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Mediception Science Pvt Ltd Requires Senior Medical Writer As a Immediate Joiner ( 02 Positions)

Mediception  Science Pvt. Ltd Requires Senior Medical Writer (On Site)  as a Immediate Joiner  Details are provided below  1. Position- Senior Medical Writer ( 02 Positions)  2..Company- Mediception  3..Job Type- On Site  4. Qualification Required- Master’s Degree or Higher in a scientific or Medical Field  5. Experience- 2 to 3 Years of Medical Content Writing.   ( Industry Medical Writing Exposure is a Must)  6. Job Responsibilities-  a. Literature Search and Systematic Literature Search.  b.  Scientific Content Writing, Medical communications  c. Slide decks and Medical marketing collaterals  d. Ability to analyse and interpret complex scientific/patient data.  e. Excellent written and verbal communication skills  f. Ability to work effectively independently and in cross functional teams  7. How To Apply- Kindly send your CV to bhawana@mediception.com  CLICK HERE FOR DETAIL...
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Require Officer/Sr. Officer/Executive for Quality Control Department - B.Sc / M.Sc. / B.tech (Biotechnology)

Job Opening:

INDUS PHARMA PVT. LTD.
Vacancy for Manufacturing Plant located at Riico Industrial Area, Ghiloth, Neemrana, Rajasthan

Department: Quality Control
Designation: Officer/Sr. Officer/Executive
Experience: 03 Yrs – 06 Yrs
Qualifications: B.Sc / M.Sc. / B.tech (Biotechnology)
Job Responsibilities:-
1. Sample Analysis
Analyze raw materials, in-process samples, finished products, and stability samples to ensure compliance with specifications.
Perform chemical and physical testing, including pH, viscosity, osmolality, sterility, particulate matter, and assay of active pharmaceutical ingredients (APIs).
2. Method Development and Validation
Develop, optimize, and validate analytical methods (e.g., HPLC, GC, UV-Vis Spectroscopy) to ensure reproducibility and reliability.
Troubleshoot and maintain analytical methods as needed.
3. Documentation
Maintain accurate and detailed records of testing, analysis, and calibration in compliance with Good Documentation Practices (GDP).
Prepare and review Certificates of Analysis (COAs), test reports, and deviation reports.
4. Regulatory Compliance
Ensure adherence to regulatory requirements, including Good Manufacturing Practices (GMP) and International Council for Harmonisation (ICH) guidelines.
Support audits and inspections by regulatory agencies (e.g., FDA, EMA).
5. Equipment Management
Operate, calibrate, and maintain laboratory instruments like HPLC, GC, UV-Vis spectrophotometers, FTIR, and more.
Ensure proper validation and qualification of laboratory equipment.
6. Microbiological Oversight (if applicable)
Collaborate with microbiology teams to ensure sterility and endotoxin testing of injectable products.
Participate in environmental monitoring programs for sterile production areas.
7. Quality Assurance Support
Assist in investigating Out-of-Specification (OOS) and Out-of-Trend (OOT) results.
Participate in root cause analysis and corrective/preventive actions (CAPA).
8. Stability Studies
Conduct stability testing of products to determine shelf life and storage conditions.
Monitor stability chambers and ensure samples are tested as per the stability protocol.

Please share your CV on :-
hr@induspharmaindia.com
+91-9990334200 (Only WA)

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