Category: Featured

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.

• Email: sdwivedi@intaspharma.com
• Email Subject: Opportunity for INTAS- IRA – ANZ (Inj. Dosses form)

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 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 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 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 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:

• Production (Vial, Ampoule and Ophthalmic)
• Sterile / Injectable Manufacturing
• Quality Assurance
• Microbiology
• Engineering and Maintenance

OSD Manufacturing

Openings are available in the following functions:

• Production
• Packing
• Quality Assurance
• Warehouse

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 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.

• Email: recruitments@biophore.com
• Interview Venue: Biophore R&D Centre, Pashamylaram, Hyderabad.

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

 

Advity is hiring a qualified professional for the position of BA/BE – QA Auditor in its Hyderabad office.
Candidates with B.Pharmacy or M.Pharmacy qualifications and 4–5 years of relevant experience are eligible to apply.
The role involves auditing bioavailability and bioequivalence (BA/BE) studies, reviewing clinical study documentation, and ensuring compliance with applicable GxP regulations and standards.
This is a full-time, on-premises opportunity for candidates with strong analytical, communication, and auditing skills.

Advity Recruitment: BA/BE – QA Auditor

Advity is inviting applications for one vacancy in its Quality Assurance department for the BA/BE – QA Auditor position. The selected candidate will be responsible for conducting clinical study audits, reviewing documentation, and supporting quality and compliance activities in Hyderabad.

Company Overview

Advity is recruiting a Quality Assurance professional to support bioavailability and bioequivalence study audits, clinical documentation reviews, and quality system compliance.

Job Role & Responsibilities

BA/BE – QA Auditor

• Department: Quality Assurance
• Number of Vacancies: 1
• Job Type: Full-time
• Work Mode: On-premises
• Location: Hyderabad
• Experience: 4–5 years
• Qualification: B.Pharmacy / M.Pharmacy

Key Responsibilities

• Conduct in-process and retrospective BA/BE study audits during clinical and statistical phases according to the audit plan.
• Ensure studies comply with study protocols, SOPs, ICH GCP and applicable GxP regulations and standards.
• Review draft study protocols, ICFs and CRFs.
• Review clinical study reports and eCTD reports.
• Review deviations and CAPA documentation.
• Review SOPs, equipment calibration and validation records, audit trails, and computer system validation documents.
• Conduct BA/BE system audits and vendor audits.

Eligibility & Qualifications

Candidates must hold one of the following qualifications:

• B.Pharmacy
• M.Pharmacy

Required experience: 4–5 years of relevant experience.

Preferred Skills

• Good communication and analytical skills.
• Ability to work as part of a team.
• Ability to complete assigned tasks within timelines.
• Knowledge of clinical study audits and quality assurance documentation.
• Familiarity with study protocols, SOPs, ICH GCP and applicable GxP requirements.

Location & Salary

• Job Location: Hyderabad, Telangana
• Work Mode: On-premises
• Job Type: Full-time

The salary is not specified in the recruitment announcement.

How to Apply

Interested and eligible candidates can submit their updated resumes by email.

• Email: hr@advityresearch.com

Candidates should ensure that their resumes clearly mention their pharmacy qualification, relevant experience, and expertise in BA/BE study audits and clinical quality assurance.

Important Recruitment Details

• Only one vacancy is advertised.
• Candidates must have a B.Pharmacy or M.Pharmacy qualification.
• The required experience is 4–5 years.
• The position is full-time and requires on-premises work in Hyderabad.

Frequently Asked Questions

1. What position is Advity hiring for?

Advity is hiring for the BA/BE – QA Auditor position.

2. What qualifications are required?

Candidates must have a B.Pharmacy or M.Pharmacy qualification.

3. How much experience is required?

The advertised experience requirement is 4–5 years.

4. What are the main responsibilities?

The role includes BA/BE study audits, clinical documentation reviews, deviation and CAPA reviews, SOP reviews, validation documentation checks, and system and vendor audits.

5. Where is the job located?

The position is based in Hyderabad and requires on-premises work.

6. How can candidates apply?

Candidates can send their updated resumes to hr@advityresearch.com.

Job Summary

Category	Details
Company	Advity
Vacancies	BA/BE – QA Auditor: 1 vacancy
Required Education	B.Pharmacy / M.Pharmacy
Experience	4–5 years

 

Aurobindo Pharma Limited is inviting applications for multiple positions at its formulation manufacturing facility in Bachupally, Hyderabad.
The vacancies are available in Production (OSD), Production (Packing), Quality Control and Administration departments.
Candidates with ITI, Diploma, B.Sc., B.Pharm., M.Pharm., M.Sc. and other relevant qualifications can apply for suitable positions.
Applicants must have relevant experience and be flexible to work in rotational shifts, with formulation experience required for the applicable roles.

Aurobindo Pharma Recruitment: Department-Wise Job Openings

Aurobindo Pharma Limited is hiring experienced professionals for its pharmaceutical manufacturing facility in Bachupally, Medchal–Malkajgiri, Hyderabad. The recruitment drive includes opportunities in production operations, packing, quality control and administration.

Company Overview

Aurobindo Pharma Limited is a pharmaceutical company involved in the manufacture of medicines and pharmaceutical formulations. The current recruitment focuses on candidates with relevant technical, quality control and facility administration experience.

Job Role & Responsibilities

1. Production (OSD) – Technical Assistant

Area: Coating and Compression

Qualification: ITI / Diploma / B.Sc.

Experience: 2–6 years

Key Responsibilities:

• Troubleshooting and handling GLATT and GANSON coating machines.
• Operating and troubleshooting FETTE and SEJONG compression machines.
• Working with equipment used in oral solid dosage (OSD) manufacturing.
• Supporting regulatory audit requirements.

2. Production (OSD) – Executive, QMS/Documentation

Qualification: B.Pharmacy / M.Pharmacy

Experience: 4–6 years

Key Responsibilities:

• Preparing and managing standard operating procedures (SOPs).
• Supporting change control, exceptions, PNC, QRM and audit preparation.
• Handling CAPA activities.
• Managing electronic batch manufacturing records (E-BMR), electronic logs (E-log), and balance integration.
• Supporting regulatory audit requirements.

3. Production (Packing) – Executive

Area: Packing

Qualification: B.Pharmacy / M.Pharmacy

Experience: 2–6 years

Key Responsibilities:

• Handling OSD packing lines, including bottle, blister, dry powder and sachet packing.
• Working with E-log and E-BPAR documentation.
• Supporting QMS documentation, including initiation of PNC, MNC and exceptions.
• Troubleshooting track-and-trace (serialization) systems.

4. Quality Control – Executive

Area: Finished Product Analysis

Qualification: B.Pharmacy / M.Sc.

Experience: 2–6 years

Key Responsibilities:

• Performing finished product analysis for OSD formulations.
• Working with HPLC and UV dissolution instruments.
• Supporting quality control activities in a pharmaceutical manufacturing facility.

5. Administration – Executive

Area: Housekeeping

Qualification: Any Degree / Post Graduation

Experience: 6–10 years

Key Responsibilities:

• Managing housekeeping and general administration activities.
• Coordinating pest control, linen control and laundry facilities.
• Overseeing canteen services.
• Maintaining facility cleanliness and hygiene in a pharmaceutical manufacturing facility.

Eligibility & Qualifications

Candidates should have the qualifications and experience specified for their preferred position.

• ITI / Diploma / B.Sc.: Production (OSD) – Technical Assistant.
• B.Pharm. / M.Pharm.: Production (OSD) – QMS/Documentation and Production (Packing).
• B.Pharm. / M.Sc.: Quality Control – Finished Product Analysis.
• Any Degree / Post Graduation: Administration – Housekeeping.

Relevant pharmaceutical manufacturing experience is required for the applicable positions. Candidates must also be willing to work rotational shifts. Formulation experience is specifically mentioned as a requirement in the recruitment announcement.

Location & Salary

Work Location: Aurobindo Pharma Limited, Unit XII, Bachupally, Medchal–Malkajgiri, Hyderabad, Telangana.

Salary details are not provided in the recruitment announcement. Compensation may depend on the position, experience and company policies.

How to Apply

Interested candidates can send their updated resumes to the recruitment team.

• Email: hrunit-12@aurobindo.com
• Work Location: Aurobindo Pharma Limited, Unit XII, Bachupally, Hyderabad.

Applicants should mention the position they are applying for and ensure their resume includes relevant pharmaceutical manufacturing experience, technical skills and educational qualifications.

Important Instructions

• Candidates must be flexible to work in rotational shifts.
• Formulation experience is required for the applicable positions.
• Relevant experience in pharmaceutical manufacturing and the specified equipment or processes is important.
• Aurobindo Pharma states that it does not charge candidates for recruitment or authorise agents to collect recruitment fees.
• Candidates should be cautious of fraudulent job offers requesting payment.

Frequently Asked Questions

1. Which departments have vacancies at Aurobindo Pharma?

The openings are in Production (OSD), Production (Packing), Quality Control and Administration.

2. What qualifications are accepted?

Depending on the role, eligible qualifications include ITI, Diploma, B.Sc., B.Pharm., M.Pharm., M.Sc., any degree or postgraduate qualifications.

3. How much experience is required?

The advertised experience ranges from 2 to 10 years, depending on the position.

4. Are rotational shifts required?

Yes. Candidates must be flexible to work in rotational shifts.

5. How can candidates apply?

Candidates can email their updated resumes to hrunit-12@aurobindo.com.

6. Is a salary package mentioned?

No specific salary is provided in the recruitment announcement.

Job Summary

Category	Details
Company	Aurobindo Pharma Limited
Vacancies	Technical Assistant – Production (OSD); Executive – QMS/Documentation; Executive – Production (Packing); Executive – Quality Control; Executive – Administration/Housekeeping
Required Education	ITI, Diploma, B.Sc., B.Pharm., M.Pharm., M.Sc., any degree or postgraduate qualification, depending on the role
Experience	2–6 years for Technical Assistant, Packing and Quality Control; 4–6 years for QMS/Documentation; 6–10 years for Administration/Housekeeping

Cipla is inviting applications from experienced candidates for Production jobs at its pharmaceutical manufacturing facility in Bommasandra, Bengaluru.
The company has openings for Senior Operator – Production and Junior Officer – Production positions.
Candidates with a Diploma in Chemical Engineering, B.Tech./B.E. in Chemical Engineering, or M.Sc. in Chemistry can apply for the relevant roles.
Eligible candidates with experience in API production, intermediates, clean rooms, GMP and validation processes can attend the walk-in interview on 25 October 2026.

Cipla Walk-In Interview for Production Jobs

Cipla is conducting a walk-in interview to recruit experienced professionals for its Production department. The vacancies are available at the company’s Bommasandra facility in Bengaluru, Karnataka.

Company Overview

Cipla is a pharmaceutical company focused on healthcare and medicine manufacturing. This recruitment drive is intended for candidates with experience in pharmaceutical production, particularly API manufacturing, intermediates and clean-room operations.

Job Openings at Cipla

Senior Operator – Production

• Designation: Senior Executive
• Qualification: Diploma in Chemical Engineering
• Experience: 3–5 years

Job Responsibilities:

• Handle production activities involving APIs and intermediates.
• Support production planning and execution.
• Work in clean-room environments.
• Follow GMP requirements and validation processes.

Junior Officer – Production

• Designation: Senior Executive
• Qualification: B.Tech./B.E. in Chemical Engineering or M.Sc. in Chemistry
• Experience: 1–3 years

Job Responsibilities:

• Support API and intermediate production operations.
• Assist with production planning and execution.
• Follow clean-room practices and GMP requirements.
• Apply knowledge of validation processes during production activities.

Eligibility & Qualifications

Candidates must have the relevant educational qualification and pharmaceutical manufacturing experience for the position they wish to apply for.

Eligible qualifications:

• Diploma in Chemical Engineering
• B.Tech. in Chemical Engineering
• B.E. in Chemical Engineering
• M.Sc. in Chemistry

Experience requirements:

• Senior Operator – Production: 3–5 years
• Junior Officer – Production: 1–3 years

Candidates must have experience in pharmaceutical manufacturing organisations approved by regulatory authorities such as USFDA, MHRA, the European Union and other major regulatory bodies.

Walk-In Interview Details

• Company: Cipla
• Department: Production
• Interview Date: 25 October 2026, Sunday
• Interview Time: 9:30 AM to 5:00 PM
• Job Location: Bommasandra, Bengaluru, Karnataka
• Interview Venue: Cipla Ltd., Bommasandra, Jigini, Krishnapuram, Bengaluru, Karnataka – 560105.

How to Apply

Interested candidates can attend the walk-in interview directly at the specified venue during the scheduled hours.

Candidates must carry two copies of their resume. The company will shortlist CVs according to its terms and conditions and reserves the right to conduct an evaluation process.

Candidates can scan the QR code provided in the recruitment poster to access the application process.

Important Instructions

• Carry two copies of your updated resume.
• Relevant pharmaceutical manufacturing experience is required.
• Experience in API production, intermediates and clean-room operations is relevant to these vacancies.
• Candidates should be familiar with GMP requirements and validation processes.
• Shortlisting will be based on the company’s terms and conditions.

Frequently Asked Questions

1. Which positions are available at Cipla?

Cipla is recruiting for Senior Operator – Production and Junior Officer – Production.

2. What qualifications are required for these Production jobs?

Candidates need a Diploma in Chemical Engineering, B.Tech./B.E. in Chemical Engineering, or M.Sc. in Chemistry, depending on the position.

3. How much experience is required?

Senior Operator – Production requires 3–5 years of experience. Junior Officer – Production requires 1–3 years.

4. When is the Cipla walk-in interview?

The interview is scheduled for 25 October 2026, from 9:30 AM to 5:00 PM.

5. Where will the interview take place?

The interview will take place at Cipla Ltd., Bommasandra, Jigini, Krishnapuram, Bengaluru, Karnataka – 560105.

6. What documents should candidates bring?

Candidates must carry two copies of their resume.

Job Summary

Category	Details
Company	Cipla
Vacancies	Senior Operator – Production; Junior Officer – Production
Required Education	Diploma in Chemical Engineering; B.Tech./B.E. in Chemical Engineering; M.Sc. in Chemistry
Experience	Senior Operator: 3–5 years; Junior Officer: 1–3 years

4C Pharma is hiring for the position of Drug Safety Associate – MICC in Hyderabad, Telangana. Candidates with 1–5 years of core MICC experience and a bachelor’s or master’s degree in Pharmacy, Life Sciences, Nursing, or a related healthcare field are eligible to apply. This is a full-time, work-from-office opportunity involving night shifts. Immediate joiners and candidates with a maximum notice period of 30 days are preferred.

Company Overview

4C Pharma is recruiting professionals for its Drug Safety Associate – MICC team in Hyderabad.

Job Role & Responsibilities

• Handle medical information inquiries from patients and healthcare professionals.
• Document adverse events (AEs) and product complaints accurately.
• Ensure timely reporting and escalation of safety information according to SOPs and regulatory requirements.
• Provide accurate medical information using approved scripts and guidelines.
• Maintain data accuracy, confidentiality, and quality standards.

Eligibility / Qualifications

Educational Qualifications:

• Bachelor’s or Master’s degree in Pharmacy.
• Life Sciences.
• Nursing.
• Related healthcare fields.

Experience: 1–5 years of core MICC experience.

Required Skills:

• Strong communication skills.
• Calling and inquiry-handling experience.
• Accurate documentation.
• Attention to detail.
• Relevant pharmacovigilance knowledge.

Additional Requirements:

• Willingness to work night shifts.
• Ability to work from the Hyderabad office.
• Immediate joiners or candidates with a maximum notice period of 30 days are preferred.
• Male candidates are preferred, as stated in the recruitment announcement.

Location & Work Mode

• Location: Hyderabad, Telangana
• Work Mode: Work from Office (WFO)
• Shift: Night shifts
• Experience: 1–5 years

Application Process

Interested candidates can share their updated resumes via email.

Email: sushmitha.r@4cpharma.com

Candidates should highlight their core MICC experience, medical information calling skills, adverse event documentation experience, and relevant pharmacovigilance knowledge in their resumes.

Summary Table

Company	4C Pharma
Department Vacancies	Drug Safety Associate – MICC
Qualification	Bachelor’s or Master’s in Pharmacy, Life Sciences, Nursing, or a related healthcare field
Experience	1–5 years of core MICC experience
Location	Hyderabad, Telangana