Neuland Laboratories Released Job Openings On 10/11/2022.Neuland Laboratories is a leading manufacturer of active pharmaceutical ingredients (APIs) and an end-to-end chemistry-related solutions provider for the pharmaceutical industry.
Vacancy Details:
Neuland Laboratories Recruiting M.Sc,B.Sc in Chemistry Graduates with 03– 05+ Years of Experience for Production Documentation Position.
Important Details :
- Working Location: Hyderabad
- No of Vacancies:NA
- Details of Salary:₹ 3,00,000 – 4,00,000 P.A.
- Opening date for online Application: 10/11/2022
- Mode of application :Walk In
- Time And Venue : 11th November – 17th November , 10.30 AM – 4.00 PM
Neuland Laboratories Limited Unit-1, Survey No: 474, 347, 490/2: Veerabhadraswamy Temple Road,, Jinnaram,, Bonthapally Village, Telangana 502313Contact – Priyanka ( 7995556801 )
For more Latest pharma jobs https://pharmapage.in/
Job Description/Skills Required
- Preparation of batch manufacturing of records.
- Receipt and issuance of batch manufacturing records from quality assurance department.
- Executed batch manufacturing records reviewed i.e. all the critical process parameters, In-process checks, Packaging details, out put yield for any deviations obtained during batch process after that completed BMRs submitted to QA.
- Preparation of standard operating procedures.
- Training conducting to all employees on SOPs, BMRs, Validation protocols through Learning Management software.
- Preparation of validation protocols (Process validation, Cleaning validation, Intermediate Hold time study) and executed.
- Handling of Change controls, Incident & Deviations, CAPA, OOS investigations.
- All the quality deviations are evaluated, critical deviations are investigated, and the conclusions are recorded and timely closed.
- Out of Specification (OOS) investigations are performed and evaluated each step by step. To avoid OOS in future CAPA is initiated for necessary actions.
- In audit compliance, based on the customer complaints investigations is performed against the customer compliant. If the complaints are Major or Minor investigation shall be completed with the target date without any delay.
- During manufacturing, Plant inspection i.e. reviewing of online BMR, equipment log books, identification status labels of accessories and cleanliness of surrounding areas.
- Conducting on regular basis shop floor persons training and brain storming on production activities like targets, GDP, audit compliance and process improvements.
Share your Resumes PriyankaPandey@neulandlabs.com & subrahmanyamg@neulandlabs.com
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