Macro Care Hiring freshers as SAS programmers , Bio - Stats and Clinical data management CDM @ hyderabadd

Macro care is hiring freshers for SAS, BIO-Stats and CDM at Hyderabad Location.

Here  following are are the details

Position 1: Bio statisticians  

Qualification: M.Sc Bio-statistics/ stats + Trained / Certified in Bio-Statistics .

Position 2: SAS Programmers

Qualification: MCA / M.Sc Stats / B.Tech(IT/CSE) + Trained/ Certified in SAS Programming

Position 3: Clinical Data Management 

Qualification: B.Pharma/ M.Pharma/ Life sciences Degree + Diploma / Certified in Clinical Data Management .

Contact Details:

Sikanth K
Mobile: 9000904033
Mail: srikanth.kanchi@makrogrp.com

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Biocon Limited Hiring M.Pharma Freshers for Hyderabad and Delhi

Biocon Limited Hiring M.Pharma Freshers for Hyderabad and Delhi

Position: Medical Scientific Liaison

Experience: 0-4 Yrs

Location: Delhi, Hyderabad

No.Of Positions: 2

Job Description

• To meet KOL's and Investigators to develop a mind space for Biocon and provide scientific support in the form conducting CMEs.
• Conduct medical and orientation program to newly inducted sales executives and sales managers.
• Effectively role out of initiatives for market insights, market research, surveys, pilot projects etc.
• Provide latest information, relating Product, Disease and Therapy area to doctors (customers).

Company Profile

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world. Today, Biocon together with group companies employs more than 5000 employees with approxmimately Rs 2500 crore turnover and is expected to grow further during the current financial year .

Contact Info: 

Contact Company:Biocon Limited

Telephone:91-80-67751744

Address :20th KM Hosur Road Electronic City, BANGALORE,Karnataka,India

Website:http://www.biocon.com/

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Dr.Reddy's Hiring Regulatory Affairs manager for solid orals and injectables Plant

Dr.Reddy's Hiring Regulatory Affairs manager for solid orals and injectables Plant

Experience: 10 - 13 Yrs

Job Location: Hyderabad

Salary: INR 8,00,000 - 15,00,000

No. Of Openings: 1

Job Description

Exposure to plant regulatory activities, especially for US/ EU markets with hand full of experience on all dosage forms including solid orals and injectables.
To collaborate with cross functional teams to provide appropriate regulatory strategies and to guide on critical regulatory requirements to meet the quality submissions and timely approvals.
To participate in the deficiency meetings and review the pending deficiencies along with Cross-Functional Teams to ensure the adequacy and timely submission of responses.
To coordinate and collaborate with core regulatory teams with respect to function related activities like: Technical/regulatory related issues of pending deficiencies, Review status of the filed products at the agency and other function related activities for better collaboration.
To review critical changes and approve the change controls and determine the impact on regulatory filing.
To lead and/or participate in cross-functional project team discussions and work effectively to identify and assess regulatory risks. Discuss the regulatory risk and strategies with departmental seniors that mitigate risk and ensure its implementation.
Enable the audits by acting as a SPOC, provide regulatory support/data to plant cross functional teams (CFT) for audits by the regulatory authorities / agencies.
Involve and provide regulatory support to plant CFT regarding OOS / OOT / Other Product related issues / plant related activities.
Training of plant personnel to impart Regulatory Awareness/Regulatory Updates.

Company Profile

Dr. Reddy's Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses - Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products - Dr. Reddy's offers a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars and differentiated formulations. Major therapeutic focus is on gastro-intestinal, cardiovascular, diabetology, oncology, pain management and anti-infective. Major markets include India, USA, Russia-CIS and Europe apart from other select geographies within Emerging Markets.

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Pharmaceutical AR&D jobs in Bangalore

Open Drive for Analytical Research & Development 18,19 and 20 Oct, 16 at Apotex, Bangalore Corporate Office.

Apotex Research Private Limited (ARPL) based at Bangalore is engaged in in the development, bio-clinical evaluation, manufacturing, and distribution of safe and efficacious generic pharmaceutical formulations for the global market.

Inviting applications for the given position:

Analytical Research & Development / Analytical Operations (Research Scientist/Sr. Research Scientist): M. Pharm/M.Sc. with 2-7 years of experience, with exposure to product development activities for regulated markets, exposure to solids orals / semi solids will be added advantage. Exposure to USFDA, MHRA, Health Canada, TGA Markets.

Interview Venue: Apotex Research Private Limited, Plot No. 1&S, Bommasandra Industrial Area, 4th Phase, Jigani Link Road, Bangalore-560099

Time: 9.00 AM to 4.00 PM

Job Location: Bangalore

Note: Experience in a Pharmaceutical manufacturing unit with exposure to Solid oral dosage forms (tablets and capsules) is a must.

Candidates from Quality Control Department can apply to the above open position.

Required Documents: Candidates are requested to carry 2 copies of resume, passport photo, pay slips, Education certificates, salary annexure and previous experience certificates.
Desired Candidate Profile
Education-
UG:B.Pharma - Pharmacy
PG:M.Pharma - Pharmacy
Doctorate:Ph.D - Advertising/Mass Communication

Job Summary:- Performing and reporting of analytical method validations, analytical method transfers, archival of analytical method validation documents. Review of validation documents and preparation of validation protocol and reports wherever applicable.

Job Responsibilities:-

1. Responsible for initiation, execution and completing of exhibit stability sample analysis.
2. Responsible for all activities in analytical research and development including cGLP, documentation, and implementation of departmental quality systems.
3. To assist the Sr. Research scientist/Team Leader/Group Leader in the day to day functioning of the analytical research and development laboratory.
4. Maintenance and management of stability samples and inventory.
5. Works as a member of a team to achieve all outcomes.
6. Communicating the requirements for the leaders and within the team members for effective CGLP procedures and departmental quality systems to achieve all outcomes.
7. Performing the activities with established regulatory compliance and safety requirements.
Job requirements:-

1. A post graduate degree in pharmacy/chemistry from a recognized college.
2. Desired candidate should have a minimum of 2years of experience as a laboratory Analyst.
3. Should have competent verbal and written communication skills.
4. Experience of working on online modules/software would be an added advantage.
5. Hands on experience in stability samples testing (Solid oral dosage form) and completion within stipulated timeline by following GLP.
6. Hands on experience in multimedia dissolution study analysis of test products and innovator products.
7. Hands on experience in calibration and qualification of instruments.
8. Knowledge on preparation of various documents like SOPs, formats, protocols, reports, analytical data etc.
9. Knowledge on technology transfers/method validation.
10. Should have well versed knowledge on regulatory guidelines and thorough knowledge on CGMP activities.

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