10 Opening(s)
4.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 14.00 LPA
CFD & Moldflow
Job ID : 410001
Experience : 4 - 10 Years
Qualification : B.E. /B. Tech or ME /M.Tech (Mechanical, Aero, Automobile, Thermal)
Location : Chennai
No of Positions : 03
Skill Set : CFD, STAR CCM+, Preon LAB, SIMERICS
Domain : Automotive
CTC Range : 14 LPA
Job Description:
Familiarity with the 3D CFD ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
5.00 LPA TO 7.00 LPA
Job Description – R&D Parenteral (Formulation) Specialist
Company: Concept Pharma Pvt. Ltd. Position: R&D Parenteral (Formulation) Specialist Experience: 2–5 Years CTC (Budget): Negotiable Location: Aurangabad
Key Responsibilities
Support the R&D team in formulation development of parenteral products, including Small Volume Parenterals (SVP) and Large Volume Parenterals (LVP) in both powder and liquid dosage forms.
Perform sterile ...
2 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 2.50 LPA
We are hiring a Junior Microbiologist in Ahmedabad.🔬 We’re Hiring | Jr. Microbiologist📍 Changodar, Ahmedabad | 🕒 Full-time
🎓 Qualification: B.Sc / M.Sc (Microbiology / Biochemistry / Biotechnology)💼 Experience: 0–1 year (Freshers welcome)💻 Skills: Basic computer knowledge🗣 Languages: Hindi & English
🔍 Key Responsibilities:✔ QC analysis & routine microbiological testing✔ Lab equipment ...
2 Opening(s)
1.0 Year(s) To 7.0 Year(s)
Not Disclosed by Recruiter
Responsibilities:
Independently plan, execute, and monitor laboratory-scale reactions for new product development or process improvement.
Troubleshoot reaction-related issues and optimize parameters to achieve desired yields and purity.
Conduct analytical testing using spectroscopy techniques (IR, NMR, UV, etc.) and interpret data for structural confirmation.
Maintain detailed experiment records, observations, and analytical results in lab notebooks.
Support ...
1 Opening(s)
0 To 1.0 Year(s)
2.00 LPA TO 2.40 LPA
Position: QC Officer
Location: Daman
Experience: 0 - 1 Years
Industries: Engineering
Responsibilities:
Quality Lab testing
Moulding expereince prefered
Colour Matching
Audit documentation
Spectra lab, Calibration of Spectra meter & Other Instrument.
Process control in Production.
Sample testing (Inward Raw material & In-process sample test )
Responsible for maintaining all ISO standards Documentation ...
3 Opening(s)
1.5 Year(s) To 6.0 Year(s)
3.00 LPA TO 7.00 LPA
Key Responsibilities:
1. Method Development & Validation
Develop analytical methods for assay, dissolution, related substances, and stability testing.
Conduct method validation as per ICH guidelines (accuracy, precision, specificity, linearity, robustness).
Optimize and troubleshoot existing analytical methods.
2. Instrument Handling
Operate analytical instruments such as HPLC, GC, UV, FTIR, KF, Dissolution Apparatus, etc.
Perform daily calibration and ensure ...
3 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 6.00 LPA
Process standardization – Carry out lab trails and pilot plants trails to fine tune the process.Scale up of process from pilot scale to commercials plant scalePrepare standard operating proceduresStudy deviations plant batches and rectifications.To carry out lab experiments for synthesis of various products.Carry out testing (e.g. acid value, OH value, ...
4 Opening(s)
1.0 Year(s) To 8.0 Year(s)
1.50 LPA TO 6.00 LPA
Key Responsibilities:
Analytical Operations:
Perform routine and non-routine analysis using HPLC, GC, UV and other instruments.
Conduct and support analytical method validations as per regulatory requirements.
Review and approve analytical data, test reports, and batch release documents.
Ensure proper calibration and qualification of laboratory instruments.
QMS & Compliance:
Manage Quality Management System (QMS) activities including:OOS, Deviations, CAPA, ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
2.40 LPA TO 5.00 LPA
The Project Coordinator is responsible for planning, tracking, and coordinating pharmaceutical laboratory projects across departments such as R&D, Quality Control, Regulatory Affairs, and Production. The role ensures timely execution of tasks, documentation, and compliance with industry standards and project deadlines.
🎯 Key Responsibilities:
Coordinate day-to-day activities of pharmaceutical lab projects (R&D, method ...
1 Opening(s)
13.0 Year(s) To 22.0 Year(s)
Not Disclosed by Recruiter
Roles & Responsibilities:
Responsible for overall performance and day to day activities of quality control dept.
Overall supervision of quality control activities during incoming material, mechanical lab, in-process, proto
tower inspection and final inspection of finished goods.
Responsible to maintain product quality as per quality assurance plan, customer requirements and
applicable national ...