235 Pharmaceutics Jobs

Production Manager (Tablets, Capsule, Liquid and Ointment) Job description Approval Tablets, Capsule, Liquid and Ointment Experience 15 Yrs and Above Role & responsibilities : Thorough Knowledge of formulation manufacturing. The role involves managing production teams Optimizing processes, and ensuring efficient and safe production workflows Manage day-to-day production operations, ensuring timely and efficient manufacturing. Ensure compliance with GMP, safety, and environmental regulations. Timely getting work done as per planning Troub le shooting and managing all aspect of production. Reporting to Plant Head. Interested send their updated resume to Email Id hrd.recruitmentconsultants@gmail dot com & WhatsApp or Call - 9.2.1.1.6.1.8.4.4.8 / 9.7.1.7.2.2.1.3.8.9

As a Senior Team Leader / Senior Group Leader at Syngene located in Bangalore within the Biopharmaceutics department, you will be part of an innovation-focused global discovery, development, and manufacturing organization. Syngene International Ltd., established in 1993, offers integrated scientific services to various industries worldwide, including pharmaceuticals, biotechnology, nutrition, animal health, consumer goods, and specialty chemicals. Collaborating with renowned clients such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife, you will lead a team of scientists in developing preclinical and clinical formulations of new chemical entities (NCEs). Your responsibilities will include providing scientific leadership in the Pharmaceutics domain to identify clinically developable drug candidates through pre-formulation activities such as physicochemical characterization and polymorphism. You will lead projects and guide the team in developing formulations for pre-clinical studies, GLP toxicology studies, Phase I (FIH), and Phase II clinical studies. A good understanding of drug degradation mechanisms, biopharmaceutics risks, novel drug delivery systems, and analytical principles will be essential in your role. To qualify for this position, you should hold a Ph.D. or Post-Doctorate in Pharmaceutics, Industrial Pharmacy, Pharmaceutical Technology, or related fields with 9-17 years of relevant industrial experience. Your technical skills should encompass Pharmaceutics, Physical Pharmacy, Dosage Form Design, Drug Delivery, Chemical Degradation, and Biopharmaceutics. Moreover, your behavioral skills should demonstrate leadership abilities, effective collaboration in matrix teams, excellent communication skills, and the capacity to mentor team members. Syngene is an Equal Opportunity Employer committed to fostering a diverse and inclusive work environment where individuals are empowered to contribute their best towards achieving project objectives.,

Aster Medcity is looking for Pharmacist Pharmacy to join our dynamic team and embark on a rewarding career journey Reviewing and interpreting prescription ordersPreparing and dispensing medicationsAdvising patients on the safe and effective use of their medications, including potential side effects and interactionsMonitoring patients for adverse reactions and ensuring that any necessary changes to their medication regimen are made in a timely mannerKeeping accurate and up-to-date records of patients' medication history and any adverse reactionsCollaborating with other healthcare professionals to provide comprehensive care to patientsStaying current on developments in the field of pharmacology and medication therapy

Responsible for Pharmacy Sales, Purchase, Inventory & Team Management Oversee the overall operations of the pharmacy, ensuring safe and efficient dispensing of medications. Supervise and manage pharmacy staff, including pharmacists, technicians, and support staff. Ensure compliance with all regulatory requirements (e.g., FDA, CDSCO, local drug control authorities). Monitor inventory levels, place purchase orders, and manage stock to avoid shortages or expiries. Implement and monitor SOPs for drug storage, dispensing, labeling, and documentation. Maintain accurate records of prescriptions, controlled substances, and billing. Provide guidance on drug usage, interactions, and dosages to patients and healthcare providers. Train and mentor new team members, ensuring adherence to safety and quality standards. Coordinate with doctors, nurses, and other departments for smooth operations. Address customer or patient complaints professionally and promptly.

Responsibilities of a Medical Representative: Client Meetings Sales Target Achievement Product Information Dissemination Documentation and Reporting Handling Objections & Queries Event Participation Annual bonus Travel allowance Performance bonus Sales incentives

Work with doctor at community center Dispense medicines as per prescription Counsel patients on dosage and usage Maintain stock and records Ensure proper storage and handling of medicines Required Candidate profile Fresher pharmacist required Must have valid Karnataka pharmacist license Work with doctor at community center Dispense medicines as prescribed Counsel patients on dosage Manage stock and storage

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols. Should have knowledge in Clinical Data Management EDC Edit Checks SAE Reconcillation Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

We have urgent vacancies for pharmacist and sr. pharmacist for TATA 1 mg @Bigbasket in Chennai. Job Description Designation: Pharmacist & Sr. Pharmacist Job Locations- Mugalivakkam, Navalur, Medavakkam, Virugambakkam, Thoraipakkam, West Tambaram Key Responsibilities: . Customer support and prescription validation . OTC order processing and clarification calls . Inventory and order management . Picking, packing, and handover to delivery riders . Cash-on-delivery (COD) cash handling . Root Cause Analysis for delayed orders . Stock receiving, audits, and shrinkage control . Store operations and manpower coordination . End-to-end store and customer fulfillment management Preferred Qualifications: . Pharma or B. Pharma with valid state license . 1- 3+ years of pharmacist experience . Proficient in MS Office and system tools . Strong communication skills in English,Tamil. . Comfortable with shift and weekend work . Experience in team and inventory management.

Role & responsibilities Dispense medications to patients according to prescriptions and provide guidance on usage. Maintain accurate records of patient interactions, including medication dispensed and dosage instructions. Monitor inventory levels of pharmaceuticals and manage stock accordingly. Provide counseling to patients about their medications, including potential side effects and interactions with other drugs. Ensure compliance with regulatory requirements for handling controlled substances Preferred candidate profile D/B/M PHARMACY SSC - ANY DEGREE WITH RETAIL PHARMACY EXPERIENCE

As an Assistant Professor/Professor in a Pharmacy college located in Poonamallee, Chennai, you will be responsible for delivering high-quality education in the field of Pharmacy. If you are interested in this opportunity, please forward your profile to hrasst2@ssiet.in. The ideal candidate for this position should possess an M.Pharm with Ph.D/Pharm.D qualification. For the role of Pharm.D, a minimum of 3 years of experience is required. As an Assistant Professor in Pharmacognosy/Pharmaceutics, you should have at least 3 years of experience. For the position of Professor in Pharmaceutics, Pharmacology, or Pharmaceutical Chemistry, a minimum of 10 years of experience is preferred. This is a permanent position with a day shift schedule. Immediate joiners are preferred. The educational requirement for this position is a Master's degree, and candidates with relevant work experience of 3 years are preferred. If you are interested in joining our team and meet the qualifications mentioned above, we encourage you to apply. Thank you for considering this opportunity.,

Dear Candidate, Greetings from Medplus.. About Company :- Medplus - India's Largest Organized Pharmacy Retail Chain. We are immediately hiring freshers for the role Pharmacy Aide/Customer Service Associate(CSA) in Medplus Pharmacy . Qualification required:- Min 12th/Diploma/Any Arts UG Degree/B.Pharm/D.Pharm. Experience required :- Freshers or Experienced any one can apply. Work Location :- Chennai(Nanganallur/Keelkattalai/Tambaram/Kundrathur/S.Kolathur/Kovilambakkam/Urapakkam) Interested candidate can call or WhatsApp the resume to Karthick HR Mobile No :- 9789747555 Thanks, Karthick HR Medplus 9789747555

Job Title: Intern CMC (Formulation) Duration: 12 Months (1 year) Location: Hyderabad Department: CMC (Formulation) Reporting To: Lead Scientist - CMC (Formulation) Stipend: Paid Qualifications: Master s degree in Pharmaceutical Sciences (Pharmaceutics) or related discipline from a reputed institution. Strong academic background in pharmaceutics Basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) is an advantage. Proficient in MS Office (Word, Excel, PowerPoint) and scientific writing. Excellent communication, organizational, and problem-solving skills. Position Summary: The Formulation R&D Intern will support the development of pharmaceutical dosage forms through hands-on laboratory work, data analysis, and documentation. This internship is designed to provide comprehensive exposure to formulation science, regulatory requirements, and industrial practices in a dynamic and collaborative environment. Key Responsibilities: Formulation Development: Assist in the design and optimization of formulations for various dosage forms including tablets, capsules, suspensions, emulsions. Conduct pre-formulation studies such as solubility, pH stability, hygroscopicity, and compatibility testing. Participate in excipient selection and formulation trials based on physicochemical properties and target product profile. Laboratory Work: Prepare lab-scale and pilot-scale batches under supervision. Operate and maintain laboratory equipment such as mixers, granulators, tablet presses, and dissolution testers. Documentation & Compliance: Maintain accurate and detailed laboratory notebooks and batch records. Prepare technical reports and summaries of experimental findings. Ensure compliance with Good Laboratory Practices (GLP) Cross-Functional Collaboration: Work closely with Analytical R&D, Quality Control, Regulatory Affairs. Participate in project meetings and contribute to formulation strategy discussions Location: Ferring India FHPDC R

Applications are invited for the post of Project Research Scientist I ( Non-Medical ) for the Indian Council of Medical Research (ICMR) funded project in School of Bio Sciences and Technology, Vellore Institute of Technology (VIT) Vellore- 632014, Tamilnadu. Title of the Project : 3D printed nano-engineered sublingual patch with viral-mimetic nanoparticles for non-invasive delivery of Insulin Qualification (Essential) : First Class Post Graduate Degree, including the integrated PG degree in Nanomedicine / Pharmaceutics / Nano-formulations / Chemical engineering/Chemistry and other related fields. Qualification ( Desirable) : Candidates with Ph.D., having hands-on experience in the area of nano-formulations / drug delivery systems esp. lipids / polymers-based nanoparticulate systems will be preferred. Candidates with above research area with animal handling experience will be given high preference. Stipend : Rs. 56,000/- + 10 % HRA per month Sponsoring Agency : Indian Council of Medical Research (ICMR) Duration : 1 year extendable to one more year maximum based on the performance of the candidate. The post is temporary and co-terminus with the duration of the project. Principal Investigator Co-Principal Investigators : : Dr. Sankar Ganesh Devaraj, Assistant Professor Senior, School of Bioscience and Technology (SBST), Vellore Institute of Technology Vellore- 632014, Tamilnadu. Dr.Arunkumar Palaniappan, PhD, MRSC. Associate Professor, Department of Biotechnology, BITS Pilani - Dubai Campus, Joint Appointment with Department of Pharmacy, BITS Pilani -Hyderabad Campus. Dr. Sunil P M., Director, Centre for Stem Cells and Regenerative Medicine Oral and maxillofacial pathology, Sri Anjaneya institute of Dental Sciences. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (30/07/2025) through online http://careers.vit.ac.in To apply online http://careers.vit.ac.in , Indicate project title, and the post applied for in the application. No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date, which will be intimated by email. The selected candidate will be expected to join at the earliest. JOB Location: VIT Vellore, Tamil Nadu.

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols Recruit, screen, and enroll study participants while maintaining accurate documentation and records Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Clin Infotech is offering the internship opportunity for BDS MDS Dental Graduates Should have Knowledge in Pharmacovigilance Should Have knowledge on Argus & MEDDRA Applicants Should Complete Certification in Pharmacovigilance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Clin Infotech is offering internship Opportunities for B.Pharm and M.Pharm Freshers who are willing to start a career in Clinical Research Pharmacovigilance clinical data management sas Medical writing and Medical coding Required Candidate profile Clinical Research Internship includes of Hands on Experience on softwares in Clinical Research Pharmacovigilance clinical data management Domain. B.Pharm M.Pharm and Pharm D Are Eligible to Apply

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Urgent Walk in For M.Pharmacy fresher Completed Clinical Data Management Training only Eligible CDM Certification is Mandatory Knowledge of Clinical Data Management Plan, study phase conduct phase and Close out phase Required Candidate profile Strong knowledge of cGMP and relevant regulatory requirements: This includes understanding manufacturing processes, quality control procedures, and validation requirements.

Manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. Conducts research to ensure these products are safe. Ordering, tracking, and managing IP and trial materials. Required Candidate profile Knowledge of the pharmaceutical industry, terminology, and practices. - Knowledge of FDA regulations and their practical implementation. - Strong verbal and written communication skills.

This position requires a sound knowledge of medical coding and the denial management process for multiple specialties. Applicants must be proficient in ICD-10 and CPT medical coding and have obtained a Certified Professional Coder (CPC) credential Required Candidate profile Should have strong knowledge In Medical Coding Anatomy Physiology and Medical Terminology Should have Good Communication Skills

We are currently hiring for DSA I role with a minimum of 1 year experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Required Candidate profile A minimum of 1 year pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT) are Eligible

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Perform triage & intake of ICSR received daily in ARGUS databases within the agreed timelines Processing literature, spontaneous clinical trial and solicited cases Responsible for coding events, indications and patient history based on MEDDRA Required Candidate profile EDUCATION: M.Pharm/Pharm D/Life sciences / Microbiology / Biotech /Biochem /Nursing / BDS EXPERIENCE: Strong Knowledge in pharmacovigilance With Certification or its equivalent.

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.