Wednesday, 22 April 2015
Submission Writer-Novartis Healthcare Pvt. Ltd. -Hyderabad / Secunderabad
1. To author, review and independently manage high quality clinical
and safety documents: non registration Clinical Study Reports (CSR),
Development Safety Update Reports (DSUR), Clinical Trial Registry
Database (CTRD), Risk Management Plans (RMP), Periodic Safety Update
Reports (PSUR). 2. Lead for outsourced Narrative projects. Coordinate
other outsourced activities in OSM. 3. Core member of Clinical Trial
Team (CTT)/ participate in Safety Management Team (SMT). 4. Actively
participate in planning of data analyses and presentation to be used in
CSRs. 5. Act as documentation consultant in CTTs and SMTs to ensure
compliance of documentation to internal company standards and external
regulatory guidelines. 6. May act as Program Writer ensuring adequate medicalwriting
resources are available for assigned program and consistency between
documents. 7. Act as liaison between CTTs, CSTs and publishing teams to
ensure timely delivery of final documents for publishing. 8. Support the
development of OSM through participating in OSM initiatives and other
related activities. 9. Contribute to development of processes within
OSM. May contribute to cross-functional initiatives. 10. Fostering
cross-functional communication to optimize feed-back and input towards
high quality documents. 11. Maintain audit, SOP and training compliance.
Minimum university life science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desirable. Fluent English (oral and written). HYDERABAD ONLY: Masters with 3-5 years of relevant experience. PhD or degree in medicine (MBBS/MD or Alternative medicine) with 1-3 years of relevant experience 2 years medicalwriting experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus strong knowledge of the medicalwriting processes. Excellent communication skills (written, verbal, presentations) Operational knowledge of clinical trial reporting. Very good understanding of biostatistics principles. Ability to prioritize and manage multiple demands and projects. Good knowledge of and some experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). Ability to define and solve complex problems (Problem-solver) Broad knowledge and future oriented perspective Proven track record in matrix environment Experience in contributing to global, cross functional projects.
Minimum university life science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desirable. Fluent English (oral and written). HYDERABAD ONLY: Masters with 3-5 years of relevant experience. PhD or degree in medicine (MBBS/MD or Alternative medicine) with 1-3 years of relevant experience 2 years medicalwriting experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus strong knowledge of the medicalwriting processes. Excellent communication skills (written, verbal, presentations) Operational knowledge of clinical trial reporting. Very good understanding of biostatistics principles. Ability to prioritize and manage multiple demands and projects. Good knowledge of and some experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). Ability to define and solve complex problems (Problem-solver) Broad knowledge and future oriented perspective Proven track record in matrix environment Experience in contributing to global, cross functional projects.
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Document Review Team Lead-Bengaluru/Bangalore, Mumbai, Delhi-PPD
Job Description
Due to continued growth, PPD is recruiting for a Document Review Team Lead to join our Global Medical Writing team.Responsibilities:
Supervises the overall operational activities of project(s) within the Document Review group including but not limited to: Provide short-term and long-term resource planning in order to assign project activities to appropriate and available staff. Hold regularly scheduled meetings with staff and provide updates to senior management. Assist staff to forecast project-related timelines for completion. Hires and evaluates employees. Recommends salary levels and promotions.
Oversees the preparation of Document Review deliverables and may serve as lead reviewer on large review projects. Organizes processes for completion of projects within established timelines. Evaluate timeliness and quality of deliverables and provide updates to senior management. Provide input and review group SOPs and WPDs; evaluates compliance with SOP/WPD on an ongoing basis. Builds client relationships, identifies, and resolves complex client management issues.
May support marketing presentations to potential clients on the capabilities of the Document Review group.
Provides input on training programs for Document Review. Ensures that reviewers on assigned project are adequately trained in document review skills.
Qualification Required:
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years) or equivalent and relevant combination of education, training, & experience.
1+ year of leadership responsibility
Knowledge, Skills & Abilities:
Experience mentoring personnel and coordinating the work of project teams
Ability to supervise, evaluate, and mentor departmental personnel
Ability to delegate tasks and facilitate completion of assignments
Effective management skills, including the ability to create and modify budgets, project timelines, allocate resources, and forecast departmental workload
Demonstrated innovation in developing new ideas related to process improvements
Strong document and quality review knowledge
Proficient in Microsoft (MS) Word and MS Excel
Advanced organizational, analytical and interpersonal skills to manage several complex projects in parallel and manage rapidly changing priorities
Ability to independently assess client needs and work with project team members in producing compliant deliverables
Ability to independently learn new technologies
Advanced editorial/proofreading skills
Strong leadership to a diverse staff
Ability to work on extremely complex problems where analysis of situations or data requires an evaluation of intangible variables
Ability to exercise independent judgment in developing methods, techniques, and evaluation criteria for obtaining results
Desired Profile
Education:UG -Any Graduate - Any Specialization, Graduation Not Required
PG - Any Postgraduate - Any Specialization, M.Sc - Any Specialization, Chemistry, Biology, Statistics, M.Pharma - Pharmacy
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H and LS Medical Writer- 4 - 6 YearsChennai-Accenture
Job Description
Schedule : Full-time
Ph.D. in Life Sciences or Pharmacy/M.D. in Pharmacology or Physiology or Public Health/ M.B.B.S./ B.D.S./ B.A.M.S with 4 to 6 years of experience in clinical development including supporting/ leading activities related to reconciling, writing, editing and/or managing the production of high quality clinical documents that are components of regulatory marketing approval may apply.
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Ph.D. in Life Sciences or Pharmacy/M.D. in Pharmacology or Physiology or Public Health/ M.B.B.S./ B.D.S./ B.A.M.S with 4 to 6 years of experience in clinical development including supporting/ leading activities related to reconciling, writing, editing and/or managing the production of high quality clinical documents that are components of regulatory marketing approval may apply.
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Walk-in @ Quintiles for PV on 25-apr-2015(fresher & Experienced)-Bengaluru/Bangalore
Hi,
Greetings from Quintiles!!!
We are hiring candidates for Pharmacovigilance Positions.
Its an exclusive walk-in event for both freshers and experienced on Saturday, 25th Apr 2015.
Timings: 8:00 AM
Interview Venue Details
Quintiles Research India Pvt Ltd.
Prestige Technologies Park ll,
Etamin Block, 3rd floor, B-wing,
Sarjapur-Marathalli Outer Ring Road,
Bangalore-560 103
Landmark: J.P Morgan company, same campus last block
Etamin Block, 3rd floor, B-wing,
Sarjapur-Marathalli Outer Ring Road,
Bangalore-560 103
Landmark: J.P Morgan company, same campus last block
Contact: Shamshuddin/Kavya L
Requirement : Candidates only with Life Science background with good knowledge in Pharmacovigilance can apply.
To Prioritize and complete the assigned trainings on time.
Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information; determining initial/update status of incoming events; database entry; coding AE and Products, writing narratives, Literature related activities.
Assuming other workflow responsibilities for the assigned project as directed by Operations team member or Manager.
Ensure to meet the expected productivity and quality standards
Ability to identify quality problems, if any, and bring them to the attention of a senior team member/ mentor.
Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
Perform other duties as assigned.
Desired Candidate Profile
Education-
UG: B.Sc
- Any Specialization, Any Specialization, Any Specialization, B.Pharma -
Pharmacy, Pharmacy, Pharmacy, BDS - Dentistry, Dentistry, DentistryPG:Post Graduation Not Required, M.Sc - Any Specialization, Anthropology, Bio-Chemistry, Biology, Botany, Nursing, Zoology, Other, M.Pharma - Pharmacy, M.Tech - Any Specialization, Bio-Chemistry/Bio-Technology, Biomedical
Pharmacovigilance Practice Head - IMS Health-Bengaluru/Bangalore, Gurgaon
- Role Purpose:
Grow and manage the pharmacovigilance (PV) services delivery practice at IMS Healths Global Delivery Center (across Bangalore, Gurgaon, and Colombo offices)
Principal Accountabilities:
Enable pharmacovigilance/adverse events tracking (PV/AE) business deals by supporting the onshore teams in the sales cycle, through building/enhancing suitable collateral for the practice, including pitch decks, proposals, project plans, audit plans, SOPs, etc.
Manage the PV team across different locations
Liaise with technology team to drive the PV/AE engagements successfully, and leverage automation to enhance productivity as well as quality
Ensure all projects are managed with pristine quality, and within the timelines agreed upon
Drive operational excellence in the PV practice, and streamline PV processes
Drive the culture of metrics and reporting these on a periodic basis, to enhance the quality and operational rigor of the practice
Ensure rigor in documentation and establish best practices
Track resourcing and profitability on engagements
Prepare the team for pharma company PV audits and to successfully undergo these audits
Establish processes for training as well as certifications required for the PV practice
Hire smart candidates (fitness for purpose) and groom them
Drive productivity, smart processes, and policies
Drive thought leadership and innovation
Educational requirements Life Sciences degree, preferably B.Pharm + M.Pharm (or B.Pharm + MBA), or MBBS from a reputed institute, with respectable scores throughout the academic career
10+ years of experience in pharmacovigilance (post-marketing surveillance experience is highly necessary as opposed to AE tracking in clinical trials)
Experience in both agency/vendor/partner (must-have) and pharma (good-to-have) preferred
Experience of driving the preparation for audits, and successfully undergoing stringent audits by pharma companies as a PV agency/partner to a pharma company
Training certifications in pharmacovigilance/adverse events tracking
Excellent communication skills
Experience in onshore/offshore model preferred
Knowledge of and exposure to unstructured data/social media data would be a plus
High comfort level and affinity to using technology tools in the field of adverse events tracking
Drive for excellence in work, passion for quality, ability to operate at scale without compromising quality, team building and leadership abilities
Social adaptability, willingness to adapt to international cultures, work environments and business processes
Additional Requirements:
Excellent presentation skills
Drive for perfection, strong attention to detail, and impeccability in delivering publishable output
Ability to communicate effectively in a complex global business set up since the job will involve routine interaction with international stakeholders
The candidate should be willing to go through assessment tests and series of interviews, which are, as a practice, administered for recruitment across all levels (including senior-most) in the Nexxus Social Media team, of which the PV team is an integral part.
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Clinical Research Coordinator TECH OBSERVER 1 - 2 yrs Mumbai
CTC: 1,25,000 - 1,50,000 P.A
Job Description
Recruitment,coordination & follow up of trial subjects, covering informed consent, adhering to safety and compliance issues;sample collection & shipment;Administer study drug;Coordination & management of Clinical Trial;
Salary: 1,25,000 - 1,50,000 P.A
Role Category:R&D
Role:Clinical Research Associate/Scientist
Desired Candidate Profile
Education-
UG: B.Pharma - Pharmacy, B.Sc - Any Specialization
PG:Post Graduation Not Required, M.Pharma - Pharmacy, M.Sc - Any Specialization
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
Good Communication skills
Willing to travel within City
Job Description
Recruitment,coordination & follow up of trial subjects, covering informed consent, adhering to safety and compliance issues;sample collection & shipment;Administer study drug;Coordination & management of Clinical Trial;
Salary: 1,25,000 - 1,50,000 P.A
Role Category:R&D
Role:Clinical Research Associate/Scientist
Desired Candidate Profile
Education-
UG: B.Pharma - Pharmacy, B.Sc - Any Specialization
PG:Post Graduation Not Required, M.Pharma - Pharmacy, M.Sc - Any Specialization
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
Good Communication skills
Willing to travel within City
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Walkin - in Interview in Quintiles on 25th April 2015 Quintiles -2 - 7 yrs Bengaluru/Bangalore
CTC: 2,00,000 - 7,00,000 P.A
- Walk-in Interview in Quintiles on 25th April 2015.
Desired Profile :
Candidates with experience from 2 to 7 years in Clinical Research /CRC / CPC / CTA /Lab/ Clinical trails are welcome.
Excellent Communication skill is mandatory.
Willing to work in shift.
Venue Details
Wing A, GroundFloor, Etamin Block,
Prestige Technology Park II
Sarjapur Marathahalli, Outer Ring Road,
Bangalore - 560103.
Contact Person: Sudhamani/Thenmozhi
Time : 8.00AM
Salary: 2,00,000 - 7,00,000 P.A
Role:Clinical Research Associate/Scientist
Role:Clinical Research Associate/Scientist
Desired Candidate Profile
Education-
UG: Any Graduate - Any Specialization, Graduation Not Required
PG:Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
PG:Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
Research Scientist- Microbiology & Genetics/biotechnology-Bhopal
Job Summary
Research scientist will work in a dynamic, fast-paced, team-oriented and collaborative environment to be part of our success. This candidate will use their skills and knowledge in Microbiology, Genetics, Molecular Biology, Virology and Bacteriology to develop and optimize new products.
Job Description
- Design, execution and coordinate in vitro enzymatic and cell based assays.
- Manipulate microbial genetic material for the development of new products.
- Develop and perform small scale fermentation studies.
- Conduct analysis of pharmaceutical and biologic products using traditional microbiological techniques such as dilution, pour plating, and filtration.
- Perform a wide range of general Microbiology and Molecular testing to include: PCR, PCR design, primer design, PCR optimization, DNA extraction from bacteria, DNA sequencing, DNA gel electrophoresis, protein extraction, BCA assay, PAGE, Western blotting, Western blot optimization, silver staining, antibody sourcing, bacteriology and fermentation.
- Candidate may also perform: cloning, subcloning, restriction digests, ligations, transformations, Southern blots and protein expression.
- Culturing bacterial and mammalian cell lines. Collect, analyze and present data at both internal meetings with other scientists and collaborators as well as at external scientific meetings.
-Perform program/project management tasks to facilitate pre-clinical to clinical development of vaccine candidates.
- Interface with external research collaborators to manage pre-clinical research studies.
- Responsible for preparation of study protocols, reports and reports for regulatory filings for product development.
- Monitor critical study phases at CROs to ensure protocol adherence and compliance with GLP standards, as necessary.
- Prepare study design, study data, and program updates.
- Work with cross functional development group to bring research stage molecules to market.
- Independently review the scientific literature for advances in product development.
-Assist in preparation of Preclinical study design and Plans.
- Analysis of the data from those studies.
- Review reports for finalization.
-Capable to write up of manuscript and publish the research work.
Research scientist will work in a dynamic, fast-paced, team-oriented and collaborative environment to be part of our success. This candidate will use their skills and knowledge in Microbiology, Genetics, Molecular Biology, Virology and Bacteriology to develop and optimize new products.
Job Description
- Design, execution and coordinate in vitro enzymatic and cell based assays.
- Manipulate microbial genetic material for the development of new products.
- Develop and perform small scale fermentation studies.
- Conduct analysis of pharmaceutical and biologic products using traditional microbiological techniques such as dilution, pour plating, and filtration.
- Perform a wide range of general Microbiology and Molecular testing to include: PCR, PCR design, primer design, PCR optimization, DNA extraction from bacteria, DNA sequencing, DNA gel electrophoresis, protein extraction, BCA assay, PAGE, Western blotting, Western blot optimization, silver staining, antibody sourcing, bacteriology and fermentation.
- Candidate may also perform: cloning, subcloning, restriction digests, ligations, transformations, Southern blots and protein expression.
- Culturing bacterial and mammalian cell lines. Collect, analyze and present data at both internal meetings with other scientists and collaborators as well as at external scientific meetings.
-Perform program/project management tasks to facilitate pre-clinical to clinical development of vaccine candidates.
- Interface with external research collaborators to manage pre-clinical research studies.
- Responsible for preparation of study protocols, reports and reports for regulatory filings for product development.
- Monitor critical study phases at CROs to ensure protocol adherence and compliance with GLP standards, as necessary.
- Prepare study design, study data, and program updates.
- Work with cross functional development group to bring research stage molecules to market.
- Independently review the scientific literature for advances in product development.
-Assist in preparation of Preclinical study design and Plans.
- Analysis of the data from those studies.
- Review reports for finalization.
-Capable to write up of manuscript and publish the research work.
Desired Candidate Profile
Education-
UG: B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy, M.Sc - Bio-Chemistry, Biology, Microbiology
Doctorate:Ph.D - Pharmacy, Bio-Chemistry/Bio-Technology, Biotechnology, Microbiology
PG:M.Pharma - Pharmacy, M.Sc - Bio-Chemistry, Biology, Microbiology
Doctorate:Ph.D - Pharmacy, Bio-Chemistry/Bio-Technology, Biotechnology, Microbiology
Preclinical Research Scientist-Bhopal
Preclinical research scientist will work in a dynamic, fast-paced, team-oriented and collaborative environment to be part of our success. This will include establishing the capabilities for testing of products in preclinical models and/or managing CRO studies aimed at providing proof of concept.
Job Description
- Design, execution and coordinate in vitro/ in vivo Pharmacology, DMPK & Toxicology studies including critical tips/suggestions in life phase of experiments, cross checking the raw data files, draft and final report reviewing and discussing the study results to intra- department teams, and project team members.
- Develop in vitro and in vivo animal model systems and techniques to evaluate efficacy and mechanism of action of nutraceuticals/pharmaceutical products.
- Monitor critical study phases at CROs to ensure protocol adherence and compliance with GLP standards, as necessary.
- Present study design, study data, and program updates.
- Support integrated project goals; pro-active role for departmental budget and timeline commitment, provide technical and professional advice to junior scientists.
- Work with cross functional development group to bring research stage molecules to market.
- Independently review the scientific literature for advances in model development.
-Assist in preparation of Preclinical Safety Development Plans.
- Analysis of the data from those studies.
- Review reports for finalization.
-Write up of manuscript and publish the research work.
Desired Candidate Profile
Education-
UG: B.Sc - Bio-Chemistry, Biology, B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy, M.Sc - Any Specialization, Bio-Chemistry
Doctorate:Ph.D - Bio-Chemistry/Bio-Technology, Biotechnology, Pharmacy
PG:M.Pharma - Pharmacy, M.Sc - Any Specialization, Bio-Chemistry
Doctorate:Ph.D - Bio-Chemistry/Bio-Technology, Biotechnology, Pharmacy
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Research Associate -analytical Formulations @ Alembic Research Centre
Job Description
1. Development of analytical methods such as Assay, Related Substances, Dissolution for new formulations for solid orals formulations.
2. Identification of unknown impurities in stability samples using LCMS/MSMS
3. Responsible for resolving issues occur during routine analysis and stability studies.
4. Generation, isolation and charactisation of unknown impurities crossing identification threshold using LCMS.
5. Complete analysis of generic drug products targeted for US,UK market.
6. Trouble shooting in method development.
7. Calibration of analytical Instruments i.e. LCMS, HPLC, UPLC.
8. Preparation of method transfer sheets and standard test procedures.
9. Ensuring regulatory compliance by maintaining of appropriate requisite documentation/record
1. Development of analytical methods such as Assay, Related Substances, Dissolution for new formulations for solid orals formulations.
2. Identification of unknown impurities in stability samples using LCMS/MSMS
3. Responsible for resolving issues occur during routine analysis and stability studies.
4. Generation, isolation and charactisation of unknown impurities crossing identification threshold using LCMS.
5. Complete analysis of generic drug products targeted for US,UK market.
6. Trouble shooting in method development.
7. Calibration of analytical Instruments i.e. LCMS, HPLC, UPLC.
8. Preparation of method transfer sheets and standard test procedures.
9. Ensuring regulatory compliance by maintaining of appropriate requisite documentation/record
| Experience | 2 - 5 Years |
| Industry Type | Pharma / Biotech / Clinical Research |
| Role | Analytical Chemistry Associate/Scientist |
| Functional Area | Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology |
| Education | UG - B.Sc - Any Specialization, Chemistry, B.Pharma - Pharmacy PG - M.Sc - Any Specialization, Chemistry, M.Pharma - Pharmacy Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required |
| Compensation: | Not disclosed |
| Location | Vadodara/Baroda |
| Keywords | Assay Dissolution Method Development |
| Contact | Human Resources Alembic Pharmaceuticals Limited |
| Website | http://www.alembic-india.com |
| Job Posted | 2015-04-21 12:12:04.0 |
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Research Executive (Phd Organic Chemistry)-Mumbai
CTC : 3,50,000 - 6,00,000 P.A
- Running & monitoring chemical reactions, work up, isolation and characterization of products.
Synthesis of various multi step agrochemicals/PGR/intermediates
Maintaining chemical inventory, taking care of lab, equipment's/instruments
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Manager Global Primary Research - Noida
CTC: 7,00,000 - 12,00,000 P.A
Email your resume with Subject : Manager Global Primary Research (Healthcare, pharmaceuticals, medical devices) - Noida (Job Id : 2283) to : jobs@thesearchhouse.com
After Emailing your resume you may call : 9811112343
View more jobs matching your profile on The Search House website. http://www.thesearchhouse.com
Recruiter Name:Jyoti
Email Address:
Website:http://www.thesearchhouse.com
Telephone:9811112343
- Responsible for healthcare / pharmaceutical / medical devices primary research operations end to end
- Managing and mentoring a team of analysts/lead analysts for various global telephone primary research projects
- Responsible for managing top lines and bottom lines for healthcare primary research vertical
- Responsible for smooth delivery of primary research projects end to end
- Manage client accounts from a relationship perspective
- Drafting project scope (business proposal) as per client's requirements, studying, analyzing and estimating effort required for execution
- Understand research objectives based on client type and accordingly design/define the work approach; project scope and timelines
- Develop work plan for projects with a visibility on client engagement process, interim deliverable, etc. in an organized manner as per prioritization
- Responsible for the quality of the work being done in the team; review work thoroughly to ensure consistently high quality output, value addition and adherence to timelines; be able to judge required level of own involvement on projects, execute parts of projects if situation so demands
- Provide analysts with effective verbal/ written feedback; counsel analysts on technical as well as business skills and guide them on best practices
- Contribute to different organisational tasks such as hiring, training and other organisational initiatives
- Strong educational background in pharmacy, biotech, life sciences, biomedical or clinical research
- 2-3 years of experience in managing teams and projects for healthcare/pharma primary market research through CATI (Telephone)
- Demonstrated skills in both people management and client management
- Experience in business development is a plus
Email your resume with Subject : Manager Global Primary Research (Healthcare, pharmaceuticals, medical devices) - Noida (Job Id : 2283) to : jobs@thesearchhouse.com
After Emailing your resume you may call : 9811112343
View more jobs matching your profile on The Search House website. http://www.thesearchhouse.com
Desired Candidate Profile
Education-
UG: B.Tech/B.E. - Any Specialization, B.Pharma - PharmacyRecruiter Name:Jyoti
Email Address:
Website:http://www.thesearchhouse.com
Telephone:9811112343
Research Associate/ Content Writer-Hyderabad / Secunderabad
CTC: 1,50,000 - 2,00,000 P.A
PG:MBA/PGDM - Finance, HR/Industrial Relations, Marketing, M.Tech - Any Specialization, M.Sc - Any Specialization, Chemistry, Maths, Physics, M.Pharma - Pharmacy
- Content writing for spectrum / Pharmaplus books
- Preparing copy right free material/ books.
- Preparing Content for MBA, B.Tech (all streams), Competitive books/ Materials.
- Content to be written in easy, meaningful and as per the requirements of the students.
Desired Candidate Profile
UG: B.Tech/B.E. - Any Specialization, Civil, Computers, Electrical, Electronics/Telecommunication, Mechanical, B.Pharma - Pharmacy, B.Com - CommercePG:MBA/PGDM - Finance, HR/Industrial Relations, Marketing, M.Tech - Any Specialization, M.Sc - Any Specialization, Chemistry, Maths, Physics, M.Pharma - Pharmacy
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Research Associate - Analytical R&D ( Male )-Hyderabad / Secunderabad
CTC: 1,00,000 - 4,00,000 P.A
Knowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms.
Handling of dissolution apparatus for Tablets, Capsules, Oral Liquids and Oral Suspensions.USP Type-I, USP Type-II & USP Type-IV.
Knowledge about the handling of analytical instruments like HPLC,GC, UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc.
Knowledge about the calibration of HPLC,GC,UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc.
Knowledge about regulatory guidelines and requirements.
Knowledge about method transfer activities.
Knowledge about the safety aspects.
Knowledge about GLP and GMP.
Knowledge about the qualification of equipment and instruments.
Qualification M.Pharm./M.Sc. (Analytical Chemistry/Organic Chemistry)
Forward CV's : ideal9@idealconsultants.com/ call at 9989059750
Knowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms.
Handling of dissolution apparatus for Tablets, Capsules, Oral Liquids and Oral Suspensions.USP Type-I, USP Type-II & USP Type-IV.
Knowledge about the handling of analytical instruments like HPLC,GC, UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc.
Knowledge about the calibration of HPLC,GC,UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc.
Knowledge about regulatory guidelines and requirements.
Knowledge about method transfer activities.
Knowledge about the safety aspects.
Knowledge about GLP and GMP.
Knowledge about the qualification of equipment and instruments.
Qualification M.Pharm./M.Sc. (Analytical Chemistry/Organic Chemistry)
Forward CV's : ideal9@idealconsultants.com/ call at 9989059750
Research Associate - Formulation R&D ( Male )-Hyderabad / Secunderabad
CTC; 1,00,000 - 4,00,000 P.A
Knowledge of Oral and Injectable dosage forms.
Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions.
Handling of Injectable Liquid and Lyophilized Formulations.
Knowledge about the handling of Cytotoxic materials.
Knowledge about the safety aspects.
Knowledge about GLP and GMP.
Knowledge about the qualification of equiment and instruments.
Knowledge about regulatory guidelines and requirements. Candidate Should have experience in pharma Industry
Qualification M.Pharmacy (Pharmaceutics/Industrial Pharmacy)
Forward CV's : ideal9@idealconsultants.com/ call at 9989059750
Knowledge of Oral and Injectable dosage forms.
Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions.
Handling of Injectable Liquid and Lyophilized Formulations.
Knowledge about the handling of Cytotoxic materials.
Knowledge about the safety aspects.
Knowledge about GLP and GMP.
Knowledge about the qualification of equiment and instruments.
Knowledge about regulatory guidelines and requirements. Candidate Should have experience in pharma Industry
Qualification M.Pharmacy (Pharmaceutics/Industrial Pharmacy)
Forward CV's : ideal9@idealconsultants.com/ call at 9989059750
Research Associate/sr. Research Associate - Bio Analytical-Macleods Pharmaceuticals Ltd.-Mumbai
CTC : 2,00,000 - 4,00,000 P.A
LC-MS/MS method development
Data analysis and report preparation of Bio analytical and ADME studies
Documentation and accountable for overall scientific data and reports
Review of Method Validation reports and Bioanalytical report
PG:Any Postgraduate - Any Specialization, Post Graduation Not Required, M.Pharma - Pharmacy
LC-MS/MS method development
Data analysis and report preparation of Bio analytical and ADME studies
Documentation and accountable for overall scientific data and reports
Review of Method Validation reports and Bioanalytical report
Desired Candidate Profile
Education-
UG: B.Pharma - PharmacyPG:Any Postgraduate - Any Specialization, Post Graduation Not Required, M.Pharma - Pharmacy
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J&J to increase wearable insulin patch-pump production
Johnson & Johnson will scale up
manufacturing of a three-day wearable patch pump used to deliver
insulin, in preparation for a post 2016 launch.
Anti-fungal shows promise for cancer breakthrough in preclinical tests
An anti-fungal drug shows potential to treat a range of cancers, according to research
from the Repurposing Drugs in Oncology
(ReDO) project, but the drugmakers will need a financial incentive to pursue a licence for new indications.
PPD pushes further into Asia with new Chinese central lab
CRO Pharmaceutical Product Development
(PPD) has opened a central laboratory in Shanghai, China, in order to
meet growing client demand for scientific and technical services there.
HLS and Harlan create hairless mouse model
Huntingdon Life Sciences and Harlan
Laboratories have launched a highly immunocompromised hairless mouse
model for oncology and immunology research.
Read More at
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