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22 April 2024

Hiring for regulatory affairs (US market) at Centaur Pharma - Experienced candidates only

Hiring for regulatory affairs US market; Expertise in authoring CMC documentation for ANDA filings and post-approval submissions with hands-on experience on using eCTD software. Review the documents against the FDA guidance assuring regulatory compliance
20 April 2024

Recruitment for Professor, Associate Professor, Assistant Professor at Santoshimata College of Pharmacy

Santoshimata College of Pharmacy was established in the year 2023 A/P Panhalsathe by a philanthropic society called Santoshimata Bahhudesiya Shaikshanik Seva Sanstha (SBSSS), Yeola. At present, this institution is offering B. Pharmacy, D. Pharmacy. The motto of our society is to provide quality education and training, which is achieved by providing state of the art infrastructural facilities and faculty.
Post : Professor, Assistant Professor, Associate Professor
20 April 2024

Job for M.Pharm, B.Pharm, MSc in Quality Assurance Department at Unison Pharmaceuticals

Unison Pharmaceuticals Private Limited was established in 1981 with a vision of providing quality & most affordable medicines across the nation. With more than 3 decades of medical service to the society, Unison is today one of the fastest growing company in Gujarat State. The base of operation being a single state, the company has very strong footing in the market. The company strictly believes in ethics and moral values throughout the operations of the business.
Quality Assurance Department
19 April 2024

Vacancy for M.Pharm, B.Pharm in Production Department at Leben Life Sciences

Leben Life Sciences Pvt. Ltd. (LLS) is an established pharmaceutical formulation company for more than four decades. LLS has following openings for its EU-GMP Approved Global Standard OSD & Semi-solids Formulation manufacturing facility at Akola (M.S.)
Production Department
Officer / Sr. Officer
Experience : 2 to 5 yrs
Section : Semi-Solids mfg. (Cream,Ointment & Gel)
Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. Today, Intas is present in more than 85 countries worldwide and is growing at 20% CAGR. Around 70% of its revenues come from the international markets, particularly the highly regulated markets of EU and US. At Intas, every day and everyone works to create a world of good health, happiness and hope.
Officer / Sr. Officer
Department : Parenteral (Sterile) Complex Skid / NDDS
Qualification : B.Pharma / M.Pharma
Experience : 2-5 Years
Skills : For Staff Level require good knowledge in "Complex Skid / NDDS
Technician
Department : Parenteral (Sterile) Complex Skid / NDDS / Aseptic / Manufacturing Clean Area / Lyphilizer/ Visual
Qualification : ITI / Diploma Eng / D.Pharma
Experience : 2-7 Years
Skills :
• For Technician Level require good knowledge in Skid / NDDS / Aseptic (PFS / Vials Liquid) / Manufacturing Clean Area / Lyphilizer /Visual Inspection.
Job Location : Intas Pharmez, Ahmedabad
Walk in Interview
Date : 25th April, 2024 (Thursday)
Time : 09:00 am
Venue : Intas Pharmaceutical Limited Plot no. 05 to 14, Pharmez, Near Village Matoda, Sarkhej - Bavla Highway 8-A, Taluka- Sanand, Dist- Ahmedabad.
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19 April 2024

Require Senior Research Scientist at Reliance Life Sciences

Reliance Life Sciences is a medical biotechnology-led company engaged in research and development, manufacturing and marketing of differentiated medical products and services, used to treat patients primarily in intensive and critical care units in hospitals. Three core businesses of RLS are plasma proteins, biosimilars, and later generation oncology pharmaceuticals. In addition, it has initiatives in clinical research, molecular medicine, regenerative medicine, genetherapy, peptides and oligonucleotides.
More than 30,000 Takeda employees working in more than 70 countries are committed to improving quality of life for patients, who remain at the center of everything we do. Takeda Pharmaceutical Company Limited is a global, research and development-driven organization working internally and with external partners to translate science into life-changing medicines. Takeda focuses on the core therapeutic areas of oncology, gastroenterology, neuroscience and providing vaccines that address the most important infectious diseases. Novel products, especially in oncology and gastroenterology, as well as our presence in emerging markets, fuel our growth.
Post : Senior Clinical Research Associate
Job Description
Objectives
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and Takeda requirements
Accountabilities :
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with study protocol and applicable regulatory requirements
• Work with CROs to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure site documents are available for filing in the Trial Master File (TMF) and verify that documents are maintained in accordance with GCP and local regulatory requirements
• Ensure 100% adherence to monitoring and study plan
• Support clinical quality in managing CAPAs and other study audit observations
• Support Clinical Operations Lead/ Clinical Operations Manager in performing CRO oversight as per agreed parameters
• Ensures adherence to study budget through constant monitoring for allocated study(ies)
• Ensures dissemination of study updates to relevant stakeholders as per agreed timelines
Candidate Profile
• Master’s or Ph. D degree in scientific discipline or healthcare with >5 years’ experience in clinical trials industry as Clinical Research Associate
• Good working knowledge of GCP and local clinical trial rules and regulations
• Organizational and problem-solving skills
• Superior communication, strategic, interpersonal, and negotiating skill
• Proven/ stable performance records over past 2-3 years
Additional Information
Experience : >5 years
Qualification : Master’s or Ph. D degree in scientific discipline or healthcare
Location : Mumbai, Maharashtra
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Research & Development
End Date : 20th May 2024
Apply Online
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19 April 2024

Work as Senior Clinical Scientist at Bristol Myers Squibb

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions.
19 April 2024

MSD looking for Specialist Quality

Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
Post : Specialist Quality
18 April 2024

Walk in Drive for M.Pharm, B.Pharm, M.Sc in Multiple Department at Sun Pharma - Only for Female

Sun Pharmaceutical Industries Limited is taking this opportunity to balance employment and the medications to the world. We arc hereby inviting candidates who are interested to join India's No. I company in Pharmaceutical sector.
Manufacturing / Packing (Parenteral)
Post : Technician to Senior Executive
Experience : 2-8 Years
Qualification : ITI/ Diploma/B.Pharma / M.Pharma