Sanket Bhardwaj

Company: Hetero DrugsLocation: TSIIC Pharma SEZ Polepally, Unit VI, Jadcherla, Mahabubnagar, Telangana 509202Date: 15th June 2024 (Saturday)Time: 9.00 a.m. to 2.00 p.m. QA Department Area of Work: QMS/ValidationsQualifications: B. Pharma/ M. Pharma/ M.ScPositions: Engineering Department Area of Work: Process Engineer/ Electrical Engineer/ Water System/ HVACQualifications: B.Tech/ DiplomaPositions: What to Bring: Note: Preferred for immediate joiners. … Read more

Associate Content Editor – Chemical Patent Abstraction Company: Clarivate Location: Noida, Uttar Pradesh Industry Type: Pharma / Healthcare / Clinical Research Functional Area: Intellectual Property Experience: 0-1 year Qualification: M.Pharm End Date: 20th June, 2024 Responsibilities: Candidate Profile: Additional Information: Application Deadline: 20th June, 2024 Apply Online>>>

Date Posted: 13 June 2024Location: BangaloreIndustry: Pharma / Healthcare / Clinical ResearchApplication Deadline: 20th June 2024 About AstraZeneca: AstraZeneca is a leading global biopharmaceutical company, with a meaningful impact on the UK economy through significant investments in jobs and wealth creation. A report commissioned in 2009 highlights AstraZeneca’s contributions beyond its medicines, including the economic … Read more

Positions: Qualifications: Experience: Responsibilities: Quality Assurance: Production: Job Location: Interview Details: Additional Information: Company Overview: For further details, attending the walk-in interview as specified is recommended.

Interested candidates are requested to share their CVs to devalmodi@torrentpharma.com by the 30th of June 2024

Positions Open for Regulatory Affairs Expert: 1. US Market – Post Approval 2. US Market – CMC 3. EU Market – Module 3 4. EU Market – Module 1 Job Location APL Research Centre -1, Sy No. 313 & 314, Bachupally, Hyderabad Application Details For further details or to apply, please reach out to the … Read more

The Safety Science Specialist will manage the receipt and processing of all adverse event reports, both spontaneous and solicited from clinical trials. This role involves data entry, review of adverse events, writing patient narratives, coding adverse events, and ensuring compliance with regulatory requirements. Key Responsibilities: Application Link

Available Positions Job Location Documents Required Contact Information Walk-in Interview Details This is a great opportunity for individuals with relevant qualifications and experience in pharmaceutical production, quality assurance, quality control, engineering, and warehouse management. Don’t miss out on the chance to work with one of the leading pharmaceutical companies. Make sure to bring all required … Read more

Job Responsibilities Apply Online>>>

Positions Available Quality Control (Microbiology) : Officer to Sr. Executive Qualifications: M.Sc. (Microbiology)Experience: 2 to 5 years in injectable dose forms.Skills Required: Quality Control (Investigator) : Asst. Manager/ Dy. Manager Qualifications: B.Sc./ M.Sc./M.TechExperience: 8-12 years in biotechnological products investigation and planning.Skills Required: Quality Control (Analyst-Biotech): Officer / Executive Qualifications: B.Sc./ M.Sc./M.TechExperience: 2-6 years in biotechnological … Read more