ICHOR Biologics Pvt. Ltd – Mega Walk-In Interview for IPQA/QA (Validations) on 26th May’ 2023

Mega Walk-In Interview for IPQA/QA (Validations)

Date & Time: 26-05-2023 Friday

Timings : 10 am – 4 pm 

Venue Address: ICHOR BIOLOGICS Pvt. Ltd, Sy. No: 222P, Thurkapally Shameerpet (M), Telangana.

Contact No : 9121514444/8367563333/9059662289

 

You should carry below mentioned documents:

1. Updated Resume / CV

2. Last 3 Months Pay slips

3. Adhaar & Pan Card

4. Latest Appraisal salary break up

5. All Educational Documents Xerox Copies

Email Resume : Marksans Pharma Hiring For Manager – R & D

Marksans Pharma Ltd. is an Indian pharmaceutical company having a global footprint. Our strengths lie in research, manufacturing and marketing of finished dosage pharmaceutical formulations. “The essence of our culture is built on meeting global standards in every aspect of our business.” These envisioned words of Mr. Mark Saldanha, our Chairman and Managing Director, reflect the extreme passion and enthusiasm that drives the organization. Marksans Pharma, headquartered at Mumbai (India) is a global pharmaceutical company. We are actively engaged in R&D and offer CRAMS to global pharmaceutical companies.

Urgent Requirement

Organization: Marksans Pharma Ltd

Location : Navi Mumbai

Department :Research & Development

Required : Manager – R & D

Experience :10-15 years

Interested Candidate can send their resume on audrey.fernandes@marksanspharma.com

Responsibilities:

Responsible for preparation and review of SOPs, protocols, reports, policies etc of Formulation Development (FD) dept.

Planning, execution and monitoring of projects of formulation activity from project feasibility stage to commercial.

Demonstrates understanding of machine principles & process related to equipment and processes across scales to transfer processes/ products

Planning, monitoring and execution of formulation development activity from project feasibility stage to commercial.

Mentoring scientists for QbD based formulation development of various generic dosage form

Coordination with analytical department for various analytical activities.

Coordination with external department team as per project requirement for all required project activities.

Design the scheme of experiments. Interpret the results from various analytical instruments like HPLC, UV, GC, IR, etc.

Visualize the developmental needs of the product.

Submit samples for conducting pilot and pivotal Bio studies of pilot and Exhibit batches respectively in consultation with team.

Understand the safety and environmental aspect.

Solve the problems and queries related to the development of the formulation and discuss them with the Tech Lead.

Understand/familiarize with the problems faced during Scale-up.

Interaction with inter department for regulatory filing documentation requirements.

Understanding regulatory queries, providing scientific justifications and responding to regulatory queries as and when required on time for respective products.

Desired Candidate :

Having leadership experience of handling a group of scientists.

Candidate must have experience for formulation equipment / instruments installation, operation & performance qualification.

Having experience of mentoring and handling of FD team members and good inter-departmental communications are required.

Having good experience in Reverse Engineering of Innovator’s product.

Having experience of successful technology transfer from R&D to Plant scale.

Regards,

Audrey Fernandes

Asst.Manager-HR

9152988980

Fresher – B.Sc/B.Pharma/B.Sc /M.Sc (For Q.C department) Walk In 24 May – 25 May At Coral Drugs

Coral Drugs. is a Manufacturer & Exporter of Pharmaceutical Products based in INDIA. We have been following a steady growth path on the pillars of its philosophy of “Quality, Integrity and Core Values”. Incorporated in March1994 and headquartered in Mumbai – India Coral Drugs has over 20 years of experience in Manufacturing of Pharmaceutical formulations. Coral Laboratories Limited manufactures various pharmaceutical formulations at three different locations all over India.

Coral Drugs, Walk-In Interviews 

Designation:Q.C department

Qualification: B.Sc/B.Pharma/B.Sc /M.Sc

Experience: 00 Years

Job Location:Sonipat/ Sonepat,Haryana

Salary: NA

Time and Venue

24 May – 25 May , 9.30 AM – 3.00 PM

Coral Drugs Pvt Ltd , Unit-1, 55-58, HSIIDC, Industrial state, Murthal Sonipat -131039, Haryana

Contact – Jagbir Singh ( 8199986208 )

Job description

Good analytical skills

Good communication skills

Only B.Pharma/M.Pharma/B.Sc /M.Sc are required,

Share CV at hrcdpl-3@coraldrugs.com or at 8199986208

Cliantha Research Limited – Walk-In Interviews for M.Sc / B.Pharm / M.Pharm on 27th May’ 2023

Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL. Cliantha Research is headquartered in India with facilities in Ahmedabad, Noida and Vadodara.

We are conducting walk-in interviews for following..!!!

Position:Research Scientist

Qualification: M.Sc / B.Pharm / M.Pharm

Experience: 1 to 6 yrs

Salary: 2-5 Lacs P.A.

Location: Ahmedabad

Time and Venue:

27 May , 2.00 PM – 5.00 PM

3rd Floor, Commerce House II, Opp. Pushparaj Tower, Judges Bungalows Road, Bodakdev, Ahmedabad – 380054, INDIA

Report Specialist

Roles and Responsibilities:-

A. Prepare Sample analysis report and Method validation report in compliance with standard operating procedure.

B. Ensure report is prepared as per respective regulatory and sponsor requirement.   

C. Handle Sponsors or regulatory queries on lab reports.

D. To ensure that lab reports are released within their timelines.

E. Maintain documents and databases for the assigned projects.

F. Compile copies of Method validation report and Sample analysis report for archiving.

Report Viewer

Roles and Responsibilities:-

A. To ensure that the data is entered in a timely fashion to meet deadlines.

B. To ensure 100% validation data review for the completeness of documentation and in compliance with all applicable standard operating procedures and regulation.

C. Ensure quality and integrity of data.

D. Maintain documents and databases for the assigned projects.

E. Ensure the completeness of documentation pertaining to a method validation.

F. Report to the Study Director/R&D supervisor for method validation related any deviations.

G. Review of Analytical Laboratory system for GLP Compliances.

H. Compile method validation for archiving.

I. Ensure reconciliation of forms after completion of method validation.

J. Preparation of summary tables of Method validation.

K. To assist Project manager/Analyst for preparation of Analytical procedure.

L. Responsible for all activities of Lab archivist in absence of Lab Archivist or as and when require.

Email Resume : Torrent Pharmaceuticals Hiring For Clinical research Scientist

Torrent Pharmaceuticals The flagship company of the Torrent Group, Torrent Pharmaceuticals Limited is a major player in the Indian pharmaceuticals sector with the vision of becoming a global entity. Torrent Pharma enjoys dominance in the niche therapeutic areas like, cardiovascular and central nervous system, gastro-intestinal, pain management and oral anti-diabetic segments. Torrent Pharma owes its success in the domestic market to its thrust on frontline research, strategic marketing and world-class manufacturing. It is among the largest spenders on R&D and has set up one of the most advanced research centers in the country at an investment of Rs. 200 crores so far. It has discovered and patented the AGE (Advanced Glycosylation End Product) Breaker Compound which has potential to treat heart diseases and diabetes related vascular complications. Its manufacturing facilities have received quality certifications from various international regulatory authorities. It is this success that Torrent Pharma attempts to replicate in the international market now. It has already established fully-owned subsidiaries in Australia , Brazil , Germany , Japan , Mexico , Philippines Russia and USA and has over 1000 product registrations in more than 50 countries worldwide.

Torrent Pharmaceuticals Recruiting For Following:

Qualification: M.Pharma

Experience : 01-06+years

Role: Clinical research Scientist

Job Location: Ahmedabad

Interested Candidates may share their CVs on vilshashah@torrentpharma.com

Job Description

-Feasibility assessment/ new product evaluation

-Literature review and BA/BE study designing

-BE Study Monitoring

-Preparation of documents for regulatory submission (i.e BENOC, Import license application etc.)

-Establishment and maintenance of study documents

-Document preparation for dossier submission (i.e clinical overview, non-clinical overview, summery tables etc.)

-Review of BE study documents i.e protocol, reports, ICF etc.

-Preparation/review of medical write up

-Coordination for serious adverse event reporting and safety update to Regulatory agency.

NCHEM LABORATORIES – Walk-In Interviews for Freshers & Experienced From 27 May – 5th June 2023

Nchem Laboratories is engaged in manufacturing and export of business chemical compounds for an expansion of industrial necessities. With roots that pass lower back to as long as 3 years, it has grown into a incredibly matured and experienced corporation. Our wonderful increase charge over time reaffirms our religion that a committed and efficient service to trade and enterprise will important make an growth in our purchaser base who look up to us as a chemical supply. Our customer base and annual sales are developing at a fast pace. We constantly search for excellence in first-class, uncompromising reliability and dependability maintaining in thoughts efficient, effective customer support and their delight as prime situation.

We are conducting walk-in interviews for following..!!!

Role: Chemical Research Scientist

Qualification: Ph.D/Doctorate in Chemistry

Experience: 0-5 yrs

Location: Hyderabad

Interview Venue and Work Location :

27 May – 5th June , 9.30 AM – 5.30 PM

NCHEM LABORATORIES || http://www.nchemlaboratories.com Plot No: A-28/1/8/B/Part-B/1, Road-15|| IDA NACHARAM|| Hyderabad || Telangana|| INDIA– 500076 || GST IN: 36ACHPY9227A1ZE||

Contact – K.THIRUMAL REDDY ( 9963432457 )

Desired Candidate Profile

PG: M.Sc(Science) in Organic Chemistry :

Experience for Sr. CHEMIST: 1-3 years

Scientist : 7-8 years

Viyash Life Sciences – Walk-In for Freshers & Experienced on 22nd & 27th May 2023

Viyash Life Sciences Private Limited, We are an integrated pharmaceutical company with a strong portfolio of niche APIs and advanced Intermediates. Viyash and its subsidiaries operate 10 manufacturing facilities with a combined capacity over 2000 KL and diversified capabilities in every aspect – small/large volume, potent / non-potent, regulated / semi-regulated markets. We have a robust R&D infrastructure with a combined network of 3 R&D facilities and over 160 scientists with expertise across several technologies and complex reactions.

WALK-IN-INTERVIEW @ 22nd & 27th May 2023 for Viyash Group of companies!!

Viyash Life Sciences Private Limited Invites Experienced, Dynamic & Self-Motivated Professionals for the below positions at the Hyderabad location.

Department: Chemical R&D/ Process Development/Analytical R&D

No. of Positions: 20

Experience : 0-6 Years

Qualification : B.Sc /M.Sc. Chemistry 

Work Location : Hyderabad

Salary : Salary will not be a constraint for deserving candidates

Date and Time of Walk-in : 22nd & 27th May 2023

Time: 10:00 am to 4:00 pm

Interview Venue : Symed Labs Ltd, (R&D) (A subsidiary of Viyash) Plot No: 89/A, Phase – 1, Shapur Nagar, IDA, Jeedimetla, Hyderabad, TS-500055.

Contact:Candidates can send their profiles to jagadeesh.komiri@vivash.com with subject name “Application For R&D” Contact No: +919963647532

Please Note: Candidates are requested to bring resume, Photo copies of all educational certificates, Latest increment letter, Last three months’ pay slips/Last three months bank statement, Aadhar card copy.