Sydler Remedies Pvt. Ltd Walk-in interview 2023.Sydler Remedies Pvt. Ltd Notification full details below.Intrested and eligible candidates can attend Interview on scheduled time and venue.Sydler Remedies Pvt. Ltd. Bhosari MIDC, Pune are in the manufacturing of Tablet, Capsules, Ointment, Cosmetics and Lozenges. We require multiple vacancies for our Pune & Ranjangaon plant.
Vacancy details:
- Post Name: Executive /Sr.Officer / Officer( Production / QA/QC/Store/Eng/IT/HR.)/Operators For Eng. Dept. (Boiler, Water system & HVAC)
- Section: OSD/Ayurveda/External Preparation
- Qualification: ITI/Diploma/B.Tech/B.Sc./MSc/B.Pharma/ M. Pharma/HSC
- Exp: 1 to 7 Yrs
Job Description: Greeting from Sydler Remedies Pvt. Ltd !!!!!
Important Details :
- Location: India-Aurangabad, Pune
- Post of date:18/02/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Walk-in interview Details:
Date: 20th March – 21st March
Time: 9.30 AM – 5.30 PM
Venue: Address for Walk-in drive – Unit-1 , M-190 ,MIDC , Waluj , Aurangabad-431136(Maharashtra) India
Role : RA Officer- Aurangabad
Responsibilities :
– To Coordinate with relevant department for arranging documents
– To prepare / compile dossier for allocated products / countries
– To coordinate for Legalization of documents
– To prepare documents required for products
– To do internet surfing for clinical literatures
– To review BMR / BPR, cross check of basic documents like COA / RMS etc
– To prepare Specifications as per pharmacopoeia
– To coordinate with DHL for dispatches of dossier / samples
– To make timely entries of submissions / dispatches
Knowledge :
- Should be aware about basic requirements for preparing dossiers for ROW countries
- – Should be aware about compilation procedures / systems / steps involved in Regulatory activities
Skill :
- Should be aware about Microsoft office [word / Excel/ PPT]
- – Should take initiative for work
- – Should able to handle multitask activities
Educational Qualification : B. Pharm/M. Pharm
Experience :
Should have knowledge Regulatory affairs and CTD /ACTD Dossier compilation
Preference to be given to candidate having minimum 1-3 years experience of RA Department
Role : Sr. Executive/ Executive Maintenance
Responsibilities :
– To perform for the smooth running the equipments of Production (Tablet, Capsule & Ointment) Department.
– To Ensuring operations of Production (Tablet, Capsule, & Ointment) area as per Standard Operating Procedures.
– To attend breakdown / problem to minimum breakdown time in Production (Tablet, Capsule & Ointment) Department.
To perform for the smooth running of the Utility (HVAC, Air compressor, Boiler in utility Department.
To perform for the smooth running the Water Plant ( RO EDI )
Knowledge :
He must have Proper knowledge in Pharma machine
(Tablet, Capsule , Ointment & Pharma Utility ) repairing
Skill :
– Flexible in work
– Multitasking Skill
Educational Qualification : Diploma / ITI
Experience : 2- 3Years (Should be from Pharmaceutical plant)
Role : QC Executive (Instrumentation) – Auranganbad
Responsibilities :
ROLE IN HEIRARCHY
1. QC Aanalyst will execute all the exercises and tasks given by the superiors and work towards achieving all the objectives and goals set by the department.
2. Responsible to assist the superiors in all respects.
3. Responsible to guide all the subordinates in all respects.
4. Monitor all the activities and effective completion of the tasks and responsibilities delegated to the subordinates in the department.
5. Responsible for all the duties of the senior executive in his/her absence.
6. ROLE IN ROUTINE
7. Carry out the analysis of the samples received.
8. Responsible for analysis of Raw materials, Packing materials, intermediates, finished products and stability samples.
9. Responsible for guiding subordinates and trainees for conducting analysis.
10. Responsible for filling of the records and the preparation of the analysis reports for the activities and analysis performed.
11. Responsible for analysis on HPLC/UV/KF.
12. Responsible for calibration of HPLC/UV/KF
13. Responsible for Analytical Method Validation on HPLC/UV/KF.
14. Responsible to to ensure that all the activities are carried out as per GLP
ROLE IN DOCUMENTATION
15. Responsible to assist the superior for maintaining all documentation of the department.
16. Responsible to prepare new documents under the guidance of the Superior.
Knowledge:
1. Analytical Chemistry
2. GLP
3. HPLC
4. UV
5. KF
6. Calibration and Analytical Method Validation
Skill:
1. Hands on experience on HPLC/UV/KF
2. Good communication skills
3. Computer skills
4. Has to be good in calculations
Qualification : B. Pharm/ M. Pharm/ B. Sc./ M. Sc.
Experience :
Minimum 2 – 3 Years of experience in HPLC/UV/KF Handling
Must be FDA Approved in Chemical and Instrumentation section
Preference from Pharmaceuticals
