Thursday 20 November 2014

Career as Regulatory Affairs Specialist in PPD Pharmaceuticals

PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations.
Post: Regulatory Affairs Specialist

Qualifications:- Bachelor's Degree.
·         0-2 years experience.
·         English language as well as local language where applicable.
·         Attention to detail and quality of documentation.
·         Good interpersonal skills.
·         Familiar with computers and their applications, e.g. Word, Excel, Power Point.

Additional Information:
Experience:
 0- 2 Years
Location:
 Haryana
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Job Code: 119818
End Date: 13th December, 2014
 
Click Here To Apply Online>>

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Thursday 18 September 2014

Career as Regulatory Affairs Specialist in PPD Pharmaceuticals

PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 32 countries and more than 9,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients.

Post: Regulatory Affairs Specialist

Qualifications
Required are:
·         Bachelor or higher graduate degree in science-related field.
·         At least 2 years of professional experience within Regulatory
·         Having relevant exposure in handling regulatory requirement for Europe or International market which includes Initial MA, Variations, Renewals & PSURs etc.
·         Sound knowledge of CMC, CTD dossiers and various ICH guidelines.
·         Additional knowledge about labelling, familiarity with globally-deployed regulatory publishing tools, processes and systems will also be an advantage.
·         Very good English language skills
·         Attention to detail and quality of documentation
·         Effective oral and written communication skills
·         Ability to work on own with minimal supervision
·         Suitable experience working in the pharmaceutical/CRO industry is preferred

Additional Information:
Experience: 
Min. 2 Years
Location:
 Mumbai
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Job Code: 112491
End Date: 30th September, 2014

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Tuesday 19 August 2014

Vacancy in Roche for the post of Executive - Regulatory Affairs

Roche Diagnostics India, with a sales turnover of INR 150 crores, nurtures an open, flexible and challenging work environment, which allows for rapid career progression.

Post: Executive - Regulatory Affairs

Candidate Profile
Education: Post Graduate
Experience-  4-5 years  in handling regulatory documentation, registration and licensing of drugs / devices

Additional Information: 
Job ID: 2958365503
Qualification: Post Graduate
Location: Delhi
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: DRA

End Date: 30th August, 2014

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Thursday 31 July 2014

Vacancy in Roche for the post of Executive - Regulatory Affairs

Roche Diagnostics India, with a sales turnover of INR 150 crores, nurtures an open, flexible and challenging work environment, which allows for rapid career progression.

Post: Executive - Regulatory Affairs

Candidate Profile
Education: Post Graduate
Experience-  4-5 years  in handling regulatory documentation, registration and licensing of drugs / devices

Additional Information: 
Job ID: 2958365503
Qualification: Post Graduate
Location: Delhi
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: DRA
End Date: 30th August, 2014
 
Apply through Recruiters Portal>>

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Tuesday 20 May 2014

B. Pharma -Quality Assurance / Regulatory Affair by healthy life pharma in Mumbai

Healthy Life Pharma
Company is looking for fresher B. Pharma or M. Pharma. Post is regulatory affair & quality assurance. Making of dossier, FDA work, and Quality assurance documentation work.
Experience: 0 to 1 yrs
Role Category:  R&D
Role:  Pharmacist/Chemist/Bio Chemist
Education: B. Pharma/ M.Pharma

Contact Details:
Recruiter Name: HR MANAGER
Email Address: job.healthparmacy@gmail.com
Telephone: 912267415973

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Sunday 27 April 2014

Opening as Pharmacist - Regulatory Affairs by Narula Exports in Delhi

Opening(s): 1
Job Description:
Advises programs on regulatory requirements, coordinates and presents regulatory data needs, and negotiates with and influences management, colleagues and partners to ensure regulatory data requirements are met.

Salary: INR 2,25,000 - 3,00,000 P.A. P.f., Bonus & Leave encashment
Role: Pharmacist/Chemist/Bio Chemist

Education:
UG - B. Pharma - Pharmacy
PG - M. Pharma - Pharmacy 


Experience: 2 to 5 yrs.

Contact us:
Recruiter Name: Parveen Kumar Narula
Address: Narula's Tower-1, 25, Central Market, Punjabi Bagh West NEW DELHI, Delhi, India
Email Address: hr@narulaexports.com
Telephone: 11-91-45459999

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Wednesday 23 April 2014

Applications are invited as Research Associate, Research Associate R&D, Executive AgroTech, Executive QA, Executive Production, Executive International Regulatory Affairs in Himalaya Drug Company

Himalaya's story began way back in 1930. A curious young man riding through the forests of Burma saw restless elephants being fed the root of a plant, Rauwolfia serpentina, which helped pacify them. Fascinated by the plant's effect on elephants, this young man, Mr. M. Manal, the founder of Himalaya, wanted to scientifically test the herb's properties.

Research Associate
No of vacancy: 1
Reference Code: RAFOOD171013
Department: R&D
Qualification: M. Sc/M. Pharma (Chemistry/Analysis)

Research Associate R&D
Reference Code: RAFAD
Department: R&D Centre
Qualification: M. Pharma
Person Specification:
·         Proficient in computer applications.
·         Good communication skills.
·         Should have a relevant experience of 2-3 years.

Executive AgroTech
No of vacancy: 1
Reference Code: EXATB20092013
Department: Agrotech
Qualification: M. Sc(Botany)/ M. Pharma(Pharmacology)
Person Specification:
·         Should have an experience of 4 to 5 years in Pharma sector.
·         Should have experience in identification of herbs.
·         Should be computer proficient.
·         Should be proficient in English.

Executive QA
No of vacancy: 3
Reference code: EQA04092013
Department: Quality Assurance
Qualification: M.sc/B. Pharma
Person Specification:
·         Should have an experience of 2-3 Years in the field of Quality Assurance
·         Good analytical skills and excellent communicator - Oral, Written and presentation skills.
·         Strong Microsoft Office skills

Executive Production
Department: Production
Reference Code: EXEP040813
Job Description:
·         Ability to operate production machines and effectively handle manpower
·         Should have exposure to contract manufacturing

Executive International Regulatory Affairs
Qualification: B. Pharma/M. Pharma
Location: Bangalore
Experience and Other Requisites:
·         Should have an experience of 3 to 4 years.
·         Should have good communication skills.
·         Should have good knowledge of cGMP.
·         Capable of handling and training workmen

Department: International Regulatory Affairs
Reference Code: EXEIRA040813
Job Description:
·         Co-ordination with internal departments.
·         Requirements to be catered specific to the specific countries
·         Dossier compilation / Planning / Execution.
·         Document review & archivals.

Qualification: B. Pharma/M. Pharma
Location: Bangalore
Experience and Other Requisites:
·         Should have an experience of 2 to 3 years.
·         Should have proficiency in using MS Office applications

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Sunday 13 April 2014

Vacancy for Senior Executive - Regulatory Affairs @ Roche

At Roche, 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.
Roche Diagnostics India, with a sales turnover of INR 150 crores, nurtures an open, flexible and challenging work environment, which allows for rapid career progression. Favoured by its geographic location in the heart of Europe, the Basel area is one of the most dynamic economic regions in Switzerland — a great place to live and work.

Post: Senior Executive - Regulatory Affairs - Delhi

Candidate Profile
Qualification - Graduate / Post Graduate in Bio-Chem / Molecular Biology / MicroBiology with Minimum - 4-5 years of experience in handling regulatory documentation
Preferred - Post Graduate - with 5 yrs experience

Additional Information: 
Job ID: 2749871511
Qualification: Graduate / Post Graduate
Location: Delhi
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: DRA
End Date: 30th April, 2014

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Tuesday 1 April 2014

Vacancy for B. Pharma & M. Pharma as DGM - Regulatory Affairs (Formulation) @ Antal International

Antal International Ltd is an international recruitment company which network comprises 132 offices in 32 countries. The head office is based in London, The United Kingdom. The company offers international recruitment services including retained executive search and selection, contingent recruitment in permanent, interim and contract / temporary staffing.One of the key products of ’’Antal International’’ is a regular research on hiring and firing trends in job markets around the world – Antal Global Snapshot.

Post: DGM - Regulatory Affairs (Formulation)

Additional Information:
Experience:
 15-20 yrs
Location: 
Goa
Education: B. Pharma & M. Pharma
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Last Date: 10th April, 2014
Interested candidates can send the updates resume atumargi@antal.com

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Saturday 29 March 2014

Vacancy for Senior Executive Regulatory Affairs in CRO - client of plug HR | B. Pharma, M. Pharma

We are a Contract Research Organization located at Ambernath, Maharashtra.

Post: Senior Executive Regulatory Affairs

Skill Requirements
1. Dossier review, knowledge, effective communication skills, team player and positive attitude
2. Reading skills, writing skills and reasoning ability
3. Excellent computer knowledge in MS Office (e.g. Word, Excel, PowerPoint, PDF)
Interested candidates can email resume with to anura.wadia@plughr.com with the below details
• Current CTC
• Expected CTC
• Current location
• Notice period
• Contact number & email

Candidate Profile
Educational Qualifications: B Pharma / M Pharma
Work Experience: 7+ years
compilation of dossiers to various regulatory markets – US, UK & ROW.

Additional Information:
Experience: 7+ years
Location:
 Ambernath
Education Level: B. Pharma, M. Pharma
Industry Type: Pharma/Biotech/Clinical Research
End Date: 5th April, 2014

Interested candidates can email resume with toanura.wadia@plughr.com with the below details
Current CTC, Expected CTC, Current location, Notice period, Contact number & email.

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Thursday 20 March 2014

M. Sc Chemistry Candidates need to apply at Manager-Quality Assurance & Regulatory Affairs (API) | Aspiring-Solutions hiring for its leading API Client

Our client is a manufacturer & exporter of API, Intermediates and Specialty Chemicals since 1979 with their well-equipped manufacturing facility located at Dombivli.

Post: QA & RA Manager (1 Nos.)

Job description:
-Hardcore experience of min. 5-8 years in RA & QA (API/ Bulk Drugs Mfg Co. only)
-M. Sc Chemistry Candidates may only apply

Candidate Profile:
M. Sc Chemistry Candidates need to apply.
Local Candidates Only.

Salary: Open upto 8 lacs PA

Additional Information:
Education: M. Sc
Experience: 5-8 yrs
Location: Dombivli East
Industry: Pharma/Biotech
Last Date: 26th March, 2014

where to forward CV: aspsol.recruitments@gmail.com (Please mention your current etc, expected etc and notice period)

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Thursday 30 January 2014

B. Pharma - Quality Assurance / Regulatory Affair at Healthy life pharma

Company is looking for fresher B.Pharma or M.Pharma. Post is regulatory affair & quality assurance. Making of dossier, FDA work. Quality assurance documentation work.

Post: Quality Assurance / Regulatory Affair

Education: B. Pharma, M. Pharma

Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Contact Details:
Recruiter Name: HR MANAGER
Email Address: job.healthypharma@gmail.com
Telephone: 912267415973

For more details: Click here



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Wednesday 29 January 2014

Urgently Required B. Pharma as Quality Assurance / Regulatory Affair in healthy life Pharma

Company is looking for fresher B. Pharma or M. Pharma. Post is regulatory affair & quality assurance, Making of dossier, FDA work and quality assurance documentation work.

Job Description


The job is under any category of regulatory affair /quality assurance chemist, technical knowledge should be clear. Basics should be clear. Awareness of recent guidelines, making of dossier, FDA work, and Quality assurance documentation work.

Industry:

Pharma / Biotech / Clinical Research

Functional Area:

Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Role Category:

R&D

Education:

UG - B. Pharma - Pharmacy
PG - Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required.

Note:- Mail your resume to job.healthylifepharma@gmail.com

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Monday 27 January 2014

Job as Regulatory Affairs Manager - Semi & Non regulated markets in Leading Pharma | B.Pharm, M.Pharm, B.Sc, M.Sc

Leading Pharma co. with huge range of products ranging from sterile preparation to oral solid dosage forms with international markets.

Post: Regulatory Affairs Manager-Semi & Non regulated markets (1 opening, Male Candidates Preferred)

Job Description:
-Knowledge of Regulatory requirement for different countries (For Regulated / Non regulated Market)
- 5-10 years experience in Regulatory related work.
-Knowledge of latest guidelines of all countries
-Good coordination skill with related depart.

Candidates should be well versed in preparation of pdf dossiers in ACTD / CTD formats. Self initiative taking. Pro Active. CANDIDATES MUST HAVE EXPERIENCE IN NON REGULATED AND SEMI REGULATED MARKET
Should Manage all activities related to Product registration. Coordination with QA and Production people for dossier requirement. Awareness of preparation of COAs, Specifications etc.
Checking of RM COA recd. From suppliers. And Finish product COA recd. etc

Candidate Profile:
Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc
Experience: 5-10 yrs exp handling Semi/non regulated markets.
Male candidates shall be preferred on priority as visiting FDA offices shall be in concern.

Additional Information:
Education: B.Pharm, M.Pharm, B.Sc, M.Sc
Experience: 5-10 yrs
Location: Andheri East, Mumbai
Industry: Pharma/Biotech
Key Skills: DRA
Last Date: 16th Feb, 2014

If the position interests you, kindly send across your updated CV (word format) at aspsol.recruitments@gmail.com
Kindly mention your current CTC, expected CTC and notice period. Also enclose your photograph with the application

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Thursday 23 January 2014

Vacancies for B.Pharm, M.Pharm, M.Sc in Par Formulations in department of Regulatory Affairs, Production, QC, Technical services, Preference for Tamil Nadu natives


Par Formulations Pvt. Ltd. a subsidiary of Par Pharmaceutical Companies Inc. (USA) is an USFDA approved facility located in Chennai facilitating Research & Development and engaged in manufacturing solid 6 semi solid dosage forms. Par Pharmaceutical Inc., is the 5th largest Generic Pharmaceutical Company in the US market and leader in Product Development and In-Licensing of generic pharmaceuticals with state of the art manufacturing facilities. In order to expand the operations of the Research & Development and Manufacturing unit in Chennai, we seek suitable candidates for the following positions:

Post: General Manager / Dy. General Manager / Manager / Reviewer / Assistant Manager / Team Leader / Analyst / Supervisor / Technician

Position: Quality Control- General Manager / Dy. General Manager / Manager / Reviewer / Assistant Manager / Team Leader / Analyst
Qualification: M.Pharm (Analysis) / B.Pharm / M.Sc. Chemistry
Experience: 2-15 years

Position: Production- General Manager / Dy. General Manager / Manager / Asst. Manager / Supervisor / Technician
Qualification: M. Pharm / B.Pharm / D.Pharm/ Diploma in mechanical / ITI
Experience: 2-15 years

Position: Regulatory Affairs - General Manager / Dy. General Manager/ Manager / Assistant Manager
Qualification: M. Pharm
Experience: 5-15 years

Position: Technical Service- General Manager / Dy. General Manager / Manager / Asst. Manager
Qualification: M. Pharm/ B.Pharm
Experience: 2-15 years

All positions are based in Chennai and the candidate will be employed in the USFDA facility.

Preference will be given to Tamilnadu natives. 

Technical expertise on specific areas is mandatory. Compensation will be based on candidate's experience and expertise.

Interested candidates are requested to forward their resume to parformhr@parpharm.com

Par Formulations Private Limited, Chennai
(A Group Company of Par Pharmaceutical Companies, Inc. USA)

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