JOB OBJECTIVE :
To working in an organization with hard work and commitment to accomplish the goal set by the management and improving my skills and try to developing systems through innovation with team spirit and collaboration.KEY ROLES -RESPONSIBILITIES :
** Effectively interfacing with people at all levels, managing healthy work place environment and inculcating bonded teamwork with high work ethics.
** Planning the work activities within the time lines; providing direction to Quality control personnel and defining priorities on a day-to-day operational basis.
** Coordinate with production department for day to day activity for timely release of Raw materials, In-process, Finished goods, & Packaging material samples.
** Analyzed work problems and evaluated resolutions to prevent delays in the production area
** Responsible to Ensure the Systems, facilities, Procedures are in Adequate.
** Induction training for new employees.
** Prepare and Review of method validation data, stability protocols, and sampling protocols.
** Experience in operational knowledgeand trouble shooting of Analytical instruments like GC, HPLC, UV Spectrophotometer etc.
** Supervise control activities like OOT,OOS failure investigation.
** Implementation of change control system related to quality control
** Possess excellent interpersonal, analytical, troubleshooting and team building skills with proven ability in establishing quality systems.
** Basic understanding of ICH guidelinesWORKING PLATFORM :
** Prepare and Review of raw data of analysis, SOP’s, STPs, Protocols, Reports and COA’s etc. as per GMP practices.
** Modifying the standard operating procedures as convenient unless exceeding the GMP requirement based on pharmacopeia and customer requirements.
** Setting up and maintaining controls and documentation procedures in on-line
** Prepare and Review of compilation data for stability studies/Holding time data.
** To monitor Control samples of Finished Products and scheduling of Accelerated / long-term Stability studies and drug intermediates for Holding time studies.
** Keen role in handling and educating trainees and subordinates.
** To ensure and control Good laboratory practices in QC laboratory.
** Minimizing the instruments / equipment breakdowns by the implementation of preventive maintenance schedule through Annual Maintenance Contract.
** To ensure the Performance Qualifications and calibrations of instruments related to laboratory.CORE COMPETENCIES :
** An effective communicator with excellent relationship management skills and strong analytical, problem solving & organizational abilities.
** Handling quality related activities involving resource planning and co-ordination with Internal Departments.ANALYTICAL SKILLS :
** Analytical method validation
** Preparation of SOP’s/STP’s /Protocol / Reports.PROFESSIONAL EXPERIENCE :
M/s. Sponsored links :
Vindhya organics private Limited. – Hyderabad ( Intermediates)
Worked as a Manager – Quality control department from May-2014 to Nov -2014
M/s. Dymes pharmachem Limited. – Hyderabad (API & Intermediates)
Worked as a Manager – Quality control department from Jan-2007 to Mar -2014
M/s. Symed Labs Limited. – Hyderabad (API & Intermediates)
Worked as a Assistant Manager – Quality control department from May-2003 to May -2006
M/s. Sipra Labs Limited.- Hyderabad ( Analytical laboratory)
Worked as Quality control Group leader from Sep-1998 to May-2003.EDUCATION :
Master of Science (Chemistry) from Nagarjuna University – Guntur. (Andhra Pradesh)PERSONAL PROFILE :Name : RaguveerContact address :
Hyderabad.Phone : +91 - 9848815571Place : Hyderabad.Date :
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