1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.00 LPA TO 3.00 LPA
Job responsibilities are to Assist Regulatory manager:
Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD,
ACTD as well as country specific format for countries
Preparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbal
products for country specific format in countries of African Region, Cambodia, Myanmar, CIS
To manage ...
2 Opening(s)
1.0 Year(s) To 2.0 Year(s)
1.44 LPA TO 2.40 LPA
URGENT OPENINGS FOR PHARMACIST POSITION AT KARJAT HOSPITAL
HOSPITAL STAFF (RECRUITMENT SERVICES AND STAFFING) 100% FREE JOB( India’s industry leader in Recruitment and Staffing of healthcare professionals over a decade)We have achieved global reputation for our standard employment assistance in the medical and healthcare domain.
LOCATION-KARJAT
SALARY 12K TO 20K
MALE/FEMALE ANY
FOR MALE-ROTATIONL SHIFT
FOR ...
2 Opening(s)
1.0 Year(s) To 2.5 Year(s)
2.40 LPA TO 3.50 LPA
Job Title: Pharmacist - Delhi Regsitered license Location: DelhiShift Timing: 11:30 AM 8:30 PMType: Full-time
Key Responsibilities:
Dispense medicines accurately as per doctors prescription
Maintain proper storage, labeling, and inventory of medicines
Ensure compliance with drug laws and clinic policies
Manage stock, expiry dates, and reorder levels
Provide basic guidance to patients on medication usage
Maintain pharmacy records and billing (if applicable)
Eligibility ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 3.60 LPA
Job Responsibilities :
Qualification:- Bsc/Msc/B.pharm/M.Pharm
Job profile:
1. Coordinate with various outsourced manufacturing sites for QA related work on daily basis
2. Maintain control samples as per SOP's
3. Coordinate artwork with designer and manufacturing site.
4. Artwork designing as per countries requirements
5. Coordination with FDCA liasoining agent for approvals
Job Types: Full-time, Permanent
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 3.60 LPA
Regulatory Affairs Officer (RA)
Qualification: B.Pharm/ M.Pharm
Experience: Minimum 3 years in regulatory affairs for the ROW (Rest of the World) market, with a total of 3 to 5 years of experience.
Job Description:
Preparing dossiers as per country-specific guidelines.
Compiling and reviewing documents.
Coordinating with QA for documentation.
Addressing queries raised by respective countries' FDA.
Bond: 18-month ...
5 Opening(s)
6.0 Year(s) To 9.0 Year(s)
Not Disclosed by Recruiter
Qualification:
Respiratory/Pain/Digestive Health/Skin Health: Bachelor's and Master’s in Pharmaceuticals/PhD/MBBS with relevant post-qualification experience in the scientific and business research space
Oral Health: Bachelor's in Dental Sciences (BDS) or M.Pharm with Oral Care/ Consumer health experience. Good understanding of Dental Sciences with robust domain knowledge; clinical experience with deep understanding of the oral ...
1 Opening(s)
1.6 Year(s) To 3.0 Year(s)
2.40 LPA TO 2.70 LPA
Hiring for MNC Pharma QA Officer ( IPQA)
POSITION : Officer
Education : B.Sc/M.Sc/D.Pharm/M.Pharm.
Experience : Min, 2+years from Pharma Industry.
Salary: 2,20,000/- to 2,60,000 LPA.
Location:- ( Aurangabad.)
Role & Responsibility
Checking and ensuring online completion of documents and line clearance activity.
To carry out line clearance activity at dispensing, manufacturing , & packaging
Performing Sampling activity like in process, ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.20 LPA TO 2.80 LPA
Job Location : Mahape, Nearest Station Ghansoli (Navi Mumbai)
Look for people from Navi Mumbai or Mumbai Only
Only Female Candidates required
Qualification : B.Pharm / M.pharm
Experience : 1yr – 3yr
Salary : 1.42lpa – 2 .80lpa
Profile :
Experience in preparing Dossiers in CTD, ACTD, Country Specific Dossiers.
Countries : ROW and Latum
Job Description:
Dossier Preparation along ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
Not Disclosed by Recruiter
CORE JOB RESPONSIBILITIES:
•Conduct comprehensive research of internal reports, scientific literature, databases, and regulatory documents relevant to formulation development, dosage forms, dissolution, biorelevant media, and drug disposition (ADME), pharmacokinetics (PK), pharmacodynamics (PD), pharmacology, and toxicology/toxicokinetics.
•Extract, curate, and critically evaluate data from tables, figures, and published sources; organize datasets into standardized formats ...