PHARMA WISDOM

Pharma, Life Science, Healthcare, Engineering Job Updates

Recent Updates

Monday 27 August 2018

Urgent Openings in QC - 2 to 5 Years Experienced Candidates @ Jadcherla & Hyderabad

UNICHEM LABORATORIES - Walk-In Interviews for QC & Production on 2nd September, 2018 @ GOA

HETERO - Walk-In Interviews for Multiple Positions in Production / QA / Micro / P&D on 1st September, 2018

Granules India Limited - Walk-In Interviews on 29th, 30th & 31st August, 2018 @ Hyderabad

17:43:00 2
Walk-In Interview for Officer – QC @ Granules India Limited
Department: Quality Control
Position: Officer
No. of Openings: 20
Experience: 2 – 5 years
Date & Time: 29th August - 31st August, 9 AM onwards
Venue:
Granules India Ltd 
Plot no 15A/1,
Phase-III, Jeedimetla,
Hyderabad-500055
Job Description:
- Monitoring of cGLP followed by laboratory personnel during routine operations to ensure adherence to procedure.
- Handling of HPLC , IV.
- Ensuring training of analysts in Laboratory techniques, Quality Control procedures and principles of cGLP / cGMP /General analytical methods instrumentation etc.
- Implementation QMS.
- Qualification of Laboratory Instruments (IQ/OQ/PQ)
- Planning of day to day Laboratory activities
- Maintain Real time documentation and Laboratory safety around the clock
- Review of analytical documents followed as per cGMP and Quality Policies.
- Handling of customer complaints.
- Checking the audit trails and analytical reports.
- Responsible for GLP compliance in the QC Department .
- Preparation and review of Method transfer/Validation protocols
- Review of Instrument Calibration data.
- Handling of Incidents, OOS, Change controls, OOT and all other cGMP record.
- Implementation of CAPAs
- Monitoring implementation of changes as per change control.
- Stability Management
- Preparation and review of specification and test procedures (STPs), General test procedures (GTPs) and cleaning methods.
- Preparation and review of Standard operating procedures (SOPs) and Validation Protocols.
- Review of Analytical Raw data sheets With respect to STPs, GTPs and SOPs.
- Preparation of Certificate of Analysis (COA) for Finished Products, and for Raw materials and intermediates.
- Review of BPCRs
- Preparation and review of Lab Metrics.
- Timely support to the regulatory activities in view of Revision of specifications and Test Methods

*** Thank you for Visit ***
More Updates Visit daily @ www.pharmawisdom.blogspot.com


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Zydus - Walk-In Interview for Multiple Positions on 1st September, 2018 @ Ahmedabad

16:49:00 0
WALK - IN INTERVIEW – 01st September’18, Saturday at Zydus Biologics based at Ahmedabad
Zydus Cadila is one of India’s leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group’s state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centres are spread across Ahmedabad, Baroda and Mumbai (Thane).
We invite candidates for the following positions based at Ahmedabad for our Quality Control and Quality Assurance Department of Zydus Biologics (ZB) based at Ahmedabad.
Executive/Sr. Executive/Asst. Manager
Quality Control –  Physico Chemical
M.Sc/M.Pharm /B-Tech/M Tech with 2-5 years of hands on experience of handling equipment & tests such as Reverse phase HPLC, Size exclusion chromatography, Ion exchange chromatography, Glycon Analysis, Gel Electrophoresis/SDS PAGE Analysis, IEF, Osmolality, HCP/HCD, Spectroscopy. Must have experience of Analysis of Fermentation Biotechnology based complex molecules (Biosimilars, Therapeutic proteins and peptides).
Quality Control –   Bioassay
M.Sc/M.Pharm /B-Tech/M Tech with 2-5 years of hands on experience in executing of in-vitro cell based bioassays by  Proliferation assays, Cytotoxicity assays, Apoptosis assay, Cytopathic assay, Receptor – ligand binding assay, Kinetic assays, Mycoplasma testing and Cell bank preparation
Quality Assurance - Analytical
M.Sc.(Biotechnology)/B. Pharm with 5 - 8 years of hands on experience in Reviewing the regular commercial, CT, exhibit batch release analytical data of Biosimilar products. Must have experience of handling OOS, change control, deviation, investigation, CAPA and QMS activities. Must be familiar with cGMP requirements and have experience on GMP documentation.
Quality Assurance – Documentation Cell
B.Sc/M.Sc./B. Pharm with 3 - 5 years of hands on experience in issuance, archival, retrieval and control of documents. Management of Document archival room.  Hands on experience in MS Office. Preference will be given to those who have an experience on GMP documentation  and must have handled Documentum software and SAP. 
For all the positions, candidate having exposure to regulatory requirement of documentation and cGMP/GLP is essential.
Interested candidates may “Walk-in” for an interview along-with their updated CVs, Salary Slip and relevant documents as per below schedule.
Date                      : 01st September 2018, Saturday
Location              : Ahmedabad
Timings               : 09:30 AM – 02:00 PM
Venue                   : Zydus Biologics, Plot Survey No. 40/P, 23, 25P, 42, 37,  Sarkhej-Bavla NH-8A,  Changodar, Opp.    Ramdev, Masala, Ahmedabad – 382213
Contact Person    : Dipak Panchasara


*** Thank you for Visit ***
More Updates Visit daily @ www.pharmawisdom.blogspot.com


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