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 15.0 Year(s)
Not Disclosed by Recruiter
Position: Associate - (Formulation Development – OSD Oral Solid Dosage)Work location: MDC AndheriWorking days: 5 days/weekWork timings: 8.5 Hrs.Contract: Auto renewablePayroll: Talisman staffingExperience Required: 1–2 years in formulation development (Tablets & Capsules)
Education: M.Pharm
Key Responsibilities:
Work on OSD (Oral Solid Dosage) manufacturing activities within R&D, including formulation development of tablets and capsules
Adhere to site-specific Standard ...
1 Opening(s)
5.0 Year(s) To 6.0 Year(s)
7.00 LPA TO 8.50 LPA
Job Title: Sr. Executive/Manager – Production Planning
Company: Concept Pharmaceuticals Ltd.Location: Aurangabad, MaharashtraExperience: 5+ YearsCTC: Negotiable ( based on interview & experience )
About the Company
Concept Pharmaceuticals Ltd. is a leading pharmaceutical manufacturing company committed to delivering high-quality healthcare products that meet global standards. With a strong focus on innovation, quality, and customer satisfaction, we continue ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 4.80 LPA
Position: QC Executive
Location: Daman
Experience: 5 - 7 Years
Industries: Pharma
Responsibilities:
Incoming Material Inspection
Inspect and test incoming raw materials, packaging materials, and components as per approved specifications and sampling plans.
Communicate non-conformances to the supplier and QA & Purchase department.
In-Process Quality Control
Perform in-process checks during production (e.g., dimensional ...
1 Opening(s)
6.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 15.00 LPA
Position: R&D Manager
Location: Silvassa
Experience: 6 - 12 Years
Industries: Pharma
Responsibilities:
Strong technical knowledge of emulsion systems, surfactants, actives, preservatives, and sensorial formulation.
Skilled in technical documentation, dossier creation, and regulatory alignment.
Excellent client communication and presentation skills — ability to translate science into a market story.
Commercial ...
2 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 6.00 LPA
Key Responsibilities:
Handle QMS activities including CAPA, Change Control, Deviation, and OOS/OOT.
Prepare, review, and maintain QMS documentation as per cGMP and regulatory guidelines.
Support internal audits, external audits, and regulatory inspections.
Ensure timely closure of quality incidents and continuous improvement initiatives.
Coordinate with cross-functional teams for compliance and quality culture.
Requirements:
B.Pharm / M.Sc (Chemistry) with ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 7.00 LPA
Position: QC Executive
Location: Silvassa
Experience: 6 - 10 Years
Industries: Pharma
Responsibilities:
Analytical Testing:
Perform routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples using HPLC, GC, UV, IR, etc.
Conduct assay, dissolution, impurity profiling, and related substance testing as per pharmacopeial standards (USP, BP, IP, etc.).
Instrument Operation & ...