Centaur Pharmaceuticals Private Limited has business interest in Formulations, CRAM, API, CRO along with its own in-house R&D setup. Centaur ranks among India’s top 50 pharmaceutical companies by prescriptions (SMSRC) and by Stockistsales audit (AWACS AIOCD).
Job Title: Medical Representative (Management Trainee)
Job Summary:
The Medical Representative (MR) is responsible for promoting and detailing the company’s products to doctors, pharmacists, and other healthcare professionals in a specified geographical region. The MR plays a crucial role in increasing product awareness, driving sales, and providing product information to healthcare professionals.
Key Responsibilities:
- Promote Products: Visit doctors, clinics, hospitals, and pharmacies to promote and sell pharmaceutical products. Conduct detailed product presentations to healthcare professionals.
- Establish Relationships: Build and maintain strong, long-term relationships with key healthcare professionals including doctors, pharmacists, and medical staff.
- Achieve Sales Targets: Meet and exceed sales targets and performance metrics set by the company.
- Product Knowledge: Stay up-to-date with product information, industry trends, competitor products, and medical literature.
- Market Intelligence: Gather and report on competitor activities, customer feedback, and market trends to the management team.
- Medical Conferences and Events: Attend medical conferences, events, and seminars to enhance product knowledge and network with healthcare professionals.
- Reporting: Provide regular reports on sales activities, market feedback, and performance against targets.
- Sample Distribution: Distribute product samples to doctors and medical professionals to encourage product usage.
- Training and Development: Participate in ongoing training to remain knowledgeable about the latest industry developments, new products, and compliance standards.
Required Qualifications and Skills:
- Bachelor’s degree in Pharmacy, Life Sciences, or related field (a medical background may be preferred).
- Previous experience in medical sales, pharmaceutical sales, or a related field is an advantage.
- Strong communication and interpersonal skills.
- Knowledge of medical terminology and industry regulations.
- Self-motivated with a target-driven approach.
- Ability to work independently and as part of a team.
- Willingness to travel within a specified region.
Preferred Qualifications:
- Experience in promoting pharmaceutical products to healthcare professionals.
- A valid driver’s license (if required for the job).
Working Conditions:
- Field-based position with frequent travel within the designated region.
- May require evening or weekend work to attend medical conferences or events.
JOB DESCRIPTION- REGULATORY AFFIARS
Position: Asst. Manager
Qualification: M.Pharm /B.Pharm/M.Sc. having 8+ years’ experience in EU/ LATAM market
Job profile:
- Responsible for the designated regulatory projects with respective deadlines
- Expertise in authoring CMC documentation for EU MAA and post-approval submissions with hands-on experience on using eCTD software
- Good coordination skills with stakeholders on regular basis to source the documents in accordance with project timelines
- Review the documents against the Agency guidances assuring regulatory compliance
- Keep knowledge up to date about regulatory guidelines
- Manage administration of regulatory documentation and ensure the traceability of regulatory history (filing, archiving, database etc)
Position: Sr.Officer/ Executive
Qualification : M.Pharm /B.Pharm/M.Sc. having 4-6 years experience in US market
Job profile:
- Author and compile CMC documentation for ANDA filings and post-approval submissions
- Coordination with stakeholders on regular basis to source the documents in accordance with project timelines
- Review the documents against the FDA guidances assuring regulatory compliance
- Keep knowledge up to date with regard to regulatory guidelines
- Hands-on experience on using eCTD software
Position: Officer
Qualification : M.Pharm /B.Pharm/M.Sc. having 2-3 years experience in US market
Job profile:
- Author and compile CMC documentation for ANDA filings and post-approval submissions
- Coordination with stakeholders on regular basis to source the documents in accordance with project timelines
- Review the documents against the FDA guidances assuring regulatory compliance
- Keep knowledge up to date with regard to regulatory guidelines
- Hands-on experience on using eCTD software
Position: Asst. Manager/ Sr.Exexcutive
Qualification : M.Pharm /B.Pharm/M.Sc. having 8+ years experience in US market
Job profile:
- Responsible for the designated regulatory projects with respective deadlines
- Expertise in authoring CMC documentation for ANDA filings and all post-approval submissions
- Good coordination skills with stakeholders on regular basis to source the documents in accordance with project timelines
- Review the documents against the FDA guidances assuring regulatory compliance
- Keep knowledge up to date with regard to regulatory guidelines
- Manage administration of regulatory documentation and ensure the traceability of regulatory history (filing, archiving, database etc)
Position Vacant: PRODUCT MANAGER (2)
Job Description / Responsibilities
1. Analyzing the market, competition & conducting market research to identify opportunities, threats & key issues for Acute business.
2. Developing marketing strategies & programs to address key issues for Anti cold/ENT/Antibiotics Product portfolio.
3. Developing innovative & informative promotional programs for augmenting Field Force detailing efforts.
4. Controlling & monitoring expenses to maximize return on investment.
5. Coordinating across the Field Force and other departments to resolve various product related issues from time to time.
6. Extensive fieldwork to understand the market, evaluate implementation of strategies and monitor key competitor activities.
7. Participating as a team player in the Operating Plan every year.
Desired profile of the candidate
We currently have an opportunity for an experienced Marketer to join our flagship sales and marketing team.
In conjunction with Vice President, work to establish key-brands as next block-buster brands along with building stronger growth trajectory for their key brand: SINAREST® tablet.
The incumbent will be responsible for the successful delivery and marketing of company’s brands and services offerings, including:
Qualification: BSC/MSC/ B PHARMA /M PHARMA/MBA
Min.Exp. 2-4 years
Location of posting : MUMBAI
Research Associate – Bioanalytical
Qualification :- BSC/ MSC (Chemistry, Bioanalytical Science)
Experience :- 1 to 5 years
Preferably :- Male Candidates (Rotational Shifts)
Job Description :-
- Performs Bio-Analytical method development and validation for the quantification of drugs.
- Active involvement in method development of drug in biological matrix.
- To write and revise SOPs as per need and maintain awareness of and adherence to all current SOPs.
- Investigates and corrects analytical, instrumental, and procedural problems, if necessary in consultation with supervisor.
- To update team member about safety precautions during analysis.
- Subject Sample Analysis.
- Reporting to the Group Leader of day to day activities.
- Documents all the work and results of all assignments as required.
- Sets-up and ensure calibration of analytical systems and maintenance of respective instrument systems.
- Maintaining GLP in Laboratory.
- Compilation of raw data and their archiving after completion of final reports.
- Incurred Sample Re-Analysis.
Interested candidates kindly send your resume to the following email IDs: nrane@centaurlab.com & hrd@centaurlab.com
