Author: Sudheer vanguri

Cronus Pharma is inviting applications for opportunities in pharmaceutical analytical method validation and method verification.
The openings are suitable for interns, trainees and candidates with at least 6 months to 1 year of experience.
Candidates looking to restart their careers are also encouraged to apply.
The opportunity includes hands-on learning, professional guidance and exposure to analytical laboratory activities.

Cronus Pharma – Analytical Department

Cronus Pharma – Method Validation & Method Verification

Function: Analytical Method Validation & Method Verification

The opportunity is open to candidates interested in building or restarting their careers in the pharmaceutical analytical field.

Cronus Pharma – Eligible Candidate Categories

The recruitment announcement invites applications from:

• Interns
• Candidates with at least 6 months to 1 year of experience
• Trainees
• Candidates looking to restart their careers
• Individuals interested in Analytical Method Validation and Method Verification

Cronus Pharma – Method Validation & Verification

Cronus Pharma – Key Opportunities

Selected candidates will receive:

• Hands-on exposure to Method Validation & Method Verification activities
• Learning and development opportunities
• Guidance from experienced professionals
• Career growth opportunities within the organization

Eligibility & Qualifications

Cronus Pharma – Educational Qualification

The provided recruitment announcement does not specify a particular educational qualification.

Candidates interested in pharmaceutical analytical careers can apply based on the eligibility categories mentioned in the announcement.

Experience Requirements

Cronus Pharma – Analytical Method Validation

The opportunity is open to:

Interns | Trainees | Candidates with 6 Months–1 Year Experience | Career Restart Candidates

Career Development Opportunity

Cronus Pharma – Analytical Careers

The position is intended for individuals who are enthusiastic about learning and developing their careers in pharmaceutical analytical activities, particularly Method Validation and Method Verification.

Job Location

Cronus Pharma – Location

Job location is not specified in the provided recruitment announcement.

How to Apply

Interested candidates can share their updated resume at:

Email: sguttula@cronuspharma.com

Candidates should send their updated CV for consideration for the Method Validation & Method Verification opportunity.

Job Summary

Beta Drugs Limited is hiring professionals and freshers across multiple departments at its Baddi, Himachal Pradesh operations.
The openings cover Microbiology, Production, Quality Assurance, Quality Control and Engineering functions.
Opportunities are available for experienced candidates as well as Apprenticeship Trainees with qualifications ranging from 12th, ITI, B.Pharm., B.Sc., M.Sc. and B.Tech.
Interested candidates can apply by sharing their updated CV with the recruitment team and mentioning the position applied for in the subject line.

Beta Drugs Limited – Microbiology Department

Beta Drugs Limited – Junior Officer – EM, GPT, MLT

Qualification: B.Tech. / M.Sc.
Experience: 1–2 Years

Beta Drugs Limited – Microbiology Skills

The position covers activities related to:

• Environmental Monitoring (EM)
• GPT
• MLT

Beta Drugs Limited – Production Department – Injection

Beta Drugs Limited – JMA – Lyophilizer

Qualification: 12th / ITI
Experience: 2–4 Years

Beta Drugs Limited – Lyophilizer Requirement

Candidates should have relevant experience in lyophilizer operations.

Beta Drugs Limited – Apprenticeship Trainee – Injection

Qualification: 12th / ITI
Experience: Fresher

Beta Drugs Limited – Production Department – OSD

Beta Drugs Limited – Officer – Manufacturing

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

Beta Drugs Limited – OSD Manufacturing

The position is for Manufacturing operations in the OSD production area.

Beta Drugs Limited – Apprenticeship Trainee – OSD

Qualification: 12th / ITI
Experience: Fresher

Beta Drugs Limited – Quality Assurance Department

Beta Drugs Limited – Officer / Senior Officer – Qualification & Validation

Qualification: B.Pharm.
Experience: 4–8 Years

Beta Drugs Limited – Qualification & Validation

The role is focused on Qualification & Validation activities.

Beta Drugs Limited – Officer / Senior Officer – QMS

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

Beta Drugs Limited – QMS

The role involves Quality Management System (QMS) activities.

Beta Drugs Limited – Apprenticeship Trainee – QA

Qualification: 12th
Experience: Fresher

Beta Drugs Limited – Quality Control Department

Beta Drugs Limited – Junior Officer – FG HPLC

Qualification: B.Sc. / M.Sc.
Experience: 1–2 Years

Beta Drugs Limited – FG HPLC

The position is related to Finished Goods (FG) HPLC activities.

Beta Drugs Limited – Officer / Senior Officer / Executive – Quality Control

Qualification: B.Pharm. / M.Sc. Chemistry
Experience: 5–10 Years

Beta Drugs Limited – Quality Control Experience

Candidates with relevant Quality Control experience can apply for these positions.

Beta Drugs Limited – Engineering Department

Beta Drugs Limited – Water System Technician

Experience: 6–9 Years

Beta Drugs Limited – Water System Requirement

Pharmaceutical industry experience is mandatory.

The source does not specify an educational qualification for this position.

Beta Drugs Limited – HVAC Officer + QMS

Experience: 3–5 Years

Beta Drugs Limited – HVAC & QMS

The role combines HVAC and QMS responsibilities. The source does not specify an educational qualification.

Eligibility & Qualifications

Beta Drugs Limited – Microbiology

B.Tech. | M.Sc.

Beta Drugs Limited – Production – Injection

12th | ITI

Beta Drugs Limited – Production – OSD

B.Pharm. | 12th | ITI

Beta Drugs Limited – Quality Assurance

B.Pharm. | 12th

Beta Drugs Limited – Quality Control

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

Beta Drugs Limited – Engineering

Qualification not specified in the source for Water System Technician and HVAC Officer + QMS.

Experience Requirements

Beta Drugs Limited – Department-wise Experience

Microbiology: 1–2 Years
Production – Injection JMA: 2–4 Years
Production – OSD Officer: 2–4 Years
QA – Qualification & Validation: 4–8 Years
QA – QMS: 3–5 Years
QC – Junior Officer FG HPLC: 1–2 Years
QC – Officer / Senior Officer / Executive: 5–10 Years
Engineering – Water System Technician: 6–9 Years
Engineering – HVAC Officer + QMS: 3–5 Years
Apprenticeship Trainee: Freshers

Beta Drugs Limited – Job Location

Beta Drugs Limited – Baddi

Location: Baddi, Himachal Pradesh

How to Apply

Interested candidates can share their updated CV at:

Email: hr.baddi@betadrugslimited.com

Candidates should mention the position applied for in the subject line of the email.

Job Summary

Sri Krishna Pharmaceuticals Limited is expanding its R&D Centre (Formulations) in Chennai and has announced multiple openings across Analytical R&D (ARD) and Formulation R&D (FRD).
The recruitment includes Group Leader, Officer, Scientist and Associate positions for both Solid Oral and Injectable divisions.
Candidates with M.Pharm, M.Sc. or B.Pharm qualifications can apply for the positions matching their experience.
Applications and employee referrals are invited until 30 September 2026.

Sri Krishna Pharmaceuticals – Analytical R&D Department

Sri Krishna Pharmaceuticals – Group Leader, Analytical R&D – Solid Orals

Vacancies: 2 Positions
Qualification: M.Pharm. / M.Sc.
Experience: 7–8 Years
Division: Solid Orals

Sri Krishna Pharmaceuticals – Group Leader, Analytical R&D – Injectables

Vacancies: 2 Positions
Qualification: M.Pharm. / M.Sc.
Experience: 7–8 Years
Division: Injectables

Sri Krishna Pharmaceuticals – Officer, Analytical R&D – Solid Orals

Vacancies: 4 Positions
Qualification: M.Pharm. / M.Sc. / B.Pharm.
Experience: 2–5 Years
Division: Solid Orals

Sri Krishna Pharmaceuticals – Formulation R&D Department

Sri Krishna Pharmaceuticals – Group Leader, Formulation R&D – Solid Orals

Vacancies: 1 Position
Qualification: M.Pharm.
Experience: 7–8 Years
Division: Solid Orals

Sri Krishna Pharmaceuticals – Group Leader, Formulation R&D – Injectables

Vacancies: 2 Positions
Qualification: M.Pharm.
Experience: 7–8 Years
Division: Injectables

Sri Krishna Pharmaceuticals – Scientist, Formulation R&D – Solid Orals

Vacancies: 1 Position
Qualification: M.Pharm.
Experience: 3–5 Years
Division: Solid Orals

Sri Krishna Pharmaceuticals – Associate, Formulation R&D – Solid Orals

Vacancies: 3 Positions
Qualification: M.Pharm.
Experience: 0–3 Years
Division: Solid Orals

Sri Krishna Pharmaceuticals – Associate, Formulation R&D – Injectables

Vacancies: 2 Positions
Qualification: M.Pharm.
Experience: 0–3 Years
Division: Injectables

Eligibility & Qualifications

Sri Krishna Pharmaceuticals – Analytical R&D

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

The source specifies M.Pharm. / M.Sc. for Group Leader roles and M.Pharm. / M.Sc. / B.Pharm. for the Officer position.

Sri Krishna Pharmaceuticals – Formulation R&D

M.Pharm.

All Formulation R&D positions listed in the source require M.Pharm.

Experience Requirements

Sri Krishna Pharmaceuticals – Group Leader Positions

7–8 Years

Sri Krishna Pharmaceuticals – Officer, Analytical R&D

2–5 Years

Sri Krishna Pharmaceuticals – Scientist, Formulation R&D

3–5 Years

Sri Krishna Pharmaceuticals – Associate, Formulation R&D

0–3 Years

Sri Krishna Pharmaceuticals – Job Location

Sri Krishna Pharmaceuticals R&D Centre

R&D Centre (Formulations), Chennai, Tamil Nadu

How to Apply

Interested candidates and employees wishing to refer suitable candidates can submit updated resumes directly to the HR Department or send them by email to:

vijayakumar.e@srikrishnapharma.com

Applications should be submitted on or before 30 September 2026.

Sri Krishna Pharmaceuticals – Application Instructions

Candidates should mention the Position Name in the subject line of the email.

Job Summary

Eugia Pharma Specialities Limited is conducting a Walk-In Interview for experienced professionals across Quality Assurance, MSAT, Quality Control – Microbiology, Production and Engineering departments.
The openings are available for Executive and Technical Assistant positions with relevant pharmaceutical manufacturing experience.
Candidates with B.Pharm, M.Pharm, M.Sc. Microbiology, B.Tech. Electrical, Diploma and ITI qualifications can apply for the respective roles.
The walk-in interview is scheduled for 20 September 2026, from 10:00 AM to 04:00 PM, at Legend Sarovar Portico, Baddi, Himachal Pradesh.

Eugia Pharma Specialities – Quality Assurance Department

Eugia Pharma Specialities – Quality Assurance Executive

Designation: Executive
Qualification: B.Pharm. / M.Pharm.
Experience: 2–5 Years
Required Experience: Validation / QMS / IPQA / AQA

Eugia Pharma Specialities – QA Requirements

Candidates should have relevant experience in:

• Validation
• QMS
• IPQA
• AQA
• Pharmaceutical manufacturing operations
• Sterile manufacturing environments
• USFDA / EU-GMP approved plants, preferably

Eugia Pharma Specialities – MSAT Department

Eugia Pharma Specialities – MSAT Executive

Designation: Executive
Qualification: B.Pharm. / M.Pharm.
Experience: 2–5 Years
Required Experience: Equipment Qualification / Validation

Eugia Pharma Specialities – MSAT Requirements

The position requires relevant experience in equipment qualification and validation within a pharmaceutical manufacturing environment.

Eugia Pharma Specialities – Quality Control Department

Eugia Pharma Specialities – QC Microbiology Executive

Designation: Executive
Qualification: M.Sc. Microbiology
Experience: 2–5 Years
Required Experience: Analyst / Reviewer

Eugia Pharma Specialities – QC Microbiology Requirements

Candidates should have relevant experience as a Microbiology Analyst or Reviewer in pharmaceutical manufacturing.

Eugia Pharma Specialities – Production Department

Eugia Pharma Specialities – Production Executive

Designation: Executive
Qualification: B.Pharm. / M.Pharm.
Experience: 2–5 Years
Required Experience: Manufacturing Process / QMS

Eugia Pharma Specialities – Production Requirements

Candidates should have experience in pharmaceutical manufacturing processes and QMS activities.

Eugia Pharma Specialities – Production Technical Assistant

Designation: Technical Assistant
Qualification: Diploma / ITI
Experience: 2–5 Years
Required Experience: Vial Filling / Vial Sealing / Aseptic / Autoclave

Eugia Pharma Specialities – Production Technical Assistant Requirements

Relevant experience in the following areas is required:

• Vial filling
• Vial sealing
• Aseptic operations
• Autoclave operations

Eugia Pharma Specialities – Engineering Department

Eugia Pharma Specialities – Engineering Executive

Designation: Executive
Qualification: B.Tech. Electrical
Experience: 2–5 Years
Required Experience: HVAC / Utility / Water System

Eugia Pharma Specialities – Engineering Requirements

Candidates should have relevant experience in:

• HVAC systems
• Utility operations
• Water systems

Eugia Pharma Specialities – Engineering Technical Assistant

Designation: Technical Assistant
Qualification: Diploma / ITI (Electrical)
Experience: 2–5 Years
Required Experience: HVAC / Utility / Water System

Eligibility & Qualifications

Eugia Pharma Specialities – Quality Assurance

B.Pharm. | M.Pharm.

Eugia Pharma Specialities – MSAT

B.Pharm. | M.Pharm.

Eugia Pharma Specialities – Quality Control Microbiology

M.Sc. Microbiology

Eugia Pharma Specialities – Production

B.Pharm. | M.Pharm. | Diploma | ITI

Eugia Pharma Specialities – Engineering

B.Tech. Electrical | Diploma | ITI – Electrical

Experience Requirements

Eugia Pharma Specialities – All Listed Positions

2–5 Years

The recruitment poster indicates 2–5 years of experience, with preference for candidates who have worked in sterile manufacturing and USFDA/EU-GMP approved plants.

Eugia Pharma Specialities – Walk-In Interview Details

Eugia Pharma Specialities – Walk-In Interview

Date: 20th September 2026, Sunday
Time: 10:00 AM – 04:00 PM

Eugia Pharma Specialities – Interview Venue

Legend Sarovar Portico
Industrial Town of Baddi
District Solan, Himachal Pradesh – 173205

Documents Required

Eugia Pharma Specialities – Interview Documents

Candidates attending the walk-in interview should carry:

• Updated CV
• Educational Documents
• Experience Letter
• Payslips
• CTC Documents

How to Apply

Candidates who are unable to attend the walk-in interview can send their CV to:

Email: hruegia2@eugiapharma.com

Interested candidates should carry the required documents and attend the interview at the specified venue and time.

Job Summary

Milan Laboratories (India) Pvt. Ltd. is hiring candidates for multiple positions at its Dahej, Gujarat facility.
The openings are available across OSD Production, SVP Injectable Production, OSD Packing and Engineering departments.
Candidates with ITI, Diploma, B.Sc., B.Pharm., M.Sc., M.Pharm. and B.Tech. qualifications can apply for the relevant positions.
The recruitment poster also states that freshers are welcome to apply, while relevant pharmaceutical manufacturing experience is preferred for several roles.

Milan Laboratories – Production OSD Department

Milan Laboratories – Granulation Operator

Qualification: ITI / Diploma / B.Sc.
Experience: 2–5 Years

Milan Laboratories – Granulation Operator Requirements

The position is listed under Production – OSD and is focused on granulation operations.

Milan Laboratories – Production SVP Injectable Department

Milan Laboratories – Officer – Production

Qualification: B.Sc. / M.Sc. / B.Pharm. / M.Pharm.
Experience: 2–5 Years
Preferred Experience: SVP / Injectable experience

Milan Laboratories – Officer Production Requirements

Candidates with relevant experience in SVP or injectable manufacturing will be preferred.

Milan Laboratories – Operator – Production

Qualification: ITI / Diploma / B.Sc.
Experience: 2–5 Years
Preferred Experience: SVP / Injectable experience

Milan Laboratories – Operator Production Requirements

The role is listed under Production – SVP (Injectable), with relevant SVP or injectable manufacturing experience preferred.

Milan Laboratories – Packing OSD Department

Milan Laboratories – Sachet Operator

Qualification: ITI / Diploma / B.Sc.
Experience: 3–5 Years
Preferred Experience: OSD packing / sachet machine experience

Milan Laboratories – Sachet Packing Requirements

Candidates with hands-on experience in OSD packing or sachet machine operations will be preferred.

Milan Laboratories – Engineering Department

Milan Laboratories – Water System Operator

Qualification: ITI / Diploma / B.Tech.
Experience: 2–5 Years
Preferred Experience: Water system / utility experience

Milan Laboratories – Water System Requirements

The position requires experience related to water systems or utility operations, where available.

Eligibility & Qualifications

Milan Laboratories – Production OSD

ITI | Diploma | B.Sc.

Milan Laboratories – Production SVP Injectable – Officer

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

Milan Laboratories – Production SVP Injectable – Operator

ITI | Diploma | B.Sc.

Milan Laboratories – Packing OSD

ITI | Diploma | B.Sc.

Milan Laboratories – Engineering

ITI | Diploma | B.Tech.

Milan Laboratories – Experience Requirements

Milan Laboratories – Department-wise Experience

Granulation Operator: 2–5 Years
Officer – Production: 2–5 Years
Operator – Production: 2–5 Years
Sachet Operator: 3–5 Years
Water System Operator: 2–5 Years

Milan Laboratories – Freshers

The recruitment poster states that Freshers are also welcome to apply.

Milan Laboratories – Job Location

Milan Laboratories (India) Pvt. Ltd.

Dahej, Gujarat

The recruitment poster identifies Dahej, Gujarat as the job location.

How to Apply

Interested candidates can apply through the registration form linked via the QR code in the recruitment poster.

Candidates can also contact the recruitment team through:

Phone: 7069007312 / 7069010614
Email: recruitment@milanlabs.com

Only shortlisted candidates will be contacted.

Job Summary

GEPACH International is conducting a Walk-In Interview for skilled professionals and freshers across multiple pharmaceutical functions.
The openings are available in Quality Control, Production and Formulation & Development departments.
Candidates with M.Sc., B.Pharm., M.Pharm. and M.Pharm. Pharmaceutics qualifications can apply for the relevant positions.
The walk-in interview is scheduled for 27 September 2026 at the company’s facility in Pithampur, Dhar, Madhya Pradesh.

GEPACH International – Quality Control Department

GEPACH International – Junior Officer / Officer – QC

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

GEPACH International – QC Skills

• HPLC
• GC
• Analytical Method Validation
• QMS
• RM/PM Testing

Candidates applying for the QC position should have relevant experience in these Quality Control activities.

GEPACH International – Management Trainee QC

GEPACH International – Management Trainee – QC

Qualification: M.Sc. / B.Pharm.

GEPACH International – QC Candidate Requirements

The recruitment advertisement highlights:

• Good communication skills
• Good writing skills

The source does not specify an experience requirement for the Management Trainee QC position.

GEPACH International – Production Department

GEPACH International – Officer / Senior Officer – Production

Experience: 3–6 Years
Qualification: M.Sc. / B.Pharm. / M.Pharm.

GEPACH International – Production Responsibilities

The role involves handling and monitoring tablet manufacturing activities, including:

• Granulation
• Compression
• Coating

Candidates with relevant pharmaceutical production experience can apply.

GEPACH International – Formulation & Development Department

GEPACH International – Management Trainee / Officer – Formulation & Development

Experience: 0–4 Years
Qualification: M.Pharm. (Pharmaceutics)

GEPACH International – Formulation Development Responsibilities

• Pre-formulation activities
• Formulation development for Solid Oral Dosage Forms
• Problem-solving related to formulation development

Eligibility & Qualifications

GEPACH International – Quality Control

M.Sc. | B.Pharm.

GEPACH International – Production

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

GEPACH International – Formulation & Development

M.Pharm. (Pharmaceutics)

Experience Requirements

GEPACH International – QC Junior Officer / Officer

2–4 Years

GEPACH International – Production Officer / Senior Officer

3–6 Years

GEPACH International – Formulation & Development Management Trainee / Officer

0–4 Years

GEPACH International – Management Trainee QC

Experience not specified in the recruitment advertisement

GEPACH International – Walk-In Interview Details

GEPACH International – Walk-In Interview

Date: 27th September 2026, Sunday
Time: 10:30 AM – 02:30 PM

GEPACH International – Interview Venue

GEPACH International
Plot No. A-10 & A-11, Industrial Area,
Indore SEZ Phase-II, Pithampur,
Dhar, Madhya Pradesh

GEPACH International – Interview Documents

GEPACH International – Documents to Carry

Candidates attending the walk-in interview should carry:

• Updated Resume
• Latest Salary Slips

How to Apply

GEPACH International – Application Process

Interested candidates can attend the walk-in interview at the above-mentioned venue with their updated resume and latest salary slips.

Candidates who are unable to attend the walk-in drive can share their resume at:

Email: hr@gepach.com

Job Summary

AdVity Research is hiring a Senior Analyst for its Hyderabad team.
The role is a full-time, on-premise position requiring 4–7 years of experience.
Candidates with B.Sc., B.Pharm., M.Sc., or M.Pharm. qualifications can apply.
The position involves bioanalytical sample preparation, method development and validation, LC-MS/MS analysis, documentation, and result reporting.

AdVity Research – Senior Analyst

AdVity Research – Senior Analyst

Position: Senior Analyst
Location: Hyderabad
Experience: 4–7 Years
Job Type: Full Time
Mode of Work: On Premise
Qualification: B.Sc. / B.Pharm. / M.Sc. / M.Pharm.

AdVity Research – Senior Analyst Responsibilities

Bioanalytical & Analytical Activities

• Perform bioanalytical sample preparation using different extraction techniques.
• Conduct method development and method validation.
• Perform sample analysis according to regulatory requirements.
• Handle analytical equipment, including LC-MS/MS.
• Prepare and review SOPs, protocols, and reports.
• Handle data generation, compilation, and reporting of results.

AdVity Research – Senior Analyst Skills

Preferred Skills

• Good communication and analytical skills.
• Ability to work as a team player and complete assigned tasks in a timely manner.

Eligibility & Qualifications

AdVity Research – Senior Analyst

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

Experience Requirements

AdVity Research – Senior Analyst

4–7 Years

AdVity Research – Job Location

Hyderabad

Location: Hyderabad, Telangana

How to Apply

Interested candidates can share their updated CV with the recruitment team at:

Email: hr@advityresearch.com

Job Summary

Torrent Pharmaceuticals Ltd. is hiring professionals for its Formulation Development (FnD) Department at the R&D Centre in Gandhinagar, Gujarat.
The openings are available for Executive and Assistant Manager positions in formulation development.
Candidates with M.Pharm. or PhD qualifications and relevant experience in OSD, oncology and complex generic formulations can apply.
The roles require experience with QbD, DoE, regulatory markets, formulation development documentation and technical development activities.

Torrent Pharma – Formulation Development Department

Torrent Pharma – Executive

Experience: 3–8 Years
Qualification: M.Pharm.
Location: R&D Centre, Gandhinagar, Gujarat

Torrent Pharma – Executive Required Experience & Skills

• Formulation development of OSD and oncology products.
• Exposure to regulated, semi-regulated and India markets.
• Experience with FnD documents such as:

  • Product Development Report
  • Specifications
  • MFC
  • BMR
  • Stability documents

• Experience in utilizing Quality by Design (QbD) principles.
• Experience with Design of Experiments (DoE) tools.
• Awareness of ICH and regulatory guidelines related to formulation development.

Torrent Pharma – Formulation Development Assistant Manager

Torrent Pharma – Assistant Manager

Experience: 8–15 Years
Qualification: M.Pharm. / PhD
Location: R&D Centre, Gandhinagar, Gujarat

Torrent Pharma – Assistant Manager Required Experience & Skills

• Lead end-to-end formulation strategy for complex OSD, oncology and complex generic dosage forms across regulated markets.
• Act as a subject matter expert in implementing QbD roadmaps and sophisticated DoE modelling.
• Prepare project timelines and development plans.
• Provide scientific and technical input for global regulatory submissions.
• Collaborate closely with cross-functional teams to ensure smooth project execution and timely completion.
• Ensure complete and accurate documentation of formulation development activities.

Eligibility & Qualifications

Torrent Pharma – Executive

M.Pharm.

Torrent Pharma – Assistant Manager

M.Pharm. | PhD

Experience Requirements

Torrent Pharma – Executive

3–8 Years

Torrent Pharma – Assistant Manager

8–15 Years

Torrent Pharma – Job Location

Torrent Pharma – R&D Centre

Gandhinagar, Gujarat

How to Apply

Interested candidates can share their updated resume with the Torrent Pharma recruitment team at:

shambhavi.arothe@torrentpharma.com
vilshashah@torrentpharma.com

Candidates should mention the relevant Formulation Development position while applying.

Job Summary

DevSynthesis is expanding its Discovery Chemistry Department and is looking for experienced professionals from the core CRO industry.
The recruitment is aimed at candidates with 2–8 years of relevant experience in Discovery Chemistry.
The source highlights opportunities to work on innovative projects, learning and career growth, and chemistry-focused research activities.
Interested candidates can share their updated resume with the recruitment team using the email or phone number provided.

DevSynthesis – Discovery Chemistry Department

DevSynthesis – Discovery Chemistry Professionals

Department: Discovery Chemistry
Experience: 2–8 Years
Industry Experience: Core CRO Industry

The recruitment artwork does not specify a particular designation, number of vacancies, educational qualification, or job location.

DevSynthesis – Candidate Requirements

DevSynthesis – Discovery Chemistry Experience

Candidates should have:

• 2–8 years of experience
• Relevant experience in the core CRO industry
• Professional interest in Discovery Chemistry

The source does not provide a detailed technical job description or specific instrument/technique requirements.

DevSynthesis – Career Opportunities

DevSynthesis – Growth & Development

The recruitment material highlights:

• Opportunity to work on innovative projects
• Learning and career growth
• Employee recognition and rewards
• A safe and inclusive work environment
• Opportunity to grow with a vibrant organization

Eligibility & Qualifications

DevSynthesis – Discovery Chemistry

Educational Qualification: Not specified in the source.

Experience: 2–8 Years in the core CRO industry.

No specific degree or specialization is mentioned in the recruitment artwork, so additional qualification requirements should be confirmed directly with the recruitment team.

How to Apply

Interested candidates can share their resume at:

Email: hr@dev-synthesis.com

Contact: 9392904327

Candidates can also refer suitable friends or professional contacts for the opportunity.

Job Summary

IQVIA Primary Market Research Associate Consultant Recruitment 2026

IQVIA is hiring a Primary Market Research Associate Consultant in Bengaluru, India for its Research & Intelligence (R&I) team.
The role focuses on delivering quantitative Primary Market Research (PMR) projects across healthcare and pharmaceutical markets, working with global clients and multiple therapy areas.
Candidates will support end-to-end research projects involving questionnaire design, data analysis, market research, report development, quality control, and client communication.
Applicants with a Bachelor’s or Master’s degree in Life Sciences and 3–4 years of relevant experience can apply, with an MBA and pharmaceutical consulting or market research experience preferred.

Primary Market Research Associate Consultant

About the Role

The position is part of IQVIA’s Research & Intelligence (R&I) team, which combines Primary Market Research (PMR) and Secondary Desk Research (SDR) to generate actionable insights for clients.

The role requires experience in Primary Market Research, with responsibility for managing multiple projects under tight timelines while working with global clientele.

Primary Market Research Experience: 3+ years
Relevant Experience: 3–4 years
Reporting To: Senior Consultant

Job Role & Responsibilities

The Associate Consultant will support the end-to-end delivery of quantitative PMR projects across different therapy areas and healthcare sectors.

Primary Market Research Projects

Responsibilities include:

• Support quantitative Primary Market Research projects across diverse therapy areas.
• Work on studies such as:

  • ATU
  • Demand estimation
  • Market assessments
  • Patient flow
  • Patient journey
  • Buying process
  • Segmentation
  • Strategic research initiatives

• Manage multiple PMR projects under tight timelines.
• Prioritize project requests based on criticality and business requirements agreed with stakeholders.

Questionnaire & Research Design

• Design and refine questionnaires and discussion guides.
• Incorporate guidance from senior team members to ensure research objectives are effectively addressed.
• Develop research approaches aligned with client objectives.

Data Analysis & Interpretation

• Conduct robust data analysis.
• Review tabulations.
• Code open-ended responses.
• Develop table specifications.
• Validate research outputs.
• Interpret quantitative and qualitative data and integrate different sources of data assets.
• Ensure research findings are accurate, insightful, and methodologically sound.

Reports & Client Deliverables

• Develop PowerPoint report templates.
• Prepare client deliverables.
• Synthesize research findings into clear and compelling narratives.
• Address key business questions and support strategic decision-making.

Project & Stakeholder Management

• Provide regular progress updates to project leads and managers.
• Contribute to internal discussions on research findings, implications, and recommendations.
• Manage stakeholder communication.
• Support project leads in client communications through:

  • Emails
  • Presentations
  • Conference calls

• Take ownership and accountability as an individual contributor.
• Deliver high-quality work with minimal supervision while maintaining productivity and project timelines.

Quality Control & Continuous Development

• Perform thorough quality control and final review of project outputs.
• Ensure deliverables are accurate, error-free, and client-ready.
• Contribute to personal capability development through continuous learning and performance improvement.
• Demonstrate flexibility and curiosity while working across different healthcare sectors.

Eligibility & Qualifications

Educational Qualification

Bachelor’s or Master’s degree in Life Sciences

MBA – Preferred

Experience

• 3–4 years of relevant experience
• 3+ years of Primary Market Research experience
• Preference is given to candidates with experience in consulting and market research within the pharmaceutical domain.

Healthcare Industry Experience

Candidates should have experience or an academic background relevant to healthcare sectors including:

• Pharmaceuticals
• Life Sciences
• Biotechnology
• Healthcare Services

Eligible Qualification Courses

B.Sc. Life Sciences | M.Sc. Life Sciences | B.Pharm | M.Pharm | Pharm.D | MBA

Required Skills

Candidates should have:

• Experience in quantitative PMR research.
• Experience working across a variety of therapy areas.
• Strong quantitative and qualitative interpretation and analysis skills.
• Ability to integrate different sources of data assets.
• Ability to understand the relationship between client needs, data, and its application.
• Experience designing and developing questionnaires and discussion guides according to client objectives.
• Excellent interpersonal communication skills.
• Strong oral and written communication skills.
• Innovative thinking abilities.
• A solution-oriented approach.
• Ability to work independently and manage project timelines.
• Strong proficiency in:

  • MS Word
  • PowerPoint
  • Excel

Healthcare & Market Research Areas

The role provides exposure to a broad range of healthcare sectors, including:

• Pharmaceutical Research
• Life Sciences
• Biotechnology
• Medical Devices
• Healthcare Services
• Primary Market Research
• Quantitative Market Research
• Healthcare Consulting
• Patient Journey Research
• Market Assessment
• Segmentation Studies
• Demand Estimation
• Patient Flow Studies

Job Location & Details

Company: IQVIA

Job Title: Primary Market Research Associate Consultant

Location: Bengaluru, India

Job Type: Full Time

Job Requisition ID: R1554086

Department: Research & Intelligence

Experience: 3–4 years relevant experience

Primary Market Research Experience: 3+ years

How to Apply

Interested and eligible candidates can apply online through the official IQVIA Careers portal.

Apply Now – IQVIA Primary Market Research Associate Consultant

Job Summary