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CV Sr. QA Manager

Sr. QA Manager

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CV/Resume ID no.: 87567

Location (Residence): Chandigarh, India
Citizenship: India
  Native: Hindi
  Other: Punjabi
Education & Experience: Work Authorization & Relocation:

Years of Experience: 13 years
Authorized to work in:
   European Union, UK (in particular), United States, Australia, Cameroon, Canada, Czech Rep., France, Germany, Hong Kong, India, Singapore, United Arab Emirates, United Kingdom, United States
Present Location:
   Anywhere (International)
Category Subcategory Ability Experience
Management QA/QC Experienced 17 years
Quality (QA/QC) Quality Assurance Experienced 17 years
Quality (QA/QC) Quality Assurance Experienced 15 years
Administration Administration Experienced 17 years
Technician Level Laboratory Experienced 22 years
Health & Safety Health & Safety Basic 7 years
CV/Resume Details
1. Summary (Cover Letter) - CV/Resume Part 1 [Mandatory]

To apply the concept hitherto learnt, continue with my learning process and climb the corporate ladder
in the field of latest Analytical technology by dint of multi skilled task, hard work, sincerity, dedication and
pursue a career of challenge and responsibility in Quality assurance.

2. Work Experience - CV/Resume Part 2 [Mandatory]

1) Presently working with “Ranbaxy Laboratories Ltd., Poanta Sahib, (H.P.)” as “Sr. Manager (QA)
Grade – A3” since July 2002 till date.

Job Responsibilities:
1) Presently working on technology transfer for contract manufacturing of products at various vendors.
2) Monitoring independently laboratory of Primary, Secondary packaging materials and their development.
3) Implementation of on-line inspection system and procedures.
4) Conducting of internal quality audits in the organization to fulfill contract manufacturing requirement.
5) Conducting of external audits at the vendor site, vendor rating and their approvals for cost reduction projects.
6) Implementation of calibration procedures, SOP’s, working instructions of all Operational machines as well as
QA/QC. Lab. Equipments as per regulated market guidelines.
7) Conducting training classes at all levels.
8) Issuing and monitoring Batch production record including yield reconciliation.
9) Implementation of Cleaning system and Cross contamination controls.
10) Implementation of Cross functional investigations.
11) Complaint handling and their redressal, product stability studies and product recall system.
12) Implementation of validation & stability study activities and Validation Master plan & checking their execution.
13) Implementation of Change/Deviation control procedure by listing out deviations and to implement proper corrective
14) Preparation of Raw & Packaging material specifications, test procedure and operational procedures including

Master formula.
15) Implementation of market feed back system regarding product quality and stability.
16) Implementation of regularity approvals in Personnel Hygiene System, OHSAS–18001, ISO 9001 (QMS), ISO
14000 (EMS), USFDA, TGA, MHRA, MCC, ANVISA, WHO-GMP and non regulated.
17) Implementation of product release system, Implementation as per cGLP, cGMP.
18) New Research and development activities related to PDL.
19) Commissioning, Validation & verification qualification as per IQ, DQ, OQ, VQ of all Laboratory equipments & plant
20) Process Validation – LVP, SVP, Anticancer drugs, Tablet, Capsules & Injectables (Dry powder).
21) Preparation of Site Master File, Master Batch Records, Updation of BMR, BPR, MBR and GMP files.
22) Release of Batch, Handling of Market complaints, Product Recalls, Designing & Approval of Art works of Unit
cartons, Labels, Literatures, Shipper, Blister Foils, Aluminum Foils, HDPE, Glass bottles, etc.
23) Co-ordination with PDL (Local AR&D) for Validation, Exhibit batches of new product.
24) To set up the Quality, Process and Audit system.
25) Build up Quality team and consciousness among the business process and each individuals mind.
26) Leading Total Quality Assurance and establishment of Quality control tools.
27) Coordinate for the all Quality activities at different locations of planning, production, procurement, packaging &
complaint control.
28) Establishment of Quality Assurance facility and procurement of inspection for new infrastructure.

2) Worked with “Saboo - Berlac Ltd., Chandigarh” as “Sr. Executive – QC/QA” from June 2000
to June 2002.

3) Worked with “ICI India Ltd., Mohali” as “Production Associate - Chemical” from December 1997
to June 2000.

4) Worked with “Honey Bee Natural Products Ltd., Lalru” as “Production cum Agmark–QC Chemist
From October 1995 to October 1997.

Extra Skill: Proficient in Computers with MS Word, MS Excel, Power Point, Tally 7.5, SAP 640, JD etc.

3. Education & Training - CV/Resume Part 3 [Mandatory]

Highest Qualification
Master of Science (M.Sc)
Field of Study : Chemistry (Analytical)
Major : Specialization in Commercial Methods of Chemical Analysis.
Grade/Class/%age : Grade A / 1st Class / 63.0
Post Graduation Date : April 1995

Other Qualification (s)/Certification/Programme/On job training(s) attended
• Approved Agmark Chemist from Directorate of Marketing and Inspection (Govt. Of India)
• Skill for Fire fighting, NCC, NSS, First aid.
• Summer Training for Three months in Pepsi Foods Ltd., Seasonal Plant (Hoshiarpur, Punjab)
• Proficiency in Computers ms WORD, Excel, Power point, SAP 630, AS400.
• Proficiency in Handling Laboratory instruments & their calibrations of Potentiometer, Polarimeter, Refractometer, Conductivity meter, UV-Visible-FTIR Spectrophotometer, Flame photometer, Mettler automatic titrator, Karl Fischer titrator, Machbeth Colour matching spectrophotometer, Glossometer, Melting and Boiling point tester, Heugmann gauges, Busting strength tester, Tensile Tester, Rub resistance tester and other separation chromatography technique like Paper, column, TLC, HPLC, GC, GLC etc.

4. Computer Skills - CV/Resume Part 4 [Mandatory]
Computer skill like Windows XP, MS word, Power point, Excel, Tally 4.5-5.5, Internet, SAP 630, AS 400 etc.
5. Other Skills - CV/Resume Part 5 [Optional]
Process validation, Preparation of RM’s and PM’s, Intermediate, Finish product specification and Approvals, Preparation of SOP’s & STP’s, Packaging design & development, Facing Quality Management systems & Audits like OHSAS, QMS, EMS, customer complaint and their redresals, Trainer for cGMP, cGLP, 5s, SQC & SPC, Kaizen, Six Sigma, Vendor development and rating, Third
party inspections, Active member of Commissioning Team for Pharma formulation and paint projects, Coordinator for HRD, Canteen and Employee retention committee.
6. Additional Information - CV/Resume Part 6 [Optional]
Main Subject Studied
A Cement & Mineral analysis.
B Food & Brevages analysis.
C Oil, Fats & Wax analysis.
D Soil analysis.
E Fertilizer analysis.
F Water Effluent & Waste water analysis.
G Mineral’s & Alloy analysis.
H Drug analysis (Ayurvedic & Allopathic)
I Soap and Detergents Analysis.
J. Paint and Varnishes Analysis.
K. Food and Brewages Analysis
Dissertation cum Research work
Physico-chemical & biological study of Compound Herbal Drug made with combination of Curcuma
longa (Haldi), Zingerber officinale (Adrak), Piper nigrum (Pipli), Piper longa (Laung).


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Sr. QA Manager
CV/Resume ID no.: 87567

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