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Teva Pharmaceuticals need Sr. Scientist - Microbiology

 

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Teva Pharmaceutical Industries Ltd.  is a leading global pharmaceutical company, committed to increasing access to high-quality healthcare by developing, producing and marketing affordable generic drugs as well as Innovative and specialty pharmaceuticals and active pharmaceutical Ingredients. Headquartered In Israel, leva Is the world's largest generic drug maker, with a global product portfolio of more than 1,250 molecules and a direct presence in approximately 60 countries. Teva employs about 40,000 people around the world and reached $13.9 billion in net sales in 2009.

Post : Sr. Scientist - Microbiology

Job  Responsibilities 
POSITION SUMMARY    
Works under minimal direction from the manager, reviews all testing documentation and determines the significance of microbes in products or raw materials.  Work is reviewed for soundness of judgment and overall quality and efficiency. Writes, updates, and evaluates new test methods and procedures. Attends team meetings and coordinates projects on cross-functional teams and within the laboratory.  

ESSENTIAL AREAS OF RESPONSIBILITY        

  • Conduct final review of documentation.    
  • Write, update and evaluate new test methods, SOPs, LPMs, using USP, NF, method validation.    
  • Coordinate testing/direction of the laboratory (non-supervisory role).     Assist in administrative functions.    
  • Train other analysts in laboratory techniques.    
  • Perform routine microbiological testing of all samples.     Perform routine testing to support other departments.     Calibration/validation of instrumentation.    
  • Represent department on project and cross-functional teams and committees.    
  • Follows Teva Safety, Health, and Environmental policies and procedures.    
  • Performs other duties as assigned or as business needs require.    
  • Documentation and microbe reviews completed within timelines and are complete and accurate.    
  • Validation packets are reviewed and any issues resolved in timely manner.    
  • Research notebooks and identifications are evaluated and reviewed in a timely manner.    
  • Procedures are complete, accurate, understandable and up-to-date.    
  • Projects are coordinated and completed in a timely manner.

Candidate Profile :
Master’s degree in microbiology, biology or related science with four (4) years of experience in a pharmaceutical, chemical or biochemical manufacturing environment.    
B.S in microbiology, biology or related science with eight (8) years of experience in a pharmaceutical, chemical or biochemical manufacturing environment.

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Skills/Knowledge/Abilities:     

  1. Excellent organizational skills and attention to detail, self-driven and motivated.    
  2. Excellent computer skills including MS Office, Windows and LIMS.    
  3. Excellent at multitasking, handling multiple projects at one time, and changing priorities based on business needs.    
  4. Excellent interpersonal and communication skills.    
  5. History of significant contribution to cross-functional teams and projects.    
  6. History of significant project management role on cross-functional teams and projects.    
  7. Specialized or Technical    
  8. Working knowledge of Microbial Limits Testing and identification procedures and/or other microbiology methods, and proficiency in most of these techniques.    
  9. Excellent knowledge of FDA, USP, ICH, cGMP, and cGLP requirements in a pharmaceutical quality control laboratory.

TRAVEL REQUIREMENTS 
Potential for up to 10% domestic travel.     

PHYSICAL REQUIREMENTS
Lift/move up to 10 lbs. and occasionally 25 lbs.    

Individual may be required to handle hazardous and non-hazardous materials.
Individual may be required to wear Personal Protection Equipment.    
Not allergic to chemicals or biosubstances found in the laboratory or production facilities.

Additional Information:
Experience : 4 years
Qualification : Master’s degree in microbiology
Location : US-VA-Forest
Industry Type :  Pharma / Biotech / Clinical Research
Functional Area : QC
Last date : 24th August, 2016

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