Showing posts with label EXPERIENCE. Show all posts
Showing posts with label EXPERIENCE. Show all posts

Saturday 31 July 2021

COVALENT LABORATORIES LTD WALK ON INTERVIEW ON 1st, AUGUST, 2021 @ HYDERABAD


ABOUT COMPANY :

Covalent Laboratories Private Limited, an ISO 9001:2008 & ISO 14001(2004) accreditated pharmaceutical company and WHO GMP certified for all its products, is specialized in the manufacturing of Cephalosporins.

It has a wide range of products and is fast expanding to meet the present and future market demands for the high value, low volume drugs. Covalent Laboratories manufactures the Active Pharmaceutical Ingredient (API) in bulk quantities for both domestic and international markets. All the drugs manufactured me -ets USP / BP / JP standards.

Covalent Laboratories, which is professionally managed and has well equipped Quality Assurance and Quality Control Lab, focuses on higher production standards for superior quality products that surpass the international standards.

Covalent Laboratories aims at reducing the production cost to give the best price to its customers through its aggre- ssive process development lab.



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HEMA LABORATORIES WALK IN INTERVIEW FOR QA DEPARTMENT FROM 1st, AUGUST TO 6th, AUGUST, 2021 @ HYDERABAD



ABOUT COMPANY :

Hema Laboratories was established by K.Siva Rami Reddy in the year 2017,with a grand vision of being the “most preferred supply partner to fulfill the requirements of pharmaceutical customers worldwide

The management aimed to achieve this vision with quality & affordability of products as our highest priority. It is one of the fastest growing manufacturers of Active Pharmaceutical Ingredients (API’S),Intermediates & Specialty chemicals.

Customer Satisfaction is a powerful engine in optimizing the companies profitability through the various imparts it can have, notably on a Quality, Commitment & Affordability Quality is a founding principle at Hema Labs. Since our beginnings,we have placed it at the centre of our concerns, even embedding it in our internal values.

At Hema Laboratories we offer a range of challenging and rewarding career opportunities in an open, diverse and supportive work environment. It is a place where we are free to explore and encouraged to voice new ideas.

As an innovative driven pharmaceutical company with sales US $ 2.8 million, the diversity of job opportunities at Hema runs wide and deep. This is what distinguished us from the rest and inspires us to Excel, Innovate and lead.

The company believes in bringing together the best and the brightest talents it can find in the industry.

If you believe that you can show your talent and sharpen your skills, doors of Hema Laboratories are always open.
Note:you may email your resume to : hr@hemalaboratories.com


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Friday 30 July 2021

MAITHRI DRUGS PVT LTD WALK IN DRIVE FOR FRESHERS & EXPERIENCE CANDIDATES ON 2nd, AUGUST, 2021 @ HYDERABAD

                                                         


ABOUT COMPANY :

Maithri Drugs is one of India's fast-growing pharmaceutical companies. Maithri's strategic focus is on active pharma ingredients (APIs). The company is widely recognized for its excellent research & development and aggressive growth strategies. Our 30 US DMFs and 9 CEPs in a short span attest to our R&D excellence.


Maithri's manufacturing facility is located in Hyderabad. This facility is audited and approved by the US FDA. In addition, our facility is certified according to the standards of  DCGI, WHO GMP, and ISO 9001:2015 We have a portfolio of 65 products and are continually expanding. Our products cover a broad range of therapeutic categories including CNS, anti-anaemics, anti-bacterial, anti-diabetic, anti-fungal, anti-hyperthyroidism, anti-inflammatory, anti-viral, antihypertensive, cardiovascular, etc. 


Maithri Drugs serves hundreds of customers spread across 35 countries. We have a constant goal of producing high-quality products and providing unparalleled customer service.


VACANCY DETAILS :

Dear Team,


Maithri Drugs R&D Technology Center, Gummadidala: R&D (API) Department walk-in drive on 02/08/2021

VACANCIES: Trainee's (Fresher's)/ Junior Executive’s/ Executive’s/ Senior Executive's

QUALIFICATION: B.Sc (Chemistry)/ M.Sc (Organic Chemistry)

ELIGIBILITY CRITERIA: 0-7 yrs of work experience -  B.Pharm & M.Pharm candidates are NOT ELIGIBLE

JOB REQUIREMENTS:
1. Need to have sound knowledge in API R&D.
2. Need to have experience in process developmemt R&D

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.

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


INTERVIEW VENUE & JOB LOCATION:  Maithri Drugs R&D Technology Center, Gummadidala. Landmark:  2nd gate beside IPC Church, Gummadidala



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AUROBINDO PHARMA LTD HIRING CANDIDATES FOR QA DEPARTMENT (IPQA/ QMS/ VALIDATION/ CSV ) @ NAIDUPETA , NELLORE

                   

                                           


ABOUT COMPANY :


Founded in 1986 by Mr. P. V. Ramprasad Reddy, Mr. K. Nityananda Reddy and a small group of highly committed professionals, Aurobindo Pharma was born of a vision. The company commenced operations in 1988-89 with a single unit manufacturing Semi-Synthetic Penicillin (SSP) at Pondicherry.

Aurobindo Pharma became a public company in 1992 and listed its shares on the Indian stock exchanges in 1995. In addition to being the market leader in Semi-Synthetic Penicillins, it has a presence in key therapeutic segments such as neurosciences, cardiovascular, anti-retrovirals, anti-diabetics, gastroenterology and anti-biotics, among others.


VACANCY DETAILS :


Send Resumes Who are willing to relocate Nayudupeta Only 

Send RESUMES On and before 01/08/2021


COMPANY : Aurobindo Pharma Ltd

JOB LOCATION : Nayudupeta , Nellore (Dt), Andra Pradesh

DEVISON : Formulation

DEPARTMENTS: QUALITY ASSURANCE 

Designation :  Executive/ Sr.executive

QUALIFICATION : B.Pharm/ M.Pharm
             
EXPERIENCE : Should have minimum experience of 4- 10 years.

Quality Assurance: Executives/ Senior Executives

(Qualifications – CSV / Equipment /QMS/IPQA)

 

Analytical Quality Assurance: Executives/ Senior Executives


Candidate with 4 – 10 years of formulations experience & should have USFDA or other Regulatory audits exposure.



In subject Mention your " AUROBINDO"

Interest candidates send resume to globalpharmanews@gmail.com



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MAITHRI DRUGS PVT LTD WALK IN DRIVE FOR QA DEPARTMENT ON 31st, JULY, 2021 @ HYDERABAD

                                                       


ABOUT COMPANY :

Maithri Drugs is one of India's fast-growing pharmaceutical companies. Maithri's strategic focus is on active pharma ingredients (APIs). The company is widely recognized for its excellent research & development and aggressive growth strategies. Our 30 US DMFs and 9 CEPs in a short span attest to our R&D excellence.


Maithri's manufacturing facility is located in Hyderabad. This facility is audited and approved by the US FDA. In addition, our facility is certified according to the standards of  DCGI, WHO GMP, and ISO 9001:2015 We have a portfolio of 65 products and are continually expanding. Our products cover a broad range of therapeutic categories including CNS, anti-anaemics, anti-bacterial, anti-diabetic, anti-fungal, anti-hyperthyroidism, anti-inflammatory, anti-viral, antihypertensive, cardiovascular, etc. 


Maithri Drugs serves hundreds of customers spread across 35 countries. We have a constant goal of producing high-quality products and providing unparalleled customer service.


VACANCY DETAILS :

Maithri Drugs Private Limited, Bonthapally: QA Department walk-in drive on 31/07/2021

VACANCIES: Assistant Manager/ Deputy Manager

QUALIFICATION: M.Sc/ M.Pharm/ B.Sc/ B.Pharm

ELIGIBILITY CRITERIA: 10-15 yrs of work experience in pharma industry

JOB REQUIREMENTS:
1. Knowledge on OOS, OOT's, Deviations and need to establish the CAPA.
2. Need to evaluate the risk assessments as part of Integrated Quality Management, Facilities, Equipment and Utilities, Materials Management.
3. Need to interact with various regulatory health authorities regarding Submission / Amendment / Variations / Approvals etc..,
4. Should be able to face the regulatory authority and customer audits
5. Preparing and Reviewing of SOP's, STP's, process and method related documents.
6. Knowledge in handling quality related complaints, return goods and recalls.
7. To verify the change management and approving impact on changes that potentially impact intermediate or API quality.
8. To verify product quality reviews.
9. Should be well versed with water system qualifications, clean room qualifications and air handling unit qualifications.
10.Should have through knowledge on QMS systems and should be able to handle quality assurance department.

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.

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

INTERVIEW VENUE & WORK LOCATION: Maithri Drugs Pvt Ltd, Bonthapally, Landmark: Lane Beside Bharat Petroleum Bunk, Bonthapally




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MARKSANS PHARMA LTD HIRING CANDIDATES FOR QA / PRODUCTION / PACKING DEPARTMENTS @ VERNA , GOA

                               

ABOUT COMPANY : 

"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.

Our key focus areas lie in the OTC & prescription drugs that have wide-ranging applications across fields like Oncology, Gastroenterology, Antidiabetic, Antibiotics, Cardiovascular, Pain Management, Gynaecology, among others.

We have established world-class manufacturing facilities by leveraging state-of-the-art technology, incorporating best practices and adhering to stringent regulatory compliances. Our plants are approved by prestigious US FDA, UK MHRA, Australian TGA and other foreign health authorities.

Our R&D capabilities include dossier development, chemical synthesis, process optimization, formulation development, analytical development and conducting stability studies. We have a team of over 50 experienced scientists specializing in formulation development and analytical development.

We possess end-to-end capabilities – from Lab scale development to Pilot scale up and from commercializing the product for large scale manufacturing to marketing globally.

The company has achieved global recognition within a very short span of time and has major global expansion plans for the near future.


VACANCY DETAILS 

*Urgent Requirement*

Organization: Marksans Pharma Ltd
Location : Verna, Goa

Department : Quality Assurance
Position : Officer - IPQA
Experience: 1 to 4 years
Qualifications: Bpharm / Mpharm

Department : Softgel (Production) 
Required : Officer (Bpharm/Mpharm) 
Experience :1-4 years

Department : Packing 
Required : Officer (Bpharm/Mpharm) 
Experience :1-4 years

Department : Production
Required : Operator (ITI/Diploma ) 
Experience :2-5 years
For Compression
Experience in handling of (Cadmach, Fette and Sejong preferred) 

Email : Neha.rao@marksanspharma.com 
Email :Joshua.dcosta@marksanspharma.com

*Note - Kindly mention the subject of the mail as "Application for the post of IPQA/ Packing Officer"*

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Thursday 29 July 2021

JUBILANT BIOSYS WALK IN INTERVIEW ON 31st, JULY, 2021 AND 1st, AUGUST, 2021 @ BANGALORE




ABOUT COMPANY :

Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centers in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies.

Jubilant Pharmova Ltd is an integrated global pharmaceutical and life sciences company engaged in pharmaceuticals, life science ingredients, drug discovery solutions and India branded pharmaceuticals.

The Pharmaceuticals segment, through its wholly-owned subsidiary Jubilant Pharma Limited, is engaged in manufacturing and supply of APIs, solid dosage formulations, radiopharmaceuticals, allergy therapy products and contract manufacturing of sterile injectables and non-sterile products through six USFDA approved manufacturing facilities in the US, Canada and India and a network of over 50 radiopharmacies in the US.

The Life Science Ingredients segment is engaged in specialty intermediates, nutritional products and life science chemicals through five manufacturing facilities in India. The drug discovery solutions business is served by Jubilant Biosys and the India branded pharmaceuticals business is an Indian venture with a range of pharmaceutical offerings for the domestic market, focusing primarily on products to treat medical conditions in the field of cardiology and diabetology.

Jubilant Pharmova Limited has a team of around 7,700 multicultural people across the globe and is committed to delivering value to its customers in over 100 countries. The Company is well recognized as a ‘Partner of Choice’ by leading pharmaceuticals and life sciences companies worldwide.



VACANCY DETAILS :

Walk-in Interviews for Research Associate/ Senior Research Associate for Jubilant Biosys Noida @ Hotel Sai Vishram, Bengaluru on 31st July & 01st August ( Saturday & Sunday)

Experience- 1 - 8 years

Qualification : M.Sc / M.Pharma (Organic Chemistry / Medicinal Chemistry)

Date: 31st July  & 01st August' 2021 (Sat-Sun)

Time: 9:00 AM- 06:00 PM

VENUE: HOTEL SAI VISHRAM
144/C-1, OPP BOMMASANDRA INDUSTRIAL AREA, HEBBAGODU,BENGALURU

Eligible and Interested candidates will come for Walk-in Drive as per above details with updated CV or mail profile at rahul.verma@jubilantbiosys.com



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SUN PHARMACEUTICAL INDUSTRIES LTD WALK IN INTERVIEW ON 1st, AUGUST, 2021 @ PAONTA , HIMACHAL PRADESH




ABOUT COMPANY :

Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of over US$ 4.5 billion. Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe.

We manufacture and market a large basket of pharmaceutical formulations covering a broad spectrum of chronic and acute therapies. It includes generics, branded generics, specialty, complex or difficult to make technology-intensive products, over-the-counter (OTC), antiretrovirals (ARVs), Active Pharmaceutical Ingredients (APIs) and Intermediates. Our broad portfolio of more than 2000 high quality molecules covers multiple dosage forms, including tablets, capsules, injectables, inhalers, ointments, creams, and liquids.

Every year, we sell over 30 billion doses covering neuro-psychiatry, cardiology, gastroenterology, anti-infectives, diabetology, oncology, ophthalmology, dermatology, urology, nephrology and respiratory among others.

The first among Indian pharmaceutical companies to realise and embrace the importance of investing in research, we invest up to 7-8% of our global revenues into Research and Development (R&D) every year.

Our core strength lies in our ability to excel in developing generics and technologically complex products backed by our dedicated teams in formulations, process chemistry, and analytical development.

Our capabilities extend beyond the development of differentiated products, including liposomal products, inhalers, lyophilized injections, nasal sprays, and controlled release dosage forms.

Our R&D is led by a strong team of more than 2000 scientists.

From humble beginnings in 1983, Sun Pharma has grown to become one of the largest generic pharmaceutical companies worldwide. We are the largest pharmaceutical company in India.

In the US, we are among the top 10 generic pharmaceutical companies and are ranked second by prescriptions in the generic dermatology market.

We are the largest Indian company in emerging markets with a presence in over 80 markets. Brazil, Mexico, Russia, Romania and South Africa are some of our key emerging markets.

We are present across all major markets in Western Europe, Canada, Australia, New Zealand, Japan and China among others.

Our presence in emerging markets and the developing world enables our teams to cross-sell and build brands with ease.




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AURORE LIFE SCIENCES WALK IN INTERVIEW FOR PRODUCTION ON 31st, JULY, 2021 @ HYDERABAD


ABOUT COMPANY :

Established in 2017, We are a pure-play Active Pharmaceutical Ingredient (API) company keen on delivering superior products in a regulatory compliant environment.

We are backed up with manufacturing facilities in India with a combined manufacturing capacity of 600 KL and our flagship facility in Hyderabad in approved with USFDA, EDQM, WHO Geneva, COFEPRIS, KFDA amongst other regulatory agencies. Our facilities, coupled with a dedicated R&D setup, complement our strategy to be a fully integrated API company with complete control of key starting materials, advanced intermediates and high-quality final product.

With a strong team of R&D experts that complements our strategy, Aurore is rapidly emerging as the most preferred API and key API intermediates supply partner for leading global pharmaceutical companies.

With a robust portfolio of niche and differentiated molecule spread across major therapeutic divisions, we are rapidly establishing ourselves as a reliable partner to serve unmet demands of the market.

 

Aurore Life Sciences is a pure-play API manufacturer with a diverse portfolio of capabilities in delivering efficiencies to generic players globally. Founded in 2017 by a team with vast experience across the pharmaceutical value chain, the company is on a mission to become the most preferred partner for pharmaceuticals.

At Aurore, we aim to push the boundaries to manufacture and deliver high quality products that can be relied upon by both customers and regulators. Our thrust on rapidly adding capabilities have led us to acquire, integrate and expand our reach across the geographies.



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Wednesday 28 July 2021

RAKS PHARMA PVT LTD (DIVISON OF AMNEAL PHARMACEUTICALS) HIRING CANDIDATES FOR QC DEPARTMENT @ VIZAG


ABOUT COMPANY :

We at Raks are dedicated to develop and manufacture active pharmaceutical ingredients and intermediates. We are committed to create value through intellectual property, quality systems and customer relation across the globe. We are research driven company providing cost effective and environmental friendly technologies with safety and quality as primary focus.

M/s. RAKS Pharma was conceptualized to become a significant API player so as to manufacture & supply APIs & Drugs Intermediate to Regulated & Non-Regulated Market from its present manufacturing site in Visakhapatnam (Andhra Pradesh), and upcoming unit in Dahej (Gujarat) India.

Raks is an interesting blend of consistency in maintaining both quality standard and growth in terms of addition of new products to its existing list of API's and intermediates. To realize this goal it has a team of experienced, dedicated and highly motivated professionals in all fields of the business.

Founded by a group of highly committed Technocrats in year 2009, today Raks Pharma is a partner of choice for pharmaceutical companies across the globe to source Active Pharmaceuticals Ingredients and their intermediates.




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JUBILANT GENERICS HIRING CANDIDATES FOR IT / PRODUCTION / QA (07th, AUGUST, 2021) @ ROORKEE


ABOUT COMPANY :

We are a global vertically integrated pharmaceutical company engaged in research and development, manufacture, sale and distribution of prescription and OTC pharmaceutical products, with global presence in more than 50 countries, including United States, Europe, Canada, Japan, Australia and Rest of the World. We offer a wide range of proprietary finished dosage formulation catering to different therapeutic segments, including CVS, CNS, gastro-intestinal, etc. in multiple dosage forms including:

  • Immediate-release oral solids
  • Modified release oral solids
  • MUPS based products
  • Chewable tablets
  • Powder for oral solutions & Suspensions

Jubilant Generics is a subsidiary of Jubilant Pharma.

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to our customers across geographies. We organise our pharma business into three segments. Firstly, ‘Specialty Pharmaceuticals’ comprising Radiopharmaceuticals (including Radiopharmacies) and Allergy Therapy Products. Secondly, our ‘CDMO’ segment, comprising Parenteral Contract Manufacturing and Active Pharmaceutical Ingredients. Finally, the ‘Generics’ segment is for our Finished Dosage Formulations business.

We supply our products and services to customers in over 85 countries. We have four manufacturing facilities in North America and two in India, coupled with research and development centers in North America and India. Additionally, we have a distribution network of more than 50 radiopharmacies in the United States.

Jubilant Pharmova is an integrated global pharmaceuticals company having three business segments Pharmaceuticals, Contract Research and Development Services and Proprietary Novel Drugs.

Jubilant Pharmova Limited has a team of around 5,800 multicultural people across the globe and is committed to delivering value to its customers. The Company is well recognized as a ‘Partner of Choice’ by leading pharmaceuticals worldwide.




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CADILA PHARMACEUTICALS LTD WALK IN INTERVIEW ON 31st, JULY, 2021@ ANKALESHWAR , GUJARAT


ABOUT COMPANY :

Cadila Pharmaceuticals Ltd. is one of the largest privately-held pharmaceutical companies in India. Over the past seven decades, we have been developing and manufacturing affordable medicines for patients around the world.

Our innovation-led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and a strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standard in clinical research and medical practice. We want to be valued not only for our pharmaceutical products but also for the way we conduct our research and business activities.

We lead our industry in demonstrating the application of cutting-edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.



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USV PHARMA PVT LTD HIRING CANDIDATES FOR QUALITY ASSUARANCE (QA) @ SAVLI-MANJUSAR , VADODARA, GUJARAT



Come & Join an exciting journey of Growth and Development

*USV Private Limited*– A leading Pharmaceuticals Company is hiring for its new state-of-the-art formulations manufacturing facilities at Vadodara. The location of the plant is at Savli-Manjusar, Vadodara, Gujarat.

We required following personnel for QA function, Qualification required B.Pharma/M.Pharma

*IPQA – Officer/Sr. Executive (Exp - 3-7 yrs.)* Responsible for in process checks, Batch execution document review, AQL, shop floor investigation & Sampling of regular batches as well as validation batches at various stage of Manufacturing & Packing. Candidate should have good knowledge about GMP guidelines. Candidate having exposure or knowledge about MES or any other electronic system for manufacturing execution will be preferred.

*IPQA- Section Head - Asst. Manager/ Dy. Manager (Exp. 9 - 12 yrs.)* Require good knowledge of QMS/CAPA. The candidate must possess good Investigation, Problem solving & troubleshooting skills. Candidate having exposure or knowledge about MES or any other electronic system for manufacturing execution will be preferred.

*QMS – Executive/ Asst. Manager (Exp. 5-8 yrs)* Person independently handling the QMS activities and involved in the investigation of all events like Market Complaints, Deviation & CAPA, Product recall and trend evaluation of QMS events. He should have good knowledge of master documents and must possess communication skill..

*QMS (Investigations) - Executive/ Asst. Manager (5-8 yrs)* - Responsible for QMS events investigation i.e. Deviation/ Complaint/ Recall/ OOS/OOT/Incident. He must be well versed with investigation tools. A person having good knowledge of regulatory norms. He also need to possess good communication skills.

*Validation / Qualification - Executive/Asst. Manager (Exp. 5-8 yrs)* - Responsibility involves conducting all type of validation/qualification activities in the plant (both process & utilities). The candidate should have good knowledge of GMP guidelines & regulatory requirement. Must possess sound problem solving/ troubleshooting skills. 

*Documentation - Officer/Executive (3-6 yrs Exp)* - Responsible for documents preparation / issuance/ retrievals. Also responsible for master formula records. A person having good knowledge regulatory expectation. He must possess good communication and presentation skills.

Share your CV at ajeet.rawat@usv.in

Date of Posting: Jul 28, 2021
www.usvindia.com

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