Category: Featured

ICON Hiring – Pharmacovigilance Manager | Drug Safety | Chennai

ICON is hiring a Pharmacovigilance Manager for its Drug Safety team in Chennai.
The role focuses on overseeing pharmacovigilance activities, safety monitoring, regulatory compliance, and delivery of drug safety operations.
Candidates with a Bachelor’s degree or higher in Life Sciences, Pharmacy, Medicine, Nursing, or a related healthcare/scientific discipline can apply.
The position requires strong pharmacovigilance experience along with mandatory line management experience and is offered in a hybrid work model.

Company Overview

ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster.

The organisation highlights integrity, collaboration, agility, and inclusion as key values.

Job Details

Pharmacovigilance Manager – Drug Safety

• Company: ICON
• Job Title: Pharmacovigilance Manager
• Job ID: JR158715
• Job Reference: JID 53215
• Department: Drug Safety
• Business Area: ICON Full Service & Corporate Support
• Location: Chennai, India
• Work Model: Hybrid

Pharmacovigilance Responsibilities

Drug Safety & Pharmacovigilance Operations

• Lead the pharmacovigilance team in the collection, evaluation, and reporting of adverse events.
• Ensure compliance with regulatory guidelines and internal standards.
• Oversee pharmacovigilance and drug safety delivery.
• Resolve operational issues and support the development of team capability.
• Develop and implement pharmacovigilance processes and policies to improve safety monitoring activities.

Safety Data & Risk Management

• Monitor and analyse safety data trends.
• Prepare risk assessments.
• Present safety findings to relevant stakeholders.
• Ensure pharmacovigilance activities comply with global regulatory requirements and internal quality standards.

Cross-Functional Collaboration

• Collaborate with Clinical, Regulatory, and Quality Assurance teams.
• Ensure comprehensive safety assessments.
• Support timely reporting of safety data.
• Communicate with clients, senior management, cross-functional teams, and external stakeholders.

Team Management Responsibilities

The role includes mandatory line management responsibilities, including:

• Workload management
• Coaching and mentoring
• Staff development
• Performance reviews
• Setting objectives
• Providing performance feedback
• Managing employee development plans
• Supporting succession planning
• Recruitment and onboarding
• Training and capability development

Eligibility & Qualifications

Educational Qualification

Candidates should have:

• Bachelor’s degree or higher in:

  • Life Sciences
  • Pharmacy
  • Medicine
  • Nursing
  • Related healthcare or scientific discipline

Pharmacovigilance Experience

Candidates should have strong Pharmacovigilance experience with exposure to areas such as:

• Case processing
• Safety reporting
• Aggregate reporting
• Pharmacovigilance operations
• Drug safety activities

Mandatory Line Management Experience

Line management experience is mandatory.

Candidates should have experience leading a small to medium-sized team, including workload management, coaching, mentoring, and staff development.

Key Skills & Requirements

• Strong understanding of global Pharmacovigilance regulations.
• Knowledge of GVP/GCP requirements.
• Understanding of SOPs, quality systems, and regulatory compliance expectations.
• Resource and capacity planning.
• Project delivery and timeline management.
• Workload forecasting and risk management.
• Metric generation and reporting.
• Data analysis and trend identification.
• Continuous process improvement.
• Strong written and verbal communication.
• Client and stakeholder interaction.
• Presentation and meeting leadership.
• Training delivery.
• Stakeholder influence across different organisational levels.
• Experience supporting audits and inspections.
• Experience with quality improvement initiatives in a regulated environment.

Project Management

Project management experience is preferred, particularly experience involving:

• Project delivery
• Resource planning
• Workload forecasting
• Risk management
• Stakeholder communication

Software & Reporting Skills

Proficiency in:

• Microsoft Excel
• Microsoft PowerPoint
• Microsoft Word
• Reporting and analytics tools

The role involves preparing management reports, dashboards, presentations, and business updates.

Eligible Qualification Courses

B.Pharm | M.Pharm | Pharm.D | B.Sc. Life Sciences | M.Sc. Life Sciences | MBBS | MD | B.Sc. Nursing | M.Sc. Nursing | Related Healthcare or Scientific Degree

Location & Work Mode

Location: Chennai, India
Work Model: Hybrid
Department: Drug Safety
Job Type: ICON Full Service & Corporate Support

What ICON Can Offer

The source states that ICON offers benefits designed around employee well-being and work-life balance. Benefits may include:

• Annual leave entitlements
• Health insurance options
• Retirement planning offerings
• Global Employee Assistance Programme
• Life assurance
• Flexible country-specific benefits
• Childcare-related benefits
• Gym membership discounts
• Subsidised travel passes
• Health assessments

Benefits may vary according to the country and applicable employment terms.

How to Apply

Interested and eligible candidates can apply through the official ICON careers page:

Apply for Pharmacovigilance Manager – ICON

Job ID: JR158715

The source also provides the direct application workflow:

ICON Application Page

Job Summary

SUN Pharmaceutical Industries Ltd. is hiring for QC Analyst positions in its Quality Control department.
The opening is available at the Officer / Senior Officer level for experienced pharmaceutical professionals.
Candidates with M.Sc, B.Pharm or M.Pharm qualifications and 3 to 6 years of experience can apply.
Experience in FP Analysis, RM Analysis and Stability is required for this Quality Control opportunity.

SUN Pharmaceutical Industries Ltd. – QC Analyst

Position Details

Position: Officer / Senior Officer
Department: Quality Control
Location: Dewas
Experience: 3 to 6 Years

SUN Pharmaceutical QC Analyst – Skills Required

Candidates should have experience in the following areas:

• FP Analysis
• RM Analysis
• Stability

Eligibility & Qualifications

Candidates with the following qualifications are eligible to apply:

B.Pharm | M.Pharm | M.Sc

Educational Qualification

• B.Pharm
• M.Pharm
• M.Sc

Experience Required

3 to 6 Years

Relevant experience in pharmaceutical Quality Control, particularly FP Analysis, RM Analysis and Stability, is required.

How to Apply

Interested candidates can share their updated resumes at the following email addresses:

nidhi.rathore1@sunpharma.com
Preksha.jhanshikar@sunpharma.com

Candidates are requested to mention the relevant position while applying.

Job Summary

Macleods Pharmaceuticals is inviting applications for an experienced Bioanalytical Analyst – LC-MS position.
The opening is suitable for candidates with 2 to 4 years of experience in bioanalysis and analytical laboratory activities.
Eligible candidates include M.Pharm, M.Sc. Analytical Chemistry, M.Sc. Chemistry and B.Pharm graduates.
The role involves bioanalytical method development, validation, biological sample analysis and GLP-compliant laboratory activities.

Macleods Pharmaceuticals – Bioanalytical Analyst (LC-MS)

Position Details

Position: Bioanalytical Analyst – LC-MS
Experience: 2 to 4 Years
Department: Bioanalytical Section
Employment Level: Experienced Candidates

Macleods Pharmaceuticals Bioanalytical Analyst – Role Profile

To assist the Project Leader in conducting bioanalysis and in maintaining the bioanalytical laboratory in compliance with the principles of GLP.

Macleods Pharmaceuticals Bioanalytical Analyst – Job Description

• To develop and validate bioanalytical methods.
• To process and analyse biological samples for drug/metabolite concentrations.
• To write and revise SOPs as per need.
• To adhere to GLP and all SOPs.
• To maintain equipment and instruments used in the bioanalytical section.
• To be responsible for housekeeping in the bioanalytical section.
• To compile raw data in data sheets and laboratory notebooks.
• To maintain equipment log books.
• To assist the Project Leader in compilation of reports.
• To calibrate and maintain records for pipettes, Handysteps and dispensers.
• To perform other responsibilities assigned by the Section Head.

Eligibility & Qualifications

Candidates with the following qualifications are eligible to apply:

M.Pharm | M.Sc. Analytical Chemistry | M.Sc. Chemistry | B.Pharm

Educational Qualification

• M.Pharm
• M.Sc. in Analytical Chemistry
• M.Sc. in Chemistry
• B.Pharm

Experience Required

2 to 4 Years

Only experienced candidates are required for this position. Freshers are requested not to apply.

Skills & Technical Requirements

Relevant experience or knowledge in the following areas will be useful:

• Bioanalysis
• LC-MS
• Bioanalytical method development
• Bioanalytical method validation
• Biological sample analysis
• GLP compliance
• SOP preparation and revision
• Laboratory documentation
• Equipment and instrument maintenance
• Raw data compilation
• Laboratory notebooks and log books

How to Apply

Interested and eligible experienced candidates can send their updated resume to:

Email: adityab@macleodspharma.com

Candidates should mention the position applied for in the subject line. Experienced candidates are specifically requested to apply.

Job Summary

Pontika Aerotech is hiring for a Quality Control position at its facility in Paonta Sahib, Himachal Pradesh.
The opportunity is open to candidates with 2–8 years of experience in pharmaceutical Quality Control.
Candidates with B.Sc, M.Sc or B.Pharm qualifications can apply for the position.
Experience in GLP, QMS and Raw Material (RM) sections is relevant to this opening.

Pontika Aerotech – Quality Control

Position Details

Position: Quality Control
Location: Paonta Sahib, Himachal Pradesh
Experience: 2–8 Years
Qualification: B.Sc / M.Sc / B.Pharm

Pontika Aerotech Quality Control – Sections

GLP – Quality Control

Candidates with experience in Good Laboratory Practices (GLP) and pharmaceutical quality control activities can apply.

QMS – Quality Control

Relevant experience in Quality Management System (QMS) activities is preferred for this Quality Control position.

RM – Quality Control

Candidates with experience in Raw Material (RM) testing and Quality Control activities are eligible to apply.

Eligibility & Qualifications

Candidates with the following qualifications are eligible to apply:

B.Sc | M.Sc | B.Pharm

Educational Qualification

• B.Sc
• M.Sc
• B.Pharm

Experience Required

2–8 Years

Relevant Quality Control experience in GLP, QMS and RM sections is applicable to this opportunity.

Job Location

Paonta Sahib, Himachal Pradesh

How to Apply

Interested candidates can apply via WhatsApp at:

WhatsApp: 8278729004

Candidates are requested to share their updated CV along with Current CTC, Expected CTC and Notice Period.

Job Summary

A pharmaceutical industry opportunity is available for QC (Analysis / RS) professionals in Mehsana.
The opening is suitable for candidates with M.Sc or M.Pharm qualifications and 3–7 years of relevant experience.
Candidates should have strong knowledge of HPLC operations, OSD Quality Control, FP, Stability, RS and impurity testing.
Interested candidates can share their updated CV along with their current and expected CTC for consideration.

Emcure Pharmaceuticals – QC (Analysis / RS) Officer / Executive

Position Details

Department: Quality Control (Analysis / RS)
Designation: Officer / Executive
Qualification: M.Sc / M.Pharm
Experience: 03–07 Years
Location: Mehsana

Emcure Pharmaceuticals – QC Analysis / RS Responsibilities & Skills

HPLC Operations

• Strong understanding of HPLC operations.
• Candidates should have relevant hands-on experience in analytical testing.

OSD Quality Control

• Must have work experience in OSD QC.
• Experience in FP and Stability testing is required.
• Good understanding of RS and impurity testing.

Analytical Quality Control

Candidates should have relevant experience in pharmaceutical Quality Control analysis and should be familiar with analytical testing requirements.

Eligibility & Qualifications

Candidates with the following qualifications are eligible to apply:

M.Sc | M.Pharm

Educational Qualification

• M.Sc
• M.Pharm

Experience Required

03–07 Years

Candidates should have relevant experience in pharmaceutical Quality Control, particularly in OSD QC, HPLC operations, FP, Stability, RS and impurity testing.

Job Location

Mehsana, Gujarat

How to Apply

Interested and eligible candidates can share their updated CV along with their current CTC and expected CTC at:

Email: bhavik.parekh@emcure.com

Candidates should mention the relevant QC position in the email subject line.

Job Summary

Damaira Pharmaceuticals Pvt. Ltd. is hiring for multiple positions at its Sterile Carbapenem Facility across Microbiology, Quality Control, IPQA, Warehouse and QA Documentation.
The company has openings for candidates with relevant science, pharmacy and graduate qualifications across different experience levels.
There are also Apprenticeship Trainee opportunities in QA, QC, Microbiology, Production, Warehouse and Engineering departments.
Interested candidates can share their updated CVs through the email addresses provided in the recruitment announcement.

Damaira Pharmaceuticals – Microbiology Jobs

Microbiology – Positions

Number of Positions: 2
Experience: 00–03 Years
Qualification: Postgraduate in Science

Candidates with a postgraduate science qualification and relevant microbiology background can apply.

Damaira Pharmaceuticals – Quality Control Jobs

Quality Control – Positions

Number of Positions: 2
Experience: 01–03 Years
Qualification: Postgraduate in Science

Candidates with relevant postgraduate science qualifications and Quality Control experience can apply.

Damaira Pharmaceuticals – IPQA Jobs

IPQA – Positions

Number of Positions: 2
Experience: 02–04 Years
Qualification: Graduate in Science

Candidates with relevant science graduation and IPQA experience are eligible to apply.

Damaira Pharmaceuticals – Warehouse Jobs

Warehouse – RM, PM & FG

Number of Positions: 2
Experience: 02–06 Years
Qualification: Any Graduate

The opening covers warehouse activities related to RM, PM and FG.

Damaira Pharmaceuticals – QA Documentation Jobs

QA Documentation – Positions

Number of Positions: 2
Experience: 02–05 Years
Qualification: B.Sc / B.Pharm

Candidates with B.Sc or B.Pharm qualifications and relevant QA documentation experience can apply.

Damaira Pharmaceuticals – Apprenticeship Trainee Jobs

Apprenticeship Trainees – Multiple Departments

Damaira Pharmaceuticals also has vacancies for Apprenticeship Trainees across multiple departments.

Eligible Qualifications: B.Sc / B.Pharm / B.Com / ITI / B.Tech / Diploma

Available Departments

• Quality Assurance
• Quality Control
• Microbiology
• Production
• Warehouse
• Engineering

Eligibility & Qualifications

Candidates with the following qualifications are eligible for the respective positions:

B.Sc | B.Pharm | B.Com | B.Tech | ITI | Diploma | Graduate Science | Postgraduate Science

Educational Qualification

• Microbiology: Postgraduate in Science
• Quality Control: Postgraduate in Science
• IPQA: Graduate in Science
• Warehouse: Any Graduate
• QA Documentation: B.Sc / B.Pharm
• Apprenticeship Trainees: B.Sc / B.Pharm / B.Com / ITI / B.Tech / Diploma

Experience Required

• Microbiology: 00–03 Years
• Quality Control: 01–03 Years
• IPQA: 02–04 Years
• Warehouse: 02–06 Years
• QA Documentation: 02–05 Years
• Apprenticeship Trainees: Experience requirement not specified

Job Location

Damaira Pharmaceuticals Pvt. Ltd.
Village Haripur, Raipur Rani, Panchkula,
Haryana – 134204, India

How to Apply

Interested and eligible candidates can send their updated CVs to the following email addresses:

hr@damaira.com
hrd@damaira.com

Candidates should mention the position or department they are applying for in the email subject line.

Job Summary

Yashashvi Rasayan Pvt. Ltd. is a leading name in the chemical manufacturing industry, committed to delivering high-quality products while ensuring sustainability and innovation.
The company is inviting applications for multiple openings at its Dahej plant across Quality Assurance, R&D, Instrumentation, Systems, Production and MEE departments.
Candidates with qualifications including B.Sc, M.Sc, B.E./B.Tech, ITI, MCP and ITI AOCP can apply for the relevant positions.
The available roles require experience ranging from 1 to 8 years, depending on the position.

Yashashvi Rasayan Pvt. Ltd. – Job Openings

Quality Assurance – QA Officer

Qualification: B.Sc / M.Sc
Experience: 1–4 Years

R&D – R&D Chemist

Qualification: B.Sc / M.Sc
Experience: 1–4 Years

Instrumentation – Instrument Engineer

Qualification: B.E. / B.Tech in Instrumentation
Experience: 3–5 Years

Instrumentation – Instrument Technician

Qualification: ITI / MCP
Experience: 3–5 Years

Systems – System Engineer

Qualification: B.E. / B.Tech in Instrumentation
Experience: 3–5 Years

Production – Production Technician

Qualification: ITI AOCP
Experience: 3–5 Years

DCS – DCS Officer

Qualification: B.E. / B.Tech Chemical
Experience: 4–8 Years

MEE – MEE Technician

Qualification: ITI AOCP
Experience: 3–5 Years

Eligibility & Qualifications

Candidates with the following qualifications are eligible for the respective positions:

B.Sc | M.Sc | B.E. | B.Tech | B.E./B.Tech Instrumentation | B.E./B.Tech Chemical | ITI | MCP | ITI AOCP

Educational Qualification

• QA Officer: B.Sc / M.Sc
• R&D Chemist: B.Sc / M.Sc
• Instrument Engineer: B.E. / B.Tech in Instrumentation
• Instrument Technician: ITI / MCP
• System Engineer: B.E. / B.Tech in Instrumentation
• Production Technician: ITI AOCP
• DCS Officer: B.E. / B.Tech Chemical
• MEE Technician: ITI AOCP

Experience Required

• QA Officer: 1–4 Years
• R&D Chemist: 1–4 Years
• Instrument Engineer: 3–5 Years
• Instrument Technician: 3–5 Years
• System Engineer: 3–5 Years
• Production Technician: 3–5 Years
• DCS Officer: 4–8 Years
• MEE Technician: 3–5 Years

Job Location

Yashashvi Rasayan Pvt. Ltd. – Dahej Plant

How to Apply

Interested and eligible candidates can send their updated resume to:

Email: palak.datta@yashrasayan.com

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

Job Summary

Lupin is conducting a Walk-In Drive for multiple positions in Production API Manufacturing, Quality Control and Quality Assurance.
The openings are available for candidates with relevant pharmaceutical manufacturing and quality experience.
Candidates with qualifications including B.Sc, M.Sc, B.E. and Diploma in Chemical Engineering can apply for the respective positions.
The walk-in interview is scheduled for 10 October 2026 at Hotel Mastiff, Ankleshwar, Gujarat.

Lupin – Production API Manufacturing Jobs

Production API – Trainee / Freshers / Associate / Officer / Sr. Officer

Qualification: B.Sc / M.Sc / B.E. / Diploma in Chemical
Experience: Minimum 2–6 Years for experienced positions

Key Skills & Responsibilities

• Responsible for adherence to SOPs and meeting targets.
• Maintain GMP and Safety practices.
• Able to handle and operate process equipment in manufacturing.
• Sound knowledge of operations of centrifuge/reactors, etc.
• Candidates should have relevant experience in pharmaceutical API manufacturing.

Lupin – Quality Control Jobs

Quality Control – Officer / Sr. Officer

Qualification: B.Sc / M.Sc. in Analytical Chemistry
Experience: Minimum 2–6 Years

Key Skills & Responsibilities

• Hands-on experience in Quality Control Laboratory.
• Knowledge of GLP, GDP, GMP and laboratory safety.
• Hands-on experience handling various instruments such as HPLC and GC.
• Awareness of Quality-QAMS software.
• Relevant experience in pharmaceutical Quality Control is preferred.

Lupin – Quality Assurance Jobs

Quality Assurance – Officer / Sr. Officer

Qualification: B.Sc / M.Sc
Experience: Minimum 2–6 Years

Key Skills & Responsibilities

• Experience in Quality Assurance activities.
• Experience in Quality Assurance, IPQA and OOS.
• Review of BPR.
• Awareness of Quality-QA software.
• Relevant pharmaceutical Quality Assurance experience is preferred.

Eligibility & Qualifications

Candidates with the following qualifications can apply for the respective positions:

B.Sc | M.Sc | B.E. | Diploma | M.Sc. Analytical Chemistry | M.Sc. Chemistry

Educational Eligibility

• Production API: B.Sc / M.Sc / B.E. / Diploma in Chemical
• Quality Control: B.Sc / M.Sc in Analytical Chemistry
• Quality Assurance: B.Sc / M.Sc

Experience Required

• Production API: Minimum 2–6 Years for experienced positions
• Quality Control: Minimum 2–6 Years
• Quality Assurance: Minimum 2–6 Years

The recruitment poster also indicates opportunities for freshers in the Production API category.

Walk-In Interview Details

Interview Date

10 October 2026 (Saturday)

Interview Time

9:00 AM to 4:00 PM

Interview Venue

Hotel Mastiff
Plot No. C/4/2 & 3, Opposite Railway Station,
Ankleshwar GIDC, Ankleshwar,
Gujarat – 393001

Important Eligibility Note

Highest degree must have 1st Class / 60% marks, or candidates should have 5 years of experience with 2nd Class.

Candidates should have relevant pharmaceutical/API manufacturing or quality experience according to the position applied for.

How to Apply

Interested and eligible candidates can attend the Lupin Walk-In Interview on 10 October 2026, between 9:00 AM and 4:00 PM, at Hotel Mastiff, Ankleshwar.

Candidates can also send their profiles to:

Email: prachipatill@lupin.com
Email: jameshktare@lupin.com

Contact

Phone: 7391040115

Job Summary

Corey Pharmaceuticals is inviting applications for the position of Trainee Chemist.
This opportunity is suitable for candidates with an M.Sc. in Organic Chemistry looking to begin or develop their career in the pharmaceutical industry.
The role offers an opportunity to work with an innovative, science-driven pharmaceutical company.
Interested candidates can share their updated resume with Corey Pharmaceuticals for consideration.

Corey Pharmaceuticals – Trainee Chemist

Position Details

Position: Trainee Chemist
Qualification: M.Sc. in Organic Chemistry

Eligibility & Qualifications

Candidates with the following qualification are eligible to apply:

M.Sc. in Organic Chemistry

Educational Qualification

• M.Sc. in Organic Chemistry

Experience Required

The recruitment poster does not specify any particular experience requirement. Candidates with relevant educational qualifications may apply.

Job Role & Responsibilities

The available information specifies the position as Trainee Chemist. Detailed job responsibilities are not mentioned in the recruitment announcement.

Candidates interested in pharmaceutical research and chemistry-related work can submit their resumes for consideration.

How to Apply

Interested and eligible candidates can send their updated resume to:

Email: info@coreypharmaceuticals.com

Candidates should mention the position applied for clearly in their application.

Job Summary

Ajanta Pharma is conducting a Walk-In Interview for multiple positions across Manufacturing, Quality Control, Quality Assurance and Maintenance departments.
The openings are available for candidates with relevant experience in pharmaceutical manufacturing, OSD operations, analytical testing, validation, QMS and engineering maintenance.
Candidates with qualifications ranging from 10th/12th, ITI and Diploma to B.Pharm, M.Pharm, B.Sc, M.Sc and engineering degrees are eligible for different positions.
The walk-in interview will be held on 11 October 2026 at Hotel Legend Sarovar Portico, Baddi, Himachal Pradesh.

Ajanta Pharma – Manufacturing & Packing Jobs

Manufacturing / Packing – Sr. Officer / Officer

Qualification: B.Pharm / M.Pharm
Experience: 02 to 08 Years

Key Skills & Responsibilities

• Exposure to OSD manufacturing operations.
• Experience in granulation and pellet coating.
• Capsule filling operations.
• Primary packing and secondary packing.
• QMS activities, including investigation of OOS and OOT.
• Handling deviations and incidents.
• Experience with investigation tools.

Manufacturing / Packing – Associate / Operator

Qualification: 10th / 12th + ITI / Diploma / D.Pharm / B.A. / B.Com
Experience: 02 to 10 Years

Key Skills & Responsibilities

• Exposure to OSD manufacturing operations.
• Experience in granulation and pellet coating.
• Capsule operations.
• Primary packing, including blister packing, sachet filling and bottle line operations.
• Secondary packing, including cartoning and labelling.

Ajanta Pharma Quality Control Jobs

Quality Control – Sr. Officer / Officer / Executive

Qualification: D.Pharm / B.Sc / M.Sc / B.Pharm
Experience: 03 to 12 Years

Key Skills & Responsibilities

• Exposure to analysis of Solid Oral Dosage (FP).
• Instrumentation analysis.
• In-process testing and stability analysis.
• Experience in Analytical Method Validation.
• Experience in PMQC.
• Dissolution testing.
• QMS activities.

Ajanta Pharma Quality Assurance Jobs

Quality Assurance – Sr. Executive / Executive

Profile: OOS/OOT
Qualification: M.Sc / B.Pharm / M.Pharm
Experience: 08 to 13 Years

Key Skills & Responsibilities

• Good exposure to investigations against OOS and OOT.
• Handling deviations and incidents.
• Risk assessment.
• Impact assessment.
• Quality investigation and compliance activities.

Ajanta Pharma Maintenance Jobs

Maintenance – QMS / Qualification – Sr. Officer / Officer

Qualification: B.E. Mechanical / Instrumentation
Experience: 04 to 10 Years

Key Skills & Responsibilities

• Preparation of SOPs.
• Raising Change Controls.
• Handling deviations, incidents and CAPA.
• Knowledge of SOP requirements.
• Qualification activities including URS, DQ, IQ, OQ and PQ.
• Exposure to e-LOG systems.

Maintenance – HVAC – Sr. Officer / Officer

Qualification: B.E. Electrical
Experience: 02 to 10 Years

Key Skills & Responsibilities

• Preventive and breakdown maintenance.
• Troubleshooting and inspection of plant equipment.
• Condition monitoring.
• Spare parts management.
• Exposure to audits and regulatory inspections.

Eligibility & Qualifications

B.Pharm | M.Pharm | B.Sc | M.Sc | D.Pharm | B.A. | B.Com | D.Pharm | B.E. Mechanical | B.E. Electrical | Instrumentation | Diploma | ITI | 10th | 12th

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

Experience Required

• Manufacturing / Packing – Sr. Officer / Officer: 02–08 Years
• Manufacturing / Packing – Associate / Operator: 02–10 Years
• Quality Control – Sr. Officer / Officer / Executive: 03–12 Years
• Quality Assurance – Sr. Executive / Executive: 08–13 Years
• Maintenance – QMS / Qualification: 04–10 Years
• Maintenance – HVAC: 02–10 Years

Walk-In Interview Details

Interview Date

11 October 2026 (Sunday)

Interview Time

09:00 AM to 04:00 PM

Interview Venue

Hotel Legend Sarovar Portico
Industrial Town of Baddi
Himachal Pradesh

Documents to Carry

Interested candidates attending the walk-in interview should carry:

• Updated resume
• CTC breakup
• Passport-size photograph

For Candidates Unable to Attend

Candidates who are unable to attend the interview may forward their updated CV to:

Email: referral.dhi@ajantapharma.com

Note: AC bus facility is available from Bharuch and Ankleshwar for the Dahej location.

How to Apply

Interested and eligible candidates can attend the Ajanta Pharma Walk-In Interview on 11 October 2026, between 09:00 AM and 04:00 PM, at Hotel Legend Sarovar Portico, Industrial Town of Baddi, Himachal Pradesh.

Candidates should carry their latest resume, CTC breakup and passport-size photograph.

Job Summary