Assistant Manager Quality Control/Analytical Services
Resume:
Muhammad Rukhsar
**********@*****.***
OBJECTIVE
Wish to Work with an organization that provides me dynamic and challenging environment for professional growth and personal enrichment and where my professional knowledge can be used for the development of disadvantage segments of society.
PROFESSIONAL EXPERIENCE
Personal Information
Father Name:
Said Karam
Date of Birth;
02-04-1992
Passport#.
AY9342961
Current Address (KSA);
HOTAT Sudair Riyadh
KSA.
Cost:
Safi
Religion;
Islam
Section;
Sunni
Dimensions.
5.8 (feet’s)
Weight.
64 kg
Blood Group;
B+
IQAMA Status:
Transferable Iqama
Available
Professional Trainings / Courses.
Laboratory Quality Management System ISO 17025:2017
Estimation of Uncertainty Measurement- GUM
Good Pharmaceutical Quality Control Laboratory (GPPQCL) WHO TRS. 957
Team building through motivation.
WHO guidelines on cGMP and WHO prequalification procedure
Receiving Complete training with certificates on HPLC, FTIR and UV Spectrophotometer.
Receiving Complete training with certificate on Advanced Microsoft Excel . Instrumentation:
HPLC Isocratic & Gradient with (Manual, Autosampler both Shimadzu (10,20,30 and 40 Series)
HPLC Hitachi and Sykam
HPLC Software’s T2000(Hitachi), LC solution [Shimadzu], Lab Solution[shimadzu] with 21CFR part 11Compliance.
UV Software’s UV2300(Hitachi), UV1800 (Shimadzu)
FTIR software’s LC solutions (Shimadzu), Lab Solutions (Shimadzu) with 21CFR Part 11Compliance.
HPLC Detector Used (UV, UV Visible, PDA, RID)
Karl Fischer (Mettler Toledo and Metrohm from Switzerland) MERCK PHARMACEUTICAL INTERNATIONAL (Multinational Group) (PVT) LTD. QUETTA PAKISTAN
(WHO-Pre-Qualified Lab / ISO/IEC 17025:2017)
Designation: Assistant Manager Analytical Services/QC Tenure: March 2022 to July 2024
HERBION PHARMACEUTICAL (PVT) LTD. ISLAMABAD-PAKISTAN Designation: Executive Quality Control
Tenure: J a n -2021 to Feb-2022
FOCUS & RULZ PHARMACEUTICAL (PVT) LTD. ISLAMABAD-PAKISTAN Designation: Sr. Quality Control Analyst/Chemist
Tenure: J u n -2017 to Oct-2020
GLOBAL PHARMACEUTICAL (PVT) LTD. ISLAMABAD -PAKISTAN Designation: Quality Control Analyst/ Chemist
Tenure: S E P -2015 to JUN-2017
Used Spectacle.
No
Marital status.
Un Married
Languages.
Urdu: Native speaker
English: Good command
Pashto: Mother Language
Interest:
Plying Cricket,
Reading books,
Internet, TV & IT
Physical Fitness:
Normal
Academic Qualification
BS(Hons)Organic Chemistry
Abdul wali khan University
Mardan KPK Pakistan-2015
Intermediate:
Pre-Engg-2011 BISE
Mardan
Matriculation
Science-2008
Personal Qualities:
Ability to work in a team
as a professional.
Reasoning ability
including strong
analytical and problem-
solving abilities.
Strong people
management
experience.
Love and wish to work
in challenging
environment.
Highly Proactive and
Expert in Acting with
Urgency
Positive attitude
towards work and
cheerful personality.
Good communication
proficiency in written
& oral English.
Patient and understanding.
Computer Skill.
Good Command MS Office,
MS Excel, Internet
Browsing,
Atomic Absorption, Gas Chromatography, Dissolution Apparatus, Disintegration Apparatus, Muffle Furnace, pH meter, Conductivity meter, Melting Point, Moister Analyzer etc.
PROFESSIONAL / TECHNICAL SKILLS
Extensive knowledge of Good Manufacturing Practice (also cGMP) Compliance requirements for Quality Operations, application of compendial methods and experience with wide range of analytical techniques.
Operate, maintain, and calibrate analytical instruments.
Perform routine and non-routine analysis of raw materials, intermediates, and finished products using analytical techniques.
Conduct assays, HPLC, GC, and other tests according to established protocols and procedures.
Managed, coordination and execution of all validation- and qualification activities for laboratory equipment as per applicable guidelines.
Creating and updating qualification project/ work plans and timelines for laboratory equipment.
Efficient management of Laboratory inventories such as Reference Standards, HPLC/GC Columns, Instrument spares, glassware, and other consumables.
Managed / Participate in out-of-specification and failure investigations and recommend corrective actions.
Participate in proficiency testing (PT) Scheme (LGC UK) and inter laboratory compression program (ILC).
Managed root cause analysis as identified through the internal audits or identified through NC reports/ Deviations or customer’s feedback.
Managed & performed intermediate checks of Equipment’s for performance verification / internal calibrations.
Managed and monitored Risk assessments / Risk register.
Perform validations / Verifications / transfers of analytical methods in accordance with applicable policies or guidelines.
Participate in External / Internal audit in Organization.
Has conducted inspections and physical test of raw materials, during manufacturing and packaging component samples and prepared test reports.
Developed local processes and procedures to ensure compliance with corporate quality standards related to QMS and other international requirements.
Drive Team engagement, effective communication, and the development of supervisors within QC lab.
Calculate/ prepare Measurement Uncertainty and develop sheets for MU calculations/ MU budget.
Assign and distribute work according to the priority, plan and skill and the capacity of individual or team.
Submitted lot of CTD, s (Common technical documents) related data to drug regulatory Authority through Proper Protocol.
Performed Comparative Dissolution Profile of different Products
Perform Stability Study of new products through proper protocol.
Perform pharmaequilence testing of new products.
Prepared STM, s(Standard Testing Methods) of new developed products. REFERENCES
References are available upon
request.
.
CV@ M.Rukhsar https://www.linkedin.com/in/muhammad-rukhsar-285757118/ Page 2 of 2
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