Author: Sudheer vanguri

Gland Pharma is offering career opportunities across Quality Assurance, Quality Control and Production functions at its VSEZ, Vizag location.
The openings are focused on injectable manufacturing, with positions requiring experience in quality systems, microbiology, validation and production operations.
Candidates with B.Sc, B.Pharm, M.Sc Microbiology, M.Sc and Diploma qualifications can apply for the relevant positions.
Interested candidates should submit their details before the 4 October 2026 application deadline.

Gland Pharma Quality Assurance Department

Gland Pharma Quality Assurance: QA Role

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

Gland Pharma Quality Assurance: Key Responsibilities

• Ensure implementation and compliance of site-wide Quality Management Systems (QMS) in line with regulatory and internal requirements.
• Conduct Analytical Quality Assurance (AQA) review of laboratory documents and data.
• Perform regular in-process QA activities in sterilization, dispensing, compounding, filling, vial sealing and external washing.
• Perform visual inspection, labelling and packing.

Eligibility & Qualifications

B.Sc | B.Pharm

Candidates with 2–4 years of relevant Quality Assurance experience can apply.

Gland Pharma Quality Control – Microbiology Department

Gland Pharma Quality Control Microbiology: Role Details

Qualification: M.Sc Microbiology
Experience: 3–5 Years

Gland Pharma Quality Control Microbiology: Key Responsibilities

• Testing and method validations.
• Culture handling, water and bioburden testing.
• Raw material and BET testing.
• Testing of water, finished products and stability samples.
• Autoclave and sterility testing.
• Observation of canisters.

Eligibility & Qualifications

M.Sc Microbiology

Candidates with 3–5 years of relevant Quality Control – Microbiology experience can apply.

Gland Pharma Quality Control – Validations Department

Gland Pharma Quality Control Validations: Role Details

Qualification: B.Sc / M.Sc / B.Pharm
Experience: 1–6 Years

Gland Pharma Quality Control Validations: Key Responsibilities

• Method transfer and method validations.
• Preparation and review of stability protocols.
• Preparation and review of analytical method transfer and analytical method validation protocols and reports.

Eligibility & Qualifications

B.Sc | M.Sc | B.Pharm

Candidates with 1–6 years of relevant Quality Control and validation experience can apply.

Gland Pharma Production Department

Gland Pharma Production: B.Sc / B.Pharm Role

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

Gland Pharma Production: Key Responsibilities

• Responsible for routine activities involving sterilization, dispensing, compounding, component preparation, GLR and TS operations.
• BPR preparation and review.
• Filling, vial sealing and external washing.
• Visual inspection, labelling and packing.

Eligibility & Qualifications

B.Sc | B.Pharm

Candidates with 2–4 years of relevant pharmaceutical production experience can apply.

Gland Pharma Production Department: Diploma Role

Gland Pharma Production: B.Sc / Diploma Role

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

Gland Pharma Production: Key Responsibilities

• Responsible for routine production activities involving sterilization, dispensing, compounding, component preparation, GLR and TS operations.
• BPR preparation and review.
• Filling, vial sealing and external washing.
• Visual inspection, labelling and packing.

Eligibility & Qualifications

B.Sc | Diploma

Candidates with 1–2 years of relevant production experience can apply.

Gland Pharma Recruitment: Eligibility & Qualifications

Eligible Qualifications

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

The required qualification and experience vary according to the department and position.

Experience Requirements

• Quality Assurance: 2–4 Years
• Quality Control – Microbiology: 3–5 Years
• Quality Control – Validations: 1–6 Years
• Production: 2–4 Years
• Production: 1–2 Years

Gland Pharma Injectable Manufacturing: Job Location

Work Location

VSEZ, Vizag

The advertised opportunities are associated with Gland Pharma’s injectable manufacturing operations.

How to Apply

Interested candidates can apply by submitting their details and updated resume to the following recruitment email addresses:

hr.vizag@glandpharma.com
nagababu.mutyala@glandpharma.com

Application Deadline

4 October 2026

Details to Include

Candidates should provide their relevant educational qualification, experience and contact details while applying.

Job Summary

Aurobindo Pharma Limited is conducting Walk-In Interviews for multiple opportunities at its Unit XV, Parawada, Visakhapatnam facility.
The openings are available across the Production, Packing and Quality Control departments for technical assistants, executives and quality control professionals.
Candidates with ITI, Diploma, B.Sc, B.Pharm and M.Pharm qualifications and relevant experience can apply for the respective positions.
The walk-in interviews are scheduled for 3rd and 4th October 2026, from 8:00 AM to 6:00 PM.

Aurobindo Pharma Production Department: Technical Assistant

Position Details

• Department: Production (Mfg)
• Position: Technical Assistant
• Qualification: Inter / ITI / Diploma / B.Sc
• Experience: 2–8 Years
• Area of Exposure: Compression, Granulation, Capsule Filling / Coating

Eligibility & Qualifications

Intermediate | ITI | Diploma | B.Sc

Candidates with 2–8 years of relevant pharmaceutical manufacturing experience can apply.

Aurobindo Pharma Production Department: Executive

Position Details

• Department: Production (Mfg)
• Position: Executive
• Qualification: B.Pharm / M.Pharm
• Experience: 2–8 Years
• Area of Exposure: Compression, Granulation, Capsule Filling / Coating

Eligibility & Qualifications

B.Pharm | M.Pharm

Candidates with 2–8 years of relevant production experience in pharmaceutical manufacturing can apply.

Aurobindo Pharma Packing Department: Technical Assistant

Position Details

• Department: Packing
• Position: Technical Assistant
• Qualification: Inter / ITI / Diploma / B.Sc
• Experience: 2–8 Years
• Area of Exposure: OSD Primary / Secondary (Cartonator)

Eligibility & Qualifications

Intermediate | ITI | Diploma | B.Sc

Candidates with relevant experience in pharmaceutical packing operations can apply.

Aurobindo Pharma Packing Department: Executive

Position Details

• Department: Packing
• Position: Executive
• Qualification: B.Pharm / M.Pharm
• Experience: 2–8 Years
• Area of Exposure: OSD Primary / Secondary

Eligibility & Qualifications

B.Pharm | M.Pharm

Candidates with 2–8 years of relevant pharmaceutical packing experience can apply.

Aurobindo Pharma Quality Control Department: Executive

Position Details

• Department: Quality Control
• Position: Executive
• Qualification: M.Pharm / B.Pharm
• Experience: 2–5 Years
• Area of Exposure: RM, IP, FP, AMV

Eligibility & Qualifications

B.Pharm | M.Pharm

Candidates with 2–5 years of relevant Quality Control experience can apply.

Aurobindo Pharma Recruitment: Eligibility & Qualifications

Eligible Qualifications

Intermediate | ITI | Diploma | B.Sc | B.Pharm | M.Pharm

The required qualification varies according to the department and position.

Experience Requirements

• Production Technical Assistant: 2–8 Years
• Production Executive: 2–8 Years
• Packing Technical Assistant: 2–8 Years
• Packing Executive: 2–8 Years
• Quality Control Executive: 2–5 Years

Aurobindo Pharma Walk-In Interview Details

Walk-In Dates

3rd & 4th October 2026

Interview Time

8:00 AM – 6:00 PM

Interview Venue

Hotel Bhargav Grand
Betchukol, Kokrla, Guntur Highway-34
Contact: +91 9127151000

Work Location

Aurobindo Pharma Limited, Unit XV
Parawada, Visakhapatnam, Andhra Pradesh

Aurobindo Pharma Employee Benefits

The recruitment advertisement highlights several employee benefits, including:

• Night Shift Allowance
• Attendance Bonus
• Subsidised Canteen & Transport
• Plant located near residential areas
• Access to nearby schools, medical facilities and recreational areas
• Special benefits to early joiners
• World-class facility and modern equipment
• Group Accidental Policy
• Fast Track Career Progression
• Relocation Reimbursement
• Subsidised Health Insurance

How to Apply

Interested and eligible candidates can attend the walk-in interview at the venue mentioned above.

Documents to Bring

Candidates should carry:

• Updated resume
• Educational documents
• PAN Card
• Aadhaar Card
• Recent appointment letter with CTC
• Last 6 months’ payslips
• Last 6 months’ bank statements

Registration

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

For recruitment-related communication:

WhatsApp: 7095826999
Email: Prasanth.Kandula@aurobindo.com

Job Summary

Emcure Pharmaceuticals is conducting a Walk-In Interview for candidates interested in opportunities at its Sanand Injectable Unit.
The recruitment includes openings in Quality Control, Production, and Packing departments.
Candidates with qualifications such as M.Sc, B.Sc, B.Pharm, ITI, Diploma, and 12th can apply for the relevant positions.
The interview is scheduled for 4 October 2026, from 10:00 AM to 3:00 PM, at Emcure Research Centre, Ahmedabad.

Emcure Pharmaceuticals Quality Control Department: Executive / Officer / Technician

Profile & Position Details

• Department: Quality Control
• Designation: Executive / Officer / Technician
• Experience: 2–8 Years
• Qualification: M.Sc / B.Sc / B.Pharm / ITI / Diploma

Key Responsibilities & Profile

• HPLC – IP / FP / Stability
• AMV – Documentation
• QMS – Investigation
• QC – Reviewer
• ITI – Instrumentation
• HPLC candidates with preference for experience on Waters HPLC with Empower software

Eligibility & Qualifications

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

Candidates with 2–8 years of relevant Quality Control experience can apply.

Emcure Pharmaceuticals Production Department: Officer / Operator

Profile & Position Details

• Department: Production
• Designation: Officer / Operator
• Experience: 2–6 Years
• Qualification: B.Sc / Diploma / ITI

Key Responsibilities & Profile

• Complex Injectable
• Filling
• Vial Washing
• Batch Manufacturing
• Leak Test
• Terminal Sterilization

Eligibility & Qualifications

B.Sc | Diploma | ITI

Candidates with 2–6 years of relevant pharmaceutical production experience can apply.

Emcure Pharmaceuticals Packing Department: Operator

Profile & Position Details

• Department: Packing
• Designation: Operator
• Experience: 1–6 Years
• Qualification: B.Sc / Diploma / ITI / 12th

Key Responsibilities & Profile

• Visual Inspection
• Labelling
• Blister Packing
• Secondary Packing

Eligibility & Qualifications

B.Sc | Diploma | ITI | 12th

Candidates with 1–6 years of relevant packing experience can apply.

Emcure Pharmaceuticals Recruitment: Eligibility & Qualifications

Eligible Qualifications

M.Sc | B.Sc | B.Pharm | ITI | Diploma | 12th

The qualification required depends on the department and designation.

Experience Requirements

• Quality Control: 2–8 Years
• Production: 2–6 Years
• Packing: 1–6 Years

Relevant experience in pharmaceutical manufacturing, injectable operations, Quality Control or packing is applicable according to the position.

Emcure Pharmaceuticals Walk-In Interview Details

Walk-In Date

4 October 2026, Sunday

Interview Time

10:00 AM – 3:00 PM

Job Location

Sanand – Injectable Unit

Interview Venue

Emcure Research Centre
At. Visat, Behind Ishan Square, Gandhinagar Highway,
Near Tapovan Circle, Chandkheda, Ahmedabad.

Documents to Carry

Candidates should bring updated documents, including:

• Updated CV
• CTC proof
• Salary slips

How to Apply

Interested and eligible candidates can attend the walk-in interview at the venue mentioned above.

Candidates should carry their updated CV, CTC proof and salary slips for the interview.

Job Summary

CRAMSN Research Park is hiring professionals for multiple opportunities across its Research & Development and related functions.
The openings cover Kilo Lab (Pilot Scale Manufacturing), CRO R&D, CDMO R&D, R&D Peptide, Logistics, DQA, Project Management, Formulations Project Management, and AR&D.
Candidates with qualifications including Diploma, B.Tech Chemical, M.Sc, MBA Logistics/SCM, and MBA Project Management can apply for the relevant departments.
Experience requirements range from freshers to 13 years, depending on the department and role.

CRAMSN Research Park Kilo Lab: Pilot Scale Manufacturing

Department Details

• Department: Kilo Lab (Pilot Scale Manufacturing)
• Experience: 3–13 Years
• Qualification: Diploma / B.Tech Chemical

Eligibility & Qualifications

Diploma | B.Tech Chemical

Candidates with 3–13 years of relevant experience in pilot-scale manufacturing or related pharmaceutical and chemical operations can apply.

CRAMSN Research Park CRO R&D Department

Department Details

• Department: CRO R&D
• Experience: 2–6 Years
• Qualification: M.Sc

Eligibility & Qualifications

M.Sc

Candidates with 2–6 years of relevant R&D experience can apply for opportunities in the CRO R&D function.

CRAMSN Research Park CDMO R&D Department

Department Details

• Department: CDMO R&D
• Experience: 2–6 Years
• Qualification: M.Sc

Eligibility & Qualifications

M.Sc

Candidates with 2–6 years of relevant R&D experience can apply for the CDMO R&D department.

CRAMSN Research Park R&D Peptide Department

Department Details

• Department: R&D Peptide
• Experience: 2–6 Years
• Qualification: M.Sc

Eligibility & Qualifications

M.Sc

Candidates with 2–6 years of relevant experience and an M.Sc qualification can apply for opportunities in the R&D Peptide function.

CRAMSN Research Park Logistics Department

Department Details

• Department: Logistics
• Experience: 2–6 Years
• Qualification: MBA (Logistics, SCM)

Eligibility & Qualifications

MBA Logistics | MBA Supply Chain Management

Candidates with 2–6 years of relevant logistics or supply chain management experience can apply.

CRAMSN Research Park DQA Department

Department Details

• Department: DQA
• Experience: Fresher
• Qualification: M.Sc Chemistry

Eligibility & Qualifications

M.Sc Chemistry

Freshers with an M.Sc. in Chemistry can apply for the DQA opportunity.

CRAMSN Research Park Project Management Department

Department Details

• Department: Project Management
• Experience: 5–10 Years
• Qualification: MBA Project Management

Eligibility & Qualifications

MBA Project Management

Candidates with 5–10 years of relevant project management experience can apply.

CRAMSN Research Park Formulations Project Management

Department Details

• Department: Formulations Project Management
• Experience: 5–10 Years
• Qualification: MBA Project Management

Eligibility & Qualifications

MBA Project Management

Candidates with 5–10 years of relevant experience in project management can apply for this opportunity.

CRAMSN Research Park AR&D Department

Department Details

• Department: AR&D
• Experience: 4–8 Years
• Qualification: M.Sc

Eligibility & Qualifications

M.Sc

Candidates with 4–8 years of relevant experience can apply for the AR&D opportunity.

CRAMSN Research Park Recruitment: Eligibility & Qualifications

Eligible Qualifications

Diploma | B.Tech Chemical | M.Sc | M.Sc Chemistry | MBA Logistics | MBA Supply Chain Management | MBA Project Management

The required qualification varies according to the department.

Experience Requirements

• Kilo Lab (Pilot Scale Manufacturing): 3–13 Years
• CRO R&D: 2–6 Years
• CDMO R&D: 2–6 Years
• R&D Peptide: 2–6 Years
• Logistics: 2–6 Years
• DQA: Fresher
• Project Management: 5–10 Years
• Formulations Project Management: 5–10 Years
• AR&D: 4–8 Years

CRAMSN Research Park Job Location

Work Location

CRAMSN Research Park
Pashamylaram, Patancheru,
Hyderabad, Telangana

The recruitment is for opportunities associated with Research & Development and related functions.

How to Apply

Interested candidates can share their updated CV with the recruitment contacts:

Mani Shankar
Email: manishankar.d@msnlabs.com

Email: manishankar.dadi@cramsn.com

Candidates should mention their relevant qualification, experience and department of interest in their application.

Job Summary

Zenotech Laboratories Limited is conducting a Walk-In Recruitment Drive for experienced professionals in its Production Department.
The openings are available across Cyto, Gen-Inj and Lupride manufacturing areas for Senior Officer and Operator positions.
Candidates with B.Pharm, M.Pharm, B.Sc, M.Sc Organic Chemistry, ITI or Diploma qualifications and relevant production experience can apply.
The walk-in interviews are scheduled for 5 and 6 October 2026, with the work location at Zenotech Laboratories Limited, Turkapally, Hyderabad.

Zenotech Laboratories Production Department: Senior Officer

Zenotech Laboratories Cyto Production: Senior Officer

• Sub-Department: Cyto
• Position: Senior Officer
• Experience: 2–3 Years
• Qualification: B.Pharm | M.Pharm | B.Sc | M.Sc Organic Chemistry

Key Responsibilities

• Supervision of dispensing, compounding and filtration activities.
• Ensure cGMP, SOP and BMR compliance.
• Maintain line clearance and conduct in-process checks.
• Manage batch documentation and reconciliation.
• Coordinate with IPQA, QC, Microbiology and Engineering.
• Handle deviations, change controls and investigations.
• Support audit and regulatory inspection readiness.

Zenotech Laboratories Gen-Inj Production: Senior Officer

Position Details

• Sub-Department: Gen-Inj
• Position: Senior Officer
• Experience: 2–3 Years
• Qualification: B.Pharm | M.Pharm | B.Sc | M.Sc Organic Chemistry

Key Responsibilities

• Supervision of dispensing, compounding and filtration activities.
• Ensure cGMP, SOP and BMR compliance.
• Maintain line clearance and conduct in-process checks.
• Manage batch documentation and reconciliation.
• Coordinate with IPQA, QC, Microbiology and Engineering.
• Handle deviations, change controls and investigations.
• Support audit and regulatory inspection readiness.

Zenotech Laboratories Lupride Production: Senior Officer

Position Details

• Sub-Department: Lupride
• Position: Senior Officer
• Experience: 2–3 Years
• Qualification: B.Pharm | M.Pharm | B.Sc | M.Sc Organic Chemistry

Key Responsibilities

• Supervision of dispensing, compounding and filtration activities.
• Ensure cGMP, SOP and BMR compliance.
• Maintain line clearance and conduct in-process checks.
• Manage batch documentation and reconciliation.
• Coordinate with IPQA, QC, Microbiology and Engineering.
• Handle deviations, change controls and investigations.
• Support audit and regulatory inspection readiness.

Zenotech Laboratories Production Department: Operator

Zenotech Laboratories Microfluidizer Production: Operator

• Sub-Department: Microfluidizer
• Position: Operator
• Experience: 2–3 Years
• Qualification: ITI | Diploma

Key Responsibilities

• Ensure cGMP and SOP compliance.
• Perform machine operation and changeover activities.
• Carry out CIP/SIP and disinfectant filtration.
• Operate autoclave, Buer and Martin Christ equipment.
• Support aseptic manufacturing and media fill activities.
• Maintain online documentation and batch records.
• Follow cleaning, sanitization and fumigation procedures.
• Support audit and inspection readiness.

Zenotech Laboratories Gen-Inj Production: Operator

Position Details

• Sub-Department: Gen-Inj
• Position: Operator
• Experience: 2–3 Years
• Qualification: ITI | Diploma

Key Responsibilities

• Ensure cGMP and SOP compliance.
• Perform machine operation and changeover activities.
• Carry out CIP/SIP and disinfectant filtration.
• Operate autoclave, Buer and Martin Christ equipment.
• Support aseptic manufacturing and media fill activities.
• Maintain online documentation and batch records.
• Follow cleaning, sanitization and fumigation procedures.
• Support audit and inspection readiness.

Zenotech Laboratories Lupride Production: Operator

Position Details

• Sub-Department: Lupride
• Position: Operator
• Experience: 2–3 Years
• Qualification: ITI | Diploma

Key Responsibilities

• Ensure cGMP and SOP compliance.
• Perform machine operation and changeover activities.
• Carry out CIP/SIP and disinfectant filtration.
• Operate autoclave, Buer and Martin Christ equipment.
• Support aseptic manufacturing and media fill activities.
• Maintain online documentation and batch records.
• Follow cleaning, sanitization and fumigation procedures.
• Support audit and inspection readiness.

Zenotech Laboratories Production Jobs: Eligibility & Qualifications

Senior Officer Positions

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

Candidates applying for the Senior Officer positions should have 2–3 years of relevant pharmaceutical production experience.

Operator Positions

ITI | Diploma

Candidates applying for Operator positions should have 2–3 years of relevant experience in pharmaceutical manufacturing or production operations.

Zenotech Laboratories Production Recruitment: Experience

Required Experience

2–3 Years

Relevant experience in pharmaceutical manufacturing and production operations is required for the advertised positions.

Zenotech Laboratories Walk-In Interview Details

Walk-In Dates

5 October 2026 and 6 October 2026

Interview Timing

9:00 AM to 2:00 PM

Work Location

Zenotech Laboratories Limited
Turkapally (V), Shamirpet (M),
Medchal-Malkajgiri (D), Hyderabad,
Telangana – 500101

How to Apply

Interested candidates can apply through the online application link provided in the recruitment advertisement:

Online Application: https://forms.office.com/r/Y5XkYcUKKY

Candidates can also share their resumes through the following recruitment email addresses:

hr1@zenotech.co.in
pushpagalla.hr@zenotech.co.in

Documents Required

Candidates should carry or submit the following documents as applicable:

• Updated CV
• Last 4 months’ payslips
• 2 years of increment documents
• Copy of appointment letter with breakup
• CTC details
• All educational certificates
• Two passport-size photographs
• Aadhaar Card
• PAN Card

Job Summary

Inductive Quotient Analytics Hiring – Market Research Analyst | Life Sciences & Healthcare | Hyderabad

Inductive Quotient Analytics is hiring a Market Research Analyst – Life Sciences & Healthcare in Hyderabad for a full-time opportunity. The role is suitable for freshers and candidates with 0–1 year of experience who are interested in market research, industry intelligence and secondary research across pharmaceutical, biotechnology, medical device and healthcare sectors.

Market Research Analyst – Life Sciences & Healthcare

Job Details

• Company: Inductive Quotient Analytics
• Position: Market Research Analyst
• Location: Hyderabad, Telangana
• Experience: Fresher / 0–1 year
• Employment Type: Full-time
• Work Mode: On-site

About Inductive Quotient Analytics

Inductive Quotient Analytics is an AI-powered Full-Service CRO, ClinTech, HealthTech and Data Intelligence partner supporting pharmaceutical, biotechnology, medical device and life sciences organizations.

The company provides services across clinical research, functional service provider models, medical device support, regulatory and medical writing, clinical data management, biostatistics, statistical programming, pharmacovigilance, real-world evidence and AI-enabled clinical trial technology solutions.

Job Summary

The selected candidate will work on market research, industry intelligence and secondary research within the pharmaceutical, biotechnology, medical device, clinical research and healthcare sectors.

The role involves researching companies, clinical trials, products, therapeutic areas, industry developments and key professionals using publicly available databases and online sources.

This is primarily a research and analytical role and does not involve field sales or telecalling.

Key Responsibilities

Market & Secondary Research

• Conduct online and secondary research on:

  • Pharmaceutical organizations
  • Biotechnology companies
  • Medical device companies
  • CROs
  • Hospitals
  • Healthcare organizations

• Research clinical trials using ClinicalTrials.gov, CTRI, WHO ICTRP and other global registries.
• Collect and validate information on companies, products, pipelines, therapeutic areas, clinical studies and industry developments.
• Identify relevant professionals and decision-makers through company websites, LinkedIn, conferences and public sources.

Industry Intelligence & Data Research

• Research product approvals, new clinical trials, funding, partnerships, expansions and other industry developments.
• Support competitor research, conference intelligence, market segmentation and company profiling.
• Prepare daily and weekly research reports and summaries.

Data Management

• Organize and maintain accurate research information in HubSpot CRM and internal databases.
• Review data for:

  • Completeness
  • Accuracy
  • Consistency
  • Duplicate records

Eligibility & Qualifications

Educational Qualification

Candidates should have a Bachelor’s or Master’s degree in any of the following:

• Pharmacy
• Life Sciences
• Biotechnology
• Clinical Research
• Biomedical Sciences
• Microbiology
• Biochemistry
• Healthcare Management
• Statistics
• Economics
• Commerce
• Related discipline

Experience

• Freshers / 0–1 year of experience
• Candidates interested in market research, industry intelligence and secondary research within healthcare and life sciences can apply.

Required Skills

• Strong internet and secondary research skills.
• Good analytical and logical-thinking ability.
• Strong attention to detail and data accuracy.
• Ability to understand and summarize technical and business information.
• Good written and verbal communication skills.
• Basic knowledge of Microsoft Excel, Word and PowerPoint.
• Interest in pharmaceutical, healthcare, clinical research or medical device industries.
• Willingness to learn clinical trial registries, HubSpot CRM, LinkedIn and research databases.

Additional Advantage

Knowledge of pharmaceutical products, clinical trials, therapeutic areas or medical devices will be an advantage.

Eligible Qualification Courses

B.Pharm | M.Pharm | B.Sc. Life Sciences | M.Sc. Life Sciences | Biotechnology | Clinical Research | Biomedical Sciences | Microbiology | Biochemistry | Healthcare Management | Statistics | Economics | Commerce

Location & Work Mode

Location: Hyderabad, Telangana
Work Mode: On-site
Employment: Full-time
Experience: Fresher / 0–1 Year

How to Apply

Interested and eligible candidates can apply through the LinkedIn job posting.

Apply for Market Research Analyst – Inductive Quotient Analytics

Job Summary

Amneal Hiring – Trainee Officer, Quality Control Lab | Ahmedabad

Amneal is hiring a Trainee Officer – Quality Control Lab in Ahmedabad for its Quality Control team. The role involves in-process and finished-product testing, analytical evaluation, laboratory documentation, GMP/GLP compliance, and quality control activities within a pharmaceutical manufacturing environment.

Trainee Officer – Quality Control Lab

Job Responsibilities

• Perform in-process and final product quality analyses and laboratory testing according to established specifications and regulatory requirements.
• Interpret and evaluate laboratory analytical results for accuracy and precision against predetermined quality standards.
• Identify ongoing quality issues within the laboratory and implement preventive measures to avoid potential production disruptions.
• Operate various measuring devices and testing equipment using predetermined methods and prescribed specifications to accept or reject products.
• Test random samples of finished goods to verify compliance with quality specifications.
• Report laboratory process deviations and finished-goods defects to relevant stakeholders in a timely manner.
• Support continuous improvement initiatives by suggesting enhancements to laboratory quality processes and testing methodologies.
• Maintain accurate and complete documentation of laboratory quality testing activities in compliance with GMP and GLP requirements.

Eligibility & Qualifications

Educational Qualification

• B.Pharm – Required
• M.Pharm – Preferred

Note: The supplied job listing also displays “Degree Level: Master of Science” in the Job Info section, which does not align with the qualification section stating B.Pharm as required and M.Pharm as preferred. The qualification section has therefore been retained as provided rather than reconciling the discrepancy.

Experience

The source lists:

• 1 year or more
• The experience field also displays “1 – 4 Years”

The exact intended experience range is therefore not fully clear from the supplied listing.

Required Skills

• Analytical Testing & Evaluation
• Chemical Testing and Analysis
• Data Entry
• Documentation & Record Control
• Equipment Cleaning & Maintenance
• Good Documentation Practices (GDP)
• Laboratory Safety
• Material Handling and Storage
• Sample Preparation Techniques
• Technical Documentation

Quality Control Laboratory – Key Areas

The position involves laboratory quality control activities related to:

• In-process testing
• Finished-product testing
• Analytical testing and evaluation
• Sample preparation
• Chemical testing and analysis
• Laboratory documentation
• GMP and GLP compliance
• Equipment operation and maintenance
• Quality issue identification
• Deviation reporting
• Continuous improvement

Location & Job Details

Position: Trainee Officer, Quality Control Lab
Job Category: Quality Control
Location: Ahmedabad City, Gujarat, India
Job Schedule: Full Time
Job Identification: 8695
Posting Date: 7 September 2026
Apply Before: 30 September 2026

The supplied listing shows the following locations under Job Info:

• Plot No. 15, 16, 17, Pharmez Special Economic Zone (SEZ), Ahmedabad, Gujarat – 382110
• 882/1-871, Village Rajoda, Ahmedabad, Gujarat – 382220

How to Apply

Interested and eligible candidates can apply through the official Amneal India Careers portal.

Apply for Trainee Officer, Quality Control Lab – Amneal

Job Summary

**Adaptis Pharma Hiring PV Professionals 🔥**
**Pharmacovigilance Executive | MICC & ICSR | Pune**
**M.Pharm | Pharm.D 
**MICC | ICSR | Case Management | PV Databases**

Apply Here ❤️  https://pharmastuff.org/job/pharmacovigilance-pune-pv-executive-adptis-pharma

Amgen Hiring – Data Management Sr Associate | Clinical Development | Hyderabad

Amgen is hiring a Data Management Sr Associate for its Clinical Development team in Hyderabad. The role focuses on supporting high-quality clinical trial data delivery through database build testing, data cleaning, query management, reconciliation, and lock preparation across the clinical study lifecycle.

Company Overview

Amgen is a biotechnology company focused on developing medicines for serious illnesses across areas including Oncology, Inflammation, General Medicine, and Rare Disease. The company describes its culture as collaborative, innovative and science-based.

Data Management Sr Associate – Clinical Development

Job Details

• Position: Data Management Sr Associate
• Career Category: Clinical Development
• Location: Hyderabad, India
• Work Mode: On Site
• Employment Type: Full Time
• Job Requisition ID: R-255251

Job Responsibilities

Clinical Data Management

• Execute study data management activities across the clinical study lifecycle.
• Perform database build testing, data cleaning, query management, reconciliation and lock preparation with limited oversight.
• Support core Data Management roles, including:

  • Data Delivery Leads
  • Database Designers
  • Data Acquisition Leads

• Own time-sensitive deliverables and ensure high-quality execution.
• Contribute to the setup and maintenance of EDC/non-CRF data structures.
• Support local laboratories, coding dictionaries and non-CRF data integrations.

Study Timelines & Data Delivery

• Track progress against data management timelines, study timelines and deliverables.
• Identify potential risks or delays.
• Escalate issues with clear documentation and applicable mitigations.
• Coordinate with local internal teams, global team members and external partners, including FSPs, when required.
• Help ensure aligned and efficient delivery of study activities.

Process Improvement

• Identify opportunities to improve repeatable data management processes.
• Contribute to best practices and knowledge sharing across the team.

Eligibility & Qualifications

Basic Qualifications

Candidates must meet one of the following requirements:

• Master’s degree, or
• Bachelor’s degree with 2 years of clinical execution experience, or
• Associate’s degree with 6 years of clinical execution experience, or
• High school diploma/GED with 8 years of clinical execution experience

Preferred Qualifications

• 3 years of work experience in a life sciences or medically related field.
• At least 1 year of biopharmaceutical clinical research experience obtained through clinical trials in a biotechnology, pharmaceutical or CRO company.
• Experience working in Data Management on global clinical trials.

Eligible Qualification Courses

Master’s Degree | Bachelor’s Degree | Associate’s Degree | Relevant Life Sciences Qualifications

The source specifies degree levels rather than particular courses such as B.Pharm, M.Pharm or Pharm.D, so specific pharmacy courses have not been added as a mandatory requirement.

Location & Work Mode

Location: Hyderabad, India
Work Mode: On Site
Employment: Full Time

The supplied job posting identifies the role as On Site.

How to Apply

Interested and eligible candidates can apply through the official Amgen careers portal.

Apply for Data Management Sr Associate – Amgen

Job Summary

GlobalData Hiring – Analyst / Senior Analyst | Healthcare | Hyderabad

GlobalData is hiring Analysts and Senior Analysts for its Healthcare – Pharma team in Hyderabad. The role focuses on researching advanced drug modalities such as ADCs, cell and gene therapies, bispecific antibodies, and RNA-based therapies, and capturing detailed scientific information for pharmaceutical and biotech intelligence databases.

Company Overview

GlobalData is a productivity and intelligence platform that combines proprietary data, human expertise, and AI to support organizations with strategic planning, innovation, risk management, and sustainable growth.

The Healthcare – Pharma team is expanding its coverage of advanced drug modalities and is looking for researchers with strong scientific knowledge and a structured, detail-oriented approach.

Analyst / Senior Analyst – Healthcare

Position Details

• Position: Analyst / Senior Analyst
• Team: Healthcare – Pharma
• Location: Hyderabad
• Work Area: Drug intelligence, scientific research, data curation and taxonomy

Education

Candidates should have one of the following qualifications:

• M.Pharm or M.S. (Pharm) in Pharmacology, Biotechnology or a related specialisation
• M.Sc. or M.Tech in Biotechnology, Biochemistry, Molecular Biology, Immunology, Genetics, Microbiology or a related life-science discipline
• PhD in a relevant field such as Immunology, Cell and Gene Therapy, Nucleic Acid Chemistry or Antibody Engineering

Experience

• 2–5 years of relevant experience in:

  • Pharmaceutical or biotech R&D
  • Academic research
  • CROs
  • Pharmaceutical intelligence
  • Scientific data curation

• Candidates with a PhD and 2+ years of industry or postdoctoral experience are also encouraged to apply.
• Hands-on laboratory or research experience in at least one advanced modality is strongly preferred.
• Relevant modalities include:

  • Cell therapy
  • Gene therapy or gene editing
  • Antibody-drug conjugates (ADCs)
  • Nucleic acid therapies
  • Antibody engineering

• Experience in cell-based therapies is particularly valued.
• Experience with taxonomy or ontology development, biomedical data curation or scientific classification is highly desirable.

Scientific Knowledge & Skills

Candidates should have:

• In-depth understanding of at least one advanced drug modality and working knowledge of others.
• Strong foundation in molecular biology, immunology and pharmacology.
• Understanding of drug targets and mechanisms of action.
• Good knowledge of the drug development lifecycle, from discovery through post-marketing.
• Familiarity with drug naming conventions, including WHO INN nomenclature for biologics and cell and gene therapies.

Taxonomy & Data Skills

• Ability to break complex scientific information into well-defined and mutually exclusive attributes.
• Understanding of taxonomy principles, including:

  • Hierarchies
  • Controlled vocabularies
  • Synonym management

• Familiarity with MeSH, NCI Thesaurus, Gene Ontology or ChEBI is an advantage.
• Advanced Microsoft Excel skills, including pivot tables, lookups and data validation.
• Basic SQL or scripting knowledge is an advantage.
• Ability to use AI-assisted research tools responsibly and verify their output carefully.

Research & Communication

• Strong systematic secondary research skills across:

  • PubMed
  • Clinical trial registries
  • Patent databases
  • Regulatory sources
  • Conference abstracts and presentations

• Strong attention to detail and critical-thinking skills.
• Ability to identify incorrect, incomplete or conflicting information.
• Clear written English and ability to document definitions, rules and decision rationale.
• Ability to work independently as well as within a global team.
• Ability to manage multiple assignments and meet deadlines.

Key Responsibilities

Modality Research & Data Capture

• Conduct in-depth secondary research on drugs across different modalities and development stages.
• Research drug development from discovery and preclinical stages through clinical development and approval.
• Extract detailed technical attributes such as:

  • Construct design
  • Delivery systems
  • Chemistry
  • Engineering features

• Research information from scientific publications, conference abstracts and posters, patents, clinical trial registries, regulatory documents and company disclosures.
• Interpret complex, incomplete or ambiguous technical information and determine what can be reliably captured.
• Maintain clear source references.
• Track new drugs, pipeline events and emerging technologies within assigned modalities.

Taxonomy Development & Classification

• Contribute to the design and development of modality taxonomies.
• Develop hierarchical categories, attribute fields, controlled vocabularies and permitted values.
• Write definitions, inclusion and exclusion criteria, and classification rules.
• Build and maintain synonyms and naming conventions.
• Classify and map drugs to the relevant taxonomy.
• Apply classification rules consistently across records.
• Document curation guidelines, decision logs and worked examples.

Data Quality & Database Management

• Create, review and update drug records in GlobalData databases.
• Identify missing, outdated or inconsistent information.
• Cross-check information across multiple sources.
• Perform quality checks on research and database outputs.
• Flag data-quality issues and work with relevant team members to resolve them.

Collaboration & Delivery

• Work with analysts, subject matter experts and managers to resolve scientific and classification questions.
• Collaborate with product, data and technology teams to translate taxonomies into database structures and search features.
• Share modality knowledge with the wider team.
• Support quality improvement initiatives.
• Manage assigned work and deliver within agreed timelines.
• Collaborate with global teams across different time zones.

Eligible Qualification Courses

M.Pharm | M.S. (Pharm) | M.Sc. Biotechnology | M.Sc. Biochemistry | M.Sc. Molecular Biology | M.Sc. Immunology | M.Sc. Genetics | M.Sc. Microbiology | M.Tech Biotechnology | PhD in relevant field

How to Apply

Interested and eligible candidates can apply through the official GlobalData careers listing for Analyst / Senior Analyst – Healthcare in Hyderabad.

Apply for Analyst / Senior Analyst – Healthcare at GlobalData

Job Summary