www.metholcrystals.com Bhagat Aromatics Ltd : Noida : Pharma, Chemist QC/QA

[mskavi]

Bhagat Aromatics Ltd
http://www.metholcrystals.com

Bhagat Aromatics : Noida : Pharma, Senior Chemist QC/QA
Keywords: Pharma

Company Profile
We as Bhagat Aromatics Limited, are Pioneer in manufacturing of Menthol Crystals, Mint Oil, and Essential Oils. We are very successfully manufacturing above Products for last 30 Years. We are well-established name in the Indian Industry as well as we are Government recognized Export Trading House Supplying to more than 45-50 Countries (USA, Europe, Middle East and African Continent) round the Globe.

Assistant Manager and Senior Chemist QC/QA

Experience:
1 - 4 Years
Location:
Noida
Compensation:
Best in the industry.
Education:
UG - B.Pharma - Pharmacy;B.Sc - Any Specialization

PG - M.Pharma - Pharmacy;M.Sc - Any Specialization
Industry Type:
Pharma/ Biotech/Clinical Research
Functional Area:
Production, Maintenance, Quality
Posted Date:
10 Sep


Job Description
SHALL BE RESPONSIBLE FOR - ENSURING COMPLETE IN-PROCESS QUALITY CONTROL ANALYSIS, MAINTENANCE CALIBRATION & TROUBLESHOOTING OF
ANALYTICAL EQUIPMENTS, CONDUCTING STABILITY STUDIES, TRAINING NEW STAFF, DEVELOPING & VALIDATING THE STABILITY INDICATING
CHROMATOGRAPHIC METHODS, PREPARE CLEANING VALIDATING PROTOCOLS FOR PROCESS DEVELOPMENT & SOP TO MEET THE LATEST TREND OF
GUIDELINES, VALIDATING TEST METHODS, FACE LL AUDITS, SUPERVISE MICROBIOLOGY SECTION ACTIVITIES, CONDUCT TESTS & INSPECTIONS TO
ENSURE DEVELOPMENT OF PRODUCTS COMPLY TO SET QUALITY STANDARDS, UPDATING ANNUAL PRODUCT QUALITY REVIEW THROUGH STABILITY,
PERFORM VENDOR AUDITS OF RAW & PACKING MATERIAL, HANDLING OUT OF SPECIFICATION THROUGH INVESTIGATION, DOCUMENTATION FOR USFDA,
UKMHRA & TGA.
Will be responsible for Quality assurance of one or multiple sites mfg activities .Will ensure the product complies with the order being executed in respective manufacturing site .Will prepare SOPs and technical documents wherever required, Preparation and submission of Dossier for International Registration of Drug Product .Will coordinate with QA of the mfg sites, R & D, Production, ADL, QA, QC, Medical, Purchase & Packaging Development departments and public testing labs for material testing. Will in involve field work are visiting manufacturing sites whenever our production is in process.

Responsible for handling Queries related to Drug Product Registration. Review of the Dossiers before submission to authority.

Desired Candidate Profile
Having sound experience quality assurance
having sound pharmaceutical background,
leadership skills
communication skills

Contact Details
Executive Name:
Abhilash Kumar Pandey

Address:
Bhagat Aromatics Ltd
C 33 and 34,
Sector 7
Noida,UP,INDIA 201301

Email Address:
bhagat@mentholcrystals.com

Telephone:
91-120-4044300

Reference ID:
QC/QA1

[Guest-IJT]

Respected Sir,

I am looking for a Job for the post of staff nurse.I have attached my resume herewith for your reference.

Siby Joseph
No: 942,1st Floor srk illam,
Kacharanahalli cross Road
Bangalore— 560084
Ph: - 09739189075,
E-mail:- sibybglr AT gmail .com

Career Profile
- Proven record of reliability and responsibility.
- Remain calm and professional throughout critical incidents.
- Strong analytical skills, capable of assessing conditions and implementing appropriate intervention.
- Possess special sensitivity to meeting diverse needs in varied situations.
- Develop rapport with patients, family, staff and physicians.
- Relate well to people from a variety of cultures.

Skills and Certification
- Operated and maintained monitors of bio-medical equipment
- Medical terminology and medication administration skills
- Maintained sterile fields and application of dressings
- Catheter, IV, and suctioning training
- Charting and documentation of patient care
- Acute and chronic care experience
- P.C. and Microsoft Office literate

Professional Background
- Diploma in General Nursing And Midwifery
From Karnataka Nursing Board, Securing 60% marks.
Karnataka Nursing Council Reg No: -- 120784

Professional Experience
Have been working as the staff nurse for the past one year.
Mahajan Neuro Center & General Hospital Pvt. Ltd,
Bareily, Uttar Pradesh.
2008 /A[/U]pril — 2009/May.

Personal Details
Name: - Siby Joseph
DOB: - 22nd July 1982
Marital Status: - Single
Languages Known: - English, Hindi, Malayalam.
Sex: - Male
Hobbies: - Listening music, Reading books.
Nationality:- Indian
State of Domicile:- Kerala

Permanent address: - Siby Joseph,
Thachethu house,
Pasuppara p.o,
Alampally, Idukki (dist),
Kerala (state), 685502,
Ph: --- 04869 246302.

I hereby declare that the details furnished above are true to the best of my
knowledge and belief.

Place: - Bangalore (signature)

Siby joseph

[Guest]

CURRICULUM VITAE
Anil Kumar Singh
Email : anil_prince2008 AT rediffmail.com ;
EXPERIENCE : 7.4 Years

CAREER OBJECTIVE
To be actively involved in an environment where each assignment is a challenge, an environment
which contributes to my professional growth and to achieve a challenging position in Pharmaceu-
tical Industry.
SPECIAL TRAINING
- (SAP) System Application Product in data processing.
WORKING EXPERIENCE
- Working with ACME FORMULATION PVT. LTD. at Chaukiwala, Nalagarh (H.P) as a
Sr. Executive Q.A. from Sep .2009 to till date.
- Worked with ANKUR DRUGS AND PHARMA LIMITED at Manakpura, Baddi (H.P) a Sr. QA Officer from Jan.2006 to Aug.2009.
- Worked with MEDICAMEN BIOTECH LIMITED Joint venture of MISSION PHARMA as a
Q.A. officer from Jan.2004 to Jan. 2006.
JOB RESPONSIBILITIES
- Independently Handling of IPQA activities of all the sections (Tablets, Capsules, Liquid & Dry Syrup)
in blocks like ( General, Cephalosporin and Beta Lactum Blocks.)
- Preparation of Master Formulation records.
- Preparation of Batch Manufacturing Records.
- Preparation of Batch Packing Records.
- Preparation of Process Validation Protocols and Reports.
- Perform all validation activities.
JOB RESPONSIBILITIES
- Preparation of Annual Product Review.
- Preparation, Review & Control of SOP’s.
- Approved Art work new launched products.
- Preparation of FDA documents.
- Self Inspection & Internal Audits.
- Provide Training and maintain training records.
- Handling of IPQA Persons and provide training.
- Handling of market complaints.
- Handling Log of Change Control, Deviation & Market Complaints.
- Issuance of BMR on Shop floor as per requirement.
- Handling of all the documents related to Q.A.
- Review of BMR and BPR before dispatch the batches.
- Handling of Master documents and Control all the documents before issue.
- Implement GMP at all levels of activities and operations.
- Carrying out in-process checks as per the frequency mentioned in the Standard Operating Procedures / Batch records during Manufacturing / Packaging.
- Carrying out in-process samplings on all stages.
- Involving in the process validation activities.
- Monitoring of On line Documentation.
- Equipment qualification.
- Issuing DQ, IQ, OQ, PQ formats of all equipments on shop floor.
- Preparation of site master file.
- Preparation of various documents related to QA.
EDUCATION QUALIFICATION
- BSC from Agra University with Second Division.
- Intermediate from U.P state board with second Division.
- S.S.C from Bihar Board with Second Division.

[Guest]

Im Rishi Kant Pathak . im graduate from Agra university in 2008. I have three year experience of pharma company documentation of production department . But i want to join QA. So ser if you nhave any vacancy please call me .....