M.pharma - PHARMA STUFF

Venus Remedies Urgent Hiring for Quality Assurance / Formulation & Development (Apply on WhatsApp)

April 29, 2024 by Ranjeet kashyap

Exciting Opportunity at Venus Remedies Limited!

Position: Jr. Research Associate / Sr. Executive / Executive

Department: Quality Assurance / Formulation & Development

Education: M.Pharm / B.Pharm

Experience: 1 to 5 Years

Salary: Not Disclosed

Location: Baddi

Company Overview: Venus Remedies Limited is a leading multinational pharmaceutical firm operating in 70 countries, renowned for its R&D focus and contributions to antimicrobial resistance.

Department	Position	Experience Required	Qualifications
Quality Assurance	Sr. Executive / Executive	2 to 5 Years	B.Pharmacy
Formulation & Development	Jr. Research Associate	1 to 3 Years	M.Pharma

Job Location: Baddi, HP

Requirements:

Exposure to injection plant operations is essential.

How to Apply:
Interested candidates can share their resume via:

Email: Hra_staff5@Venusremedies.Com
WhatsApp: 9882859675

Doctor of Philosophy (PhD) Program in Pharmaceutics

April 29, 2024 by Ranjeet kashyap

Location: Mahidol University Faculty of Pharmacy, Thailand
Application Deadline: May 31, 2024

Position: Doctor of Philosophy (PhD) Program in Pharmaceutics (International Program)

Department: Mahidol University Faculty of Pharmacy, Thailand

Education: Holders of a Master’s or Bachelor’s degree in Pharmacy

Job Description:
Join our comprehensive PhD program in Pharmaceutics, equipping you with advanced skills in pharmaceutical sciences. Apply by May 31, 2024.

Who Can Apply:

Program Plan	Eligibility
Plan 1.1	Research Only (Regular and Special Programs) – Holders of a Master’s degree in Pharmaceutics or related fields with at least one international research publication.
Plan 2.1 & 2.2	Coursework + Research (Regular Program Only) – Holders of a Master’s or Bachelor’s degree in Pharmacy, Pharmaceutics, or related fields.

Teaching Schedule:
Regular Program: Weekdays
Special Program: Weekdays (Out of Office Hours) and Weekends

Research Focus Areas:

Innovative Pharmaceutical Products and Drug Delivery Systems
Advanced Biomaterials
Novel Biopharmaceutical Evaluation Techniques
Advanced Manufacturing Process Engineering

Contact Details:
Program Director: Assoc. Prof. Dr. Satit Puttipipatkhachorn (Satit.Put@Mahidol.Ac.Th)
Program Secretariat: Assoc. Prof. Dr. Jiraphong Suksiriworapong (Jiraphong.Suk@Mahidol.Ac.Th)

Scholarship:
Full and partial scholarships available for Thai and international students.

Scan for more information & apply: [Insert QR Code]

Doctor of Philosophy Program in Pharmaceutics at Mahidol University Faculty of Pharmacy - Apply Now

ICON Hiring for Senior Pharmacovigilance Reporting Associate

April 28, 2024 by Ranjeet kashyap

Experience: Not disclosed

Salary: Not disclosed

Location: Not specified

About Us: Join ICON, where diverse teams empower us to advance patients’ lives through drug development.

Role Overview:
As a Senior Pharmacovigilance Reporting Associate, you’ll ensure timely and accurate safety reporting to stakeholders.

Apply Now

Key Responsibilities:

Responsibility	Qualifications/Experience
Submit SAE reports, periodic reports, line listings within project timelines	Bachelor’s degree in relevant field
Maintain understanding of safety reporting systems and SOPs	Experience in pharmacovigilance
Provide oversight to ensure compliance with regulatory requirements
Collaborate with project team members, clients, investigators, vendors
Maintain databases, prepare for audits and inspections
Mentor junior associates, participate in meetings
Maintain understanding of therapeutic areas

Benefits:

Competitive salary packages
Annual bonuses based on performance
Health benefits for employees and families
Retirement plans and life assurance
Professional growth opportunities

Equal Opportunity Employer: ICON is committed to a discrimination-free workplace.

How to Apply: Apply through the provided link.

Apply Now

[FRESHERS] Intas Pharmaceuticals Hiring for Regulatory Affairs, Finance, R&D, Research Scientist/ Sr Research Scientist

April 28, 2024 by Ranjeet kashyap

Company: Intas Pharmaceuticals
Experience: 3-12 Years
Education: MSC/MTECH/MPHARM Biotechnology
Location: Ahmedabad, India
Salary: Not Disclosed

Description:
Intas Pharmaceuticals invites professionals for Regulatory Affairs, Finance, R&D, and Research Scientist roles. Join our team and advance your career.

Opportunities:

Position	Department	Qualification	Experience
Senior Executive/Assistant Manager/Manager	Regulatory Affairs	MSC/MTECH/MPHARM Biotechnology	3-12 Years
Senior Executive	Finance & Accounts	ICWA Inter / MBA Finance	3-6 Years
Research Scientist	R&D ADL	PhD/MSC/MTECH Biotechnology	0-9 Years
Research Scientist/Senior Research Scientist	R&D Drug Product Development	M. Pharm	6-12 Years

Responsibilities:

Regulatory Affairs:

Prepare registration applications for global markets.
Maintain regulatory registrations and provide support for audits.
Stay updated with regulatory guidelines.

Finance & Accounts:

Process service bills and purchase requisitions.
Manage asset-related documents and conduct inventory management.

R&D ADL:

Conduct chromatographic and electrophoresis techniques.
Develop and validate analytical methods for biotherapeutic products.

R&D Drug Product Development:

Prepare and review protocols, reports, and SOPs.
Plan and execute drug product development studies and manage project timelines.

How to Apply:
Visit Intas Pharmaceuticals Careers to apply.

[Freshers Welcome] Clinical Research Associate Hiring at Trialcraft Pharma

April 28, 2024 by Ranjeet kashyap

Company: Trialcraft Pharma

Experience: Freshers | Salary: Not Disclosed

Trialcraft Pharma specializes in project management and clinical trial monitoring for pharmaceuticals.

Position: Clinical Research Associate (Freshers Welcome)

Department: Clinical Trials, Clinical Research

Education: B.Pharm, M.Pharm, M.Sc, B.Sc, Pharm.D, Life Sciences

Job Location: Not specified

Description:

Join Trialcraft Pharma as a Clinical Research Associate, where freshers are welcomed to contribute to clinical trials and research.

Qualifications:

Qualifications	Details
Proficiency in protocol development	Demonstrate expertise in developing clinical trial protocols and conducting research.
Familiarity with clinical operations and research methods	Understand clinical operations and research methodologies for effective trial management.
Strong analytical and problem-solving skills	Exhibit strong analytical abilities and critical thinking to address challenges in research.
Attention to detail and precision in work	Maintain keen attention to detail, ensuring accuracy and quality in all aspects of work.

Business Development Manager – Multiple Locations

April 28, 2024 by Ranjeet kashyap

Company: Biozenta Lifescience Pvt. Ltd.

Experience: 2-3 Years | Salary: Not Disclosed

Locations: Mohali, Delhi

Founded in 2018, Biozenta is a leading pharmaceutical manufacturing company specializing in antiviral, injections, pills, and cancer drugs.

Position: Business Development Manager (BDM)

Department: Business Development

Education: Bachelor’s Degree in Science, Marketing, or related field

Job Location: Mohali, Delhi

Responsibilities:

Responsibilities	Details
Develop and implement strategic sales plans	Achieve company goals by identifying new business opportunities and staying abreast of market trends.
Build and maintain strong client relationships	Foster partnerships with clients and stakeholders, ensuring excellent communication and rapport.
Collaborate with cross-functional teams to drive sales	Work collaboratively across departments to drive sales initiatives and meet targets efficiently.
Provide timely sales reports and forecasts	Generate accurate sales reports and forecasts, contributing to informed decision-making and strategy planning.

Biozenta Hiring for Business Development Manager Multiple Location

PV RA MW Coordinator – Work From Home

April 28, 2024 by Ranjeet kashyap

Company: Thermo Fisher Scientific

Experience: 1-3 years | Salary: INR 5-7 Lakhs

Education: B.Pharm, M.Pharm, M.Sc, B.Sc, Pharm.D

Location: Work From Home

Description:
Join our Clinical Research Services team at Thermo Fisher Scientific, supporting safety and regulatory document coordination with precision and confidentiality.

Responsibilities:

Responsibilities	Details
Review safety and regulatory documents	Ensure accurate processing and timely uploads to electronic trial master files.
Maintain document quality and confidentiality	Track data, redact sensitive information, and ensure compliance with IT security standards.
Coordinate project meetings and facilitate communication	Ensure effective collaboration and support project-specific training and audit readiness.
Manage project expenses and budget	Oversee expenses, manage translations, and ensure cost-efficiency while adhering to budget parameters.
Archive regulatory documents and submissions	Contribute to seamless information flow and compliance by archiving essential documents and submissions accurately.

Apply Now

[Freshers + Remote] BD Hiring in Regulatory Affairs BD

April 28, 2024 by Ranjeet kashyap

Company: BD
Experience: 0 – 3 Years
Education: B.Pharm, M.Pharm, M.Sc, B.Sc, Pharm.D
Location: Remote
Salary: Not Disclosed

Description:
Join BD’s Regulatory Affairs team remotely. Review labels, organize documentation, assist in regulatory activities, and maintain compliance.

Responsibilities:

Key Responsibilities
Review and approve labels, labeling, and promotional materials.
Collect and organize labeling documentation for review.
Perform gap analysis for labeling projects.
Assist in regulatory activities for US and OUS labeling.
Review protocols, reports, and articles for data support.
Draft and route SOPs, work instructions, and policies.
Stay current on advertising, promotion, and labeling regulations.
Support team meetings outside standard hours.

Skills & Competencies:

Excellent verbal and written communication skills.
Ability to analyze and interpret scientific, technical, and regulatory documents.
Attention to detail and adaptability to business priorities.
Proficiency in SAP, Microsoft Word/Excel/PowerPoint.
Efficient time management.

Apply Now

Join Whatsapp

[Freshers] Stanex Hiring in R&D, QC, HPLC – Urgent Needed / Trainee

April 28, 2024 by Ranjeet kashyap

Company: Stanex Drugs And Chemicals Pvt Ltd
Location: Hyderabad

Experience:

0 Years / Freshers

Salary:

Not Disclosed

Education:

B.Pharm, M.Pharm, M.Sc, B.Sc, M.Tech

Department:

Research & Development, Quality Control

About Stanex:
Stanex is a leading player in the pharmaceutical and healthcare space, aiming to become an integrated multinational pharmaceutical organization.

Position Overview:
Stanex is urgently hiring for the roles of R&D, QC, and HPLC Officer/Trainee. Freshers with the mentioned educational backgrounds are welcome to apply.

Benefits:

Competitive salary package
Opportunity to work in a reputable pharmaceutical company
Career growth prospects

Apply now and join Stanex in its mission to contribute to the healthcare industry.

Gracure Pharmaceuticals: Hiring Regulatory Affairs Executive/Manager in New Delhi,M.pharma

April 28, 2024 by Ranjeet kashyap

Anacipher: Hiring Biostatistician in Hyderabad

Experience: 3 to 16 Years

Salary: Not Disclosed

Education: M. Pharma Degree

Location: Moti Nagar, New Delhi

Position: Regulatory Affairs Executive/Manager

Department: Regulatory Affairs

Job Description:

Collaborate for timely regulatory approvals.
Develop cost-effective regulatory strategies.
Plan and execute regulatory activities.
Innovate strategies for dossier flexibility.

Requirements:

M. Pharma Degree
3 to 16 years of regulatory affairs experience

How to Apply: Send CVs to rajat.gupta@gracure.com and aakansha.agarwal@gracure.com