1. Cover Letter
Dear Sir,
I have come to know through some reliable sources about your requirement for
department Production your organization. In respect this I am here by attaching my
resume for your kind perusal.
I am working as a Chemist (sterile Production) with one of the leading
PharmaceuticalCompany M/S Wockhardt Ltd, Ankleshwar.7 year of experience in
the field of sterile Production. My resume will let you know regarding my work
profile.
I hope that my experience will suit to your requirement and you will give me a
chance to work your esteemed Organization.
Thanking you sir,
Yours sincerely,
Surendherreddy a

2. CURRICULAM VITAE
Surrender Reddy.A
H.no 158/b pragathinagar hydrabad
E-mail Id: rsurender51@gmail.com
Cell: 91-8463964311
Summary:
A post graduate in Organic Chemistry and having 7 Years of experience in the
areas of API Sterile production with validation activities.
Objective:
Looking forward to a very challenging career, which will help me in contributing
my best for theorganizationas well as helping my desires to learn new technologies
and think globally.
Personal Skill:
Comprehensive problem solving abilities, ability to deal with people diplomatically,
highly motivated to learn and gain new things team facilitator.
Computer Skill:
Completed a courseon Fundamentalsof Computer and very fluent in working any
of the operating systems MS office.
Educational Qualification:
Master degree in Science (Organic Chemistry) from Dr. BAMU Mardtwada
University, Aurangabad. (MH).

3. Career Profile:
 As a working with a Aurobindopharmacy As a Assistant -Production
October- 2016 stilldate.
 As a working with WOCKHARD LTD. As a Chemist-ProductionsinceMarch-
2012. To SEPTEMBER- 2016.
 As a CHEMIST in Surya PharmaceuticalLtd. From July-2011 to March-2012.
 As an Officer in Orchid chemical & Pharmaceuticals. From January-2010 to
July-2011.
CURRENT JOB PROFILE:
1. Working as a Chemist in Sterile API production.
2. Understandingtechnology of themanufacturingof sterileproduct.
3. Execution, planning and control in co-ordination with team member.
4. Monitor &control the operation to ensure consistent quality, delivery of
budgeted volumes, manufactured under strict cGMP condition.
5. Ensurethe cGMP, GDP during manufacturing operationsand other activities
in the plant.
6. Documents review with respect to data integrity.
7. Implement company’s safety policy and ensurefollowing of safety procedures
and use of PPE’s.
8. Coordination with various departments like Quality Assurance, Quality
Control, Microbiology and maintenance during validation as well as
production.
9. Full involvement During Audit preparations.
Other Activity Exposure:
1. Knowledge of GMP practices and SOP’s etc.
Equipment Handling:

4. 1. Moist Heat Sterilizer Make MACHINE FABRIK
2. Dry Heat Sterilizer Make TRITON ENGINEERING
3. Pressure Filter Drier Make OMCA ITALY
4. Multicolumn Distillation Unit Make PHARMA LAB
5. Pure Steam Generator Make PHARMA LAB
6. Ultra filtration System Make PHARMALAB
7. Non Viable particle counter Make Solair
8. Filter integrity tester Make IT-4 MILLIPORE & SARTOCHECK-4 Plus
SARTORIOUS
AUDIT FACED
 USFDA(2015).
 WHO(2014).
 BIOPHARMA(ITALY) Customer Audit
Personal Profile:
Name : Surender Reddy Appam
Father’s Name : IndhersenreddyAppam
Date of Birth : 13th
May 1984
Sex : Male
MaritalStatus : Married
Religion : Hindu
Languages Known: English, Hindi& Telugu
Permanent Address : Surenderreddyappam

5. H.No 74/3, Degaon,
Bhainsa, Adilabad,
Telangana- 504102
Expected Salary : As per Company Norms
Ph Nos. : 91-9974608195,
8905677955
E-Mail : rsurender51@gmail.com
Declaration:
I, Surender Reddy Appam hereby declarethat all theabove mentioned particulars
are trueto thebest of my knowledgeand belief
(SURENDER REDDY A.)