PHARMA WISDOM

Emcure Pharmaceuticals Ltd - Openings for MSTG (Manufacturing Science & Technology Group) / AMV (Analytical Method Validation) 20 Positions 

Walk-In for Formulation-Analytical Development

Dates: 2nd and 3rd Feb 2021

Time: 10am to 5pm.

Venue:

Granules India-Formulation plant-R&D Center- Gagillapur plant-Near Kazipally-Near Gandimaissamma x roads- Medchal road-Hyd-

Dept: Analytical R&D (Formulation)

Qualification: M.Sc or M.Pharm

Experience: 4 to 7 years

Requirement: Method development - HPLC, Dissolution, Good knowledge on mass balance - Assay, Related substances.

• Instruments: Dissolution, HPLC, GC,
• Software: Empower and Awareness on custom calculations
• Knowledge on QMS and GXP.
• Placement at Granules - Formulation plant - R&D center-Gandimaissamma x roads-Gagillapur (Near Kazipally)- Hyd.

Please bring the following with you

*Passport size Photograph

*Latest copy of CV;

*All educational certificates

*Latest Increment Letter

*3months Pay Slips

Contact: 9866479173

Mail: sharad.chandra@granulesindia.com

Walk-In for Quality Control (AMV)

Qualification: M.Sc or B.Pharm or M.Pharm

Experience: 4 to 7 years

Requirement: Method validation, Method transfer & Regular/Stability analysis of Dissolution, Assay, Related substances and Residual solvents

• Instruments: Dissolution, HPLC, GC, UV, IR & KF
• Software: Empower and Awareness on custom calculations
• Knowledge on QMS and GXP.

Please bring the following with you

*Photograph

*Latest copy of resume

*All educational certificates

*Latest Increment Letter

*3months Pay Slips

Contact: 7995144462

Mail: Ramanavenkat.Kamkol@granulesindia.com / Shilpa.Nookaraju@granulesindia.com

Venue:

Granules India Limited

Sy No. 160/A, 161/E, 162 & 174/A,

Gagillapur Village, Dundigal-Gandimaisamma Mandal,

Medchal-Malkajgiri District – 500 043,

Telangana,India

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Walk- In Interview @ RLFC (R&D , AR&D & AMV)

Openings: 50

Date: 23rd January - 29 January, 2021

Time: 9.30 AM - 4.00 PM

Venue:

R L Fine Chem Pvt. Ltd. C-10, 1st Cross,

KSSIDC Industrial Estate, Yelahanka New Town, Yelahanka,

Bangalore - 560 064, India,

R&D: Junior / Research Associate (1-6 Years)

Qualification: M.Sc. Organic Chemistry

Experience in multi-step synthesis process development of organic molecules

AR&D: Junior / Research Associate (1-6 Years)

Qualification: M.Sc. Analytical Chemistry/ Organic Chemistry

Experience in Method Development, Validation, routine analysis, documentation & regulatory support. Exposure in handling HPLC, GC, UV, IR etc.

AMV: Junior / Research Associate (1-6 Years)

Qualification: M.Sc. Analytical Chemistry/ Organic Chemistry/ Chemistry

Experience in Analytical Method Validation

Note : No Walk-ins on 24th & 26th

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Alembic Pharma Ltd - Pre-Planned Walk-In Interviews on 19th Dec' 2020

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MACLEODS PHARMA LTD
WALK IN INTERVIEW at Mumbai on 13/12/2020
Vacancies for Analytical Method Validation & Development (API) at our R&D Center - Mumbai.
Research Associate/ Sr. Research Associate - AMV (API)
Edu: M.Sc.
Exp: 2 to 7 yrs of in instruments like HPLC/GC for Method Validation (API).
Candidates with QC Validation exp. can be considered.
Research Associate/ Sr. Research Associate - AMV (Formulation)
Edu: M.Pharm/ M.Sc.
Exp: 2 to 7 yrs of relevant exp. in handling HPLC for Method Validation (Formulation).
Candidates with QC Validation exp. can be considered.
Research Associate/ Sr. Research Associate - AMD (API).
Edu: M.Sc.
Exp: 2 to 7 yrs experience handling various instruments like HPLC/GC/ ICPMS/LCMS/NMR or XRD for Method Development (API).
Please WALK IN along with CV and CTC proof (Annexure) on following date & place AT 9:30am to 5:00pm.
Sunday, 13th Dec 2020.
Venue:
MACLEODS HOUSE,
B.D.Sawant Marg,
Off Western Express Highway Opposite Hindustan Unilever Ltd.,
Chakala, Andheri(E), Mumbai-400099.
advaitc@macleodspharma.com; Mayurim@macleodspharma.com
In case of any query, please revert on 9892506453/ 8291331272/ 8356923637

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Greetings from Macleods Pharma

Position : Research Associate - GC and HPLC

Department : Analytical Method Validation

Location : Mumbai

Job Responsibilities:

• Perform method Validation of Active Pharmaceutical ingredients using Gas Chromatography and high performance Liquid chromatography.
• Method transfer to manufacturing sites.
• Re-qualification of impurity standards, DMF Queries, Customer Queries, Absence studies and Batch analysis of samples.
• Preparation of Method validation protocol (MVP), method validation reports (MVR) & method validation raw data.
• To work in a validation protocol and Report drafting and complies.
• To work as per GLP and GMP .
• Must have exposure to cleaning validation and verification parameters.
  Must have exposure to process complete validation in APIs.
• Operate analytical instruments like HPLC, GC, GC-MS, UV Spectrophotometer and Dissolution Tester.
• Trouble shoot as and when Required.
• Conduct force degradation studies and routine analysis for stability.

Kindly share your updated resume on Advaitc@macleodspharma.com

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Research Associate - Analytical Method Validations (Respiratory)

Location: Nashik / Aurangabad

Roles and Responsibilities

This role is based out of Glenmark's Aurangabad Manufacturing plant and involves supporting R&D team with Analytical Validations and Development process of Respiratory portfolio dosage forms (Inhalers, Aerosols of various indications, Nebulizers, Tablets / capsules etc.) for Global Markets. The goal of this role is to deliver services with an accuracy in results and within agreed timelines set by Group leader.

• Perform Method Validation at Manufacturing Plant and R&D site - Ensure that all tasks assigned by the functional manager/Seniors are completed within time and with appropriate quality. Conduct/Execute validation activity as per protocol. Daily online calculation of validation related activity
• Prepare Validation Protocol and Report as per guideline and regulatory requirement
• Calibration and qualification of Instruments - Ensure that all tasks completed as per SOP and according to GLP procedure within time
• Follow current GLP System in the lab maintain the quality and accuracy of the work throughout the year

Desired Candidate Profile

Education (degree / diploma) - M.Pharm - Pharmaceutics Chemistry / Ph. D / M.Sc. Analytical Chemistry

Experience - Should have 2 to 6 years total work experience in Analytical Method Development
Knowledge and Skills (Functional / Technical) - Should be well acquainted with handling below equipment like HPLC/UPLC/Spray View etc.

Other requirements (licenses, certifications, specialized training) - Experience in handling ANDA

Interested candidates who meet the above criteria can send their CVs to Dhurjuti Dhibar (Dhurjuti.Dhibar@glenmarkpharma.com ) and Bhushan Wadgaonkar (Bhushan.Wadgaonkar@glenmarkpharma.com)

Sr. Research Officer / Research Scientist - MDI Formulations

Roles and Responsibilities:

The role involves support to various activities that are involved in formulation development process of MDI dosage form for US/EU/ROW and India market. The goal of this role is to deliver commercialization of formulations in MDI dosage for India/ROW or regulated markets and other Services with accuracy in results within agreed timelines.

Below listed are a few deliverables in the role:

• Literature and patent search - Should perform literature search from reference book, Should have some basic understanding of patent and generic formulation development.
• Subject knowledge - Should think and come up with Novel/Innovative formulation ideas or strategy
• Documentation and data review - Should review relevant data like in vitro study , characterisation studies
• Regulatory requirements - Should have knowledge towards development activities as per regulatory/IP requirements etc.
• Competitor product procurement and characterization, Evaluation/optimization of excipients and primary packaging Materials
• Pre formulation development - knowledge of Pre-formulation studies
• Process Finalization - know basic mfg. process during development
• Stability studies and report writing - aware stability conditions and keep track and evaluate stability data
• Technology transfer of the product at Plants and Exhibit Batches at Plant (as per the Requirement of Regulatory)

Desired Candidate Profile

Education (degree / diploma) - M. Pharm - Pharmaceutics /Ph. D

Experience - Should have minimum of 6 to 10 years of work experience in Formulation and Development of MDI dosage formulations preferably for US/EU Mkts.
Other requirements (licenses, certifications, specialized training)-

• Updated technical knowledge. Relevant to MDI dosage form
• Should aware of FDA guidance to take out RLD details etc.
• Should aware of basic understanding of technology to initiate developmental work related to MDI dosage form
• Should have experience in handling ANDA
• Should be well conversant with commercialization of few formulations in MDI dosage for India/ROW or regulated market
• Should be thorough in documentation to provide MFC and BOM based on development and facility available.

Interested candidates who meet the above criteria can send their CVs to Dhurjuti Dhibar (Dhurjuti.Dhibar@glenmarkpharma.com) and Bhushan Wadgaonkar (Bhushan.Wadgaonkar@glenmarkpharma.com)

Research Officer - Analytical Development

Roles and Responsibilities

The role involves support to various activities that are involved in Analytical Development process for various dosage forms like Tablets, hard / Soft Gelatin capsules, Nasal, Nebulizers & NMEs for different Markets.

Desired Candidate Profile:

• Initial Sample Analysis - Analysis for Assay, Related substance, Dissolution profile, BRS & APSD.
• Stability Study Analysis
• Method development as per QbD approach with reference from latest research articles.
• In-Vitro study & Characterization study to be perform as per approved protocol
• Working standard preparation & Standardization as per SOP, STP and according to GLP.
• Analytical Technology transfer and Validation support at different site.
• Calibration and qualification of Instruments

Suitable candidate can send their profiles on Bhushan.Wadgaonkar@glenmarkpharma.com, Dhurjuti.Dhibar@glenmarkpharma.com.

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