PHARMA WISDOM

Walk- In Drive for MSc Fresher's & Experience in R&D Department API Division- R&D Center.

Openings: 120

Experience: 0 to 4 Year in API - R&D- M.Sc Fresher's & Experience, Process R&D, CRO -R&D

Eligibility Criteria:

Should have M.Sc Fresher's (Organic Chemistry) and Passed out in   2018, 2019 & 2020 only.

Should have 60% in throughout the Academical Career.

Position: Executive Trainee / Executive 

Department:  Research & Development (R&D - API)

Only Male Candidates

Date of Interview: 26.02.2021 (Friday)

Interview Time: 9.00 AM to 11.00 AM

Venue Details:

MSN Laboratories Pvt. Ltd.,

R&D Center, Plot No 12, IDA Pashamylaram

Patancheru Mandal, Sangareddy Dist

Hyderabad

Ph No : +91-8452304799/4899

040-30438786

Work Location : R&D Center, Pashamylaram

Walk- In Drive for Regulatory Affairs Dept. in API Division- R&D Center.

Regulatory Affairs API RA Dept. in API Division,

Openings: 70
Job Title: Executive / Senior Executive Experience: 1 to 8 years in API RA field Education: B Pharma / M Pharma / M.Sc
Department: Regulatory Affairs
Job Profile:
1. Collecting and reviewing the documents received from various departments R&D, AR&D, QA, QC and Production etc at each and every stage of manufacturing of drug substances to minimize the errors at the time of submission to regulatory agencies.
2. Hands on experience on the preparation of DMFs and their registration processes in the major regulatory regions [US, Canada, Europe etc]..
3. Hands on experience on preparation of drug master files, Applicants Parts, Tech Pack, life cycle management [updates and amendments] and drafting of response to deficiencies and customer DMF review comments for all global regions.
4. Should have hands on experience on eCTD regulatory submission tools.
5. Should have knowledge on the requirements to respond to the deficiencies.
6. Participation in the cross functional team meetings and providing regulatory inputs to the Product Development Teams.
Job Title: Junior Manager / Assistant Manager Experience: 1 to 8 years in API RA field Education: B Pharma / M Pharma / M.Sc
Department: Regulatory Affairs
Job Profile:
1. Good scientific conceptual background to the level to evaluate the processes and procedures in the area of Quality, R&D, AR&D and Production.
2. Manageable communication in English [should be able to manage regulatory and scientific discussions in the internal and external meetings and one to one interactions within the organization and with customers]
3. Manageable knowledge on the regulatory and quality guidelines from various regulatory agencies ICH, FDA, EMA, Health Canada, ANVISA, PMDA, MFDS, CFDA etc.
4. Thorough knowledge and hands on experience on the DMF registration and marketing authorization application systems in the major regulatory regions [US, Canada, Europe etc]..
5. Hands on experience on preparation of drug master files, life cycle management and drafting of response to deficiencies and customer DMF review comments for all global regions.
6. Should have knowledge on product developmental and the quality systems to ensure the regulatory compliance.
7. Should have hands on experience on eCTD regulatory submission tools.
8. Conducting meetings for the deficiencies received from various regulatory agencies and should have knowledge on the requirements to respond to the deficiencies. Ensuring that the accurate and adequate responses are sent to the authorities within the timelines defined by agencies.
9. Thorough review and ensuring that the regulatory submissions are adequate and error free with minimum open issues and closing of open issues before filing or before the receipt of deficiencies.
10. Participation in the cross functional team meetings and providing regulatory inputs to the Product Development Teams.
11. Reviewing the documents received from various departments R&D, AR&D, QA, QC and Production etc at each and every stage of manufacturing of drug substances to minimize the errors at the time of submission to regulatory agencies.
12. Review and assessment of change controls and providing guidance to the team on proposed changes.
13. Ensuring that the regulatory databases are properly maintained and updated on time to time for each regulatory activity.
Drug Regulatory Affairs API RA Dept.

Exp : 1 to 8 Years
Position: Junior Executive / Executive /Senior Executive / Junior Manager

Date of Interview: 06.03.2020 (Saturday)

Interview Time: 9.00 AM to 1.00 PM

Venue Details:

MSN Laboratories Pvt.Ltd.,

R&D Center, Pashamylaram

Ph No : +91-8452304799

040-30438786

Work Location : MSN LS II & R&D Center

REGULATORY AFFAIRS/EXPERIENCE-BULK DRUGS/API-HYDERABAD

Department: Regulatory Affairs

Designation: Executive/Sr. Executive

Industry: Pharma/API

Experience: 2 to 6 years

CTC: Negotiable

Job Location: Sanath Nagar, Hyderabad

Roles and Responsibilities

• Preparation of Drug Master Files (DMF) in CTD / eCTD / Nees format for US, European Countries, Canada, Australia, Japan, GCC, Turkey and Korea as per customer/ business requirement.
• Preparation of amendments/ Annual Reports to USDMFs, CEP variations, EDMF Updates, Biannual updates to Canada DMFs and Annual updates to Korea DMFs, Japan DMFs.
• Review and approval of change controls.
• Submission of notifications to the customers pertaining to regulatory submissions as per the applicability.
• Responding to deficiency letters received from various regulatory agencies like USFDA, EU Agencies, TGA, Health Canada etc.
• Hands-on experience in Electronic submissions-Lorenz.
• Maintaining query database and response timelines.
• Tracking of variation submission timelines (Amendments, Annual Reports) to various Health Authorities
• Responsible for organizing meetings to address queries and variation submissions.
• Rendering customer support by preparing technical packages, Applicant" s Part Drug Master Files and responding to the technical queries received from customers.

• Preparation of pharmaceutical ingredients (API) and its intermediates.
• Analytical interpretation, trouble shooting & Plant performances.

Desired Candidates Please Share Your Updated Resume vivek.s@heterodrugs.com

SUN PHARMA LTD - Urgent Openings for Production / Engineering / ETP Departments - Apply Now

Dear Aspirants,

Greetings from BVR Solutions…..

We are looking for Fresher candidates with good communication skills for API & Formulation PLANTs based @ Hyderabad.

Candidates are requested to carry recent passport size photo, updated resume, photo copies of Educational Certificates.

Timings: 9.00 am

Contact:  9121514444 | 8185999958 | 7337227575

                 040-35115211

E-mail id: bvrcareers@gmail.com / hr.bvr09@gmail.com

Address: BVR SOLUTIONS, plot no: 60 1^st floor 103, near arjun theatre (opposite to siri tiffins), jalavayu vihar road, western hills, KPHB, Hyderabad..

 SUN PHARMA LTD - Urgent Openings for Production - API

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Biophore India - Walk-In Interviews for M.Sc Organic Chemistry Freshers & Experienced in R&D API on 12th & 13th Feb' 2021

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 Maithri Drugs Pvt. Ltd, Bonthapally: Production (API) walk-in drive on 13/02/2021

VACANCIES: Trainee's/Assistant's/Officer's/Junior Executive’s/ Executive's (TOTAL 30 OPENINGS)

ELIGIBILITY CRITERIA: MEN candidates only of B.Sc/B.Com/BA/Inter/SSC with minimum 0-6 yrs of work experience. Diploma, ITI, B.Tech & BE candidates are NOT ELIGIBLE

TIMINGS: Only MEN candidates may walk-in from 09:00 AM to 01:00 PM

DOCUMENTS TO BE CARRIED: Candidates are requested to carry updated resume, photocopies of educational certificates, latest increment letter, last 3 months pay slips, last 6 months bank statement and photocopy of aadhar card.

INTERVIEW VENUE & WORK LOCATION: Maithri Drugs Pvt Ltd, Bonthapally. Landmark: Bonthapally Kamaan, Beside Bharat Petroleum Bunk Lane.
GOOGLE MAP: https://goo.gl/maps/vV9L5cG9vadJVZS87 
Contact: 040 30438366, 08455 694101

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Walk In Interview for API Production Chemist (1-5 years) 11 Feb @ Gland Pharma Ltd.

Roles and Responsibilities

Dy. Chemist / Chemist for API Production Department
* Candidate with Notice Period: 1 or 2 months are preferable.

Desired Candidate Profile

Qualification: B.Sc/M.Sc

Should have experience in API/Bulk Manufacturing

Attend interview with the following Documents:

1.     Resume

2.     Educational certificates

3.     Recent Increment Letter

4.     Payslips - 03 months (Latest)

5.     Supporting Bank Account Statement

6.     Pan Card copy

7.     Aadhar card copy

Walk In Venue details

Date 11^th Feb’ 2021, 09:00 am to 12:00 noon

Gland Pharma Ltd

Plot No. 49 & 50,

JN Pharmacity, Parawada

Visakhapatnam - 531019

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Torrent Pharmaceuticals Ltd - Urgent Openings for Freshers & Experienced in Quality Assurance / Quality Control / Production / PDL / EHS Departments @ Vizag

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Biophore India - Walk-In Interviews for Freshers & Experienced in R&D - API (Synthesis / Process / CRO) on 12th & 13th Feb' 2021

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