Author: Sudheer vanguri

FDC Limited has announced an Open Interview Schedule for multiple positions at its pharmaceutical facility in Khol-Bhud, Baddi.
The openings are available in Production, Quality Control and Quality Assurance departments.
Candidates with qualifications including 12th with ITI, B.Pharm, M.Pharm and M.Sc. Chemistry can apply for the relevant positions.
The required experience ranges from 2 to 10 years, depending on the position and department.

FDC Limited – Open Interview Schedule

Interview Details

Company: FDC Limited
Location: Village Khol-Bhud, Tehsil Baddi, District Solan, Himachal Pradesh – 173205
Interview Date: 10/10/2026

Interested candidates are requested to carry their updated CV and latest CTC Annexure for the interview.

FDC Limited – Production Department

Production Supervisor

Vacancies: 4
Experience: 4–6 Years
Qualification: 12th with ITI

Area / Skills:

• Manufacturing
• Compression Machine
• Granulation Machine
• Coating Machine
• Dry Syrup Filling Machine

FDC Limited – Production Officer

Production Officer

Vacancies: 2
Experience: 2–6 Years
Qualification: B.Pharm / M.Pharm

Area / Skills:

• Manufacturing

FDC Limited – Quality Control

Quality Control Officer

Vacancies: 3
Experience: 2–4 Years
Qualification: B.Pharm / M.Pharm / M.Sc. Chemistry

Area / Skills:

• HPLC Testing
• Stability
• GC

FDC Limited – Quality Assurance

Quality Assurance Executive / Sr. Executive

Vacancies: 1
Experience: 8–10 Years
Qualification: B.Pharm / M.Pharm

Area / Skills:

• QMS
• GMP Compliance
• Deviation
• Market Complaints
• Change Control
• CAPA
• Risk Assessment
• SOP Reviews
• Regulatory Audit Exposure

Eligibility & Qualifications

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

12th with ITI | B.Pharm | M.Pharm | M.Sc. Chemistry

Educational Qualification

• 12th with ITI for Production Supervisor
• B.Pharm / M.Pharm for Production Officer
• B.Pharm / M.Pharm / M.Sc. Chemistry for Quality Control Officer
• B.Pharm / M.Pharm for Quality Assurance Executive / Sr. Executive

Experience Required

Experience requirements vary by position:

• Production Supervisor: 4–6 Years
• Production Officer: 2–6 Years
• Quality Control Officer: 2–4 Years
• Quality Assurance Executive / Sr. Executive: 8–10 Years

How to Apply

Interested candidates can attend the Open Interview on 10 October 2026.

Candidates are requested to carry:

• Updated CV
• Latest CTC Annexure

Contact Details

Department: Human Resources
Email: sushil.kumar@fdcindia.com
Contact Number: 9736880100

Interview Location

FDC Limited
Village Khol-Bhud, Tehsil Baddi,
District Solan, Himachal Pradesh – 173205

Job Summary

Eugia Pharma Specialities Limited is conducting a Walk-In Interview for multiple opportunities across Production, QA-IPQA, Microbiology, Warehouse and Quality Control departments.
The openings are available for candidates with qualifications ranging from Diploma and B.Sc. to B.Pharm, M.Pharm, M.Sc. and Biotechnology.
Candidates with 1 to 12 years of experience, depending on the position, are eligible to apply.
The walk-in interview is scheduled at Eugia Pharma Specialities Limited, Unit-III, Pashamylaram, Patancheru, Sangareddy.

Eugia Pharma Specialities – Walk-In Interview

Interview Details

Company: Eugia Pharma Specialities Limited
Unit: Unit-III
Date: 10th October 2026
Time: 10:00 AM to 03:00 PM
Venue: Eugia Pharma Specialities Limited, Unit-III, Pashamylaram, Patancheru, Sangareddy

Eugia Pharma Specialities – Production Department

Operator

Experience: 2–9 Years
Qualification: Diploma / B.Sc.

Job Profile:

• Operation of Vial / BFS / PFS / FFS / Isolator filling machines.
• Working knowledge of aseptic behaviour.
• Operation of autoclave.
• Washing and sealing activities.
• Online documentation.
• cGMP compliance.
• Compounding preparation.

Executive / Sr. Executive

Experience: 2–12 Years
Qualification: B.Pharm

Job Profile:

• Monitoring of Vial / BFS / PFS / FFS / Isolator filling line operations.
• Experience in aseptic behaviour.
• Online documentation.
• cGMP compliance.
• In-charge for shift activities.
• Compounding preparation.

Eugia Pharma Specialities – QA-IPQA

Executive / Sr. Executive

Experience: 1–3 Years
Qualification: B.Pharm / M.Pharm

Job Profile:

• Line clearance activity for washing, filling and sealing.
• Visual inspection.
• Environmental monitoring activity in Grade A, B, C and D cleanroom areas.
• In-process activity.

Eugia Pharma Specialities – Microbiology

Trainee / Assistant / Executive

Experience: 1–5 Years
Qualification: B.Sc / M.Sc Microbiology / Biotechnology

Job Profile:

• EM monitoring.
• Should be ready to work in shifts or shopfloor operations.

Eugia Pharma Specialities – Warehouse

Technical Assistant / Sr. Technical Assistant

Experience: 3–5 Years
Qualification: B.Sc.

Job Profile:

• Receipt and dispensing of raw material.
• Packing material handling.
• Cleaning.
• Upkeep of warehouse area in compliance with regulatory standards.

Eugia Pharma Specialities – Quality Control

Technical Assistant / Executive

Experience: 2–5 Years
Qualification: B.Sc / M.Sc.

Job Profile:

• Analyst testing.
• Inspection of raw materials.
• In-process testing and related Quality Control activities.

Eligibility & Qualifications

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

B.Pharm | M.Pharm | B.Sc | M.Sc | M.Sc Microbiology | Biotechnology | Diploma

Educational Qualification

• B.Pharm
• M.Pharm
• B.Sc
• M.Sc
• M.Sc Microbiology
• Biotechnology
• Diploma

Experience Required

Experience requirements vary by position:

1 to 12 Years

• Production Operator: 2–9 Years
• Production Executive / Sr. Executive: 2–12 Years
• QA-IPQA Executive / Sr. Executive: 1–3 Years
• Microbiology Trainee / Assistant / Executive: 1–5 Years
• Warehouse Technical Assistant / Sr. Technical Assistant: 3–5 Years
• Quality Control Technical Assistant / Executive: 2–5 Years

How to Apply

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

Interview Venue

Eugia Pharma Specialities Limited – Unit-III
Pashamylaram, Patancheru, Sangareddy

Date: 10th October 2026
Time: 10:00 AM to 03:00 PM

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

Job Summary

Medreich Limited Pharmacovigilance Jobs – Bengaluru

Medreich Limited is hiring Pharmacovigilance professionals in Bengaluru for a specialized role in Aggregate Reporting and Core Submissions. The position involves end-to-end authoring, scientific evaluation, and timely submission of global periodic safety reports and core regulatory submissions. The role also serves as a Subject Matter Expert (SME) for cumulative safety data analysis, signal detection, and preparation of key regulatory documents. Candidates with 4–5 years of experience and an M.Pharm/Pharm.D background are preferred.

Pharmacovigilance Aggregate Reporting and Core Submissions Specialist

Job Role & Responsibilities

The Pharmacovigilance Aggregate Reporting and Core Submissions Specialist will be responsible for:

• End-to-end authoring of global periodic safety reports.
• Scientific evaluation of cumulative safety data.
• Timely submission of periodic safety reports and core submissions.
• Analysing cumulative safety data.
• Detecting and evaluating safety signals.
• Compiling key regulatory files.
• Ensuring compliance with global Health Authority requirements.

Key Regulatory Documents

The role involves preparation and compilation of:

• Periodic Safety Update Reports (PSURs)
• Periodic Benefit-Risk Evaluation Reports (PBRERs)
• Risk Management Plans (RMPs)
• Addendums to Clinical Overviews

Eligibility & Qualifications

Experience

• 4–5 years of relevant experience in Pharmacovigilance is preferred.

Educational Qualification

• M.Pharm / Pharm background preferred.

Eligible Qualification Courses

M.Pharm | Pharm.D | Pharmacy-related qualifications

How to Apply

Interested candidates can connect with the recruitment contacts below:

Email: varsha.h@medreich.com
Email: swathi.ds@medreich.com

Candidates with relevant Pharmacovigilance, aggregate reporting, safety evaluation, signal detection, and regulatory submissions experience may apply.

Job Summary

Torrent Pharmaceuticals Ltd. is conducting a Walk-In Interview for multiple positions at its Oncology Plant in Bileshwarpura.
The recruitment drive is open for candidates across Production, Packaging, Warehouse, Quality Control and HSE departments.
Candidates with qualifications including B.Pharm, M.Pharm, B.Sc, M.Sc, ITI, Diploma, BE/B.Tech and related qualifications can apply for suitable positions.
Experience requirements range from 1 to 15 years, depending on the department and grade.

Torrent Pharmaceuticals Ltd. – Walk-In Interview

Interview Details

Company: Torrent Pharmaceuticals Ltd.
Plant: Oncology Plant, Bileshwarpura
Date: 11th October 2026 (Sunday)
Time: 09:00 AM to 03:00 PM
Job Location: Torrent Pharmaceuticals Ltd. – Bileshwarpura Plant, Ahmedabad–Mehsana Highway, Village Bileshwarpura, Tal. Kalol, Dist. Gandhinagar, Gujarat – 382729

Positions

Assistant Manager / Executive / Technical Assistant / Fixed Term Employee

Torrent Pharmaceuticals – Production Department

Assistant Manager

Experience: 10 to 15 Years
Qualification: B.Pharm / M.Pharm
Job/Skill Set: Experience in Production and Packaging, Granulation, Compression, Coating, Capsules and Documentation.

Executive / Technical Assistant / Technician / Fixed Term Staff

Experience: 2 to 8 Years
Qualification: B.Pharm / M.Pharm / ITI / Diploma
Job/Skill Set: Granulation, Compression, Coating, Capsules and Documentation.

Torrent Pharmaceuticals – Packaging (Tablet & Capsules)

Executive / Technical Assistant / Technician / Fixed Term Staff

Experience: 2 to 8 Years
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm / ITI / Diploma
Job/Skill Set: Blister Packaging, Bottle Packaging, Bulk Packaging, Secondary Line, Track & Trace System and Documentation.

Torrent Pharmaceuticals – Warehouse (Tablet & Capsules)

Executive / Technical Assistant / Technician / Fixed Term Staff

Experience: 2 to 8 Years
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm / ITI / Diploma
Job/Skill Set: Dispensing, RM/PM Handling and Documentation.

Torrent Pharmaceuticals – Quality Control (Stability)

Technical Assistant / Executive

Experience: 1 to 5 Years
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
Job/Skill Set: Stability Protocols, Stability Samples and ensuring compliance with cGMP, GDP, ICH, WHO and regulatory requirements.

Torrent Pharmaceuticals – Quality Control (GLP)

Technical Assistant / Executive

Experience: 1 to 5 Years
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
Job/Skill Set: GLP guidelines, instrument calibration, PHV/HPLC calibration, etc.

Torrent Pharmaceuticals – HSE

Executive

Experience: 2 to 8 Years
Qualification: BE + PGDIS / ADIS
Job/Skill Set: EPCB legal requirements, Work Permit System, OHS legal documents, ETP operations, Fire and Safety Knowledge, ISO 14001 and ISO 45001.

Eligibility & Qualifications

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

B.Pharm | M.Pharm | B.Sc | M.Sc | ITI | Diploma | BE / B.Tech | PGDIS | ADIS

Educational Qualification

• B.Pharm / M.Pharm
• B.Sc / M.Sc
• ITI / Diploma
• BE / B.Tech
• PGDIS / ADIS

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

Experience Required

Experience requirements vary by position:

1 to 15 Years

• Production: 2–15 Years
• Packaging: 2–8 Years
• Warehouse: 2–8 Years
• Quality Control: 1–5 Years
• HSE: 2–8 Years

Important Instructions

• Please carry your updated CV, only last 3 months’ salary slips and qualification documents.
• Candidates interviewed during the last 6 months need not apply.

How to Apply

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

Interview Venue

Torrent Pharmaceuticals Ltd. – Bileshwarpura Plant
Ahmedabad–Mehsana Highway, Village Bileshwarpura,
Tal. Kalol, Dist. Gandhinagar, Gujarat – 382729

Date: 11th October 2026 (Sunday)
Time: 09:00 AM to 03:00 PM

For queries, candidates may contact:

Email: jyotigsai@torrentpharma.com / nishantpatel@torrentpharma.com
Mobile: +91 6357344213 / +91 63595621329

Candidates can also scan the QR code provided in the recruitment advertisement for the location.

Job Summary

Hetero is conducting a walk-in interview for opportunities in its Formulation R&D Units in Hyderabad.
The openings are available across Liquids, Hormones, Solid Orals and Injectables sections.
Candidates with M.Pharmacy, B.Pharmacy and M.Sc. Chemistry qualifications can apply for the respective positions.
Experience requirements range from 2 to 7 years, depending on the R&D section and dosage form.

Hetero Formulation R&D – Walk-In Interview

Walk-In Interview Details

Company: Hetero
Department: Formulation R&D / Analytical R&D
Interview Date: 10-10-2026 (Saturday)
Interview Time: 10:00 AM – 02:00 PM
Interview Location: Hetero Corporate Office, 7-2-A2, Sanath Nagar IE, Sanath Nagar, Hyderabad, Telangana – 500018

Hetero Formulation R&D – Job Openings

FR&D – Liquids

Experience: 2–7 Years
Qualification: M.Pharmacy / B.Pharmacy

Job Profile:

• Should have experience in formulation development, process optimization, scale-up and technology transfer of liquid and solid dosage forms.
• Hands-on experience with homogenizer, RMG, FBP, compression and coating machines.
• Preparation of technical documents including MFC, PDR, stability notes and specifications.

FR&D – Hormones

Experience: 3–5 Years
Qualification: M.Pharmacy / B.Pharmacy

Job Profile:

• Should have experience in formulation development as per QbD and formulation optimization using Design of Experiments (DoE).
• Scale-up batch manufacturing.
• CFT coordination with ARD, RA, TT, Manufacturing and Purchase.
• Experience in Soft Gel or Veterinary dosage forms is preferred.

FR&D – Solid Orals

Experience: 2–7 Years
Qualification: M.Pharmacy / B.Pharmacy

Job Profile:

• Should have experience in Oral Solid Dosage formulation development, process optimization, scale-up and technology transfer.
• Experience with OSD manufacturing processes/equipment such as granulation, compression and coating.
• Technical documentation and troubleshooting.

Hetero Analytical R&D – Job Openings

AR&D – Hormones

Experience: 3–5 Years
Qualification: M.Pharmacy / B.Pharmacy / M.Sc. Chemistry

Job Profile:

• Should have experience in analytical method development for raw materials and finished products.
• Analytical testing, data interpretation, documentation and troubleshooting.
• Compliance with GLP/GMP.
• CFT coordination with RA, TT, Validation, QC and Purchase.

AR&D – Injectables

Experience: 5–7 Years
Qualification: M.Pharmacy / B.Pharmacy / M.Sc. Chemistry

Job Profile:

• Should have experience in analytical testing and method development/validation of parenteral dosage forms.
• Hands-on exposure to HPLC, GC and particle-size analysis.
• Ensure GMP/GLP compliance, documentation, stability testing and investigation of OOS/OOT results.

Eligibility & Qualifications

Candidates with the following qualifications are eligible for the respective R&D positions:

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

Educational Qualification

• B.Pharmacy
• M.Pharmacy
• M.Sc. Chemistry

Experience Required

2–7 Years, depending on the position and R&D section.

Hetero R&D Skills & Experience

Relevant experience in the following areas is applicable:

• Formulation Development
• Process Optimization
• Scale-Up and Technology Transfer
• Oral Solid Dosage
• Liquid Dosage Forms
• Hormonal Formulations
• Injectable / Parenteral Dosage Forms
• Analytical Method Development
• Method Validation
• HPLC and GC
• Stability Testing
• GLP / GMP Compliance
• OOS / OOT Investigation
• Technical Documentation
• Troubleshooting

How to Apply

Candidates who are unable to attend the recruitment drive can share their updated CV at:

Email: durgaprasad.d@hetero.com

Candidates attending the walk-in interview should carry their updated CV and relevant educational and experience documents.

Scan the QR code in the recruitment advertisement to complete the application.

Job Summary

ProPharma Hyderabad Scheduled Walk-In Drive – PV & Drug Safety Jobs

ProPharma is conducting a scheduled walk-in drive in Hyderabad for experienced professionals in Pharmacovigilance and Drug Safety. The openings cover PV ICSR Specialist and Aggregate Report Writer roles with experience requirements ranging from 1 to 8 years. Immediate joiners and candidates with a 0–15 day notice period are preferred. Email confirmation/invitation from the ProPharma Talent Acquisition team is mandatory to attend the walk-in.

ProPharma Walk-In Interview – Hyderabad

Company: ProPharma
Location: Hyderabad
Walk-In Date: Friday, 9 October 2026
Time: 10:00 AM – 6:00 PM
Hiring Preference: Immediate to 15-day notice period

Important: This is a scheduled walk-in only. Candidates must receive an official email confirmation/invitation from the ProPharma Talent Acquisition team before attending.

PV ICSR Specialist

Experience: 1–4 Years

Key Skills

• Case Processing
• Narrative Writing
• Quality Review
• Argus

Aggregate Report Writer

Experience: 2–8 Years

Key Skills

• PBRER / PSUR / DSUR Authoring
• Signal Evaluation
• Risk Management

Eligibility & Qualifications

The provided recruitment notice specifies the experience ranges and role-specific skills above. It does not specify a particular educational qualification.

Eligible Qualification

Relevant Pharmacy, Life Sciences, Clinical Research, or related qualifications may be considered based on the respective role, but the source does not explicitly state the required qualification.

How to Apply

Interested candidates should email their updated CV to:

ramya.bantupalli@propharmagroup.com

Candidates must receive an official invitation/confirmation email from the ProPharma Talent Acquisition team before attending the scheduled walk-in.

Job Summary

Lupin Hiring – Officer, Quality Assurance | Biotech / Pharma | Pune

Lupin is hiring an Officer – Quality Assurance for its Pune Biotech facility in Maharashtra.
The role involves GMP compliance, manufacturing investigations, CAPA, validation activities, batch record review, and warehouse quality oversight.
Candidates with 1–3 years of experience and qualifications in Biotechnology, Biopharmaceutics, or Pharmacy can apply.
The position focuses on ensuring manufacturing and warehouse activities comply with GMP, regulatory requirements, and approved procedures.

Job Details

Officer – Quality Assurance

• Company: Lupin
• Department: Quality Assurance
• Location: Pune Biotech, Maharashtra
• Experience: 1–3 years
• Date: October 7, 2026

Quality Assurance Responsibilities

GMP & Regulatory Compliance

• Visit the DS manufacturing and warehouse facility to ensure activities are carried out according to:

  • GMP requirements
  • Regulatory requirements
  • Approved procedures

Manufacturing Investigation & CAPA

• Participate in manufacturing investigations.
• Participate in CAPA finalization activities.
• Prepare and review Risk Assessment and Mitigation Plans.

Validation & Documentation

• Ensure process and cleaning validation activities are conducted according to approved protocols.
• Review master documents such as:

  • Study protocols
  • BPR
  • MFR
  • Other applicable master documents

Batch Release & Warehouse Activities

• Review executed Batch Processing Records for batch release.
• Review Batch Dispatch Records.
• Verify dispatch activities conducted in the warehouse.

APQR & Quality Systems

• Coordinate APQR data compilation.
• Coordinate and support APQR preparation activities.
• Prepare and review Quality System SOPs and documents.
• Review SOPs for all departments to ensure compliance with GMP requirements.

Eligibility & Qualifications

Educational Qualification

The source specifies the following qualification backgrounds:

• Master’s in Biotechnology or Biotechnology
• Post Graduation in Biopharmaceutics or Pharmacy

Experience

• 1–3 years

The source does not specify a separate minimum experience requirement for individual qualification streams.

Key Competencies

Lupin lists the following competencies for the position:

1. Strategic Agility
2. Innovation & Creativity
3. Customer Centricity

Eligible Qualification Courses

M.Sc. Biotechnology | M.Tech. Biotechnology | Post Graduation in Biopharmaceutics | M.Pharm | Other Postgraduate Qualification in Pharmacy

The source wording is “Masters in Biotechnology or Biotechnology” and “Post Graduation in Biopharmaceutics or Pharmacy.” Individual degree formats such as M.Sc. or M.Tech. are not separately specified, so the list above should be treated as a practical representation rather than an exhaustive course-wise eligibility list.

Location

Lupin – Pune Biotech
Pune, Maharashtra, India

How to Apply

The source provided does not include a direct application URL. Candidates should apply through the official Lupin Careers portal for the Officer – Quality Assurance position.

Job Summary

Annova Solutions Hiring – Medical Coder | Medical Coding | Chennai

Annova Solutions is hiring Medical Coders for its full-time opportunity in Chennai, Tamil Nadu.
The position is open to graduates and postgraduates with a Health Science background, with medical coding certifications preferred.
Candidates should have strong knowledge of anatomy, physiology, medical terminology, ICD-10 guidelines, and clinical documentation.
The role involves medical record review, accurate ICD-10 coding, quality checking, and maintaining coding standards and patient confidentiality.

Company & Job Details

Medical Coder

• Company: Annova Solutions
• Job Title: Medical Coder
• Industry: BPO/ITES
• Location: Chennai, Tamil Nadu
• Job Type: Full-Time
• Posted On: 09 July 2026
• PIN Code: 600096

Job Responsibilities

Medical Coding & Documentation

• Abstract information from documentation and assign appropriate ICD-10 codes.
• Ensure codes are accurate and sequenced correctly according to applicable guidelines.
• Ensure compliance with medical coding policies and guidelines.
• Perform coding of charts across a variety of specialties with over 99% accuracy.
• Follow up with the supervisor when documentation is insufficient or unclear.
• Review medical records and determine the accuracy and completeness of documentation.

Quality & Team Responsibilities

• Work as part of a team to achieve quality and productivity goals.
• Perform quality checking of coding completed by associates.
• Track errors and calculate associate accuracy.
• Apply subject expertise when evaluating business operations and processes.
• Maintain patient confidentiality and strict adherence to HIPAA requirements.
• Support team guidance and maintain team quality standards.

Eligibility & Qualifications

Educational Qualification

• Any Graduate or Postgraduate with a Health Science background

The source does not provide a specific list of eligible degree courses.

Preferred Certifications

The following certifications are preferred:

• AAPC
• AHIMA
• CPC
• CRC

Certification is described as preferably required in the source, not as a mandatory qualification.

Required Knowledge & Skills

Candidates should have:

• Knowledge of anatomy, physiology, and medical terminology.
• Ability to apply anatomy and physiology knowledge when interpreting clinical documentation and identifying applicable medical codes.
• Strong knowledge of ICD-10 guidelines and their implementation.
• Ability to determine valid encounters, including legibility and valid signature requirements of medical records.
• Experience or ability to perform quality checks of coding completed by associates.
• Ability to track coding errors and calculate accuracy.
• Ability to review medical records for accuracy and completeness.
• Critical-thinking skills to ensure coding activities are properly managed according to scope.
• Ability to solve moderately complex problems independently.
• Ownership mindset toward guidance, team support, and maintaining team quality.

Eligible Qualification Courses

Health Science Graduate | Health Science Postgraduate

The employer specifically states “Any graduate and postgraduate in health science background.” Individual courses such as B.Pharm, M.Pharm, B.Sc., M.Sc., BPT, BAMS, BHMS, Nursing, etc.

Location

Chennai, Tamil Nadu – 600096

 

How to Apply

Interested and eligible candidates can apply directly through the Annova Solutions careers page:

Apply for Medical Coder – Annova Solutions

Job Summary

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