Vacancy in Baidyanath for post of Production Officer | Require BAMS or B.Pharma or MD (Ayurveda)

One of India's most respected Companies, Shree Baidyanath Ayurved Bhawan (p) Ltd. (Kolkata), popularly known as Baidyanath, is the acknowledged leader of Ayurvedic know-how. Established in 1917, the Company has played a pioneering role in re-establishing ancient knowledge with modern research and manufacturing techniques.

Post: Production Officer
Key Accountability:
- To carry out proper production planning
- To carry out proper manpower allocation.
- To carry out productivity analysis.
- To properly administer BPR
- To carryout production of different categories of Ayurvedic products.
- To ensure shop floor is properly maintained as per GMP norms.
- To impart continuous on-the-job training (OJT) in the factory.
- To ensure all safety equipments are checked periodically and carry out periodic safety drills.
- To monitor moment of workmen for avoiding unnecessary unrest & production.

Requirements:
- Qualification: BAMS or B.Pharma (Ayurveda) or MD (Ayurveda)
- Experience: Minimum 5 years of Ayurvedic Production experience.
- Knowledge & Skills:
• Identification of different herbs.
• Knowledge in different categories of Ayurvedic Production like: Asava-arista, Ayurvedic medicated oil, Tablets, Pills, Capsules, Syrups, Avaleha, Pak etc.
• Must have working knowledge of Labour Laws.
• Working knowledge of different Pharmaceutical machineries.
• Working knowledge of ERP.
• Knowledge of management of Factory Production and Administration.
• Communication Skills: Must have excellent oral, written and presentation skills in English. Knowledge of Bangali and Hindi is essential.
• International Codes: Knowledge of GMP implementation. Knowledge of WHO will be added advantage.

Additional Information:
Location: Howrah works
Experience: Min. 5 years
Reporting to: Dy. Works Manger
Functional Area: Production
Last Date: 23^th Feb, 2014

Note:- Interested candidates must apply only through email along with their Salary details and recent passport size photograph. hrdsudeep@baidyanath.com

Career for Degree in Pharmacy as Associate Manager - CDA in clinical research at Parexel

PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

Post: Associate Manager GRO, CDA

Job Description
• Manage and oversee team activities including appropriate resourcing of staff, staff assignments and quality control of project deliverables and timely delivery of project deliverables.
• Monitor performance close interaction with PL/GRO Lead
• Train, mentor and allocate team members according to their ability
• Provide technical support to team members to ensure that they have the required knowledge to fulfill their duties.
• Check quality of team deliverables (e.g., on site visits, Central File documentation) and take appropriate remedial action.
• Meet and aim to exceed client expectations by recruiting, retaining and developing a skilled, experienced and motivated team.
• Maintain an agreed level of productivity/billability and staff turnover.
• Participate in and contribute to Project bids, including client presentations.
• Meet client and business needs to have all projects optimally resourced with suitably experienced staff.
• Ensure direct reports meet departmental and project productivity and quality metrics by efficient execution of their project in line with project plan.
• Meet percentage of travel and billability guidelines for staff as appropriate.
• Produce accurate resourcing plans in conjunction with the appropriate Project Team Members.
• Provide consultation, facilitate metrics collection and develop action plans in conjunction with Management/Project Leadership/Leads to keep project on time and within budget.
• May be responsible for own assignments as project team member. This includes taking the role of a senior level contributor on a project team and ensuring high quality and timely delivery of own deliverables.
• May be responsible to coordinate client or account activities for department or function.
• Prepare and submit weekly study specific status reports to Project Team, Sponsors and management and attend project team meetings.
• Serve as an on going liaison with Project Team, Sponsor and management regarding performance of direct reports.
• Manage and develop the team to ensure their performance meets and or exceeds both the business and their own personal goals/objectives
• Maintain a positive, results orientated work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced and objective manner
• Participate in formal staff review processes e.g. performance and salary reviews to corporate standards and timescales.
• Maintain a working knowledge of, and assure compliance with, applicable ICH Guidelines, Good Clinical Practices, Regulatory Agency requirements, and PAREXEL WSOPs.
• Participate in PXL and department system/standards improvement activities.
• Support efforts for generating business leads (client networking, public speaking,
• Complete routine administrative tasks in a timely manner (e.g. timesheets, metrics, travel expense claims
• Departmental or Project tasks as assigned.

• Educated to a degree level (biological science, pharmacy or other health related discipline preferred) or relevant clinical or business equivalent

Candidate Profile
• Educated to a degree level (biological science, pharmacy or other health related discipline preferred) or relevant clinical or business equivalent
• Substantial monitoring/data management experience or equal experience in clinical research

Additional Information:
Location: Andhra Pradesh - Hyderabad
Functional Area: CR
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 30^th Feb., 2014
Req ID: pare-10031245

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Opening Post for Development Scientist in Danaher

Beckman Coulter develops, manufactures and markets products that simplify, automate and innovate complex biomedical testing. Our diagnostic systems are found in hospitals and other critical care settings around the world and produce information used by physicians to diagnose disease, make treatment decisions and monitor patients. Scientists use our life science research instruments to study complex biological problems including causes of disease and potential new therapies or drugs. Hospital laboratories are our core clinical diagnostic customers. Our life science customers include pharmaceutical and biotechnology companies, universities, medical schools and research institutions. More than 275,000 Beckman Coulter systems operate in both diagnostics and life sciences laboratories on six continents. For more than 75 years, our products have been making a difference in peoples lives by improving the productivity of medical professionals and scientists, supplying critical information for improving patient health and reducing the cost of care.

Post: Development Scientist - Bangalore Development Centre-BEC001527

Job Description
Development Scientist. Associate (Professional). None The Development Scientist assists in the evaluation and implementation of new technologies. The incumbent performs experiments as defined and planned by supervisor; reviews test results for experimental error and determines if repeats are required; participates in planning studies for the development, evolution and optimization of assay(s); maintains well organized laboratory notebooks in compliance with relevant procedures; and supports post-launch to resolve performance and/or quality issues. Boundary Conditions/Authority Levels Normally receives no instruction on routine work; general instructions on new assignments
- Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained
- Participates in the analysis, design and development of system applications
- Reports status of experiments to supervisor
- Provides quality assurance for adherence to technical standards  Adheres to policies and procedures

Danaher is a Fortune 200, NYSE-listed, science and technology leader that designs, manufactures and markets innovative products and services to professional, medical, industrial and commercial customers. Our premier brands are among the most highly recognized in each of the markets we serve. The Danaher Business System provides a foundation to our 63,000 associates around the world, serving customers in more than 125 countries. In 2012, we generated $18.3 billion of revenue from five reporting segments: Test & Measurement, Environmental, Dental, Life Sciences & Diagnostics, and Industrial Technologies.

Additional Information:
Location: Bangalore
Functional Area: R&D
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 28^th Feb., 2014

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