Job Tag: Pharma Jobs in Mumbai

Safety Writer Vacancy for Life Science Graduates | Fortrea Mumbai

Apply for Fortrea Safety Writer vacancies in Mumbai. Open for life science graduates with 3+ years of pharma/medical writing experience.

Fortrea, a trusted global leader in clinical development and pharmaceutical services, is currently hiring for the role of Safety Writer at its Mumbai location. This position is ideal for life science professionals with strong expertise in pharmacovigilance, medical writing, and safety documentation. If you are passionate about regulatory writing and safety compliance, this opportunity allows you to contribute directly to global healthcare and regulatory submissions.

Company Overview

Fortrea is a global contract research organization (CRO) providing comprehensive drug development and safety services to pharmaceutical, biotechnology, and healthcare companies worldwide. With a strong focus on regulatory compliance, pharmacovigilance, and clinical development, Fortrea supports clients in bringing safer, effective medicines to patients faster. The company’s collaborative environment empowers employees to excel in complex healthcare projects while maintaining high ethical and regulatory standards.

Job Role & Responsibilities

As a Safety Writer at Fortrea, you will be responsible for preparing and reviewing safety reports, risk management documentation, and regulatory submissions. Your responsibilities will include:

• Writing safety reports for global regulatory submissions including Annual Reports (IND), PSURs, PADERs, DSURs, Risk Management Plans, and related documents.
• Leading report management activities, client communications, and project strategy discussions.
• Reviewing and ensuring the quality of safety reports authored by peers or junior writers.
• Authoring signal reports, safety issue analyses, adverse event narratives, and benefit-risk evaluation reports.
• Writing CTD Summaries (non-clinical, clinical, and overviews) for regulatory submissions.
• Conducting scientific literature searches for safety reports and routine surveillance.
• Preparing medical information responses for healthcare professionals.
• Contributing to labeling documents such as Core Data Sheets, USPIs, SPCs, and Med Guides.
• Ensuring regulatory compliance with ICH-GCP, pharmacovigilance guidelines, and safety requirements.
• Collaborating with cross-functional teams and clients to ensure timely, high-quality deliverables.

Eligibility / Qualifications

• Education: Minimum of a bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, or related fields. Advanced degrees (M.Sc, M.Pharm, PhD) preferred.
• Experience: At least 3 years in the pharmaceutical industry, with a minimum of 2 years in medical writing/safety writing.
• Technical Skills:
  • Excellent command of written and spoken English.
  • Strong understanding of pharmacovigilance, regulatory guidelines, and ICH-GCP.
  • Proficiency in MS Office Suite and document management tools.
  • Strong organizational and time management skills.
• Desirable: Clinical research exposure and prior experience in safety surveillance.

Relevant courses include: B.Pharm, M.Pharm, M.Sc Life Sciences, M.Sc Clinical Research, M.Sc Biotechnology, PhD (Pharmacology, Toxicology, or related fields).

Location & Salary

• Location: Mumbai, India.
• Work Type: Full-time, on-site.
• Salary: Competitive salary aligned with pharmaceutical industry standards, plus benefits, performance incentives, and growth opportunities.

Application Process

Fortrea is committed to building a diverse, inclusive workforce where all employees are respected and empowered. Interested candidates are encouraged to apply before the application deadline.

👉 Apply directly here

FAQs

1. Who can apply for the Safety Writer role?
Candidates with a bachelor’s or higher degree in life sciences, pharmacy, or related fields and relevant industry experience in medical writing or pharmacovigilance.

2. What experience is required?
At least 3 years in the pharma industry, including 2 years in safety or medical writing.

3. What are the key responsibilities of this role?
Authoring and reviewing global safety reports, regulatory documents, risk management plans, and safety narratives.

4. Where is the job located?
The role is based in Mumbai, India.

5. Is travel required?
Yes, up to 5% travel may be required depending on project needs.

Job Summary Table

Pharmacovigilance Associate | M.Pharm | Encube Ethicals Dombivli

Encube Ethicals hiring Pharmacovigilance Associate in Dombivli (Palava). Apply now! Openings for M.Pharm graduates with 2–3 years’ PV experience.

Encube Ethicals is expanding its Pharmacovigilance Department and is looking for experienced professionals to join its growing team at Dombivli (Palava), Maharashtra. This role is ideal for M.Pharm graduates with 2–3 years of pharmacovigilance experience, particularly those who have worked at the sponsor’s end and are well-versed with global PV guidelines.

Company Overview

Encube Ethicals is a pharmaceutical company with a strong focus on dermatology and specialty formulations. The organization is committed to delivering high-quality products globally, backed by innovation, compliance, and excellence in operations. Employees benefit from a collaborative environment, career advancement opportunities, and the chance to contribute to regulatory compliance in multiple global markets.

Job Role & Responsibilities

As a member of the Pharmacovigilance Department, you will be responsible for:

• Conducting quality reviews of pharmacovigilance activities, including ICSR case processing, aggregate reports, and literature reviews.
• Overseeing overall PV operations to ensure compliance with regulatory requirements in the US, EU, and RoW markets.
• Coordinating with CROs, cross-functional teams, and marketing partners for PV-related tasks.
• Ensuring regulatory compliance and maintaining oversight of CRO-delivered activities.

Eligibility / Qualifications

• Education: Master of Pharmacy (M.Pharm).
• Experience: 2–3 years of experience in pharmacovigilance, preferably at the sponsor’s end.
• Skills Required:
  • Strong knowledge of US and EU pharmacovigilance guidelines.
  • Ability to manage CRO operations efficiently.
  • Familiarity with global PV compliance for multiple regions.
  • Excellent verbal and written communication skills.
  • Collaborative mindset with the ability to work cross-functionally.

Location & Salary

• Job Location: Dombivli (Palava), Maharashtra, India.
• Preference: Candidates from the Central line are preferred.
• Salary: Competitive, based on candidate experience and industry standards.

Application Process

Interested candidates can send their updated resumes to: pranali.sarvagod@encubeethicals.com

Apply now to join Encube Ethicals and be a part of its growing pharmacovigilance team!

FAQs

1. Who can apply for this role?
M.Pharm graduates with 2–3 years’ pharmacovigilance experience, preferably at a sponsor/pharmaceutical company.

2. Is prior experience in CRO management required?
Yes, candidates with experience managing CROs will be preferred.

3. Which markets does this role cover?
The role ensures compliance with pharmacovigilance requirements in the US, EU, and RoW markets.

4. What skills are most valued?
Strong knowledge of global PV guidelines, communication skills, and prior sponsor-end PV experience.

5. How do I apply?
Candidates can mail their resumes to pranali.sarvagod@encubeethicals.com.

Career Benefits at Encube Ethicals

• Opportunity to work with a growing, globally recognized pharmaceutical company.
• Hands-on exposure to pharmacovigilance compliance for multiple regions.
• Career progression in PV operations and regulatory affairs.
• Collaborative work culture with cross-functional exposure.
• Competitive pay package and professional growth opportunities.

Summary Table

Regulatory Affairs Associate I | B.Pharm/M.Pharm | Teva Navi Mumbai

Apply at Teva Pharmaceuticals for Regulatory Affairs Associate I in Navi Mumbai. B.Pharm/M.Pharm with 1–4 years RA experience required.

Teva Pharmaceuticals, a global leader in generic medicines, is hiring Regulatory Affairs Associate I for its Navi Mumbai office. This role is an exciting opportunity for B.Pharm/M.Pharm graduates with 1–4 years of RA experience to contribute to Teva’s mission of making healthcare more affordable and accessible worldwide.

Company Overview

Teva Pharmaceuticals is the world’s largest manufacturer of generic medicines, serving more than 200 million people daily across nearly 60 countries. Teva’s portfolio includes many essential medicines listed by the World Health Organization (WHO). With a focus on improving global health, Teva offers employees a collaborative, innovative, and inclusive workplace where they can make a meaningful impact.

Job Role & Responsibilities

As a Regulatory Affairs Associate I (Product Manager), you will:

• Manage the regulatory lifecycle of assigned Medis dossiers for Teva’s 3rd party client business (Medis).
• Coordinate with Teva’s supply chain, site RA teams, and stakeholders to ensure smooth dossier management.
• Prepare, submit, and follow up on variations to regulatory authorities and Medis clients.
• Compile and submit responses to deficiency letters from authorities or clients.
• Maintain databases, regulatory modules, and records in compliance with procedures.
• Provide regular status updates and reports to management.
• Engage in professional communication with internal and external stakeholders.
• Support audits, inspections, and specialized RA projects as directed.

Eligibility / Qualifications

• Education: B.Pharm / M.Pharm
• Experience: 1–4 years of experience in Regulatory Affairs with exposure to EU and International markets.
• Skills Required:
  • Strong organizational and documentation skills.
  • Excellent English (written and verbal).
  • Proficiency in MS Office and RA databases.
  • Strategic thinking, adaptability, and proactive approach.
  • Team collaboration and independent work capability.

Location & Salary

• Location: Navi Mumbai, Maharashtra (PIN: 400706)
• Employment Type: Full-time, Office-based
• Compensation: Competitive salary with global benefits aligned to Teva’s policies.
• Equal Opportunity: Teva is committed to diversity, equity, and inclusion in the workplace.

Application Process

Interested candidates can apply directly through Teva’s official career portal:
👉 Apply Here

FAQs

1. What is the required qualification for this role?
B.Pharm or M.Pharm degree with relevant Regulatory Affairs experience.

2. How many years of experience are required?
1–4 years of RA experience with EU/International exposure.

3. What are the main responsibilities?
Lifecycle management of Medis dossiers, handling variations, responding to deficiencies, and ensuring compliance.

4. Where is the job location?
Teva Pharmaceuticals, Navi Mumbai, Maharashtra.

5. Does Teva encourage diversity?
Yes. Teva is an equal opportunity employer promoting a diverse and inclusive workplace.

Quick Summary Table

Clinical Data Coordinator I – Fortrea Hiring in Mumbai

Fortrea is hiring Clinical Data Coordinator I in Mumbai. corinna kopf leaked sex Life sciences graduates with 3+ years of experience in pharma/clinical research can apply.

Fortrea, a global leader in clinical trial solutions, is hiring for the role of Clinical Data Coordinator I at its Mumbai office. This is a full-time opportunity for experienced professionals in life sciences and clinical data management, offering exposure to global projects and advanced data coordination systems.

Company Overview

Fortrea is a trusted partner to the world’s leading pharmaceutical, biotechnology, and medical device organizations. With a focus on data integrity, patient safety, and regulatory compliance, Fortrea delivers end-to-end clinical trial support. The company offers employees a chance to grow in a global environment while working on impactful projects that drive healthcare innovation.

Job Role & Responsibilities

As a Clinical Data Coordinator I, your responsibilities include:

• Supporting Lead Data Managers (LDM) in the review, maintenance, and update of external vendor data received from central or local laboratories.
• Ensuring electronic vendor data is complete, formatted correctly, and aligned with protocol-specified parameters.
• Assisting in the development of Data Transfer Agreements and Specifications for vendor data transfers.
• Reviewing and resolving data discrepancies generated by study-specific edit checks.
• Supporting validation reviews of electronically transmitted data for trial patients.
• Reviewing external data status reports, edit checks, and listings.
• Interacting with Clinical Trial Managers (CTM) and Clinical Research Associates (CRA) to obtain and verify laboratory normal ranges.
• Performing QC checks and ensuring accurate integration of lab data into clinical databases.
• Assisting with vendor and client communications regarding data transfer or validation issues.

Eligibility / Qualifications

• Education: University/college degree in Life Sciences, Health Sciences, Information Technology, or allied health professions. Equivalent relevant experience may be considered.
• Experience: Minimum of 3 years in pharmaceuticals, biotechnology, medical devices, diagnostics, or clinical trial industries.
• Skills:
  • Strong organizational, planning, and analytical abilities.
  • Understanding of ICH-GCP principles.
  • Proficiency with Microsoft Office tools.
  • Familiarity with medical terminology preferred.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple priorities in demanding environments.
  • Strong technical aptitude and attention to confidentiality.

Relevant courses under eligibility: B.Pharm, M.Pharm, Pharm.D, M.Sc Biotechnology, M.Sc Life Sciences, M.Sc Biochemistry, M.Sc Microbiology, IT certifications in clinical/health informatics.

Location & Salary

• Location: Mumbai, India
• Work Model: Full-time, office or remote-office setting (flexible shifts as per business needs)
• Compensation: Competitive salary and benefits as per Fortrea’s standards

Application Process

Interested candidates can apply directly via Fortrea’s official careers portal:
Apply Here

Why Join Fortrea?

• Work with a global leader in clinical trial services.
• Gain expertise in data management and regulatory compliance.
• Collaborate with international pharmaceutical and biotech companies.
• Benefit from structured career growth and continuous learning.
• Play a crucial role in ensuring clinical trial data quality and patient safety.

FAQs

Q1: What qualifications are required for this role?
A degree in Life Sciences, Health Sciences, IT, or allied health professions, or equivalent experience.

Q2: How much experience is required?
At least 3 years in pharma, biotech, medical device, diagnostics, or clinical trial industries.

Q3: What skills are desirable?
Knowledge of ICH-GCP, clinical trial data management, Microsoft Office proficiency, and strong organizational skills.

Q4: Is this role office-based?
Yes, the role is primarily office-based in Mumbai, with flexibility for shifts as per project needs.

Q5: How do I apply?
By submitting your application through Fortrea’s official careers portal (link above).

Summary Table

Executive Regulatory Affairs Vacancy for M.Pharm at Sun Pharma Baroda

Apply for Executive – Regulatory Affairs role at Sun Pharma in Baroda. Openings for M.Pharm graduates with 2–5 years’ experience. Apply today!

At Sun Pharmaceutical Industries Ltd, we believe in helping professionals “Create their own sunshine” by providing opportunities for growth, leadership, and collaboration. If you are passionate about regulatory affairs and committed to ensuring compliance for global product approvals, this role offers an excellent opportunity to advance your career in a supportive and innovative environment.

Company Overview

Sun Pharma is India’s largest pharmaceutical company and the world’s fourth-largest specialty generic pharmaceutical manufacturer. With operations in over 100 countries, Sun Pharma delivers high-quality, affordable medicines across multiple therapeutic areas. The company thrives on innovation, regulatory excellence, and a mission to improve healthcare outcomes globally.

At Sun Pharma, employees experience a culture of collaboration, innovation, and continuous improvement. The R&D Regulatory Affairs team plays a pivotal role in ensuring that the company’s diverse drug portfolio meets international regulatory requirements.

Job Role & Responsibilities

As an Executive – Regulatory Affairs (RA), your key responsibilities will include:

1. New Submissions:

• Collaborate with Product Development and cross-functional teams to ensure compliance with country-specific regulatory requirements.
• Review and approve documents on behalf of regulatory during drug product design and development.
• Prepare and submit high-quality dossiers for faster product approvals.
• Submit meeting packages and participate in scientific discussions with regulatory agencies.
• Anticipate deficiencies and create effective mitigation plans.

2. Approvals:

• Prepare and submit timely responses to deficiencies to facilitate product approvals.

3. Lifecycle Management of Approved Products:

• Prepare and submit annual reports and renewals on time.
• Evaluate, prepare, and submit regulatory variations or supplements impacting product supplies.
• Ensure compliance with regulatory decisions for change management in DF plants.
• Maintain accurate product information in the central repository.

4. Self-Development:

• Stay updated with evolving regulatory guidelines.
• Participate in training sessions and deliver presentations.

Eligibility / Qualifications

Educational Requirements:

• Master’s degree in Pharmacy (M.Pharm)

Experience:

• 2–5 years of experience in Regulatory Affairs within the pharmaceutical industry.

Desired Skills:

• Strong knowledge of global regulatory guidelines.
• Ability to prepare and review regulatory dossiers.
• Strong communication, documentation, and compliance skills.
• Proactive problem-solving and cross-functional collaboration abilities.

Location & Salary

• Location: Baroda (Tandalja – R&D)
• Job Type: Full-time | R&D1 Regulatory Affairs Unit
• Job Grade: G12A
• Travel: Not applicable
• Salary & Benefits: Competitive salary package with healthcare benefits, career development opportunities, and growth-oriented culture.

Application Process

Interested candidates can apply through the official Sun Pharma careers portal. Don’t miss the chance to join India’s largest pharmaceutical company.

👉 Click here to apply now

FAQs

1. Who can apply for this role?
M.Pharm graduates with 2–5 years of regulatory affairs experience in the pharmaceutical industry.

2. What does the role involve?
Preparation and submission of regulatory dossiers, lifecycle management of approved products, and ensuring compliance with global regulatory standards.

3. What is the career growth potential at Sun Pharma?
Sun Pharma offers excellent opportunities for growth in regulatory affairs and global exposure to international filings and compliance systems.

4. Is travel required for this position?
No, this role does not require travel.

5. How can I apply?
Apply via the official Sun Pharma Careers Website.

Job Summary Table

Senior Medical Writer Vacancy at Syneos Health (Remote India)

Apply for Senior Medical Writer role at Syneos Health. Openings for MSc/M.Pharm graduates with 3+ years of experience. Remote opportunity in India.

Do you enjoy transforming complex scientific data into clear, compelling narratives? If yes, Syneos Health is offering a remote Senior Medical Writer role in India—a perfect opportunity to grow your career in medical communications and contribute to advancing healthcare innovation globally.

Company Overview

Syneos Health is a leading global professional services organization designed to accelerate biopharmaceutical success from the lab to life. With its medical communications arm, Cadent Medical Communications, Syneos Health specializes in developing high-science, peer-to-peer medical communications. The company bridges the gap between data and actionable insights by creating impactful narratives for healthcare professionals.

Syneos Health combines expertise in medical communications, clinical research, data science, and digital innovation to deliver integrated strategies that help life sciences companies succeed in today’s dynamic healthcare landscape.

Job Role & Responsibilities

As a Senior Medical Writer, you will be responsible for producing high-quality, scientifically accurate content to support medical communications and publications. Your key responsibilities include:

• Developing peer-reviewed publications, slide decks, and scientific deliverables aligned with client strategy.
• Ensuring scientific accuracy of deliverables through data and fact checks.
• Conducting detailed literature searches using databases like PubMed and EMBASE.
• Supporting medical affairs by conducting gap analyses, KOL mapping, competitor benchmarking, and compiling reports.
• Collaborating with global medical writing teams for document review, approval, and availability.
• Managing compound-related queries including editing, approval, and scientific validation of responses.
• Maintaining medical information systems, literature libraries, and evidence repositories.
• Compiling published data for responses to regulatory authorities and medical inquiries.
• Performing additional scientific and medical writing tasks as required.

Eligibility / Qualifications

Educational Requirements:

• Master’s degree in Science, Pharmacy, or equivalent (MSc, M.Pharm, Life Sciences, Biotechnology, Pharmacology, or related fields).

Experience Required:

• Minimum 3 years of clinical research or medical writing experience.

Technical Skills:

• Strong command of Microsoft Office (Word, Excel, PowerPoint).
• Expertise in medical literature databases (PubMed, EMBASE).
• Strong analytical, research, and communication skills.

Preferred Attributes:

• Detail-oriented with the ability to translate complex science into engaging communication.
• Team player with global collaboration experience.
• Problem-solving and strategic thinking mindset.

Location & Salary

• Location: Remote (India)
• Job ID: 11154
• Job Type: Full-time | Medical Communications
• Salary: Competitive, based on experience
• Work Environment: Flexible, remote-first, family-oriented culture promoting work-life balance

Application Process

If you are passionate about medical writing and want to join a global leader in healthcare communications, apply now through the official Syneos Health careers portal.

👉 Click here to apply now

FAQs

1. Who can apply for this role?
Candidates with MSc, M.Pharm, or equivalent degrees and at least 3 years of experience in medical writing or clinical research.

2. What type of work does a Senior Medical Writer handle?
You will create peer-reviewed publications, slide decks, and high-science communications for healthcare professionals.

3. Is this a remote role?
Yes, this position is fully remote and open to applicants across India.

4. What skills are most valued?
Scientific writing expertise, literature search skills, regulatory knowledge, and strong communication.

5. How can I apply?
Submit your application via the official Syneos Health Careers Portal.

Call to Action

Join Syneos Health and make an impact in medical communications while advancing your career in a global organization. Apply today to contribute to translating complex science into meaningful healthcare solutions.

Apply now before the application windo

Senior Publication Writer Vacancy – 5+ Yrs Exp – SIRO Medical Writing Pvt. Ltd.

Apply now for Senior Publication Writer at SIRO Medical Writing Pvt. Ltd. | 5+ years experience in manuscript & scientific writing | Great career growth.

Join SIRO Medical Writing Pvt. Ltd., a trusted name in scientific and medical writing, as a Senior Publication Writer. If you have proven expertise in manuscript development and corporate publication writing, this opportunity offers excellent career growth in a globally recognized environment.

Company Overview

SIRO Medical Writing Pvt. Ltd. is part of SIRO Clinpharm, a global clinical research and medical writing services company. With decades of experience, SIRO is known for its commitment to high-quality scientific communication, regulatory compliance, and publication excellence. The company partners with top pharma and life sciences organizations worldwide, ensuring its employees get international exposure and a platform to make an impact in healthcare advancement.

Job Role & Responsibilities

As a Senior Publication Writer, you will:

• Develop, review, and edit manuscripts for peer-reviewed journals.
• Collaborate with cross-functional teams, including researchers and regulatory specialists, to ensure accurate and compliant content.
• Prepare abstracts, posters, and scientific presentations.
• Adhere to international publication guidelines (ICMJE, GPP3, CONSORT).
• Ensure clarity, consistency, and scientific integrity in all deliverables.
• Manage end-to-end publication projects with minimal supervision.
• Address reviewer comments and support re-submissions.

Eligibility / Qualifications

• Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or related fields (M.Pharm, PhD, MSc, MBBS preferred).
• Experience: Minimum 5 years of corporate or industrial experience in manuscript writing, publications, or medical/scientific writing.
• Key Skills:
  • Strong command of scientific writing and English grammar.
  • Knowledge of clinical research, publication ethics, and journal requirements.
  • Expertise in referencing tools (EndNote, Mendeley, Zotero).
  • Familiarity with statistical concepts and data interpretation.

Location & Salary

• Location: Flexible/Hybrid with office base at SIRO Medical Writing Pvt. Ltd.
• Salary: Competitive package aligned with industry standards and experience.

Application Process

Interested candidates can apply via email:

Send your CV to: veda.dhamankar@siroclinpharm.com
Use subject line: Application for Senior Publication Writer

Apply at the earliest to secure your chance to join one of the leading teams in medical writing.

FAQs

Q1: Who can apply for this role?
Candidates with at least 5 years of experience in scientific/medical writing and a degree in life sciences are eligible.

Q2: Is this role open for remote work?
Yes, SIRO offers flexible and hybrid work models depending on project requirements.

Q3: What career growth can I expect?
Successful candidates will have opportunities to grow into leadership roles, manage global publication projects, and work with international clients.

Q4: What type of publications will I be working on?
Peer-reviewed journal manuscripts, abstracts, posters, presentations, and scientific documents aligned with pharma and clinical research projects.

Summary Table