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Pharma R&D jobs
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View similar jobs with this employerCadila Pharmaceuticals LtdJammu, Jammu and Kashmir- Ensure the cGMP compliance of QC area Key Responsibilities: • Follow up of Standard operating procedure for testing and analysis RM/FG etc.
- Indian Institute of Patent and Trademark Education...Kolkata, West Bengal
- A formulation scientist leads the design and development of formulations and processes, scaling up for manufacturing of batches for clinical and pre-clinical…
- Indian Institute of Patent and Trademark Education...Kolkata, West Bengal
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- Instapill Private LimitedHarohalli, Karnataka
- Years of Experience : 0 - 2 Years with relevant experience.
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- Kawman PharmaPark Town, Chennai, Tamil NaduCareers Join Our Team at Kawman Pharma At Kawman Pharma, we take immense pride in the trust and dedication of our more than 200 employees, who are the…
- DSK InnoSciencesHosur, Tamil Nadu
- 3-7 years experience in chemical/CRO/pharma industries.
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View similar jobs with this employerCadila Pharmaceuticals LtdPatna, Bihar- Achieve and consistently surpass the assigned Sales Budget and YPM (Yearly Performance Milestone) for the territory.
- Territory planning & time management.
- Quality HR India Pvt LtdDaman, Daman and Diu
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- Amneal PharmaceuticalsIndia
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- LupinPune, Maharashtra
- Analytical method development and validation for dissolution/in-vitro release using USP Type I, II, IV, shaking water bath, bottle rotating apparatus, or other…
- Speciality Organics Pvt LtdPithampur, Madhya Pradesh
- Plan, execute, and monitor laboratory experiments related to organic synthesis and API development.
- Handle reaction setup, reaction monitoring, and optimization…
- Indian Institute of Patent and Trademark Education...Kolkata, West Bengal
- Analyse patents in a particular domain to highlight the R&D, trends, evolutions, alternatives, and competitive intelligence in various technology domains.
- Lifechem Pharma Pvt ltdAnkleshwar, Gujarat
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- Piramal Pharma LimitedNavi Mumbai, Maharashtra
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- LupinPune, Maharashtra
- Medical writing of the device related documentation.
- Experience with EU MDR Regulation.
- Experience drafting technical documentation for both US and EU (…
Executive
Job details
Pay information not provided
Full-time
Jammu, Jammu and Kashmir
Full job description
Role Objective:- 1. Ensure the cGMP compliance of QC area Key Responsibilities: • Follow up of Standard operating procedure for testing and analysis RM/FG etc. • Follow up of Current Good Laboratories Practices. • Completion of Online Documents. • Ensure for calibration of equipments. • To ensure the delivery of product as per the production schedule. • To ensure the work discipline and cleanliness in production area. • To prepare Standard Operating Procedure. • Handling of deviation, initiation of change control and CAPA. • To impart training. • To follow safety norms in daily routine. • Monitoring and recording of Environmental condition of tablet compression / Bin-charging area as per defined frequency.
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