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Requirements:
Bachelors degree in Life Science, Engineering field or second degree in fields of quality and statistics
Proven experience in quality systems (4- 5 years) and in medical device field (minimum 3 years).
Experience working in an FDA and ISO 13485 regulated environment.
Project management skills, strong communication, problem solving, and analytical skills are required.
Leadership skills without direct authority responsibility
Strong English capabilities.

Requirements:
- Bachelor's degree in the fields of biology, biotechnology, life sciences, chemistry - mandatory - Previous experience in laboratory work is an advantage - Experience working under GMP conditions - a significant advantage - Ability to work in shifts system - including afternoon and night shifts (as needed) - Proven experience working with GC, HPLC analytical equipment mandatory
Omrix is an equal opportunity employer promoting diversity and inclusion in the workplace. This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability

Requirements:
To be eligible for the role, you need to hold a degree in Medical\Pharmaceutical\Health Sciences (MD\PhD\DMD\DVM\PharmD). Fluency in written and spoken Hebrew and English language are mandatory and previous and work experience within a pharma company is an advantage.
We would also like you to have:
Proactive approach and accountability for assigned tasks.
Good presentation and interpersonal skills.
Scientific curiosity and acumen.
Collaborative approach and capability to operate within defined timelines.
Capability for prioritization and multi-tasking.
Precision and accuracy.

Requirements:
B.Sc. in Life Science, Pharmacy/nursing qualification or equivalent, M.Sc. in Life Science would be an advantage.
Basic GCP qualification.
At least 3 years of experience as a Start-Up Team member.
At least 2 years of direct people management-Preferred.
Conceptual and strategic approach to the clinical organization development with strategic insight to trial Start-Up and supporting processes in the clinical trial conduct.
Strong track record in clinical trial execution in multifunctional team at country level, including clinical quality (audits and inspections) and training.
Strong leadership and management skills to build and manage the start-up team.
Excellent communication and collaboration skills to work closely with the CDC Director and with the TA Heads and CQTM.
Experience in executing regulatory submissions of Clinical Trial Applications (CTA) and obtaining approvals.
Fluency in Hebrew and English.

Requirements:
B.Sc. in Health Care/Scientific field. M.Sc. in Life Science- an advantage.
At least 4 years of experience as a CTM/COM.
At least 4 years of experience in direct people management. Experience in managing managers- an advantage.
Excellent leadership and management skills, with the ability to build relationships and collaborate with key opinion leaders.
Strong knowledge of regulatory requirements and attention to details as well as the ability to ensure compliance with policies and procedures.
Conceptual and strategic approach to the clinical organization development in a multi-country setting.
Strategic insight to clinical trial conduct processes and continuous improvements.
Strong track record in clinical trial execution in multifunctional team, including clinical quality (audits and inspections).
Fluency in Hebrew and English.

Requirements:
Bachelor's degree in a life sciences field.
Clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1-2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered.
Valid driver's license where applicable.
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills & Abilities:
Basic medical/therapeutic area knowledge and understanding of medical terminology.
Ability to attain and maintain a proven understanding of ICH GCPs and industry regulations and procedural documents.
Good oral and written communication skills, with ability to communicate effectively with medical personnel.
Good interpersonal skills.
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers underlying issues.
Good organizational and time management skills.
Ability to remain flexible and adaptable in a wide range of scenarios.
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving.
Ability to manage Risk Based Monitoring concepts and processes.
Ability to work in a team or independently as required.
Good digital literacy: proven knowledge of Microsoft Office and ability to learn appropriate software.
Good English language and grammar skills.

Requirements:
PhD or MSc in life sciences
3 years of industry experience with hands-on lab research
Strong bench experience with mammalian cell cultures and cell biology
Independent design and troubleshooting of experiments
Team player
Advantages:
Experience with: RT-PCR, FACS, IF, WB
Molecular biology and cloning techniques
Background in cancer research
Proteomics sample preparation experience