The resume summarizes Sanjeev Ranjan's 14 years of experience in the pharmaceutical industry, primarily in production roles but also quality assurance. His current role is QA Manager at Sigachi Industries, where he oversees quality assurance functions and ensures compliance. Previously he held production roles of increasing responsibility at several major pharmaceutical companies.

1. RESUME
SANJEEV RANJAN
A-224 ,IInd
Phase,Janapriya Arcadia
Darga Road, Kowkoor, Secunderabad
Contact: 09618255197 (m)
Email: snjv_ranjan@yahoo.com
SUMMARY:
A professional with fourteen years of experience in different areas of Pharma Industry. Primarily worked
for the Production department but also has the working experience in Quality Assurance.
JOB PROFILE
Company : Sigachi Industries Pvt. Limited – Hyderabad
Duration : From – Nov 2015 To – till date
Designation : QA Manager
Work Profile
 To be responsible for all activities in the Quality Assurance, including cGMP/cGLP,
documentation and implementation of departmental quality systems.
 Responsible for in Process document control and records retention as per cGMP.
 Review of executed Batch Production & Control Records and Process documents.
 Preparation of Standard Operating Procedures (SOP’s), and (BPCR).
 Monitoring dispatch related activities and solely responsible for timely release of Batch.
 Responsible for IPQA Checks during Production.
 Routine inspection of various departments to maintain cGMP (current Good Manufacturing
Practices) compliance at all levels.
 Responsible to investigate the root cause for the complaints received and their timely closure by
taking appropriate corrective & preventing actions required.
 Conducting regular Internal Audit for Production in order to ensure that all the set guidelines are
being followed.
 Review and compile the Deviations and change controls.
 Facing customer and regulatory audits and audit follow-ups.
 Preparation of Annual Product Quality Review and Process Validations.
Reported To : Executive Vice Chairman
Audits faced : ISO 9001: 2015 & FSSC 22000, Customer Audit
Company : Alkem laboratories Limited – Daman
Duration : From – July 2008 To – Oct 2015
Designation : Sr. Executive
Work Profile
 Coordination & Planning with QA Dept. for regular production plan and validation activities.
 Monthly, Weekly & daily planning production schedule so as to achieve the given production
target within stipulated time.

2.  Co-ordinated closely all activitieseg. Production planning, Raising of production notes& follow
ups through necessary organizational and technical interface.
 Direct supervision of all the stages of manufacturing & packing activities.Dry syrup, Capsule,
Tablet department.
 Tracing & Tracking of all documents, eg. Change Control, Deviations etc.
 Conducting Self Inspection Audits and Imparting on job training related to CGMP/regulatory
requirements.
 Preparation & reviewing of SOP’s
 Handling of CVC bulk packing line 220 BPM and 120 BPM. For U.S Market.
Reported To : Dy. GM -Production
Audits faced :USFDA,MHRA,TGA.MCC
Company : Intas Pharmaceutical Ltd. Ahemadabad
Duration : From – Sept 2006 To – June 2008
Designation : Sr. Executive
Work Profile
 Monitoring of routine Production activities.
 To carry out validation activities such as preparation of protocols & reports.
 Review & Ensure the completeness of all production records.
 Conduct the investigations as per the complaints.
 Participating in investigations pertaining to deviations OOS &Failure investigation.
 Conducting Self Inspection Audits and Imparting on job training related to CGMP/ regulatory
requirements.
Reported To : Manager-Production
Audits faced :MHRA,USFDA
Company : Strides Arcolab Ltd. Bangalore
Duration : From – Dec 2004 To – Aug 2006
Designation : Executive
Work Profile
 Preparation of IQ/OQ/PQ protocols.
 Preparation & review of SOP’s,BMR’s and MFR’s.
 Conduct the investigations as per the complaints.
 Participating investigations pertaining to deviations, OOS & return goods.
 Participate in designing Training.
 Ensure the completeness of all production records.
 Conductance of Internal Audits as delegated / assigned.
Reported To : Team Leader -Production
Audits faced :MCC, WHO
Company : Torrent Pharmaceutical Ltd. Ahmadabad
Duration : From – Aug 2004 To – Nov 2004
Designation : Sr. Technical Officer

3. Work Profile
 Production planning and manpower handling.
 Co ordination with raw material and packing material stores in order to
 Preparation, reviewing, of production related documents like SOP,BMR and BPR.
 Super vision of manufacturing processes like Granulation, blending,
 Compression in accordance with GMP requirements.
 On job training to workman to comply GMP requirements on shop floor.Assisting with QA
department in order to plan and implement process Validation, cleaning validation activity on
shop floor.
Reported To : Sr. Executive -Production
Audits faced : WHO
Company : Alkem Laboratories Ltd. Daman
Duration : From – July 2000 To – July 2004
Designation : Production Officer
Work Profile
 Production planning and manpower handling.
 Co ordination with raw material and packing material stores in order to
 Streamlining day to day production activities.
 Super vision of manufacturing processes like Granulation, blending,
 Compression in accordance with GMP requirements.
 On job training to workman to comply GMP requirements on shop floor.
 Assisting with QA department in order to plan and implement process
 Effective resources planning and utilization of men, material and machine, thereby cost reducing
and quality consciousness approaches in team.
Reported To : Manager -Production
Audits faced : WHO, MHRA,MCC South Africa
ACADEMICDETAILS
 Bachelor in Pharmacy (Karnataka University, Dharwad)
 MBA with the specialization in Operational Management (Sikkim Manipal University)
 Diploma in pharmaceutical Production Management in the year July 2001from I.P.E.R.-Pune
 Diploma in the PharmaceuticalPackaging Management year July 2002 from I.P.E.R.- Pune
SEMINARS ATTENDED
 Documentation in PharmaceuticalIndustry
 ISO-Awareness programme
SKILLS IN COMPUTER
 Operating System - DOS,MS-Office
 ERP system - End user knowledge of SAP in production
SANJEEV RANJAN
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