Current Openings At BIOCON
Designation: Senior Scientist - Process development cell culture-R&D
No Of positions: 1
Education Qualification: M.Tech or PhD in Engineering (preferably Biochemical engineering/Chemical engineering) / M.Sc candidates
Experience: 3-6 Years (Industrial experience)
Job Description:
* The ideal candidate should have hands-on experience in development of stirred tank processes in a leading biopharmaceutical company in the late stage mammalian cell culture development facility or a pilot plant.
* The candidate should have experience in design, development, scale-up and troubleshooting of cell culture process from laboratory bioreactors to pilot or production tanks.
* Ability to work with scientists in a laboratory as well as in a production set-up would be useful.
* Experience in the resolution of technical problems during manufacturing would be an added advantage.
* Understanding of regulatory compliance and guidelines e.g. FDA and EMEA desirable.
Technical / Functional Skills:
* The candidate should have lead a group of scientists in the past.
* Good verbal and written skills are needed.
* Extensive skill, knowledge, and experience are needed for this position.
* Identifying complex problems and reviewing related information to develop and evaluate options and implement solutions.
* Use logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems
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Designation: Scientist / Sr. Scientist - RND - ANF
No Of positions: 1
Education Qualification: M.Pharm/M.tech
Experience: 1-4 years
Job Description:
* Conducting analytical characterization
* Pre-formulation studies and indicative stability programs of biologicals
* Coordinating activities between the formulation group and purification/quality control groups
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Designation: Sr. Manager - Phamacovigilance
No Of positions: 1
Education Qualification: MD-Pharmacology with 6-10 yrs of experience in phamacovigilance or M.Pharm /PHD with relevant work experience.
Experience: 6-10 Years
Industry Type: Biopharmaceuticals/ Pharmaceuticals/Chemical / Biotech/Clinical Research /API
Functional Area: Phamacovigilance
Job Description:
The incumbent should provide global drug safety and phamacovigilance surveillance for marketed and investigational products. S(he) should provide case management and maintain phamacovigilance and drug safety operations. S(he) should conduct medical assessment, determine additional information needed and independently generate drug safety. S(he) will be responsible for drug safety crisis management. S(he) will overlook the signal detection and risk management activities for designated global products. S(he) should design and implement systems for drug safety collection, processing, reporting and coding. S(he) will be involved in making strategies for pre and post marketing risk management and should keep abreast of phamacovigilance methods and trends in published literature and global regulation. The position will be in the quality department and the incumbent will report to the head of quality.
Technical / Functional Skills:
* MD-Pharmacology with 6-10 yrs of experience in phamacovigilance or M.Pharm /PHD with relevant work experience.
* Experience in contract research organization or pharmaceutical / Biotechnology Company is a must.
* In-depth clinical background is needed. Should have good knowledge of EMEA, Non-EU and FDA regulation.
* Should have strong knowledge of worldwide safety regulation for marketed and investigational products.
* Should have industrial knowledge experience in drug safety and phamacovigilance and FDA and global regulations related to drug safety reporting ,ICH guidelines, and GCP and the process required to comply.
Behavioral / Management / Other Skills:
* Should have excellent oral and written communication skills. Should be able to present/articulate to large internal/external groups
* Should have very strong judgment; and exhibit tactful discretion.
* Should have analytical thinking and problem solving skills.
* Should be able to make high level decisions.
* Should be able to build a team in a short span of time.
Location: Bengaluru /Bangalore
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Department: Production
Position: Jr. Executive
Qualification: B.Sc - Any Specialization, Bio-Chemistry, Chemistry; Diploma - Any Specialization, Chemical.
Experience: 0 - 2 Years.
Location: Bangalore
Job Description:
* Handle the day to day activities of the production
* Handle day to day cell culture and purification activities in departments
Candidate Profile:
* The ideal candidate should be a diploma in chemical or petro-chemical engineering or BSc with chemistry, biochemistry with 1 to 2 years experience
* Should able to handle trouble shoot operations and function as a part of the team
* Should able handle the day to day activities of the production
* Male candidates preferred as this job involves night shifts
Department: Production
Position: Executive
Qualification:B.Tech/B.E.- Any Specialization, M.Sc - Chemistry
Experience: 2 - 4 Years.
Location: Bangalore
Job Description:
* Monitoring of daily Production activities
* Streamlining of documentation and operations
Candidate Profile:
* Should have manpower management capabilities and effective communicational abilities
* Should have the qualification or B.Tech of MSc chemistry with 1 to 2 years of relevant experience
* Should able handle the day to day activities of the production
* Male candidates preferred as this job involves material handling and night shifts
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Position: Toxicology
Location: Bangalore
Qualifications:
* Hands-on experience in designing and directing GLP tox and/or safety pharmacology studies involving protein and/or small molecule drug candidate.
* Ph.D. with 4+ years in toxicology preferably from industry.
* Knowledge and experience in regulatory submission is highly desirable
* Self-motivated, attention to detail, dedication to quality, and willingness to learn
* Ability to work independently and interdependently in a supportive multi-functional team setting.
* Working knowledge of GLP regulations
* Demonstrated in vivo experience
* Highly developed medical writing skills
Responsibilities:
* Design, conduct and carry out preclinical safety/toxicology and other preclinical studies
* Coordinate, supervise, and manage contract GLP toxicology and safety pharmacology studies
* Responsible for protocol generation, initial selection and negotiation with CROs, study monitoring, data collection and analysis, and report writing/drafting
* Assist preparation of preclinical portion of regulatory submissions such CTD, BLA and IND.
* carrying out risk assessments on potential new drugs to see they are safe to test on humans;
* assessing whether the benefits of the drug outweigh the risks;
* carrying out work on cells and tissues before tests are carried out on animals and then humans.
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Department: API Marketing
Position: Deputy Manager/Manager
Qualification: Bsc/B.Pharm + MBA
Experience: 5-8 Years
Location: Bangalore
Job Description:
* Market Survey, Market Research & Development for A.P.Is and Intermediates in Domestic as well as on International Level
* New product development.
* Managing International and Domestic business.
* Product Registration and approval of products in various countries.
* MIS Management.
Desired Profile:
* Marketing and Sales Professional with over 6 years Marketing and Sales experience in A.P.Is (Active Pharmaceutical Ingredients), Intermediates and Specialty Chemicals.
* Exceptional Communicator with consultative sales style, strong negotiation skills, exceptional problem solving abilities and a keen customer needs assessment aptitude.
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