Mahesh Pooyath

Voice: +968-********

Email: adee0m@r.postjobfree.com

Raysut, Salalah, Dhofar State, Oman.

Objective

An experienced and technically efficient researcher currently working for Oman Pharmaceutical products Co. LLC (Oman) in Formulation and Development Department as Senior Officer RnD. Looking forward for a position where my qualification and experience can contribute to the organizational growth.

Profile and Skills

Academically proficient M. Pharm (Pharmaceutics)

Self-dependable, self-motivated, initiative, keen on responsibilities.

Able to perform well in team-based environments and take feedback.

Hard working, trouble shooting, positive and scientific attitude, Ability to work without micro evaluation, Eager to learn new concepts, Ability to work independently with minimal supervision

Work Experience

Currently handling solid oral dosage forms such as immediate release tablets, extended release capsules and extended release tablets at Oman Pharmaceuticals Products LLC., Salalah, Oman.

Worked as Executive at Mylan Laboratories LTD, Hyderabad from September 2017 to May 2019

Worked in Sai Life Sciences Ltd, Pune as Research Associate from August 2015 to August 2017

Worked in Ajanta Pharma Pvt Ltd., Kandivali (W) Mumbai as Research Associate from August 2013 to August 2015.

Previously worked in Vergo Pharma research Pvt Ltd. Verna Goa as Research Trainee from

July 2012 to July 2013.

Academic

M.Pharm specialized in Pharmaceutics from Sri Ramachandra University, Porur, Chennai with 79% in 2013.

Bachelor of Pharmacy from Nehru College of Pharmacy, Pampady, Trichur, Kerala with 72 % in 2010

12th from Govt Model School for Boys, Trichur, Kerala with 71% in 2004.

10th from National High school, Trichur with 91% in 2002.

Field of Interest

Formulation R&D (FD)

Academic Project Details

“Formulation and evaluation of biodegradable sustained release microspheres of antipsychotic drug”

Job Profile Summary

Participate in establishing a formulation development strategy to meet a target product profile

Participate in planning activities and resources, as well as preparing specifications for analyses and choice of methods

With support from the analytical center, co-develop and validate analytical methods

Design study plans, including in-vitro release methods, formulation compositions, stability and compatibility studies, and in-vivo tests (in conjunction with the preclinical center)

Prepare logistics and draft protocols for experiments; conduct experiments; observe results

Conduct iterative work to refine and optimize formulations to meet product specifications

Compile and analyze data

Ensure the careful and complete documentation/archiving of all generated data, namely in our electronic lab notebook system

Conduct scientific literature research to resolve problems and make recommendations for improvement

Participate in meetings and / or teleconferences with development partners when required, communicating in English

Work closely with other team members and perform activities in response to priorities

Verify that established procedures are followed and quality standards are maintained

Achievements

Actively involved in Formulation of Mesalamine Delayed Release Tablets 1.2g for US market

Developed formulation of topical gel up to scale up level for US market.

Successfully completed development of ER tablets of an antidepressant drug (BCS class I) up to query response stage.

Successfully completed development of IR tablets with antiepileptic drugs (BCS class III) for US Market.

Completed development of IR Tablets for US and Europe markets up to query response stage (Antileprotic - BCS class II DS).

Completed development of IR Tablets (ANDA Para I) up to query response stage (antimalarial BCS class III DS).

Developed extended release matrix tablet formulation of antidiabetic drug (BCS class III).

Successfully developed Enteric coated pellets in capsule product made of antidepressant drug substance of BCS Class II.

Successfully completed USFDA query response trials and exhibit batches of IR Tablets.

Handled regulatory body, query response trials and exhibit batches for multilayered coated tablets with fixed dose combination.

Assisted in product life cycle management and supplement filings projects.

Technical Proficiency

Well versed with MS Windows, MS Office (Word, Excel, PowerPoint & DOS) and Internet Applications

General work Attitude

Effective functioning in a rapidly changing environment and adherence to organization values and mission

Consistency, precision, perseverance, directness and listening skills

Open mindedness and ability to adapt to changing situations

Strong team spirit and open sharing of all the information necessary to successfully achieve overall work goals

Desire to continuously improve and progress

Strong work ethic

Summary

A skilled Research scientist with 7 years of experience in Formulation Development, Generic Product Development, Scale-up, Tech Transfer, Good Presentation, Sound Managerial concepts, Fluent Communication, Flexibility

Personal Dossier

Father’s Name

P. Sudhakaran

Date of Birth

31 October 1986

Address

Salalah, Oman

Interest

Playing Football

Personal

Male / Married

Languages known

Hindi, English, Malayalam, Tamil and Marathi

Nationality

Indian

Permanent Address Kizhakke Varapuzha house, Peruvanam, Cherpu Post, Thrissur, Kerala,

Pin: 680561

Declaration

I hereby declare that the information furnished above is true to the best of my knowledge and belief. I assure that if offered a job in your esteemed organization I shall serve to the best of my abilities.

Date:

Place: Salalah, Oman Mahesh Pooyath

Contact this candidate