To strengthen our team, we are searching best talents for
our Bulk Drugs (API) and formulation manufacturing location based at Ratlam
(M.P.)
We have following opening at our Bulk Drugs and Formulation
manufacturing division located at Ratlam
Departments: Bulk
Drugs (API) and Formulation manufacturing
Location: Ratlam
Executive
- Q.A (API):
B.Sc/M.Sc(Chemistry)/B.Pharm/M.Pharm with 5 to 8 Years
exposure on Q.A function like Knowledge of Quality Assurance
Analytical/Manufacturing/Data integrity Review, Online Audit, Compliance,
Qualification and Validation, Q.M.S, I.P.Q.A Validation System, Qualification,
Change Control, Deviation, Market Complaints, OOS /OOT, CAPA, Batch Release
system, Well experience about current Good Manufacturing practices, Audits etc.
Chemist / Officer / Executive (QC and Stability):
B.Sc(Chemistry)/M.Sc Chemistry/B.Pharm with 2 to 10 years
experience in testing of API and formulation products (Method validation using
of HPLC, GC and Particle Size), Sampling of Raw material, Stability section.
Office
Q.C. (Instrumentation):B.E/B.Tech
(Instrumentation/Automation) with 3 years of experience in QC Instrumentation.
Should have experience of Qualification and Validation of QC instruments,
Preventive maintenance of QC instruments, Repair and maintenance of QC
instruments and Communication with Vendor.
Interested candidates can email their resume to karn.singh@ipca.com and
vidhi.bohra@ipca.com
Contact No: 07412-278358
Looking for clinical QA professionals with
field experience of Auditing clinical trial activities:
People with minimum of 2 years of
experience Sound understanding of clinical trial process and BA/BE studies is
must.
Willing to relocate to Mumbai
Multiple positions.
Interested candidate may contact on
9324681197 or
send your resume to nitin.chandurkar@ipca.com
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