LUPIN LIMITED - Walk-In Interviews on 13th February, 2021
Sunday 7 February 2021
Thursday 4 February 2021
Ipca Laboratories Limited - Walk-In Interviews for Multiple Positions in Quality Assurance / Production on 7th Feb' 2021
Walk-In
Interview for Quality Assurance & Production
Roles and
Responsibilities:
Quality
Assurance:
Section -
IPQA
Job Profile: Line Clearance & In-process checking during
Manufacturing & Packing.
Designation:
Officer / Sr. Officer
Qualification: B. Pharm. / M. Pharm.
Experience: 2 to 4 Years
Section: QMS
Job Profile:
OOS / OOT / Lab Investigation / Deviation / Documentation
Designation:
Executive / Sr. Executive
Qualification: B. Pharm. / M. Pharm.
Experience: 6 to 8 Years
Section: Lab
QA
Job Profile: Review of Analytical documents / Audit Trail Review
Designation:
Officer / Sr. Officer
Qualification: B. Sc. / M. Sc.
Experience: 4 to 6 Years
Section:
Qualification
Job Profile: Equipment / HVAC / Qualification, Computer System Validation
Designation:
Officer / Sr. Officer
Qualification: B. Pharm. / M. Pharm.
Experience: 4 to 6 Years
Production:
Section: Granulation
Job Profile: Supervision of Granulation Activities & Documentation
Designation:
Officer / Sr. Officer
Qualification: B. Pharm. / M. Pharm.
Experience: 2 to 5 Years
Job Profile: Granulation Machine Operator
Designation:
Technician / Sr. Technician
Qualification: SSC / HSC / ITI
Experience: 2 to 5 Years
Section: Compression
Job Profile: Supervision of Compression Activities &
Documentation (Knowledge of FETTE machine will be preferred).
Designation:
Officer / Sr. Officer
Qualification: B. Pharm. / M. Pharm.
Experience: 2 to 5 Years
Job Profile: Compression Machine Operator
Designation:
Technician / Sr. Technician
Qualification: SSC / HSC / ITI
Experience: 2 to 5 Years
Date: 7th February, 2021,
Time: 10.00
AM - 3.00 PM
Venue: VITS Shalimar Hotel, Valia Road, Near G.I.D.C. Reservoir, Bharuch,
Ankleshwar, Gujarat 393002.
Contact - Pradeepta Kumar Mohapatra ( 02606624407 )
Wednesday 3 February 2021
IPCA LABORATORIES LTD - Urgent Openings for Production / Quality Control / EHS Departments - Apply Now
We IPCA LABORATORIES LTD are one of the world's largest manufacturers and
suppliers of over a dozens of APIs in various location site in India over a
more then 60 years having vacancy for Ankleshwar site(APIs &
Intermediate):-
1) Department : Production
Designation : Sr. Executive
Experience : 7 to 9 years
Qualification : B.Sc/M.Sc/B.E/B.Tech Chemical
2)Department: Production
Designation: Sr. Officer
Experience: 5 to 7 years
Qualification: B.Sc/M.Sc/B.E/B.Tech Chemical
3) Department: Production
Designation: Officer
Experience: 3 to 5 Years
Qualification: B.Sc/M.Sc/B.E/B.Tech Chemical
4) Department: Production
Designation: Technician (Plant Operator)
Experience: 4 to 6 Years
Qualification: S.S.C/H.S.C/ I.T.I( AOCP)
5) Department: Q.C
Designation: Assistant Manager
Experience: 10 to 15 years
Qualification: B.Sc/M.Sc
6) Department: Q.C
Designation: Sr. Chemist - Q.C
Experience: 2 to 3 years
Qualification: B.Sc/M.Sc
7) Department : EHS
Designation: Sr. Officer(Safety)
Experience: 5 to 7 Years
Qualification: Any Graduate/Post Graduate/Diploma in Safety
LOCATION:-ANKLESHWAR, GUJARAT
Interested candidate may send their updated CV on ketan.chaudhari@ipca.com
Monday 1 February 2021
Urgent Openings for Production / QC / QA / QC-Micro / R&D / Engineering Departments @ NAGINDAS HIRALAL BHAYANI (Pharma & Plastic Unit)
Urgent Openings for Production / QC / QA / QC-Micro / R&D / Engineering Departments @ NAGINDAS HIRALAL BHAYANI (Pharma & Plastic Unit)
Location: Ankleshwar
Send Resumes to: hr@bhayanigroup.com / receptionnhb@gmail.com
Thursday 21 January 2021
RUSAN PHARMA LTD - Walk-In Interviews for Multiple Positions in Production / ADL / QA / QC Departments on 22nd & 23rd Jan' 2021
RUSAN PHARMA LTD - Walk-In Interviews for Multiple Positions in
Production / ADL / QA / QC Departments on 22nd & 23rd Jan' 2021
Tuesday 19 January 2021
Macleods Pharma Ltd | Walk-In Interviews on 24th Jan' 2021 | Apply Here
Macleods
Pharma Ltd | Walk-In Interviews on 24th Jan' 2021
Register in
below link
Monday 11 January 2021
MACLEODS PHARMA LTD - Walk-In Interviews for Quality Control / Stores / Engineering Departments on 24th Jan' 2021
MACLEODS PHARMA LTD - Walk-In Interviews for Quality Control / Stores /
Engineering Departments on 24th Jan' 2021
Saturday 19 December 2020
Rusan Pharma Ltd - Openings for Production / Quality Assurance - Apply Now
Production -
API (R&D) - Rusan Pharma ltd - Gandhidham
Opening for Manager - Production (API) with Rusan Pharma Ltd (R&D
Center)
Location: Kandla, Gandhidham (Gujarat)
Exp : 5+ Years of Exp from R&D API Background
Profile: Manager Production in R & D
Candidate can apply only if wants to relocate at Gandhidham Location.
Education:
- Masters or PhD qualification in Organic
Chemistry
Job
Description:
Development, Technology transfer and production operation in API.
Expertiseinbuildingteambystreamliningmanufacturingoperationsusingprocedurestofacilitaterobustqualitymanagementsystemswithprocessoptimizationandcontrolrespectingquality,safety
and process norms.
Route scouting, synthesis and scale-up of small organic molecules/intermediate
Plans and schedule synthesis campaigns to support large scale demands
Responsible & audit - the lab documentation in the PRD lab
Innovates solutions to synthetic/scale-up issues (chemical, physical,
preparative, application specific and analytical), transfer results and
involves in scale-up/production
Optimize process flows and methods of concerned working fields.
Plan, evaluate, document and analyse experiments, results and suggest
improvements
Co-operates in cross functional project teams to ensure timely delivery.
Education and supporting of trainees as well as interns and ensure
targeted safe work performance.
Stay up to date with scientific developments in the field of organic
synthesis and organic process research & development percolate the
developments to the peers in PRD lab.
Perform all project work to ensure effective and efficient on budget, on
time delivery of the required amount of product of the required quality.
Carry out practical experiments and demonstrate understanding of organic
chemistry, guided by line manager.
Use literature search engines to aid in selection of work plan with line
manager.
Aid in the development of processes that are suitable and robust to
transfer to pilot plant/kilo lab within budget and to the schedule assigned for
that project.
Identify problems and propose potential solutions, with supervision where
appropriate.
Document all experimental work fully and accurately in lab notebook.
Perform and interpret own routine analysis (eg NMR, HPLC, LCMS, KF).
Discuss the need for obtaining further analytical data with line manager.
Act as support chemist for project in kilo lab./pilot plant operations by
ensuring clear communication of expectations of the process to operations or
plant chemist.
Sr.
Management - Quality Assurance - API - Rusan Pharma Ltd, Ankleshwar
Opening for Sr. Management - Corporate Quality Assurance - API
(Ankleshwar)
with Rusan Pharma Ltd
Qualification : M.sc
Exp : 12+ Years - API Background
Location : Ankleshwar (API)
Responsible for managing QA activities such as deviation management,
change management, SOP compliance, batch release, supplier quality assurance,
complaint handling and document review.
Preparation, Review and Maintaining corporate QMS SOPs. (Deviation,
Change control, Audit Management, Complaints, Self Inspection, and document
reviews).
Market complaints - Investigation, CAPA analysis, resolution of
complaints & taking timely corrective action for critical and major
categories.
Managing QA activities such as deviation management, change management,
SOP compliance, batch release, supplier quality assurance, complaint handling
and document review
preparation / review of various protocols and reports such as cleaning
validation, process validation, validation master plan, computerized system
validation, etc
Communication with international corporate colleagues on various
subjects.
Preparing monthly and yearly reports with respect to QA activities and
presenting the same to corporate QA.
Preparation of the site qualification and validation master plan for
current year and tracking the progress plan on quarterly basis.
Preparation and Implementation of internal audit program.
Documentation, Validation & Qualification, Internal & External
Audit, handling Customer Complaints and indepth knowledge of Regulatory
requirements
E-Mail: corporatehr@rusanpharma.com