דרושים Microbiology ב-United States
Flex Microbiology Lab Analyst United States, Texas, Austin
The “” will be based in
Responsibilities:
- Support cleanroom IQ/OQ/PQ validations.
- Perform bioburden and endotoxin.
- Perform routine microbiological testing and data analysis.
- Participate in customer or regulatory audits.
- Collect, review and analyze test results to support irradiation process.
- Review and execute validation protocols for laboratory equipment and test methods.
- Perform review of test data with application of GDP.
- Will be required to perform change requests when required and complete them in a timely manner.
- Author, review and revise laboratory work instructions.
- Conduct and document investigations into laboratory OOS results and cleanroom excursions.
- Ensure laboratory area is always maintained in a GMP state while following all EHS and 5S guidelines.
- May be required to generate, execute and summarize special laboratory studies.
- Ensure personal training requirements are met and that training records are current.
Qualifications:
- Experience in bioburden, endotoxin, environmental monitoring
- Experience in cleanroom gowning and cleanroom behavior
- Strong analytical, mathematical and statistics skills
- Demonstrates advanced technical skills
- Demonstrates detailed functional knowledge and may lead process
- Has awareness of newtechnologies/techniques
- Typically requires a bachelor’s degree or equivalent experience and training. Typically requires a minimum of 2 years of related experience
What you'll receive for the great work you provide:
- Full range of medical, dental, and vision plans
- Life Insurance
- Short-term and Long-term Disability
- Matching 401(k) Contributions
- Vacation and Paid Sick Time
- Tuition Reimbursement
משרות נוספות שיכולות לעניין אותך
Teva Microbiology Senior Quality Control Associate United States, Pennsylvania, East Bradford Township
In this microbiology laboratory position, your main responsibilities will be scheduling and supporting microbiological laboratory testing, data review, analysis of endotoxin and bioburden samples, and evaluation of environmental monitoring (EM) activities (including preparation of EM trend reports) within a GxP-compliant QC microbiology laboratory to support pre-clinical studies, clinical development and commercial production for biological products manufactured in a GMP production facility.
• Perform microbiological testing activities (e.g., bioburden, endotoxin, special studies and qualifications) within a GxP-compliant QC microbiology laboratory to support pre-clinical studies and clinical development for biological products manufactured in a GMP production facility.
• Possess background and experience with aseptic techniques and environmental monitoring (EM) programs, including EM collection techniques.
• Conduct and write investigations independently or with minimal assistance.
• Prior experience in a GMP microbiology laboratory, and experience working with microorganism cultures and identification systems (e.g., MALDI) is a plus.
• Use and apply scientific/technical standards, principles, theories, concepts and techniques of bio-pharmaceutical drug development and GxP requirements.
• Display sound scientific/technical judgment and ability to review work for overall adequacy and accuracy.
• Demonstrate knowledge of local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, DEA, etc.) as applicable to the integral responsibilities of this position.
• Contribute actively to work on and resolve various scientific/technical problems of moderate scope and complexity.
• Work under general supervision. Follow established written procedures and processes.
• Support improving existing procedures and/or establishing new procedures.
• Contribute to completion of milestones associated with specific projects, both as an individual contributor and as part of the team.
• Frequent contact with project leaders and professional staff on goals, progress and resolution of issues. Infrequent inter-organizational and outside contacts on routine matters.
Your experience and qualifications
Required Education: Bachelor’s degree in Microbiology or other relevant scientific discipline from an accredited college or university
Required Skill: Strong proficiency in Microsoft Office applications
Preferred: Knowledge of LIMS systems and Trackwise a plus
Preferred Education: Master’s degree in Microbiology or other relevant scientific discipline from an accredited college or university
Preferred Experience: MS with 2 years or BS with 5 years experience in Microbiology or Biology within the pharmaceutical industry.
Specialized Skills or Technical Knowledge:
Strong Proficiency in Microsoft Office applications
Knowledge of LIMS system is a plus
Physical Requirments:
Ability to work in a laboratory performing microbiology
We offer a competitive benefits package, including:
- Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
- Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
- Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
- Life and Disability Protection: Company paid Life and Disability insurance.
- The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
משרות נוספות שיכולות לעניין אותך
Teva Microbiology Senior Quality Control Associate United States, Pennsylvania, East Bradford Township
In this microbiology laboratory position, your main responsibilities will be scheduling and supporting microbiological laboratory testing, data review, analysis of endotoxin and bioburden samples, and evaluation of environmental monitoring (EM) activities (including preparation of EM trend reports) within a GxP-compliant QC microbiology laboratory to support pre-clinical studies, clinical development and commercial production for biological products manufactured in a GMP production facility.
• Perform microbiological testing activities (e.g., bioburden, endotoxin, special studies and qualifications) within a GxP-compliant QC microbiology laboratory to support pre-clinical studies and clinical development for biological products manufactured in a GMP production facility.
• Possess background and experience with aseptic techniques and environmental monitoring (EM) programs, including EM collection techniques.
• Conduct and write investigations independently or with minimal assistance.
• Prior experience in a GMP microbiology laboratory, and experience working with microorganism cultures and identification systems (e.g., MALDI) is a plus.
• Use and apply scientific/technical standards, principles, theories, concepts and techniques of bio-pharmaceutical drug development and GxP requirements.
• Display sound scientific/technical judgment and ability to review work for overall adequacy and accuracy.
• Demonstrate knowledge of local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, DEA, etc.) as applicable to the integral responsibilities of this position.
• Contribute actively to work on and resolve various scientific/technical problems of moderate scope and complexity.
• Work under general supervision. Follow established written procedures and processes.
• Support improving existing procedures and/or establishing new procedures.
• Contribute to completion of milestones associated with specific projects, both as an individual contributor and as part of the team.
• Frequent contact with project leaders and professional staff on goals, progress and resolution of issues. Infrequent inter-organizational and outside contacts on routine matters.
Your experience and qualifications
Required Education: Bachelor’s degree in Microbiology or other relevant scientific discipline from an accredited college or university
Required Skill: Strong proficiency in Microsoft Office applications
Preferred: Knowledge of LIMS systems and Trackwise a plus
Preferred Education: Master’s degree in Microbiology or other relevant scientific discipline from an accredited college or university
Preferred Experience: MS with 2 years or BS with 5 years experience in Microbiology or Biology within the pharmaceutical industry.
Specialized Skills or Technical Knowledge:
Strong Proficiency in Microsoft Office applications
Knowledge of LIMS system is a plus
Physical Requirments:
Ability to work in a laboratory performing microbiology
We offer a competitive benefits package, including:
- Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
- Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
- Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
- Life and Disability Protection: Company paid Life and Disability insurance.
- The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
משרות נוספות שיכולות לעניין אותך
The “” will be based in
Responsibilities:
- Support cleanroom IQ/OQ/PQ validations.
- Perform bioburden and endotoxin.
- Perform routine microbiological testing and data analysis.
- Participate in customer or regulatory audits.
- Collect, review and analyze test results to support irradiation process.
- Review and execute validation protocols for laboratory equipment and test methods.
- Perform review of test data with application of GDP.
- Will be required to perform change requests when required and complete them in a timely manner.
- Author, review and revise laboratory work instructions.
- Conduct and document investigations into laboratory OOS results and cleanroom excursions.
- Ensure laboratory area is always maintained in a GMP state while following all EHS and 5S guidelines.
- May be required to generate, execute and summarize special laboratory studies.
- Ensure personal training requirements are met and that training records are current.
Qualifications:
- Experience in bioburden, endotoxin, environmental monitoring
- Experience in cleanroom gowning and cleanroom behavior
- Strong analytical, mathematical and statistics skills
- Demonstrates advanced technical skills
- Demonstrates detailed functional knowledge and may lead process
- Has awareness of newtechnologies/techniques
- Typically requires a bachelor’s degree or equivalent experience and training. Typically requires a minimum of 2 years of related experience
What you'll receive for the great work you provide:
- Full range of medical, dental, and vision plans
- Life Insurance
- Short-term and Long-term Disability
- Matching 401(k) Contributions
- Vacation and Paid Sick Time
- Tuition Reimbursement
משרות נוספות שיכולות לעניין אותך
