industry experience, technical knowledge, and an understanding of GMP/GLP requirements can apply.

    Company Overview

    Themis Medicare is a pharmaceutical company involved in healthcare and pharmaceutical manufacturing. The current recruitment drive focuses on quality systems, laboratory testing, and material management operations at its Haridwar facility.

    Job Roles and Responsibilities

    1. Quality Assurance (QA) Officer/Executive

    The Quality Assurance team is responsible for maintaining quality systems and supporting compliance with applicable pharmaceutical standards.

    Key responsibilities include:

    • Quality Management System (QMS) activities

    • Documentation and validation

    • Compliance with applicable quality standards

    2. Quality Control (QC) Officer/Executive/Senior Officer

    This position focuses on laboratory testing and analytical quality control activities.

    Key responsibilities include:

    • HPLC and GC analysis

    • Analytical testing of raw materials and pharmaceutical products

    • RM/PM testing

    • Method validation

    3. Store Operations (RM/PM) Officer/Executive

    The Store Operations team handles pharmaceutical materials and related inventory activities.

    Key responsibilities include:

    • Raw material handling

    • Packing material management

    • Dispensing operations

    • ERP-related activities

    Eligibility & Qualifications

    Candidates must have relevant educational qualifications and pharmaceutical industry experience.

    Educational Qualifications

    Eligible qualifications include:

    • B.Sc.

    • M.Sc.

    • B.Pharm

    • M.Pharm

    • Other relevant qualifications related to the position

    Experience Required

    • Required experience: 2–7 years in the pharmaceutical industry.

    • Industry background: Relevant pharmaceutical manufacturing experience.

    • Technical knowledge: Compliance with GMP/GLP standards and role-specific technical requirements.

    Essential Skills

    • Knowledge of pharmaceutical quality systems

    • Documentation and validation skills

    • Understanding of GMP/GLP standards

    • Analytical testing knowledge for QC positions

    • Material management and ERP knowledge for Store Operations positions

    Job Location and Salary

    Location: Themis Medicare facility, Haridwar, Uttarakhand.

    The recruitment poster does not specify salary details. Compensation may depend on the designation, relevant experience, and the company’s salary structure.

    How to Apply

    Interested candidates can apply by sending their updated resume to the recruitment email address provided in the announcement.

    • Email: hrharidwar1@themismedicare.com

    • Contact Number: 9219540131

    • Application Method: Email your updated resume or contact the recruitment team for further information.

    Candidates should mention the position they are applying for in their email subject line and ensure their resume includes relevant pharmaceutical industry experience and technical skills.

    Important Instructions

    • Candidates must have 2–7 years of pharmaceutical industry experience.

    • Applicants should have qualifications relevant to the selected position.

    • Knowledge of GMP/GLP standards is an essential requirement.

    • Candidates should provide accurate educational and employment details in their resumes.

    Frequently Asked Questions

    1. Which company is hiring in Haridwar?

    Themis Medicare is recruiting experienced professionals for its pharmaceutical facility in Haridwar.

    2. Which positions are available?

    The openings include QA Officer/Executive, QC Officer/Executive/Senior Officer (HPLC), and Store Officer/Executive for RM/PM operations.

    3. What qualifications are required?

    Candidates with B.Sc., M.Sc., B.Pharm, M.Pharm, or other relevant qualifications may apply, depending on the position.

    4. How much experience is required?

    The recruitment announcement specifies 2–7 years of experience in the pharmaceutical industry.

    5. How can candidates apply?

    Candidates can send their updated resumes to hrharidwar1@themismedicare.com or contact 9219540131.

    6. Is the salary mentioned?

    No salary information is provided in the recruitment announcement.

    Job Summary

    Category Details
    Company Themis Medicare
    Vacancies QA Officer/Executive; QC Officer/Executive/Senior Officer (HPLC); Store Officer/Executive (RM/PM)
    Required Education B.Sc. / M.Sc. / B.Pharm / M.Pharm or other relevant qualifications
    Experience 2–7 years in the pharmaceutical industry

  • Aurobindo Pharma Production Walk-In Drive

    Aurobindo Pharma Limited is conducting a walk-in drive for Production department vacancies at its API manufacturing division in Sangareddy, Telangana.
    The recruitment is being conducted for Apitoria Pharma Private Limited, a wholly owned subsidiary of Aurobindo Pharma Limited.
    Candidates with a B.Sc. or M.Sc. qualification and 0–4 years of experience in API production are eligible to apply.
    The walk-in interview is scheduled for 25 October 2026, from 9:00 AM to 2:00 PM, at Aurobindo Pharma Limited, Unit-VI, Chitkul Village, Sangareddy District, Telangana.

    Aurobindo Pharma Walk-In Drive for Production

    Aurobindo Pharma Limited is inviting applications for Production department positions at its API division in Sangareddy, Telangana. The recruitment is being conducted for Apitoria Pharma Private Limited, which is a subsidiary of Aurobindo Pharma Limited. Candidates interested in API production jobs can attend the walk-in interview with their updated resume and supporting documents.

    Company Overview

    Aurobindo Pharma Limited is a pharmaceutical company involved in the development and manufacturing of pharmaceutical products. Through Apitoria Pharma Private Limited, the company is recruiting candidates for production operations in its active pharmaceutical ingredient (API) division.

    Job Role & Responsibilities

    Production Department

    Selected candidates will be involved in production-related activities at the API manufacturing facility.

    Key responsibilities include:

    • Production management

    • Process optimization

    • Compliance and safety

    • Documentation

    • Quality Control coordination

    • Inventory and logistics

    Eligibility & Qualifications

    Educational Qualification

    Candidates must possess one of the following qualifications:

    • B.Sc.

    • M.Sc.

    Experience Required

    • 0–4 years of experience in API Production.

    • Candidates with relevant production experience may apply.

    • Male candidates are preferred for rotational shifts.

    Aurobindo Pharma Walk-In Interview Details

    Particulars Details
    Company Apitoria Pharma Private Limited, a subsidiary of Aurobindo Pharma Limited
    Department Production
    Division API Manufacturing
    Job Location Sangareddy, Telangana
    Interview Date Sunday, 25 October 2026
    Interview Time 9:00 AM to 2:00 PM
    Interview Venue Aurobindo Pharma Limited, Unit-VI, Chitkul Village, Sangareddy District, Telangana

    Documents Required

    Candidates attending the interview must bring the following documents:

    • Updated resume

    • Passport-size photograph

    • Educational certificates

    • Payslips

    How to Apply

    Eligible candidates can attend the walk-in interview on 25 October 2026, between 9:00 AM and 2:00 PM, at the venue mentioned above.

    Candidates should carry all the required documents for the interview and verification process.

    Important notice: Apitoria Pharma Private Limited does not directly or indirectly charge any fees for job applications or recruitment processing. Candidates should avoid any communication requesting payment for employment.

    Frequently Asked Questions

    1. Which company is conducting the Production walk-in drive?

    The recruitment is for Apitoria Pharma Private Limited, a subsidiary of Aurobindo Pharma Limited.

    2. What qualifications are required for the Production vacancies?

    Candidates with a B.Sc. or M.Sc. qualification are eligible to apply.

    3. How much experience is required?

    The advertised experience requirement is 0–4 years in API Production.

    4. When is the Aurobindo Pharma walk-in interview?

    The walk-in interview is scheduled for 25 October 2026, from 9:00 AM to 2:00 PM.

    5. Where will the interview take place?

    The interview venue is Aurobindo Pharma Limited, Unit-VI, Chitkul Village, Sangareddy District, Telangana.

    6. Which documents should candidates carry?

    Candidates must bring an updated resume, passport-size photograph, educational certificates and payslips.

    Job Summary

    Category Details
    Company Apitoria Pharma Private Limited / Aurobindo Pharma Limited
    Vacancies Production
    Required Education B.Sc. / M.Sc.
    Experience 0–4 years in API Production

  • Sun Pharma Walk-In Interview for Manufacturing Jobs

    Sun Pharma Laboratories Ltd. is conducting a walk-in interview for experienced professionals at its integrated manufacturing facility in Guwahati, Assam.
    The recruitment drive covers Parenteral Manufacturing and Oral Solid Dosage (OSD) Manufacturing departments.
    Candidates with 2–15 years of experience in pharmaceutical manufacturing, particularly in regulated manufacturing units, are invited to attend the interview.
    The walk-in interview will be held on 25 October 2026, from 9:00 AM to 4:00 PM, at Hotel Kinara Residency, Chandmari, Hyderabad.

    Sun Pharma Walk-In Interview 2026

    Sun Pharma Laboratories Ltd. is hiring experienced professionals for manufacturing and support functions at its Guwahati facility. The vacancies span Parenteral Manufacturing and OSD Manufacturing, offering opportunities in production, packing, quality assurance, microbiology, engineering and maintenance, and warehouse operations.

    Company Overview

    Sun Pharma Laboratories Ltd. is part of Sun Pharma, a pharmaceutical company engaged in manufacturing medicines for healthcare needs. The Guwahati facility has integrated manufacturing capabilities for oral solid dosage and parenteral products.

    Sun Pharma Departments and Open Positions

    Parenteral Manufacturing

    The following departments are included in the recruitment drive:

    OSD Manufacturing

    Openings are available in the following functions:

    Eligibility & Qualifications

    Sun Pharma is looking for qualified and experienced professionals with backgrounds relevant to pharmaceutical manufacturing operations.

    Experience Required

    • Experience range: 2–15 years

    • Preferred background: Pharmaceutical manufacturing experience

    • Additional preference: Experience in regulated pharmaceutical manufacturing units

    Candidates should have experience relevant to the department and manufacturing function for which they are applying.

    Sun Pharma Walk-In Interview Details

    • Company: Sun Pharma Laboratories Ltd.

    • Location: Guwahati, Assam

    • Interview Date: 25 October 2026, Sunday

    • Interview Time: 9:00 AM to 4:00 PM

    • Venue: Hotel Kinara Residency, Chandmari, Hyderabad

    Documents Required

    Candidates attending the walk-in interview should carry the following documents:

    • Updated resume

    • Latest salary proof

    • Educational certificates

    • Experience documents

    How to Apply

    Interested and eligible candidates can attend the walk-in interview at Hotel Kinara Residency on 25 October 2026 between 9:00 AM and 4:00 PM.

    Candidates should carry their updated resume and supporting documents for verification during the interview.

    Important: The recruitment announcement does not provide a specific application email address or online application link. Candidates should refer to the official Sun Pharma recruitment channels for any additional instructions before attending.

    Frequently Asked Questions

    1. Which company is conducting the walk-in interview?

    Sun Pharma Laboratories Ltd. is conducting the recruitment drive for its manufacturing facility in Guwahati, Assam.

    2. Which departments have vacancies?

    The drive covers Parenteral Manufacturing and OSD Manufacturing, including production, packing, quality assurance, microbiology, engineering and maintenance, and warehouse functions.

    3. How much experience is required?

    The advertised experience range is 2–15 years. Pharmaceutical manufacturing experience is preferred.

    4. When is the Sun Pharma walk-in interview?

    The interview is scheduled for 25 October 2026, from 9:00 AM to 4:00 PM.

    5. Where is the interview venue?

    The poster lists Hotel Kinara Residency, Chandmari, Hyderabad, as the interview venue, while the job location is Guwahati, Assam. Candidates should confirm the venue details before travelling.

    6. Which documents should candidates bring?

    Candidates should carry an updated resume, latest salary proof, educational certificates and experience documents.

    Job Summary

    Category Details
    Company Sun Pharma Laboratories Ltd.
    Vacancies Parenteral Manufacturing and OSD Manufacturing roles across Production, Packing, Quality Assurance, Microbiology, Engineering and Maintenance, and Warehouse
    Required Education Relevant qualifications for the respective positions; specific degrees are not listed in the poster
    Experience 2–15 years; pharmaceutical manufacturing experience preferred

  • Biophore Research Analyst and AR&D Jobs

    Biophore is conducting a walk-in interview for Junior Research Analyst and Research Analyst positions in its R&D Centre at Pashamylaram, Hyderabad.
    The openings are available in the Analytical Method Development and Analytical Method Validation departments.
    Candidates with an M.Sc., B.Pharmacy or M.Pharmacy (Analysis) qualification and 2–5 years of relevant experience are eligible to apply.
    The walk-in interview is scheduled for 24 October 2026, from 10:00 AM to 3:00 PM, at the Biophore R&D Centre, Hyderabad.

    Biophore Walk-In Interview: Research Analyst Jobs

    Biophore is inviting applications from experienced candidates for research and analytical development roles at its R&D Centre in Pashamylaram, Hyderabad. The recruitment drive focuses on Analytical Method Development and Analytical Method Validation, with experience in analytical instruments such as HPLC and GC-MS required for the relevant positions.

    Company Overview

    Biophore is recruiting candidates for its research and development operations. The advertised positions involve analytical method development, analytical method validation and the use of laboratory analytical instruments.

    Job Openings at Biophore

    1. Junior Research Analyst / Research Analyst – Analytical Method Development

    • Department: AR&D Development

    • Qualification: M.Sc. / B.Pharmacy / M.Pharmacy (Analysis)

    • Experience: 2–5 years

    • Gender Requirement: Male candidates only, as stated in the recruitment announcement.

    Key Responsibilities and Skills

    • Experience in analytical method development.

    • Knowledge of analytical instruments, particularly HPLC.

    2. Junior Research Analyst / Research Analyst – Analytical Method Validation

    • Department: AR&D Validations

    • Qualification: M.Sc. / B.Pharmacy / M.Pharmacy (Analysis)

    • Experience: 2–5 years

    • Gender Requirement: Male candidates only, as stated in the recruitment announcement.

    Key Responsibilities and Skills

    • Experience in analytical method validation.

    • Knowledge of analytical instruments, particularly HPLC and GC-MS.

    Eligibility & Qualifications

    Candidates must meet the qualification and experience requirements for the advertised research positions.

    Eligible qualifications:

    • M.Sc.

    • B.Pharmacy

    • M.Pharmacy (Analysis)

    Experience: 2–5 years of relevant experience in analytical method development or analytical method validation.

    Important: The recruitment announcement specifies that only male candidates are eligible.

    Walk-In Interview Details

    • Company: Biophore

    • Positions: Junior Research Analyst / Research Analyst

    • Interview Date: 24 October 2026, Saturday

    • Interview Time: 10:00 AM to 3:00 PM

    • Interview and Work Location: Biophore R&D Centre, Pashamylaram, Hyderabad.

    Documents Required

    Candidates should carry the following documents to the interview:

    • Updated CV or resume

    • Educational certificates, including photocopies

    • PAN card and Aadhaar card

    • Salary slips for the last three months or bank statements for the last six months

    How to Apply

    Eligible candidates can attend the walk-in interview at the Biophore R&D Centre on the scheduled date and time.

    Candidates who cannot attend the interview can share their profile by email.

    The recruitment announcement also states that Biophore is not associated with manpower consultancies for this hiring process.

    Important Instructions

    • Carry an updated resume and the required supporting documents.

    • Candidates should have relevant experience in analytical method development or validation.

    • Knowledge of HPLC is required for the advertised analytical roles, with GC-MS knowledge specified for the validation role.

    • Candidates who cannot attend the walk-in interview may email their profile to the recruitment team.

    Frequently Asked Questions

    1. Which positions are available at Biophore?

    Biophore is recruiting Junior Research Analysts and Research Analysts for Analytical Method Development and Analytical Method Validation.

    2. What qualifications are required?

    Candidates with an M.Sc., B.Pharmacy or M.Pharmacy (Analysis) qualification are eligible.

    3. How much experience is required?

    Candidates must have 2–5 years of relevant experience.

    4. When is the Biophore walk-in interview?

    The interview is scheduled for 24 October 2026, from 10:00 AM to 3:00 PM.

    5. Where will the interview take place?

    The interview will be held at the Biophore R&D Centre, Pashamylaram, Hyderabad.

    6. How can candidates apply if they cannot attend?

    Candidates who cannot attend the interview can send their profile to recruitments@biophore.com.

    Job Summary

    Category Details
    Company Biophore
    Vacancies Junior Research Analyst / Research Analyst – Analytical Method Development and Analytical Method Validation
    Required Education M.Sc. / B.Pharmacy / M.Pharmacy (Analysis)
    Experience 2–5 years