Pharmazone Hiring CRA, RA, PV, QA, Production

B.Pharm/M.Pharm Clinical, RA, PV Roles – Pharmazone

B.Pharm/M.Pharm — Multiple openings (CRA, RA, PV, QA, Production) at Pharmazone. Location: Not specified. Apply now.

Pharmazone is hiring experienced life‑science professionals across clinical, regulatory, pharmacovigilance, quality and production functions. If you hold a B.Pharm or M.Pharm and want hands‑on roles where scientific rigor meets regulatory impact, these openings are built for practical people who deliver reliable results.

Company Overview

Pharmazone is a niche service provider and contract research partner working across pharmaceutical development, GMP compliance, and pharmacovigilance services. The company partners with manufacturers, CROs, and healthcare companies to support regulatory filings, safety monitoring, quality assurance, and audit readiness. Pharmazone positions itself as a solutions‑driven firm with deep technical capability — an environment where technical ownership and regulatory discipline are valued.

Why applicants choose Pharmazone:

• Integrated service offerings across clinical research, GMP audits, quality systems and PV.
• Cross‑functional exposure that accelerates technical growth.
• Opportunities to work on compliance projects, audits, and dossier support that directly affect market access and patient safety.

Note: The job posting does not specify a single hiring location. Candidates should apply and confirm exact role location during the recruitment process.

Open Positions & Role Summary

Pharmazone seeks qualified candidates for the following roles (experience ranges shown):

Clinical Research Associate (CRA) — 1 to 5 years

CRAs manage site monitoring activities, ensure protocol compliance and maintain trial documentation. This role suits candidates who are detail‑oriented, experienced in ICH‑GCP, and capable of organizing monitoring visits, source data verification, and timely query resolution.

Key responsibilities:

• Conduct site initiation, monitoring and close‑out visits.
• Verify source documents and CRF entries.
• Ensure informed consent processes and protocol adherence.
• Prepare monitoring visit reports and follow up on action items.

Auditor (GMP Services) — 3 to 4 years

GMP auditors evaluate manufacturing and quality systems against national and international standards. Candidates should have a strong audit trail record, CAPA handling experience, and the ability to produce concise, actionable audit reports.

Key responsibilities:

• Perform GMP audits, gap assessments and mock inspections.
• Write factual, risk‑based audit reports and corrective action plans.
• Support client remediation and regulatory inspection readiness.

Production Expert (GMP Services, OSD) — 11 to 14 years

Senior operational role for professionals with deep OSD manufacturing experience. This role focuses on process robustness, technology transfer, and compliance for oral solid dosage manufacturing.

Key responsibilities:

• Oversee process optimization and scale‑up for OSD products.
• Lead GMP best practices on the shop floor, training and deviation management.
• Drive productivity improvements while maintaining product quality.

Aggregate Report Specialist (Pharmacovigilance) — 4 to 5 years

This specialist prepares aggregate safety reports (PBRERs, PSURs, DSURs) and supports signal detection and periodic safety reporting. The role requires strong safety database knowledge and regulatory submission experience.

Key responsibilities:

• Draft and compile PBRERs, PSURs and other aggregate reports.
• Coordinate with medical writers and safety data managers.
• Support global submissions and maintenance of safety databases.

Regulatory Affairs Executive — 2 to 6 years

Regulatory professionals preparing dossiers, responding to agency queries, and supporting filings across markets. The ideal candidate has hands‑on experience with dossier formats and regulatory strategy.

Key responsibilities:

• Prepare regulatory submissions and manage filing timelines.
• Maintain product regulatory files and correspondence.
• Support labeling, CMC sections, and regulatory intelligence activities.

MICC Executive — Freshers welcome (B.Pharm / M.Pharm / BDS)

MICC (Medical Information / Customer Care / Clinical Call) executives handle medical queries, product information requests and field‑level liaison duties. An excellent entry point for graduates to learn product science and pharmacovigilance basics.

Key responsibilities:

• Respond to medical and product information queries.
• Escalate safety‑related information to PV teams.
• Maintain call logs and product literature accuracy.

Eligibility / Qualifications

Pharmazone prefers candidates with formal life sciences qualifications and relevant industry exposure. Typical requirements:

• Clinical Research Associate: B.Pharm / M.Pharm / Life sciences degree with 1–5 years CRA experience.
• Auditor (GMP): Degree in pharmacy/chemistry with 3–4 years audit/GMP experience.
• Production Expert (OSD): B.Pharm / M.Pharm / B.Tech with 11–14 years OSD manufacturing experience.
• Aggregate Report Specialist (PV): M.Pharm / B.Pharm / M.Sc with 4–5 years PV aggregate reporting experience.
• Regulatory Affairs Executive: B.Pharm / M.Pharm with 2–6 years RA exposure.
• MICC Executive: B.Pharm / M.Pharm / BDS freshers accepted.

Skills & competencies across roles:

• Strong knowledge of cGMP, ICH‑GCP, and pharmacovigilance principles where applicable.
• Excellent technical writing and documentation discipline.
• Proficiency with regulatory databases, safety databases, and laboratory or QA systems (role dependent).
• Good communication skills and ability to work in cross‑functional teams.

Relevant courses (comma‑separated): B.Pharm, M.Pharm, BDS, M.Sc Pharmaceutical Sciences, Diploma in Clinical Research, Postgraduate Diploma in Pharmacovigilance, Regulatory Affairs Certification, GMP & Quality Assurance Training, HPLC/Analytical Training.

Location & Compensation

• Location: Not specified in the posting. Candidates should confirm role location during the interview or via HR.
• Employment type: Full‑time roles.
• Compensation: Competitive, experience‑based — exact packages will be discussed during selection.

How to Apply

Send your CV and a concise cover note to the HR inbox: hr@pharmazones.com.
Include the role you are applying for in the email subject line (for example: “Application — CRA / Clinical Research Associate“).

Application tips

• Use a clear subject line with the exact role name.
• Attach a one‑page summary of relevant projects or audits you led.
• Mention notice period, current CTC and expected CTC in the email body.

Selection Process

• Shortlisting based on technical fit and role experience.
• Technical interviews with hiring managers and functional leads.
• Final HR discussion to confirm compensation and joining timelines.

FAQs

Q: Can freshers apply for any role?
A: Freshers are considered for the MICC Executive position only. Other roles require prior industry experience.

Q: Is remote work allowed?
A: The posting does not mention remote work. Confirm during interview or with HR.

Q: What documents should I attach?
A: CV, one‑page project/audit summary (if applicable), educational certificates, and two professional references if available.

Q: What is the expected turnaround after application?
A: Shortlisting timelines vary. If you do not hear within 2–3 weeks, follow up via the same HR email.

Q: Does Pharmazone charge any fees for recruitment?
A: No. Applicants should not pay any fee for application, testing, or onboarding unless explicitly communicated in a formal offer.

Final checklist before applying

• Confirm the role you are applying for and mention it clearly in the email subject.
• Tailor your CV to highlight specific, measurable achievements (e.g., number of monitoring visits, audits conducted, dossiers prepared).
• Prepare to discuss specific regulatory guidelines you have worked with (ICH, GCP, GMP).

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+----------------------+-----------------------------------------------------------+
| Company              | Pharmazone                                                |
+----------------------+-----------------------------------------------------------+
| Vacancies            | CRA, Auditor (GMP), Production Expert (OSD), Aggregate PV Specialist, Regulatory Executive, MICC Executive |
+----------------------+-----------------------------------------------------------+
| Required Education   | B.Pharm, M.Pharm, BDS, M.Sc (see roles for specifics)     |
+----------------------+-----------------------------------------------------------+
| Experience           | Fresher (MICC) to 14 years (Production Expert)            |
+----------------------+-----------------------------------------------------------+

Tagged as: Pharma Jobs in Ahmedabad