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Wednesday, July 14, 2010


Hector & Streak is the premier provider of executive human capital solutions. For the last several years Hector & Streak has specialized in chief executive, board member and senior-level management search 

Job DescriptionWe are having one of the Senior position with one of our reputed client in Pharma Industry.

Position : Sr . Manager - Quality Control

Reporting to : GM - Quality Control

Location : Baddi

Compensation : Best in industry

Experience : 8 + years

Education : B.Sc / M.Sc / B.Pharma

Job Responsibilities :

Entire review of documentation (ADS, Specs/STP, SOPs, COA, Logbooks and all Validation Protocols/Reports) of the QC Department.

Up-gradation of the system to meet cGLP and other regulatory requirements.

Leading validation activity like Analytical Method Validation, Process Validation, Cleaning Validation.

Qualification and Calibration /Validation of Instrument/Equipment.

Up-gradation of the manpower of QC personnel by continuous training (system and instrumental).

Up-gradation of laboratory with instruments and adequate layout design.

Conducting stability studies of Validation/Exhibit and Post production batches for Drug substances/Drug product as per regulatory/ICH requirements.

Management of Working standards (which prepared against with Reference standard USP/BP/IP/IH etc) and HPLC/GC columns.

Testing planning of samples of Raw material, Packaging material, In process, Finished product, Stability and Microbiology .

To plan and review of the productst o mcet the quality standardsa s per guidelines.

To ensure that all raw materials, intermediates, packaging components and formulated products a re analyseda s per STPs( Pharmacopoeiaal nd/or in-house).

To ensure successful audit, inspections and visits by parties aryldrug authorities of the Company's QC activities.

To ensure that all instruments are calibrated periodically both in-house and outside agency.

To get the product analyzed and tested within time as per the sampling procedurcs giving approval of it's release.

To verify quality of raw materials and packaging materials.

To arrange for sampling of raw materials received, analyzing them and cnsure that they
are accepted only when they meet with laid down quality norms.

To ensurep rocurementa nd maintenanceo f working standards.

To review and approve the RM/PM/FP/Stability/Micro & Validation reports.

To ensure proper documentation & submission of report by analyst.

To monitor and co-ordinate all in process activities in Laboratory.

To co-ordinate for sampling, testing and results between procluction and quality control.

To coordinate with Production and store for Testing plans.

To ensure all the activitics related to stability studies for exhibit and post production stability studies.

NOTE : Man Management experience is mandatory for this position .

If interested mail me your resume in wordformat alongwith below mentioned details :

Current ctc

Expected ctc

Notice period

Thanks & Regards,

Menaj Shaikh

Hector & Streak

Email id :


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