Author: Sudheer vanguri

Labcorp Associate Data Analyst Jobs in Bengaluru

Labcorp is hiring an Associate Data Analyst for its Corporate Operations team in Bengaluru, Karnataka. Candidates with a bachelor’s degree in Science or a related field and at least 2 years of professional experience can apply. The role involves clinical and laboratory data reconciliation, resolving data discrepancies, database updates, query management, and maintaining audit-ready documentation. Candidates with knowledge of data revision processes, clinical data management, and Microsoft Office applications can explore this full-time, non-remote opportunity.

Company Overview

Labcorp is a global life sciences company providing laboratory services, diagnostic insights, and clinical research support. Its teams use scientific expertise, data, and technology to support healthcare providers, pharmaceutical companies, researchers, and patients.

Job Details

• Company: Labcorp

• Designation: Associate Data Analyst

• Job ID: 2636678

• Department: Corporate Operations

• Location: Bengaluru, Karnataka, India

• Employment Type: Full-time

• Work Mode: On-site, non-remote

• Work Schedule: Rotational shifts

• Experience: Minimum 2 years of professional experience

Job Role & Responsibilities

Data Reconciliation & Database Management

• Identify, analyze, and resolve data discrepancies between clients, including sponsors, CROs, and investigators, and internal databases.

• Perform data revisions ranging from basic to highly complex according to established data revision and data cleaning procedures.

• Update databases based on client requirements while maintaining accuracy and compliance with quality standards.

• Support data reconciliation activities and query management processes.

• Ensure timely responses to data-related requests and coordinate activities to meet project timelines.

Client Coordination & Issue Resolution

• Maintain effective communication and follow up with internal stakeholders, clients, and cross-functional teams.

• Support Workflow Leads and Client Leads in executing data reconciliation and query management activities.

• Investigate data, project, and service-related issues and escalate concerns to the appropriate teams when necessary.

• Coordinate with relevant departments to ensure complete resolution of discrepancies and operational issues.

Quality Assurance & Documentation

• Maintain audit-ready documentation and support audits and quality-related investigations.

• Assist leadership with Corrective and Preventive Action (CAPA) activities, reportable issues, and CAIRs.

• Follow departmental guidelines, company policies, Standard Operating Procedures (SOPs), work instructions, and management communications.

• Ensure data-related activities comply with Good Clinical Practice (GCP) guidelines and applicable quality standards.

Training & Process Improvement

• Attend mandatory Data Reconciliation Center (DRC) meetings.

• Participate in training related to process improvements, system updates, and data reconciliation best practices.

• Support the implementation of global processes and procedures to improve operational consistency.

• Contribute to initiatives that improve quality, productivity, operational efficiency, and customer experience.

• Perform additional responsibilities and special projects assigned by management.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Educational Qualification: Bachelor’s degree in Science or a related field.

• Experience: Minimum 2 years of professional experience.

• Data Management Skills: Strong understanding of data revision, data reconciliation, and laboratory or clinical data management processes.

• Computer Skills: Proficiency in Microsoft Word, Excel, and Outlook.

• Preferred Education: Bachelor’s or Master’s degree in Science, Life Sciences, Data Management, or a related field.

• Communication Skills: Ability to coordinate effectively with clients, internal stakeholders, and global teams.

• Analytical Skills: Attention to detail, problem-solving ability, and the capacity to resolve data discrepancies.

• Documentation Skills: Ability to maintain accurate records and follow established quality procedures.

Location & Work Schedule

The position is based in Bengaluru, Karnataka, and is listed as a full-time, non-remote role. Candidates should be prepared to work rotational shifts.

How to Apply

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

Apply Online: Labcorp Associate Data Analyst – Official Application

Applicants should highlight their experience in data reconciliation, database updates, clinical or laboratory data management, Microsoft Excel, and quality documentation.

Job Summary

Rhydburg Biotech Senior Executive – Regulatory Affairs Jobs in Dehradun

Rhydburg Biotech Ltd. is hiring a Senior Executive – Regulatory Affairs (JB-1702) for its pharmaceutical regulatory team in Dehradun, Uttarakhand. Candidates with a B.Pharm or M.Pharm qualification and at least 3 years of experience in Quality Assurance or analytical validation roles are eligible to apply. The position involves regulatory dossier preparation, analytical method validation document review, regulatory submissions, quality documentation, and compliance with applicable regulatory guidelines. The company lists a salary range of ₹25,000–₹30,000 and mentions flexible working arrangements.

Company Overview

Rhydburg Biotech Ltd. manufactures, markets, and exports generic pharmaceutical products. The company focuses on research and development, regulatory capabilities, and supplying quality products through public and private drug distribution systems.

Job Details

• Company: Rhydburg Biotech Ltd.

• Designation: Senior Executive – Regulatory Affairs

• Job Code: JB-1702

• Location: Dehradun, Uttarakhand, India

• Employment Type: Full-time

• Experience: Minimum 3 years in Quality Assurance or analytical validation roles

• Salary: ₹25,000–₹30,000

• Date Posted: October 14, 2026

• Industry: Pharma, Biotechnology, Clinical Research

Job Role & Responsibilities

Regulatory Documentation & Submissions

• Prepare, review, and maintain regulatory documents and submissions in accordance with applicable guidelines and company procedures.

• Compile and coordinate regulatory dossiers, applications, renewals, variations, amendments, and other regulatory submissions.

• Maintain regulatory trackers, submission records, approvals, licenses, certificates, and related documentation.

• Prepare and coordinate responses to regulatory queries, deficiencies, observations, and requests for additional information.

Analytical Data & Technical Document Review

• Review technical documents, product specifications, analytical data, stability data, and manufacturing information for regulatory compliance.

• Review analytical method validation documentation.

• Assess technical information for accuracy, completeness, and compliance with applicable requirements.

Quality Assurance & Cross-Functional Coordination

• Coordinate with Quality Assurance, Research and Development, Production, and other departments to obtain regulatory information and supporting documentation.

• Review quality documents, including deviations, Corrective and Preventive Actions (CAPA), change controls, SOPs, and batch-related records, for regulatory requirements and impact.

• Support regulatory audits and inspections by preparing documents and coordinating responses with QA and relevant departments.

Regulatory Compliance & Data Integrity

• Monitor updates to regulatory guidelines and assess their impact on products, processes, documentation, and quality systems.

• Ensure regulatory activities are completed within required timelines.

• Maintain accurate documentation, regulatory compliance, and data integrity.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Educational Qualification: B.Pharm or M.Pharm. A bachelor’s or master’s degree in Pharmacy is mandatory.

• Experience: Minimum 3 years of experience in Quality Assurance or analytical validation roles.

• Technical Skills: Hands-on experience reviewing analytical method validation documentation.

• Analytical Skills: Ability to interpret analytical data and review technical documentation.

• Regulatory Knowledge: Understanding of regulatory submissions, dossier preparation, quality documentation, and compliance requirements.

• Communication Skills: Good communication skills and the ability to coordinate with cross-functional departments.

Salary & Work Arrangements

• Salary Range: ₹25,000–₹30,000.

• Work Location: Dehradun, Uttarakhand.

• Employment Type: Full-time.

• Working Arrangements: The listing mentions a remote working option with defined review responsibilities and flexible working hours aligned with dossier and submission timelines.

• Role Focus: Technical documentation and regulatory responsibilities, without laboratory or shop-floor operations, as described in the listing.

Candidates should confirm the applicable remote or office arrangement with the employer before joining.

 

How to Apply

Interested and eligible candidates can apply through the official Rhydburg Biotech recruitment portal.

Apply Online: Rhydburg Biotech Senior Executive – Regulatory Affairs

Applicants should highlight their pharmaceutical qualifications, Quality Assurance or analytical validation experience, analytical method validation document review skills, and regulatory documentation expertise.

Job Summary

Thermo Fisher Scientific CRA I – FSP Jobs | Clinical Research

Thermo Fisher Scientific is recruiting for a Clinical Research Associate I (CRA I – FSP) position within its PPD® clinical research business. This opportunity is suited to candidates with a Master’s degree in Life Sciences, preferably Pharmacy, and 1–2 years of independent on-site clinical monitoring experience. The role involves clinical trial site monitoring, protocol compliance, Source Data Verification (SDV), Source Data Review (SDR), investigator site management, and regulatory documentation. Candidates with experience conducting clinical trial site visits across India are required, while oncology trial monitoring experience is preferred.

Company Overview

Thermo Fisher Scientific provides clinical research services through its PPD® clinical research portfolio. Its clinical research teams support drug development by helping ensure that clinical trials follow approved protocols, applicable regulations, and International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines.

Job Details

• Company: Thermo Fisher Scientific

• Clinical Research Business: PPD®

• Designation: Clinical Research Associate I (CRA I – FSP)

• Job Requisition ID: R-01368661

• Work Schedule: Standard, Monday to Friday

• Work Environment: Office, with on-site and remote clinical monitoring activities

• Experience: 1–2 years of independent on-site clinical monitoring experience

• Travel Requirement: May exceed 75%

Job Role & Responsibilities

Clinical Trial Site Monitoring

• Monitor investigator sites using a risk-based monitoring approach.

• Conduct on-site and remote monitoring visits to assess compliance with clinical trial protocols, regulatory requirements, ICH-GCP, and applicable SOPs.

• Perform Source Data Review (SDR), Source Data Verification (SDV), and Case Report Form (CRF) reviews, as applicable.

• Assess investigational products through physical inventory checks and records review.

• Conduct monitoring activities according to the approved monitoring plan.

• Initiate clinical trial sites in accordance with relevant procedures and compliance requirements.

• Perform clinical trial close-out activities and retrieve trial materials.

Data Quality & Risk Management

• Apply root cause analysis (RCA), critical thinking, and problem-solving skills to identify site process failures.

• Determine corrective and preventive actions to address findings and bring sites into compliance.

• Identify and reduce study-level and site-level risks.

• Document observations in monitoring reports and letters within required timelines.

• Escalate deficiencies and issues to clinical management and follow them through to resolution.

• Investigate and follow up on findings, as applicable.

• Recommend appropriate actions regarding site compliance.

Regulatory Documentation & Compliance

• Ensure essential clinical trial documents are complete and maintained according to ICH-GCP and applicable regulations.

• Conduct on-site file reviews according to project specifications.

• Maintain audit readiness and respond to company, client, regulatory audit, and inspection requirements.

• Ensure study systems and the Clinical Trial Management System (CTMS) are complete, accurate, and updated.

• Maintain compliance with approved protocols, regulatory requirements, and monitoring procedures.

Investigator Site & Project Coordination

• Maintain regular contact with investigative sites between monitoring visits to confirm protocol compliance, timely data entry, and resolution of outstanding issues.

• Facilitate communication between investigative sites, client companies, and internal project teams.

• Participate in investigator meetings when required.

• Support investigator payment processes.

• Assist in identifying potential investigators and suitable clinical trial sites when required.

• Provide trial status updates and progress reports to project teams.

• Complete administrative activities, including expense reports and timesheets.

• Contribute to project publications, monitoring tools, and process-improvement initiatives.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Educational Qualification: Master’s degree in a Life Sciences-related field, preferably Pharmacy.

• Experience: 1–2 years of independent on-site clinical monitoring experience is mandatory.

• Site Visit Experience: Hands-on experience conducting clinical trial site visits across India.

• Preferred Experience: Monitoring oncology clinical trials.

• Clinical Research Knowledge: Understanding of clinical trial processes, medical terminology, and therapeutic areas.

• Regulatory Knowledge: Working knowledge of ICH-GCP requirements, applicable regulations, and relevant procedural documents.

• Risk-Based Monitoring: Ability to manage risk-based monitoring concepts and processes.

• Analytical Skills: Critical thinking, root cause analysis, investigation, and problem-solving abilities.

• Communication: Good written and verbal English skills and the ability to communicate effectively with medical personnel.

• Organizational Skills: Strong time management, attention to detail, interpersonal skills, and adaptability.

• Computer Skills: Proficiency in Microsoft Office and the ability to learn and use relevant clinical research software systems.

Work Schedule & Travel Requirements

The role follows a Monday-to-Friday standard work schedule. Although the listing identifies an office work environment, the responsibilities include both on-site and remote monitoring activities.

Travel may exceed 75%, so candidates should be prepared to travel extensively for clinical trial site visits across India.

 

How to Apply

Interested and eligible candidates can apply through the official Thermo Fisher Scientific careers portal.

Apply Online: Thermo Fisher Scientific CRA I – FSP Recruitment

Before applying, ensure that your resume clearly highlights independent site monitoring experience, clinical trial site visits, ICH-GCP knowledge, and experience with SDV, SDR, and risk-based monitoring.

Job Summary

ICON Site Specialist I – Contracts & Budgets Jobs in Chennai

ICON is hiring a Site Specialist I – Contracts & Budgets for its Study Start-Up team in Chennai, Tamil Nadu. This opportunity is suitable for professionals with 3+ years of experience negotiating and managing clinical trial agreements (CTAs) and site budgets in a pharmaceutical, biotechnology, or contract research organization (CRO) environment. The role involves contract negotiations, budget management, clinical trial site activation, regulatory compliance, and risk mitigation. Candidates with a bachelor’s degree in Life Sciences or a related discipline and strong contract management skills can apply.

Company Overview

ICON is a global healthcare intelligence and clinical research organization that supports the development of new medicines and treatments. The company works with pharmaceutical and biotechnology organizations to advance clinical research and help bring treatments to patients.

Job Details

• Company: ICON

• Designation: Site Specialist I – Contracts & Budgets

• Job Requisition ID: JR155444

• Vacancy ID: 52543

• Department: Study Start-Up

• Business Unit: ICON Full Service & Corporate Support

• Location: Chennai, Tamil Nadu

• Work Mode: Hybrid

• Experience: 3+ years in clinical trial contract and site budget management

Job Role & Responsibilities

Clinical Trial Contracts & Budget Management

• Lead the negotiation, execution, and ongoing management of Clinical Trial Agreements (CTAs) and site budgets with investigative sites.

• Review client-requested contract changes, assess deviations, and escalate issues when required.

• Ensure contracts and amendments are complete, accurate, compliant with internal standards, and appropriately filed in contract databases.

• Maintain clear and timely documentation of site interactions and contract status updates.

Study Start-Up & Site Activation

• Collaborate with Clinical Operations and Project Management teams to support timely site activation.

• Forecast and track contract execution timelines.

• Coordinate translations and assist with submission packages for Central and Local Ethics Committees (ECs), Institutional Review Boards (IRBs), and Competent Authorities.

• Support study start-up activities in accordance with applicable regulatory requirements.

Regulatory Compliance & Risk Management

• Work with Functional Management to ensure compliance with local laws, regulatory requirements, and departmental policies.

• Identify, assess, and escalate contractual, legal, and operational risks.

• Proactively communicate issues to the CTA Lead, FSA Project Manager, Clinical Trial Manager (CTM), or Contract Manager.

• Apply departmental guidelines when evaluating contract changes and making decisions.

Team Collaboration & Process Improvement

• Manage multiple contracts simultaneously while adapting to changing timelines and business priorities.

• Mentor and guide junior Contract Associates.

• Identify opportunities to improve processes and strengthen collaboration with project teams and investigative sites.

• Provide recommendations to CTA Leads and Project or Functional Management to improve team efficiency and service delivery.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Educational Qualification: Bachelor’s degree in Life Sciences or a related discipline, or equivalent relevant experience.

• Experience: At least 3 years of experience negotiating and managing clinical trial contracts and site budgets within a pharmaceutical, biotechnology, or CRO environment.

• Regulatory Knowledge: Understanding of clinical trial regulatory and compliance requirements across jurisdictions.

• Contract Management: Experience with clinical trial agreements, site budgets, contract amendments, and execution timelines.

• Analytical Skills: Ability to evaluate contract changes, identify risks, and recommend appropriate actions.

• Communication Skills: Excellent written and verbal communication and interpersonal skills.

• Organization: Ability to prioritize multiple contracts, manage deadlines, and maintain accurate documentation.

• Teamwork: Ability to work independently, collaborate across functions, and support junior team members.

Location & Work Mode

The position is based in Chennai, Tamil Nadu, with a hybrid work arrangement. The role involves collaboration with clinical operations teams, project managers, investigative sites, and other stakeholders to support clinical trial start-up activities.

How to Apply

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

Apply Online: ICON Site Specialist I – Contracts & Budgets, Chennai

Candidates should highlight their experience in clinical trial agreement negotiations, site budget management, contract execution, regulatory compliance, and risk mitigation in their application.

Job Summary

Abbott Officer Quality Assurance Jobs – Baddi

Abbott is recruiting for an Officer – Quality Assurance position at its established pharmaceuticals division in Baddi, Himachal Pradesh. The role focuses on in-process quality assurance (IPQA), current Good Manufacturing Practices (cGMP), data integrity, and oral dosage manufacturing and packing compliance. Responsibilities include line clearance, in-process checks, batch record review, sample management, instrument calibration, and investigation support. Candidates interested in pharmaceutical quality assurance and manufacturing compliance can review the official vacancy details and apply through Abbott’s careers portal.

Company Overview

Abbott is a global healthcare company with businesses across pharmaceuticals, medical devices, diagnostics, and nutrition. This vacancy falls under the Established Pharmaceuticals Division (EPD) and involves quality assurance activities supporting oral dosage manufacturing operations.

Job Details

• Company: Abbott

• Designation: Officer – Quality Assurance

• Job ID: 31164037

• Division: Established Pharmaceuticals Division (EPD)

• Department: Quality

• Location: Village Mauza, Baddi, Himachal Pradesh, India

• Work Area: Oral dosage manufacturing facility

Job Role & Responsibilities

The selected candidate will be responsible for maintaining quality standards and ensuring compliance with pharmaceutical manufacturing procedures.

Quality Assurance & GMP Compliance

• Ensure compliance with current Good Manufacturing Practices (cGMP) in the oral dosage facility.

• Follow Good Documentation Practices (GDP) and data integrity requirements.

• Ensure manufacturing and packing processes comply with approved Batch Manufacturing Records (BMRs) and Batch Packing Records (BPRs).

• Ensure compliance with IPQA-related Standard Operating Procedures (SOPs) and records.

In-Process Quality Checks

• Perform line clearance activities before manufacturing and packing operations.

• Conduct in-process checks at different stages of batch manufacturing and packing.

• Monitor compliance with approved manufacturing and packing procedures.

Batch Documentation & Sample Management

• Collect and manage control samples, stability samples, validation samples, and other applicable samples.

• Maintain accurate sample records.

• Issue batch records and review executed batch documentation.

• Issue controlled copies of logbooks and formats.

Calibration, Investigations & Training

• Calibrate IPQA instruments and maintain associated records.

• Assist with investigation activities.

• Complete assigned SOP training in ISOtrain within the stipulated timeline.

• Follow applicable safety practices and the company’s Code of Business Conduct and Compliance (COBC).

Additional Responsibility

In the absence of the position holder, the designated Executive – IPQA will act as the authorized designee and be responsible for day-to-day operations.

Eligibility & Qualifications

The supplied vacancy details do not state a specific educational qualification or minimum experience requirement. Candidates should review the official Abbott application page to confirm the eligibility criteria.

Relevant role-related knowledge includes:

• Current Good Manufacturing Practices (cGMP).

• Good Documentation Practices (GDP) and data integrity.

• In-process quality assurance (IPQA).

• Oral dosage manufacturing and packing operations.

• Batch Manufacturing Records (BMRs) and Batch Packing Records (BPRs).

• Line clearance, in-process checks, sample management, and instrument calibration.

• SOP compliance, documentation review, and investigation support.

Location & Work Environment

The position is based at Village Mauza, Baddi, Himachal Pradesh, within Abbott’s Established Pharmaceuticals Division.

The listed significant work activity includes continuous standing for prolonged periods, defined as more than two consecutive hours during an eight-hour workday. The vacancy lists medical surveillance as not applicable.

How to Apply

Interested candidates can visit Abbott’s official careers website to review the vacancy and submit their application.

Apply Online: Abbott Officer – Quality Assurance, Baddi

Novo Nordisk Safety Surveillance Specialist Jobs – Bangalore

Novo Nordisk is hiring a Safety Surveillance Specialist for its Global Patient Safety team at Novo Nordisk Global Business Services (GBS) in Bangalore, Karnataka. This senior pharmacovigilance opportunity is intended for qualified medical professionals with at least 12 years of experience in pharmacovigilance or patient safety. The role focuses on safety signal detection, benefit-risk evaluation, risk management plans, aggregate safety reporting, and product safety strategy across Diabetes, Obesity, and Rare Diseases portfolios. Eligible candidates can apply online before October 26, 2026.

Company Overview

Novo Nordisk is a global healthcare company focused on treatments for chronic diseases, including diabetes, obesity, and rare diseases. The Global Patient Safety team monitors, evaluates, and communicates product safety throughout the medicine lifecycle, working with colleagues in Bangalore, Copenhagen, and other global teams.

Job Details

• Company: Novo Nordisk

• Designation: Safety Surveillance Specialist

• Department: Global Patient Safety, Novo Nordisk GBS

• Category: Regulatory Affairs & Safety Pharmacovigilance

• Location: Bangalore, Karnataka, India

• Experience: Minimum 12 years in pharmacovigilance or patient safety

• Educational Qualification: MBBS or MD

• Application Deadline: October 26, 2026

Job Role & Responsibilities

Medical Safety Evaluation

• Evaluate the medical safety profile of products from clinical development through post-marketing.

• Analyze complex safety data and document clear medical conclusions.

• Review safety information from clinical trials, spontaneous reports, scientific literature, and post-marketing sources.

• Identify, evaluate, and interpret potential safety signals.

• Contribute to evidence-based safety decisions throughout the product lifecycle.

Signal Management & Risk Assessment

• Establish and maintain product safety profiles through critical safety data analysis.

• Lead pharmacovigilance planning by developing and implementing safety strategies.

• Provide expert medical opinions on benefit-risk assessments.

• Contribute to risk management strategies and risk management plans (RMPs).

• Interpret epidemiological data and integrate evidence from multiple sources to support safety conclusions.

Clinical Development & Regulatory Documentation

• Contribute to clinical study designs and safety monitoring strategies for study protocols.

• Support the development and maintenance of core reference safety information.

• Participate in product labelling activities.

• Ensure accurate documentation of safety interpretations and conclusions in regulatory reports.

• Support safety governance meetings and represent Safety Surveillance in discussions with regulatory authorities, external consultants, and partners.

Team Leadership & Collaboration

• Work with global teams, including colleagues in Copenhagen and other partner functions.

• Build collaborative relationships with internal stakeholders and external partners.

• Coach and mentor team members, sharing expertise to strengthen team capabilities.

• Contribute to long-term safety strategy and process improvement initiatives.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Educational Qualification: Medical degree (MBBS or MD) from an accredited institution.

• Experience: Minimum 12 years in pharmacovigilance or patient safety, with a proven track record of delivery.

• Signal Management: Extensive experience in safety signal detection, evaluation, and management.

• Risk Management: Strong experience with risk management plans and aggregate safety reports.

• Regulatory Knowledge: Strong understanding of drug development and relevant regulatory frameworks.

• Data Interpretation: Ability to interpret epidemiological data and integrate different sources of safety evidence.

• Project Management: Strong project and stakeholder management capabilities.

• Communication: Excellent written and spoken English communication skills.

• Leadership: Innovative mindset, strategic thinking, and experience contributing to process improvements.

Important: This is a senior medical safety role requiring an MBBS or MD qualification and substantial pharmacovigilance experience. It is not an entry-level pharmacovigilance vacancy.

Location & Work Environment

The role is based in Bangalore, Karnataka, within Novo Nordisk Global Business Services. The successful candidate will work with global patient safety teams and cross-functional stakeholders, including teams in Copenhagen, as well as external regulatory and consulting partners.

 

How to Apply

Interested and eligible candidates can apply through the official Novo Nordisk careers website.

Apply Online: Novo Nordisk Safety Surveillance Specialist – Official Careers Page

Application deadline: October 26, 2026.

Job Summary

Sun Pharma Executive – Pharmacology Jobs in Vadodara

Sun Pharmaceutical Industries Ltd. is seeking candidates for the Executive – Pharmacology position at its R&D facility in Vadodara, Gujarat. This opportunity is suitable for candidates with a Master’s degree in Pharmacy (Pharmacology) or Life Sciences and knowledge of preclinical pharmacology research. The role involves in vivo efficacy and pharmacokinetic studies, cell-based in vitro assays, laboratory documentation, data analysis, and GMP compliance. Fresh candidates with strong academic knowledge and laboratory exposure may also apply, according to the job summary.

Company Overview

Sun Pharmaceutical Industries Ltd. is a pharmaceutical company with research and development activities supporting drug discovery and development. This position is part of the R&D function and focuses on pharmacology studies, laboratory procedures, scientific documentation, and regulatory compliance.

Job Details

• Company: Sun Pharmaceutical Industries Ltd.

• Designation: Executive – Pharmacology

• Business Unit: R&D1 Regulatory Affairs

• Job Grade: G12A

• Location: Vadodara, Gujarat

• Work Location: Tandalja – R&D

• Date Listed: September 22, 2026

• Experience: The job summary mentions 0–3 years; the job requirements section specifies 2+ years.

Job Role & Responsibilities

In Vivo Pharmacology

• Conduct animal handling, dosing, sample collection, and observations according to approved protocols.

• Execute efficacy and pharmacokinetic (PK) studies using mice, rats, rabbits, and guinea pig models.

• Monitor animal health, body weight, clinical signs, and study endpoints.

• Maintain accurate records of study activities and observations.

• Assist with necropsy, tissue collection, and sample processing.

• Follow institutional animal ethics committee guidelines and applicable regulatory requirements.

Cell-Based In Vitro Assays

• Perform mammalian cell culture and cell maintenance activities.

• Execute cell-based assays, including cell viability and proliferation assays, cytotoxicity assays, reporter gene assays, functional and mechanistic assays, and ELISA-based studies.

• Prepare reagents, media, buffers, and assay components.

• Analyze assay results and maintain laboratory records.

GMP Compliance & Documentation

• Follow approved SOPs, study protocols, and GMP requirements.

• Maintain laboratory notebooks, study records, logbooks, and worksheets.

• Follow data integrity requirements and ALCOA+ principles.

• Report deviations, incidents, and out-of-specification observations.

• Participate in instrument qualification, calibration, and maintenance activities.

• Support internal audits and regulatory inspections.

Data Analysis & Reporting

• Compile study data and prepare summary reports.

• Assist with statistical analysis and interpretation of results.

• Present experimental findings to departmental teams.

• Maintain complete and accurate study records.

Eligibility & Qualifications

Candidates should review the following educational and technical requirements before applying.

• Educational Qualification: Master’s degree in Pharmacy (Pharmacology) or Life Sciences.

• Experience: The job summary states 0–3 years of experience, while the job requirements section specifies 2+ years in pharmacology research, CROs, pharmaceutical R&D, or preclinical research laboratories.

• Pharmacology Knowledge: Understanding of pharmacology principles and drug evaluation.

• Laboratory Skills: Basic knowledge of laboratory animal handling, cell culture procedures, and aseptic techniques.

• Assay Knowledge: Familiarity with ELISA, spectrophotometric assays, and bioassays.

• Documentation & Compliance: Understanding of GMP, GLP, and data integrity concepts.

• Computer Skills: Familiarity with statistical software and Microsoft Excel, Word, and PowerPoint.

Behavioral Competencies

• Strong attention to detail.

• Good documentation and organizational skills.

• Scientific aptitude and analytical thinking.

• Ability to work in a multidisciplinary team.

• Good communication and presentation skills.

• Willingness to learn and manage multiple projects.

Location & Work Environment

The position is based at Sun Pharma’s R&D facility in Tandalja, Vadodara, Gujarat. The role involves laboratory-based pharmacology research, preclinical studies, cell-based assays, scientific documentation, and compliance activities.

How to Apply

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

Apply Online: Sun Pharma Executive – Pharmacology Recruitment

Candidates should review the experience criteria carefully because the job summary and job requirements sections state different experience expectations.

Job Summary

Fortrea Regulatory Operations Specialist I Jobs – Mumbai

Fortrea is hiring a Regulatory Operations Specialist I for its team in Mumbai, Maharashtra. This opportunity is suited to candidates with a scientific background in pharmaceutical, chemical, or biological sciences and 5–7 years of experience in the pharmaceutical industry, preferably in Quality Assurance. The role involves regulatory operations, document review and approval, quality issue management, CAPA, change controls, risk assessment, and compliance with client requirements. Candidates with relevant industry experience can apply through the official Fortrea careers portal.

Company Overview

Fortrea is a global contract research organization (CRO) that supports pharmaceutical and biotechnology companies in clinical development and related services. This position involves regulatory operations and quality-related responsibilities, including coordination with internal teams, clients, and business partners.

Job Details

• Company: Fortrea

• Designation: Regulatory Operations Specialist I

• Job Requisition ID: 265581

• Location: Mumbai, Maharashtra

• Employment Type: Full-time

• Work Environment: Office or remote

• Experience: 5–7 years in the pharmaceutical industry, preferably in Quality Assurance

• Application Deadline: October 17, 2026

Job Role & Responsibilities

The selected candidate will support regulatory operations, quality management, project coordination, and compliance activities.

Regulatory Operations & Document Management

• Review and approve documents, including protocols and reports related to method qualification, method validation, method transfer, investigations, and non-conformances.

• Coordinate regulatory operations involving the creation, revision, compilation, and approval of specifications, regulatory documents, and labeling documents across the product lifecycle.

• Support regulatory submissions to health authorities in the United States, European Union, Japan, and other regions, as applicable.

• Coordinate with supported departments and project teams to maintain service quality and meet agreed timelines.

Quality Assurance & Compliance

• Handle quality issues, Corrective and Preventive Actions (CAPA), and change controls related to clients and their contract laboratories.

• Support continuous improvement in quality culture and contribute to achieving Quality Key Performance Indicators (KPIs).

• Participate in relevant meetings, including Quality Assurance CSQ meetings, CAPA board meetings, quality improvement programs, and business connect meetings.

• Ensure compliance with procedures, quality standards, and customer requirements.

Risk Assessment & Stakeholder Management

• Collaborate on data-driven risk assessments, including risk identification, analysis, and evaluation.

• Develop risk mitigation plans and support CAPA initiatives.

• Build effective working relationships with stakeholders and business partners to identify improvement opportunities and meet business objectives.

• Identify potential issues, troubleshoot problems, resolve conflicts, and recommend appropriate solutions.

Eligibility & Qualifications

Candidates should meet the following minimum requirements:

• Educational Qualification: Bachelor’s or Master’s degree in a scientific discipline, such as pharmaceutical, chemical, or biological sciences, or equivalent experience.

• Experience: 5–7 years of experience in the pharmaceutical industry, preferably in the Quality Assurance department.

• Technical Knowledge: Familiarity with quality documentation, method validation, investigations, non-conformances, CAPA, and change controls is relevant to the listed responsibilities.

• Core Skills: Risk assessment, troubleshooting, stakeholder coordination, quality compliance, and continuous improvement.

Location & Work Environment

The position is listed for Mumbai, Maharashtra, with the work environment described as an office or remote setting. Candidates should confirm the applicable work arrangement with Fortrea during recruitment.

 

How to Apply

Interested and eligible candidates can submit their applications through the official Fortrea careers website.

Apply Online: Fortrea Regulatory Operations Specialist I – Official Application

Application deadline: October 17, 2026. Apply before the closing date.

Job Summary

Virchow Biotech Pvt. Ltd. is conducting a Walk-In Interview for openings across Manufacturing & R&D Biologics, LVP Operations, and Injectable facilities.
Both freshers and experienced candidates can attend the recruitment drive.
The company is inviting candidates from Biotechnology, Biochemistry, Molecular Biology, Pharmacy, Engineering, and ITI backgrounds.
Interested candidates can attend the walk-in interview at Virchow Biotech Pvt. Ltd., Unit-I, Gagillapur, Hyderabad.

Virchow Biotech Walk-In Interview – Manufacturing & R&D Biologics

Virchow Biotech Pvt. Ltd. has announced openings across its Manufacturing & R&D Biologics, LVP Operators, and Injectable Facility operations.

Walk-In Interview Details

Interview Dates: 9th October 2026 (Friday) & 10th October 2026 (Saturday)

Interview Venue:
Virchow Biotech Pvt. Ltd., Unit-I
Survey No. 172, Gagillapur, Dundigal Mandal,
Medchal Dist., Hyderabad – 500043

Departments & Openings

Manufacturing & R&D Biologics

Opportunities are available in Manufacturing and R&D Biologics operations.

LVP Operators

Candidates can apply for opportunities related to LVP operations.

Injectable Facility

Openings are also available for candidates interested in injectable manufacturing operations.

Eligibility & Qualifications

The recruitment drive is open to candidates with the following qualifications:

M.Sc – Biotechnology | M.Sc – Biochemistry | M.Sc – Molecular Biology | B.Sc – Biotechnology | B.Pharm | M.Pharm | B.Tech | M.Tech | ITI

Eligible Backgrounds

• Biotechnology
• Biochemistry
• Molecular Biology
• Pharmacy
• Engineering
• Technical / ITI

Experience

Freshers and experienced candidates can attend.

The recruitment poster does not specify a particular experience range for the individual openings.

Documents Required

Candidates are requested to bring:

• Updated Resume
• ID Proof
• Educational Certificates
• Experience Letters, if any

How to Apply

Candidates who are interested in attending the walk-in interview can visit the venue on 9th or 10th October 2026 with their updated resume and required documents.

Candidates who cannot attend the walk-in can send their CV to:

Email: hr@virchowbiotech.com
Contact: +91 91001 25845

Job Summary

Brillex Clinical Research Pvt. Ltd. is hiring for the position of Report Writer in its Clinical Research team.
The opportunity is open to Science Graduates with 2 to 5 years of experience in report writing.
The role involves preparing clinical study reports for early-phase and late-phase clinical trials while ensuring compliance with regulatory requirements.
Candidates with strong scientific writing, editing, clinical research and documentation skills are encouraged to apply.

Brillex Clinical Research – Report Writer

Brillex Clinical Research Pvt. Ltd. is looking for an experienced Report Writer to support clinical research documentation and reporting activities. The position is based in Ahmedabad, Gujarat.

Job Role & Responsibilities

The selected candidate will be responsible for preparing and reviewing clinical study reports and supporting documentation in accordance with applicable regulatory requirements.

Report Writing & Clinical Research Responsibilities

• Preparation of clinical study reports for early-phase and late-phase clinical trials in compliance with regulatory requirements.
• Strong scientific writing, editing, and formatting skills with attention to detail.
• Knowledge of clinical research regulations, including ICH-GCP guidelines, with expertise in developing and reviewing clinical study reports.
• Proficiency in communication with sponsors and cross-functional collaboration skills.
• Demonstrate excellent analytical and problem-solving skills to address various challenges while ensuring quality, compliance, and audit readiness.
• Mentor and train team members.
• Foster collaboration across cross-functional departments and drive continuous process improvements through SOP development and best-practice implementation.
• Demonstrate excellent project management and time management skills, with a proven track record of delivering high-quality documents on schedule.

Eligibility & Qualifications

Candidates with the following qualification and experience can apply:

Any Science Graduate

Experience Required

2 to 5 years of experience in Report Writing

Key Skills

• Clinical study report writing
• Scientific writing
• Editing and formatting
• Clinical research documentation
• ICH-GCP guidelines
• Regulatory compliance
• Sponsor communication
• Cross-functional collaboration
• Analytical and problem-solving skills
• SOP development
• Project management
• Time management

Job Location

Brillex Clinical Research Pvt. Ltd.
602, Ariane Legacy,
Adalaj – Gandhinagar, Gujarat, India – 382421.

How to Apply

Interested candidates with relevant experience can share their updated CV with the recruitment team.

Email: rushabhshah@brillexcro.com

Candidates are requested to mention the relevant position while sharing their resume.

Job Summary