The pharmaceutical and clinical research industry in India continues to witness remarkable growth, creating exciting employment opportunities for experienced professionals and talented pharmacy graduates. If you are looking for a rewarding career in Clinical Research, Quality Assurance, Documentation Management, or Medical Writing, then this latest hiring announcement from Panexcell Clinical Research could be the opportunity you’ve been waiting for.
Panexcell Clinical Research, a reputed Contract Research Organization (CRO) based in Rabale, Navi Mumbai, has announced multiple vacancies across its Quality Assurance and Clinical Operations departments. The organization is actively seeking immediate joiners who possess the required qualifications, relevant experience, and a passion for maintaining high standards of compliance and clinical excellence.
Whether you are an experienced QA professional with expertise in bioanalytical compliance or a pharmacy graduate aspiring to build a career in medical writing, these openings offer excellent growth prospects within a regulated clinical research environment.
About Panexcell Clinical Research
Panexcell Clinical Research is a well-established Contract Research Organization (CRO) that provides comprehensive clinical research and bioanalytical services to pharmaceutical, biotechnology, and healthcare companies.
The organization plays a crucial role in supporting drug development programs by ensuring adherence to international regulatory standards, maintaining data integrity, and delivering reliable clinical research outcomes.
With a strong commitment to quality, compliance, and scientific excellence, Panexcell has built a reputation for delivering high-quality services while providing employees with opportunities to learn, grow, and contribute to impactful healthcare innovations.
Current Open Positions at Panexcell Clinical Research
Panexcell is currently hiring for the following positions at its Rabale, Navi Mumbai facility:
| Department | Position | Qualification | Experience | Vacancies |
|---|---|---|---|---|
| Quality Assurance | Bioanalytical QA Specialist | M.Pharm / M.Sc | 5-8 Years | 01 |
| Quality Assurance | Documentation & Archival Analyst | Pharma / Science Graduate | 1-2 Years | 01 |
| Clinical Operations | Medical Writer | B.Pharm / M.Pharm | 1-2 Years | 01 |
1. Bioanalytical QA Specialist
Eligibility Criteria
Educational Qualification
Candidates must possess:
- M.Pharm
- M.Sc (Life Sciences, Chemistry, Bioanalytical Sciences, or related fields)
Experience Required
- 5 to 8 years of relevant experience
- Previous experience in a regulated CRO environment
- Hands-on exposure to bioanalytical laboratories
- Strong knowledge of GLP and regulatory requirements
Key Responsibilities
The selected Bioanalytical QA Specialist will be responsible for ensuring compliance with regulatory requirements and maintaining quality standards within the bioanalytical facility.
Major responsibilities include:
Regulatory Compliance
- Ensuring adherence to GLP guidelines
- Supporting compliance with USFDA regulations
- Ensuring alignment with EMA requirements
- Monitoring compliance with MHRA expectations
Quality Audits
- Conducting routine internal audits
- Reviewing laboratory practices
- Verifying compliance documentation
- Auditing sample management processes
Data Review
- Reviewing chromatograms
- Assessing analytical data
- Verifying method validation reports
- Evaluating study documentation
CAPA Management
- Managing deviations
- Investigating non-conformities
- Implementing corrective actions
- Tracking preventive measures
SOP Management
- Reviewing Standard Operating Procedures
- Updating regulatory documentation
- Conducting periodic SOP assessments
- Supporting employee training programs
Skills Required
Successful candidates should possess:
- Strong analytical thinking
- Regulatory knowledge
- Attention to detail
- Documentation expertise
- Audit management skills
- Communication abilities
- Problem-solving capabilities
2. Documentation & Archival Analyst
Documentation management plays a critical role in maintaining data integrity within pharmaceutical and clinical research organizations.
Panexcell is looking for highly organized professionals capable of managing critical records and supporting compliance initiatives.
Eligibility Criteria
Educational Qualification
Candidates may possess:
- B.Pharm
- M.Pharm
- B.Sc
- M.Sc
- Any Life Science Degree
Experience Required
- 1 to 2 years of experience
- Experience in pharmaceutical documentation
- Knowledge of archival procedures
- Familiarity with quality systems
Key Responsibilities
Documentation Control
The selected candidate will:
- Maintain controlled documents
- Track document revisions
- Manage quality records
- Ensure version control compliance
Archival Activities
Responsibilities include:
- Archiving study documents
- Maintaining archival inventory
- Tracking file retrieval requests
- Ensuring proper storage conditions
Regulatory Compliance
The role requires:
- Supporting inspections
- Maintaining audit readiness
- Preserving critical records
- Following retention schedules
Record Retrieval
Candidates will:
- Retrieve requested files
- Support client audits
- Assist regulatory inspections
- Coordinate document requests
Desired Skills
Ideal candidates should have:
- Excellent organizational skills
- Strong documentation practices
- Record management knowledge
- Computer proficiency
- Data integrity awareness
- Good communication skills
3. Medical Writer
Medical Writing has emerged as one of the most promising career paths for pharmacy professionals.
This position offers an excellent opportunity for B.Pharm and M.Pharm graduates who enjoy scientific writing and clinical documentation.
Eligibility Criteria
Educational Qualification
Applicants must possess:
- B.Pharm
- M.Pharm
Experience Required
- 1 to 2 years of Medical Writing experience
- Clinical documentation experience
- Scientific writing exposure
- Knowledge of clinical research guidelines
Key Responsibilities
Clinical Document Development
The Medical Writer will prepare:
- Clinical Study Reports (CSR)
- Clinical Trial Protocols
- Informed Consent Documents (ICD)
- Case Report Forms (CRF)
Scientific Literature Review
Responsibilities include:
- Conducting literature searches
- Reviewing published studies
- Summarizing scientific evidence
- Supporting protocol development
Regulatory Writing
The candidate will:
- Follow ICH guidelines
- Ensure GCP compliance
- Prepare regulatory documents
- Support clinical submissions
Content Review
Additional duties include:
- Reviewing scientific accuracy
- Editing medical content
- Formatting clinical documents
- Maintaining consistency in reporting
Why Consider a Career in Medical Writing?
Medical writing offers several advantages:
High Demand
Clinical trials continue to increase globally, resulting in growing demand for skilled medical writers.
Career Growth
Professionals can progress to:
- Senior Medical Writer
- Lead Medical Writer
- Regulatory Writer
- Scientific Communication Specialist
- Clinical Documentation Manager
Competitive Compensation
Medical writing professionals often enjoy attractive salary packages and long-term career stability.
Global Opportunities
Medical writing skills are highly transferable across:
- CROs
- Pharmaceutical companies
- Biotechnology firms
- Medical communication agencies
Location Details
Work Location
📍 Rabale, Navi Mumbai
Rabale is one of Navi Mumbai’s major industrial and pharmaceutical hubs.
The location offers excellent connectivity through:
- Navi Mumbai suburban railway network
- Thane-Belapur Road
- Mumbai-Pune Expressway
- Public transportation services
Candidates residing in:
- Mumbai
- Navi Mumbai
- Thane
- Kalyan
- Dombivli
- Panvel
can conveniently commute to the workplace.
Important Hiring Requirements
Panexcell has specified certain mandatory criteria for applicants.
Immediate Joiners Preferred
The company is prioritizing candidates who:
- Are currently unemployed
- Have completed their notice period
- Can join within a few days
- Are available for immediate interviews
Mumbai-Based Candidates Only
Currently, applications are being considered primarily from candidates residing in:
- Mumbai
- Navi Mumbai
- Thane
- Nearby Maharashtra locations
Candidates from distant locations may not be prioritized.
How to Apply?
Interested candidates should send their updated resumes directly to the HR department.
Official HR Email
Recommended Email Subject Lines
For Bioanalytical QA
Application for Bioanalytical-QA | 6 Years Exp | Immediate Joiner | Mumbai
For Medical Writer
Application for Medical Writer | 1.5 Years Exp | B.Pharm | Immediate Joiner
For Documentation & Archival
Application for Documentation & Archival | 2 Years Exp | Immediate Joiner
Using a clear subject line can help recruiters identify your profile faster and improve the visibility of your application.
Interview Preparation Tips
For Bioanalytical QA Candidates
Prepare topics such as:
- Bioanalytical Method Validation
- GLP Guidelines
- USFDA Regulations
- EMA Guidelines
- MHRA Compliance
- CAPA Management
- Audit Trail Reviews
For Documentation & Archival Candidates
Focus on:
- ALCOA+ Principles
- Data Integrity
- Document Control Systems
- Record Retention Policies
- Audit Readiness
- Electronic Documentation
For Medical Writers
Review:
- ICH-GCP Guidelines
- Clinical Study Report Structure
- Protocol Writing
- Clinical Trial Documentation
- Literature Review Techniques
- Regulatory Writing Standards
Why Join Panexcell Clinical Research?
Working with Panexcell offers several benefits:
✅ Exposure to global regulatory standards
✅ Professional growth opportunities
✅ CRO industry experience
✅ Learning-oriented environment
✅ Diverse clinical research projects
✅ Competitive industry exposure
✅ Career advancement potential
For professionals seeking long-term careers in clinical research and quality systems, these openings represent an excellent opportunity to join a reputed CRO and contribute to meaningful healthcare research initiatives.
Apply Now
Candidates meeting the eligibility criteria and available for immediate joining are encouraged to apply as soon as possible.
📧 Email Resume: hr@panexcell.com
📍 Location: Rabale, Navi Mumbai
🏢 Company: Panexcell Clinical Research
💼 Departments: Quality Assurance & Clinical Operations
⏳ Immediate Joiners Preferred
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