Author: Sudheer vanguri

**Clinipace Hiring Freshers 🔥**
**Trainee – Statistical Programming | Trivandrum**
**B.Tech | M.Sc/M.Tech Mathematics | Statistics | IT | Life Sciences**
**Freshers | SAS | R | Clinical Data | CDISC | Biometrics**

**Apply Here ❤️** 

Springer Nature Drug Safety Analyst Recruitment 2026

Springer Nature is hiring a Drug Safety Analyst for its AdisInsight Safety team in Pune.
The role focuses on validating AI-generated drug safety content from biomedical literature while supporting research, analysis, and technical activities related to pharmaceutical safety products.
Candidates with a Master’s degree or higher in Pharmacy, Life Sciences, or Medicine and 3–5 years of experience in Pharmacovigilance or a related drug safety discipline can apply.
Professionals with significant experience in signal detection and management are particularly sought for this opportunity.

Drug Safety Analyst – AdisInsight Safety

About the Role

The Drug Safety Analyst will validate AI-derived safety content generated from biomedical literature and contribute to the research, analysis, technical support, product development, and continuous improvement of Pharma Solutions safety products.

The role is intended for an established Pharmacovigilance professional who wants to apply their PV expertise in a product-focused environment while contributing to product quality, delivery, development, and global patient safety.

Job Role & Responsibilities

The Drug Safety Analyst will be responsible for:

• Evaluate and validate AI-derived or published drug safety content within regular and evolving production processes.
• Apply scientific comprehension and pharmaceutical industry knowledge when reviewing safety content.
• Conduct technical and domain research to create product and business value.
• Identify opportunities by connecting technical and domain facts with broader business perspectives.
• Communicate product development issues and opportunities clearly through discussions, presentations, and documentation.
• Collaborate with stakeholders and contribute to continuous learning and process improvement.
• Demonstrate adaptability and contribute to innovation.
• Drive results by identifying ways to improve efficiency, quality, and effectiveness.

Eligibility & Qualifications

Educational Qualification

Master’s degree or above in:

• Pharmacy
• Life Sciences
• Medicine

Experience

• 3–5 years of experience in Pharmacovigilance or a related drug safety discipline.
• Candidates with significant experience in signal detection and management are preferred.

Pharmacovigilance Knowledge Required

Candidates should have a strong understanding of PV workflows and fundamental principles covering:

Case Processing & Medical Literature

• Case processing
• ICSR criteria
• Application of ICSR criteria to medical literature
• MedDRA coding

Signal Detection & Safety Assessment

• Signal identification and validation
• Disproportionality analysis
• Signal prioritization and evaluation
• Benefit-risk assessment
• Risk management

Safety Reporting & Regulatory Compliance

• Aggregate safety reporting
• Regulatory reporting requirements
• Regulatory compliance requirements

Required Skills

Candidates should demonstrate:

• Logical and critical thinking
• Strong analytical skills
• Literature review capabilities
• Technical domain research
• Ability to identify issues, trends, and opportunities
• Ability to connect technical facts with business, product, and operational perspectives
• Strong English-language and scientific expression skills
• Attention to detail when conducting data and content checks
• Self-motivation and enthusiasm
• Collaborative attitude
• Ability to work independently with minimal or no supervision when required

Key Skills

The position combines expertise in Pharmacovigilance, Drug Safety, Medical Literature Review, Signal Detection, Safety Reporting, MedDRA, ICSR, Aggregate Reporting, Regulatory Compliance, Data Analysis, and Scientific Research.

AdisInsight Safety

AdisInsight Safety supports pharmaceutical customers with pharmacovigilance literature monitoring and provides safety intelligence covering valid ICSRs and special situations across medicines.

The platform combines automated content acquisition using AI/ML technologies with expert human validation to support the identification, categorization, and analysis of safety-related information from biomedical reference databases.

Job Location & Details

Company: Springer Nature

Brand: AdisInsight Safety

Job Title: Drug Safety Analyst

Location: Pune, Maharashtra, India

Employment Type: Full Time

Job Requisition ID: JR106531

Application Deadline: 5 October 2026

Work Area: Drug Safety / Pharmacovigilance

 

How to Apply

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

Apply Now – Springer Nature Drug Safety Analyst

Job Summary

**Cognizant Hiring Pharmacovigilance Professionals 🔥**
**TL – Pharmacovigilance | Pune | Hybrid**
**B.Pharm | M.Pharm | Pharm.D | Life Sciences | Any Graduate**
**PV Case Processing | Safety Operations

Apply Here ❤️**  https://pharmastuff.org/job/cognizant-associate-returnship-program-pharmacovigilance

Pfizer Hiring Associate Database Analyst – Clinical Database Management

Pfizer is hiring for the position of Associate, Associate Database Analyst – Clinical Database Management in its Chennai, India operations.
This full-time opportunity is part of the Worldwide Medical and Safety organization and focuses on clinical data monitoring, database management, documentation, and data quality.
The role involves supporting clinical data collection systems, data review, query management, validation, CTMS support, and clinical documentation.
Candidates with a BA/BS degree and knowledge of ICH/GCP, clinical development processes, regulatory requirements, and electronic data management systems can apply.

Associate Database Analyst – Clinical Database Management

Job Role & Responsibilities

The Associate Database Analyst will support Data Monitoring and Management (DMM) activities and help maintain the accuracy, integrity, and quality of clinical data.

Key responsibilities include:

• Engage in Data Monitoring and Management activities, including data review, query management, and investigation of logic check flags.
• Support database design activities through documentation, testing, validation, and implementation of clinical data collection tools or systems.
• Serve as the first point of contact for customers requiring assistance with Clinical Trial Management System (CTMS) questions and issues.
• Follow applicable Standard Operating Procedures (SOPs) and established working practices.
• Collaborate with Study Team Points of Contact, Document Owners, and Trial Master File (TMF) Study Owners.
• Help resolve document-related discrepancies and issues.
• Contribute to process improvement initiatives and additional projects as required.

Eligibility & Qualifications

Educational Qualification

BA/BS – Required

The position accepts candidates with any years of experience. Pfizer Associate Database Analyst – Clinical Database Management

Required Knowledge & Experience

Candidates should have:

• Demonstrated experience with ICH/GCP documentation requirements.
• Hands-on experience with electronic documentation management systems and/or web-based data management systems.
• Awareness of the clinical development process.
• Strong understanding of Good Clinical Practice (GCP) principles.
• Knowledge of regulatory requirements and relevant data standards.
• Strong oral and written English communication skills.
• Proficiency in Microsoft Office Suite.

Eligible Qualification Courses

B.A. | B.S.

Preferred Qualifications & Skills

Additional experience or skills that may be advantageous include:

• Experience with Clinical Trial Management Systems (CTMS).
• Familiarity with data validation and quality control processes.
• Ability to work collaboratively within a team environment.
• Strong problem-solving skills.
• Excellent attention to detail.
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem-solving and productivity.
• Understanding of responsible AI practices, including risk management and ethical use.

Clinical Database Management Skills

The role provides exposure to several areas of clinical research and clinical data management, including:

• Clinical Data Monitoring and Management
• Clinical Database Management
• Clinical Trial Management Systems
• Data Review and Query Management
• Database Validation
• Data Quality Control
• ICH/GCP Documentation
• Trial Master File (TMF) Documentation
• Regulatory Requirements
• Clinical Data Standards
• Electronic Documentation Management Systems

Job Location & Work Mode

Company: Pfizer

Location: Chennai, India

Job Type: Full Time

Work Location Assignment: Hybrid

Job Requisition ID: 4964296

Posted: 21 September 2026

How to Apply

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

Apply Now – Pfizer Associate Database Analyst

Job Summary

Alkem Laboratories is conducting a Walk-In Interview for its Formulation Manufacturing Facility based at Daman.
Openings are available across Quality Control, Production, Engineering and Warehouse departments.
Candidates with M.Sc., B.Pharm., Diploma, B.Sc., ITI and other specified qualifications can apply for the relevant positions.
The walk-in interview is scheduled for 20th September 2026, from 9:00 AM to 03:30 PM, at Hotel Woodland, Vapi.

Alkem Laboratories – Quality Control Department

Alkem Laboratories – QC Formulation Officer / Senior Officer

Position: Officer / Sr. Officer
Experience: 2–7 Years
Qualification: M.Sc. / B.Pharm.

Alkem Laboratories – QC Formulation Areas

• FP / Stability
• Analytical Instrumentation
• HPLC
• UV
• Dissolution
• LIMS
• Empower Software
• HPLC (Waters)

Alkem Laboratories – Production Formulation Department

Alkem Laboratories – Production Technical Associate

Position: Technical Associate
Experience: 2–6 Years
Qualification: Diploma / B.Sc. / ITI

Alkem Laboratories – Manufacturing Core Areas

• Wurster (Glatt, 21 CFR SCADA)
• Pellet Coating
• Bottom Spray (Glatt)
• Granulation
• Integrated Line
• GEA / Glatt
• Flow Coater
• Compression using KORSCH, Sejong, GEA and CADMACH
• Coating using Glatt Coater
• Liquid Manufacturing and Filling
• Sachet Filling Machine using Wraptech / Bossar

Alkem Laboratories – Production Packing Department

Alkem Laboratories – Officer / Senior Officer / Technical Associate

Position: Officer / Sr. Officer / Technical Associate
Experience: 2–6 Years
Qualification: B.Pharm. / Diploma / B.Sc. / ITI

Alkem Laboratories – Packing Primary Areas

• Blister Packing using Uhlmann / Elmach / BQS
• Bulk Packing
• Bottle Packing
• CVC
• Liquid Packing

Alkem Laboratories – Engineering Department

Alkem Laboratories – Engineering Technical Associate

Position: Technical Associate
Experience: 2–6 Years
Qualification: ITI / Diploma (Electrical)

Alkem Laboratories – Engineering Areas

• Process Equipment Maintenance (OSD)
• HVAC Operation
• Utility Area

Alkem Laboratories – Warehouse Department

Alkem Laboratories – Warehouse Officer / Associate

Position: Officer / Sr. Officer / Associate / Sr. Associate
Experience: 2–6 Years
Qualification: M.Sc. / B.Pharm. / M.Com. / B.Com. / B.Sc. / D.Pharm. / ITI / 12th

Alkem Laboratories – RM / PM Responsibilities

• Receiving and dispensing through the online system
• Handling eLog and eBMR
• Knowledge of SAP
• Knowledge of eWMS
• Knowledge of WDS systems for warehouse operations

Eligibility & Qualifications

Alkem Laboratories – Quality Control

M.Sc. | B.Pharm.

Alkem Laboratories – Production Formulation

Diploma | B.Sc. | ITI

Alkem Laboratories – Production Packing

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

Alkem Laboratories – Engineering

ITI | Diploma (Electrical)

Alkem Laboratories – Warehouse

M.Sc. | B.Pharm. | M.Com. | B.Com. | B.Sc. | D.Pharm. | ITI | 12th

Experience Requirements

Alkem Laboratories – Department-wise Experience

QC Formulation: 2–7 Years
Production Formulation: 2–6 Years
Production Packing: 2–6 Years
Engineering: 2–6 Years
Warehouse: 2–6 Years

Alkem Laboratories – Work Location

Formulation Manufacturing Facility

Daman

The recruitment advertisement states that the positions are for Alkem Laboratories’ formulation manufacturing facility based at Daman.

Walk-In Interview Details

Alkem Laboratories – Walk-In Interview

Date: 20th September 2026, Sunday
Time: 09:00 AM – 03:30 PM

Interview Venue

Hotel Woodland (Vapi)
N.H. No. 8, Near Desai Auto Mobiles,
Balitha, Vapi – Gujarat

Documents Required

Alkem Laboratories – Interview Documents

Candidates should carry:

• Copy of Resume
• Salary Breakup / Increment Letter
• Passport-Size Photograph
• Copy of Aadhaar Card
• Copy of PAN Card

How to Apply

Interested and eligible candidates can attend the Alkem Laboratories Walk-In Interview at the above-mentioned venue with the required documents.

Candidates should carry a latest updated resume and supporting employment documents.

Job Summary

Lupin is conducting a Walk-In Interview in Indore for experienced professionals across Quality Control, Quality Assurance, Production, Engineering and Process Engineering functions.
The recruitment covers Formulation, API, Nasal, Derma, MDI/DPI, OSD, Sterile and Ophthalmic operations.
Openings range from Operator and Officer to Executive-level positions, with experience requirements ranging from minimum 2 years to 10 years, depending on the role.
The walk-in interview will be held from 20th to 22nd September 2026, from 09:00 AM to 06:00 PM.

Lupin – Quality Control Department

Lupin – QC Formulation Officer – FG / In-Process

Experience: 2–5 Years
Qualification: B.Pharm. / M.Sc.
Area: Nasal / Derma / MDI & DPI

Lupin – QC Formulation Responsibilities

• Analyse finished products including Nasal, Derma and MDI/DPI products using tests such as Assay, RS, SCU, Spray Pattern, APSD (NGI), DU, FPM and physical tests.
• Operate and maintain instruments including HPLC/GC (Chromeleon), UV, pH meter and Spray Vise.
• Ensure compliance with GMP, data integrity and 21 CFR Part 11.
• Maintain accurate QC documentation.

Lupin – QC API Officer – RM Analysis

Experience: 2–5 Years
Qualification: B.Pharm. / M.Sc.
Area: Raw Material Analysis

Lupin – QC API Responsibilities

• Perform in-process, HST and stability testing of API products using HPLC, UV, GC, IR and Polarimeter.
• Maintain laboratory documentation according to cGMP, GLP and data integrity requirements.
• Support OOS/OOT investigations.

Lupin – QC Formulation Officer – OSD Stability

Experience: 2–5 Years
Qualification: B.Pharm. / M.Sc.
Area: OSD Stability Section

Lupin – OSD Stability Responsibilities

• Perform stability testing of formulation products according to approved protocols.
• Conduct analysis using HPLC, UV, dissolution and other analytical instruments.
• Maintain laboratory documentation in compliance with cGMP, GLP and data integrity requirements.
• Complete stability studies and reporting.

Lupin – QC Formulation Officer – FG / In-Process

Experience: 2–5 Years
Qualification: B.Pharm. / M.Sc.
Area: OSD FG / In-Process

Lupin – FG / In-Process QC Responsibilities

• Analyse finished products using HPLC, GC, UV and other analytical instruments in OSD formulations.
• Work with analytical quality systems including LIMS, QMS and SAP.
• Handle OOS/OOT and laboratory deviations.

Lupin – QC Formulation Officer – Sterile / Ophthalmic

Experience: 2–5 Years
Qualification: B.Pharm. / M.Sc.
Area: Sterile / Ophthalmic

Lupin – Sterile / Ophthalmic QC Responsibilities

• Analyse ophthalmic finished products using Assay, Related Substances, Dissolution, PSD by Malvern and physical tests.
• Operate and calibrate instruments including HPLC (Chromeleon), UV-Visible Spectrophotometer, IR, Dissolution Apparatus, Malvern Particle Size Analyzer, analytical balance and pH meter.
• Ensure compliance with GMP, data integrity and 21 CFR Part 11.
• Maintain accurate QC documentation.

Lupin – Quality Assurance Department

Lupin – QA Formulation Officer – IPQA

Experience: 2–5 Years
Qualification: B.Pharm. / M.Sc.
Area: Nasal / Derma / MDI & DPI

Lupin – IPQA Responsibilities

• Perform IPQA activities for MDI and DPI formulations.
• Conduct line clearance, sampling and AQL inspection.
• Manage retention samples.
• Review BMR/BPR through Pass-X.
• Prepare APQR.
• Review cleaning validation documents.
• Maintain strong knowledge of cGMP, documentation practices and pharmaceutical quality systems.

Lupin – QA Formulation Executive – IPQA & QMS

Experience: 8–10 Years
Qualification: B.Pharm. / M.Sc.
Area: Nasal / Derma / MDI & DPI

Lupin – QA Executive Responsibilities

• Perform IPQA activities for MDI and DPI formulations.
• Handle line clearance, sampling, AQL inspection and retention sample management.
• Review BMR/BPR through Pass-X.
• Support QMS reviews and deviation/OOS investigations.
• Prepare APQR and review cleaning validation documentation.
• Maintain knowledge of cGMP, GDP and pharmaceutical quality systems.

Lupin – Production Department

Lupin – Production Filling Operator

Experience: Minimum 2 Years
Qualification: ITI / B.Sc. / Diploma
Area: Nasal & Derma

Lupin – Production Filling Responsibilities

• Work in filling areas for Nasal and Topical Formulations (Derma).
• Operate and handle filling equipment.
• Experience with Nasal filling machine (DARA).
• Experience with Derma filling machines.
• Exposure to bottle filling and capping machines such as PKB.
• Experience with Sofbag filling machine (Marchesini).
• Exposure to tube filling machines such as Norden and IMA.

Lupin – Production Packing Operator

Experience: Minimum 2 Years
Qualification: ITI / B.Sc. / Diploma
Area: Nasal & Derma

Lupin – Production Packing Responsibilities

• Perform packing activities for Nasal formulations.
• Operate packing equipment including sticker labelling machines and cartoning machines.
• Handle printing and scanning systems such as Jekson.
• Experience in Nasal Spray, Solution and Suspension batch packing operations.
• Experience in BMR through PAS-X.

Lupin – Production Manufacturing Operator

Experience: 2–8 Years
Qualification: ITI / D.Pharm. / B.Sc.
Area: Sterile / Ophthalmic

Lupin – Production Manufacturing Responsibilities

• Handle clean room operations.
• Prepare steam sterilizer loads.
• Work with vessels and homogenizers.
• Perform CIP/SIP activities.
• Conduct filter integrity and glove leak tests.
• Handle bulk manufacturing and filtration.
• Maintain routine batch records and logbooks.
• Perform balance and pH meter calibration and in-process checks.

Lupin – Production Aseptic Filling Operator

Experience: 2–8 Years
Qualification: ITI / D.Pharm. / B.Sc.
Area: Sterile / Ophthalmic

Lupin – Aseptic Filling Responsibilities

• Perform aseptic practices and interventions in Grade A areas.
• Handle sterile API operations.
• Work in suspension manufacturing.
• Operate filling machines and associated systems.
• Exposure to Romaco, Dynomill and homogenizer systems.
• Work with LAF, pass box, garment cubicle and NVPC systems.

Lupin – Production Officer

Experience: 2–5 Years
Qualification: B.Pharm.
Area: Sterile / Ophthalmic

Lupin – Production Officer Responsibilities

• Supervise unit operations in unclassified, controlled, aseptic and garment preparation areas.
• Handle media fill and batch processing.
• Perform stage-wise batch reconciliation.
• Manage material receipt, return and status labelling.
• Conduct in-process checks.
• Handle aseptic filtration and filling.
• Prepare SOPs and monthly reports.
• Support gap analysis and corrective actions.
• Handle SAP activities.

Lupin – Engineering Department

Lupin – Fitter / Electrician

Experience: Minimum 5 Years
Qualification: ITI – Fitter / Electrical
Area: Process Maintenance

Lupin – Engineering Responsibilities

• Perform maintenance and troubleshooting of pharmaceutical process and packaging equipment.
• Exposure to granulation, compression, coating, filling, blistering, cartoning, labelling and utility equipment is preferred.
• Experience with GMP requirements and maintenance documentation is an added advantage.
• Knowledge of SAP-PM/CMMS systems is desirable.

Lupin – HVAC & Water System Operator

Experience: Minimum 5 Years
Qualification: ITI – Fitter / Electrical
Area: Utility Operation

Lupin – HVAC & Water System Responsibilities

• Operate AHU, chiller, cooling tower and dehumidifier systems.
• Monitor differential pressure, temperature and relative humidity.
• Operate PW/WFI systems.
• Handle pure steam generator and distribution loop systems.
• Perform sanitization and filter integrity activities.
• Work with BMS/SCADA systems.

Lupin – Process Engineering Department

Lupin – Process Engineering Officer

Experience: 5–6 Years
Qualification: B.E. / Diploma – Mechanical / Electrical
Area: Process Maintenance

Lupin – Process Engineering Responsibilities

• Plan and execute preventive and breakdown maintenance of process and packaging equipment.
• Troubleshoot mechanical, electrical, pneumatic, PLC/HMI and utility systems.
• Maintain maintenance records in SAP-PM/CMMS.
• Support audits.
• Support IQ/OQ/PQ activities.
• Handle calibration, change control, deviation and CAPA activities.
• Support spare planning and AMC coordination.

Lupin – Eligibility & Qualifications

Lupin – Quality Control & Quality Assurance

B.Pharm. | M.Sc.

Lupin – Production

ITI | B.Sc. | Diploma | D.Pharm. | B.Pharm.

Lupin – Engineering

ITI – Fitter | ITI – Electrical

Lupin – Process Engineering

B.E. Mechanical | B.E. Electrical | Diploma – Mechanical / Electrical

Lupin – Experience Requirements

Department-wise Experience

QC Formulation / QC API: 2–5 Years
QA Formulation – IPQA: 2–5 Years
QA Formulation – IPQA & QMS: 8–10 Years
Production Filling / Packing: Minimum 2 Years
Production Manufacturing / Aseptic Filling: 2–8 Years
Production Officer: 2–5 Years
Engineering: Minimum 5 Years
Process Engineering: 5–6 Years

Lupin – Regulatory Requirement

USFDA & MHRA Exposure

The recruitment advertisement clearly states that USFDA and MHRA regulatory exposure is mandatory.

Walk-In Interview Details

Lupin – Walk-In Interview Indore

Dates: 20th, 21st & 22nd September 2026
Days: Sunday, Monday & Tuesday
Time: 09:00 AM – 06:00 PM

Interview Venue

The Red Maple Marshal
Jhoomer Ghat, Rau, Indore, Madhya Pradesh

Lupin – Interview Eligibility & Documents

Documents Required

Candidates should bring:

• Latest Resume
• Last three salary slips
• Revision / Increment Letter
• Relieving letters from all previous organizations

Eligibility Conditions

• 60% marks are mandatory where experience is less than 5 years.
• Candidates interviewed by Lupin during the last 6 months are not eligible.

How to Apply

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

For recruitment-related communication:

Email: sahuikhan1@lupin.com
Mobile: 9617733913

Candidates should carry all required documents and meet the specified eligibility criteria before attending.

Job Summary

Amneal Pharmaceuticals Officer Quality Control Recruitment 2026

Amneal Pharmaceuticals is hiring for the position of Officer – Quality Control in its pharmaceutical manufacturing operations in Ahmedabad, Gujarat.
The role involves in-process and finished product quality analysis, analytical testing, documentation, and inspection in compliance with GMP and regulatory requirements.
Candidates will be responsible for evaluating analytical results, testing finished goods, identifying quality issues, and supporting CAPA and continuous improvement activities.
B.Pharm candidates are required, while M.Pharm is preferred, with 1–4 years of experience specified for the position.

Officer – Quality Control | Amneal Pharmaceuticals

Job Role & Responsibilities

The Officer – Quality Control will be responsible for conducting in-process and final product quality analyses and inspections while ensuring compliance with established internal standards and applicable regulatory requirements.

Key responsibilities include:

• Perform in-process and final product quality analyses and inspections in compliance with regulatory and internal standards.
• Interpret and evaluate analytical results for accuracy and precision against established specifications.
• Operate measuring devices and testing equipment according to predetermined testing methods.
• Accept or reject products based on prescribed quality specifications.
• Test random samples of finished goods to verify conformity with quality specifications.
• Identify and report manufacturing process deviations and defects in finished goods to relevant stakeholders.
• Identify ongoing quality issues and recommend preventive measures to avoid potential production problems.
• Maintain accurate and complete records of testing activities in accordance with GDP and GMP requirements.
• Support implementation of corrective and preventive actions (CAPA) arising from quality investigations.
• Contribute to continuous improvement by suggesting enhancements to testing methods and quality processes.

Quality & Regulatory Compliance

The position operates within a structured quality management framework aligned with:

• 21 CFR Part 210 and 211
• ICH guidelines
• Good Manufacturing Practices (GMP)
• Good Documentation Practices (GDP)
• Applicable Indian and international pharmaceutical regulations
• Data integrity and documentation requirements

Eligibility & Qualifications

Educational Qualification

B.Pharm – Required

M.Pharm – Preferred Apply for Amneal Officer – Quality Control

Experience

1–4 years of relevant experience is specified for the position.

Eligible Qualification Courses

B.Pharm | M.Pharm

Required Skills

Candidates should have knowledge or experience in the following areas:

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

Job Location & Schedule

Location: 882/1-871, Village Rajoda, Ahmedabad, Gujarat – 382220, India

Job Type: Full Time

Job Category: Quality Control

Job Identification: 8071

Posting Date: 21 September 2026

Application Deadline: 31 December 2026, 12:00 AM

How to Apply

Interested and eligible candidates can apply online through the official Amneal India Careers job posting.

Apply Now – Amneal Officer, Quality Control

Job Summary

National Forensic Sciences University Visiting / Guest Faculty Recruitment 2026

National Forensic Sciences University (NFSU), Gandhinagar Campus, School of Pharmacy, has invited Expressions of Interest (EOI) from eligible and experienced academicians, professionals, researchers, and industry experts.
The engagement is for Visiting Faculty, Guest Faculty, and Subject Experts on a temporary, part-time, and need-based basis.
Experts are required in Pharmaceutical Chemistry, Pharmaceutical Quality Assurance, Regulatory Affairs, Industrial Pharmacy, Pharmacology, and related areas.
Eligible candidates can attend the walk-in interview on 21 September 2026 at NFSU, Gandhinagar, with their CV and necessary documents. NATIONAL FORENSIC SCIENCES UNIV…

NFSU School of Pharmacy – Visiting / Guest Faculty

National Forensic Sciences University (NFSU), Gandhinagar Campus, is inviting eligible professionals and academic experts for empanelment as Visiting / Guest Faculty / Subject Experts in the School of Pharmacy.

The selected experts may be engaged to deliver lectures, conduct practical sessions, and undertake other academic activities based on the University’s requirements. NATIONAL FORENSIC SCIENCES UNIV…

Areas of Expertise / Specializations

The requirement covers the following areas:

1. Chemistry / Pharmaceutical Chemistry / Forensic Chemistry
2. Pharmaceutical Quality Assurance
3. Regulatory Affairs / Industrial Pharmacy
4. Pharmacology NATIONAL FORENSIC SCIENCES UNIV…

Eligibility & Qualifications

Qualifications and experience will be considered as per the applicable UGC, NFSU, and PCI norms.

Ph.D. Qualification

Candidates holding a Ph.D. degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or the relevant discipline are eligible, subject to:

• Minimum First Class or 60% or equivalent at the preceding degree level.
• Degree must be from a recognized university. NATIONAL FORENSIC SCIENCES UNIV…

Master’s Degree Qualification

Candidates with a Master’s degree in the relevant discipline are also eligible, subject to:

• Minimum First Class or 60% or equivalent.
• Degree must be from a recognized university. NATIONAL FORENSIC SCIENCES UNIV…

Eligible Qualification Courses

Ph.D. Pharmacy | Ph.D. Pharmaceutical Sciences | Ph.D. Chemistry | M.Pharm | M.Sc. Chemistry | M.Sc. Pharmaceutical Sciences | Master’s Degree in Relevant Discipline

Nature of Engagement

The engagement will be:

• Temporary
• Part-time
• Need-based
• Based on the academic requirements of the University.

NFSU reserves the right to engage empanelled experts depending upon its academic requirements. NATIONAL FORENSIC SCIENCES UNIV…

Honorarium / Remuneration

• ₹1,500 per lecture/session, subject to University norms and approval.
• Maximum remuneration will not exceed ₹50,000 per month, irrespective of the number of lectures/sessions assigned. NATIONAL FORENSIC SCIENCES UNIV…

Walk-In Interview Details

Interview Date & Reporting Time

Date: 21 September 2026
Reporting Time: 10:30 AM to 11:30 AM

Interview Venue

IRD Seminar Hall, National Forensic Sciences University (NFSU), Gandhinagar

Interested candidates are required to remain present at the mentioned venue along with their CV and other necessary documents. NATIONAL FORENSIC SCIENCES UNIV…

NFSU Gandhinagar Campus Contact Details

National Forensic Sciences University, Gandhinagar Campus
Sector-9, Gandhinagar
Gujarat – 382007
Phone: 079-23977102 / 103
Email: exe_registrar@nfsu.ac.in NATIONAL FORENSIC SCIENCES UNIV…

How to Apply

Eligible and interested candidates should attend the walk-in interview on 21 September 2026 at the IRD Seminar Hall, NFSU, Gandhinagar.

Candidates should carry their updated CV and other necessary documents for verification and consideration. NATIONAL FORENSIC SCIENCES UNIV…

Job Summary

Quality and Compliance Assistant | Labcorp

Labcorp is hiring a Quality and Compliance Assistant for its Corporate Affairs team in India. The role focuses on supporting quality and compliance operations, administrative activities, metric collation, Veeva Quality Systems, and customer health check discussions. Candidates with a Master’s degree in Life Sciences and 1 year of experience can apply. The position is remote-based, with a Monday to Friday schedule from 2:00 PM to 11:00 PM.

Job Details

Position

Quality and Compliance Assistant

Company

Labcorp

Job ID

2633009

Department

Corporate Affairs

Location

Bengaluru, India

Work Mode

Remote

Employment Type

Full Time

Experience

1 Year

Work Schedule

Monday to Friday
2:00 PM – 11:00 PM

Work Arrangement

Remote Based

Quality & Compliance Responsibilities

• Perform administrative tasks as required by the Quality and Compliance group.
• Support metric collation activities as required.
• Learn to use Veeva Quality Systems.
• Assist in Customer Hallmark Health Check discussions.
• Adapt techniques to new procedures or specific requirements as directed.
• Recommend modifications to processes where appropriate.
• Learn to schedule and manage multiple assignments.
• Maintain a clean and safe work environment.
• Learn to organize the work environment effectively.
• Work under regular supervision.
• Perform other related duties as assigned.

Veeva Quality Systems

The selected candidate will receive exposure to Veeva Quality Systems and support quality-related activities under the guidance of the Quality and Compliance group.

The role also involves learning established procedures and adapting to new processes according to business requirements.

Eligibility & Qualifications

Minimum Qualification

• Master’s degree in Life Sciences
• 1 year of experience in the job discipline

Preferred Qualification

An associate-level qualification in any of the following areas or equivalent is preferred:

• Laboratory Technology
• Animal Technology
• Biological Sciences
• Pharmacy
• Medical Nursing

Eligible Qualification Courses

M.Sc. Life Sciences | M.Sc. Biotechnology | M.Sc. Microbiology | M.Sc. Biochemistry | M.Pharm | Pharm.D | B.Pharm | B.Sc. Life Sciences | B.Sc. Biological Sciences | Nursing

The official posting specifically requires a Master’s degree in Life Sciences as the minimum qualification.

Key Skills

• Good English speaking, writing, and reading skills.
• Strong time-management skills.
• Good communication skills.
• User knowledge of Microsoft Office and software applications.
• Good verbal, numerical, and visual skills.
• Strong attention to detail.
• Ability to manage multiple assignments.
• Ability to adapt to new procedures and processes.
• Ability to work under regular supervision.
• Quality and compliance orientation.

Additional Requirements

• Mandatory immunizations and screening may be required.
• Limited travel may be required for business-related purposes, including site visits.
• Overtime, weekend, and holiday work may be required depending on business needs.

How to Apply

Interested and eligible candidates can apply for the Quality and Compliance Assistant position through the official Labcorp careers portal.

Apply for Quality and Compliance Assistant – Labcorp

Job ID: 2633009

Work Mode: Remote Based

Job Summary

Scientist I – Protein Biology | Thermo Fisher Scientific

Thermo Fisher Scientific is hiring a Scientist I – Protein Biology in Bangalore, Karnataka for its Research & Development team. The role focuses on antibody validation and characterization, protein biology, cell and molecular biology, and immunoassay development. Candidates with a Master’s degree and 2–5 years of experience or a PhD in Immunology, Biochemistry, Biotechnology, or Molecular Biology can apply. The position is fully onsite and involves laboratory-based research activities.

Job Details

Position

Scientist I – Protein Biology

Company

Thermo Fisher Scientific

Job ID

R-01344458

Category

Research & Development

Team

Protein Biology

Location

Bangalore, Karnataka, India

Work Arrangement

Fully Onsite

Employment Type

Full Time

Work Schedule

Monday to Friday

Work Environment

Laboratory Setting

About the Protein Biology Team

The Protein Biology team works on large-scale functional validation of antibodies, with a focus on reagent quality and specificity.

The team’s activities include:

• Data mining and processing
• Western blotting
• Immunofluorescence imaging
• Immunohistochemistry
• Chromatin Immunoprecipitation (ChIP)
• Gene silencing
• Antibody validation and characterization

The program focuses on high-quality product validation and creating product information to support research applications.

Role & Responsibilities

The selected candidate will contribute to the antibody validation workflow and support target biology validation using innovative experimental methods.

Antibody Validation & Protein Biology

• Contribute to antibody validation and characterization activities.
• Apply knowledge of key aspects of protein biology to deliver antibody validation results.
• Understand target biology validation requirements.
• Validate antibodies for reproducibility.
• Develop and generate datasets that support product differentiation.
• Demonstrate scientific proficiency in experimental planning and execution.

Experimental Design & Laboratory Research

• Design experiments carefully to meet program goals.
• Work with cell and molecular biology experimental workflows.
• Support the design and development of protein assays.
• Maintain accurate records of experimental results in data sheets and laboratory notebooks.
• Follow defined schedules and maintain strong attention to detail.

Immunoassays & Analytical Techniques

The role involves experience with immunoassay techniques such as:

• Western Blotting
• Immunofluorescence
• Immunohistochemistry
• Flow Cytometry
• ELISA
• Co-immunoprecipitation for protein-protein interaction studies

Research Data & Literature

• Regularly review scientific literature.
• Stay updated with developments in antibody validation.
• Compile and present research data in written and oral formats.
• Participate actively in team meetings.
• Communicate research findings effectively.
• Provide technical troubleshooting to resolve scientific problems.

Eligibility & Qualifications

Educational Qualification

Candidates should have either:

• Master’s degree with 2–5 years of relevant experience, or
• PhD

in one of the following fields:

• Immunology
• Biochemistry
• Biotechnology
• Molecular Biology

Eligible Qualification Courses

M.Sc. Biotechnology | M.Sc. Biochemistry | M.Sc. Molecular Biology | M.Sc. Immunology | M.Pharm | M.Tech Biotechnology | PhD in Biotechnology | PhD in Biochemistry | PhD in Molecular Biology | PhD in Immunology

Experience

Candidates should have:

• 2–5 years of experience with a relevant Master’s degree, or
• A PhD in a relevant scientific discipline.

Experience working within a research team and a proven ability to set goals, manage work-related customer concerns, and deliver work according to program objectives will be beneficial.

Technical Skills

• Strong understanding of protein biology.
• Cell and molecular biology experimental workflows.
• Protein assay design and development.
• Protein-protein interaction studies.
• Co-immunoprecipitation.
• Immunoassay development.
• Western blotting.
• Immunofluorescence.
• Immunohistochemistry.
• Flow cytometry.
• ELISA.
• Experimental planning and execution.
• Scientific data analysis and presentation.
• Technical troubleshooting.
• Literature review and scientific research.
• Basic understanding of computational biology tools.
• Basic knowledge of databases and programming languages.

Key Competencies

• Scientific proficiency and research-oriented thinking.
• Strong experimental design skills.
• Attention to detail.
• Excellent laboratory record keeping.
• Ability to work according to schedules and timelines.
• Good verbal and written communication skills.
• Ability to present scientific data clearly.
• Technical problem-solving and troubleshooting.
• Ability to work collaboratively within a research team.
• Commitment to maintaining high-quality research standards.

How to Apply

Interested and eligible candidates can apply for the Scientist I – Protein Biology position through the official Thermo Fisher Scientific careers portal.

Apply for Scientist I – Protein Biology – Thermo Fisher Scientific

Job ID: R-01344458

Location: Bangalore, Karnataka, India

Job Summary