safety compliance specialist

Prime One

<div>
 <strong>
  About Us
  <br/>
  <br/>
 </strong>
 Prime One is a leading transportation company committed to safety, compliance, and operational excellence. We&rsquo;re seeking a motivated and detail-oriented DOT Safety Risk Management Specialist to take charge of key responsibilities, including claims management and new driver orientation.
 <br/>
 <br/>
 <strong>
  Job Summary
  <br/>
  <br/>
 </strong>
 As the DOT Safety Risk Management Specialist, you will ensure compliance with DOT regulations, manage safety programs, handle claims, and lead new driver orientation programs. Your role will involve identifying risks, ensuring smooth onboarding for new hires, and driving continuous improvements in safety and compliance.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct driver orientations and training programs on DOT safety regulations and company policies.
  </li>
  <li>
   Monitor compliance with FMCSA/DOT standards and maintain safety records.
  </li>
  <li>
   Collaborate with drivers to address safety concerns and reinforce best practices.
  </li>
  <li>
   Investigate incidents, analyze trends, and implement corrective action plans.
  </li>
  <li>
   Oversee pre-employment screenings and ensure driver qualification files are up to date.
  </li>
  <li>
   Develop and promote a culture of safety through effective communication and proactive measures.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Driver Support &amp; Orientation
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Facilitate orientation for new hires, ensuring they understand company policies, safety protocols, and compliance requirements.
  </li>
  <li>
   Train new drivers on pre-trip inspections, Hours of Service (HOS), ELD use, and other key areas.
  </li>
  <li>
   Act as a safety resource for drivers, answering questions and addressing concerns.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Policy Enforcement &amp; Communication
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Enforce company policies related to safety and compliance, addressing violations promptly.
  </li>
  <li>
   Communicate safety expectations to drivers and management regularly.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Collaboration
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Work with dispatch, maintenance, and HR teams to maintain a safety culture.
  </li>
  <li>
   Partner with the operations team to address safety and compliance gaps.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Strong knowledge of DOT and FMCSA regulations.
  </li>
  <li>
   Proven experience in safety and risk management in the transportation or logistics industry.
  </li>
  <li>
   Excellent communication and training skills for new hire orientation.
  </li>
  <li>
   Familiarity with ELD platforms and safety management systems.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience leading driver training programs or orientations.
  </li>
  <li>
   Background in the Trucking and Logistics Field.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Prime One is proud to be an equal-opportunity employer and values diversity in the workplace.
 </strong>
</div>


DOT Safety Compliance Manager

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
Standard (Mon-Fri)<p></p><p><b>
Environmental Conditions</b></p>
Office<p></p><p><b>
Job Description</b></p><p></p><p>
At Thermo Fisher Scientific, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on &ndash; now and in the future.</p><p></p><div>
Join us as Senior Safety Reporting Specialist &ndash; To lead and oversee the preparation of complex safety reports, ensure compliance with international pharmacovigilance regulations, and drive continuous improvement in our reporting processes to safeguard patient health.<br>
<br>
What You&rsquo;ll Do:<br>
<ul><li>Receive, prepare and submit safety reports to applicable parties. Ensure that all reports are compliant with regulatory timelines and country legislation and monitor this on a regular basis.</li><li>Lead large scale projects effectively, ensuring safety reports are submitted in accordance with the agreed processes and regulatory timelines.</li><li>Provide input and feedback to aid the development of program and departmental procedural documents.</li><li>Sharing ideas and suggestions with team members. Take an active role in the development and implementation of ideas and suggestions.</li><li>Liaise with relevant departments around safety reporting tasks and attends various meetings as required.</li><li>Provide input, feedback and guidance to other team members and mentors new starters.</li><li>Produce metrics and have some involvement in financial project.</li></ul><br>
Education and Experience:<br>
<ul><li>Bachelor's degree or equivalent and relevant formal academic / vocational qualification.</li><li>Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 5+ years&rsquo;).</li></ul><br>
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.<br>
<br>
Knowledge, Skills and Abilities:<br>
<ul><li>Excellent knowledge of medical terminology</li><li>Excellent Microsoft Office skills and good understanding of database functionality</li><li>Excellent knowledge of procedural documents and thorough understanding of global safety reporting requirements</li><li>Good time management and multi-tasking skills</li><li>Strong attention to detail</li><li>Ability to influence at all levels of the organization</li><li>Ability to work well in a collaborative team environment</li><li>Demonstrated initiative and utilizes persuasion and negotiation skills</li><li>Excellent critical thinking and problem-solving abilities</li><li>Ability to apply knowledge, skills, and expertise to assist lower-level colleagues in safety reporting activities</li></ul><br>
Why Join Us?<br>
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You&rsquo;ll work in an environment where collaboration and development are part of the everyday experience &ndash; and where your contributions truly make a difference.<br>
<br>
Apply today to help us deliver tomorrow&rsquo;s breakthrough.</div></div><p></p>

Senior Safety Reporting Specialist, Turkey

Syneos Health

<div>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 Safety &amp; PV Specialist I (Literature Review)
 <br/>
 <br/>
 Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
 <br/>
 <br/>
 Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
 <br/>
 <br/>
 Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
 <br/>
 <br/>
 Discover what our 29,000 employees, across 110 countries already know:
 <br/>
 <br/>
 <strong>
  WORK HERE MATTERS EVERYWHERE
  <br/>
  <br/>
 </strong>
 Why Syneos Health
 <br/>
 <br/>
 <ul>
  <li>
   We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  </li>
  <li>
   We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  </li>
  <li>
   We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Job Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements.
  </li>
  <li>
   Maintains safety tracking for assigned activities.
  </li>
  <li>
   Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required.
  </li>
  <li>
   Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.
  </li>
  <li>
   Manual recoding of un-recoded product and substance terms arises from ICSRs.
  </li>
  <li>
   Identification and management of duplicate ICSRs.
  </li>
  <li>
   Activities related to SPOR / IDMP.
  </li>
  <li>
   Quality review of ICSRs.
  </li>
  <li>
   Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.
  </li>
  <li>
   Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process.
  </li>
  <li>
   Fosters constructive and professional working relationships with all project team members, internal and external.
  </li>
  <li>
   Participates in audits as required/appropriate.
  </li>
  <li>
   Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job.
  </li>
  <li>
   Minimum 2+ years of experience in Literature review
  </li>
  <li>
   Candidates with Literature review experience along with Literature Case Processing and Clinical Trial Case Processing exp are preferred
  </li>
  <li>
   Drug Safety Triager Database preferred for Literature experience
  </li>
  <li>
   Safety Database systems and knowledge of medical terminology required.
  </li>
  <li>
   Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance.
  </li>
  <li>
   Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet.
  </li>
  <li>
   Ability to work independently and in a team environment.
  </li>
  <li>
   Excellent communication and interpersonal skills, both written and spoken.
  </li>
  <li>
   Good organizational skills with proven ability to prioritize and work on multiple tasks and projects.
  </li>
  <li>
   Detail oriented with a high degree of accuracy and ability to meet deadlines.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Get to know Syneos Health
  <br/>
  <br/>
 </strong>
 Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
 <br/>
 <br/>
 No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
 <br/>
 <br/>
 http://www.syneoshealth.com
 <br/>
 <br/>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
 <br/>
 <br/>
 <strong>
  Summary
  <br/>
  <br/>
 </strong>
 Roles within Pharmacovigilance &amp; Safety job family are responsible for providing expertise on pharmacovigilance services. This includes participating in all aspects of the medical safety team's involvement in assigned trials, such as performing medical review and clarification of trial-related Adverse Events, providing aggregate reviews of safety information, and serving as an internal consultant to pharmacovigilance case processing teams. Provides and contributes trends and safety signal detection and risk management assessment and provides safety support to the clinical development teams. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.
</div>


Safety & PV Specialist I (Literature Review)

<div><p><b>Description</b>
</p>Safety &amp; PV Specialist I (Literature Review)<p></p><p>
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.</p><p>
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.</p><p></p><p>
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.</p><p></p><p>
Discover what our 29,000 employees, across 110 countries already know:</p><p></p><p><b>
WORK HERE MATTERS EVERYWHERE</b></p><p></p><p>
Why Syneos Health</p><ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul><p></p><p><b>
Job Responsibilities</b></p><p></p><ul><li>
Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements.</li><li>
Maintains safety tracking for assigned activities.</li><li>
Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required.</li><li>
Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.</li><li>
Manual recoding of un-recoded product and substance terms arises from ICSRs.</li><li>
Identification and management of duplicate ICSRs.</li><li>
Activities related to SPOR / IDMP.</li><li>
Quality review of ICSRs.</li><li>
Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.</li><li>
Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process.</li><li>
Fosters constructive and professional working relationships with all project team members, internal and external.</li><li>
Participates in audits as required/appropriate.</li><li>
Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.</li></ul><p></p><p><b>
Qualifications:</b></p><ul><li>
Bachelor&rsquo;s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job.</li><li><b>
Minimum 2+ years of experience in Literature review</b></li><li><b>
Candidates with Literature review experience along with Literature Case Processing and Clinical Trial Case Processing exp are preferred</b></li><li><b>
Drug Safety Triager Database preferred for Literature experience</b></li><li>
Safety Database systems and knowledge of medical terminology required.</li><li>
Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance.</li><li>
Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet.</li><li>
Ability to work independently and in a team environment.</li><li>
Excellent communication and interpersonal skills, both written and spoken.</li><li>
Good organizational skills with proven ability to prioritize and work on multiple tasks and projects.</li><li>
Detail oriented with a high degree of accuracy and ability to meet deadlines.</li></ul><p></p><p><b>
Get to know Syneos Health</b></p><p><br>
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.</p><p></p><p>
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.</p><p></p><p>
http://www.syneoshealth.com</p><p></p><p><b>
Additional Information</b></p><p><br>
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.</p><p><b>
Summary</b>
</p>Roles within Pharmacovigilance &amp; Safety job family are responsible for providing expertise on pharmacovigilance services. This includes participating in all aspects of the medical safety team's involvement in assigned trials, such as performing medical review and clarification of trial-related Adverse Events, providing aggregate reviews of safety information, and serving as an internal consultant to pharmacovigilance case processing teams. Provides and contributes trends and safety signal detection and risk management assessment and provides safety support to the clinical development teams.Impact and ContributionIndividual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.</div>

<div><p><b>Description</b>
</p>Safety &amp; PV Specialist I<p></p><p>
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.</p><p>
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.</p><p></p><p>
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.</p><p></p><p>
Discover what our 29,000 employees, across 110 countries already know:</p><p></p><p><b>
WORK HERE MATTERS EVERYWHERE</b></p><p></p><p>
Why Syneos Health</p><ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul><p></p><p><b>
Job Responsibilities</b></p><p></p><ul><li>
Enter information into PVG quality and tracking systems for receipt and tracking ICSR as required. Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required. Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability. Enters data into safety database. Codes events, medical history, concomitant medications, and testsCompiles complete narrative summaries. Identifies information to be queried and follows up until information is obtained and queries are satisfactorily resolved. Assists in the generation of timely, consistent, and accurate reporting of expedited reports in accordance with applicable regulatory requirements.</li><li>
Maintains safety tracking for assigned activities.</li><li>
Performs literature screening and review for safety, drug coding, maintenance of drug dictionary, MedDRA coding as required.</li><li>
Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.</li><li>
Manual recoding of un-recoded product and substance terms arises from ICSRs.</li><li>
Identification and management of duplicate ICSRs.</li><li>
Activities related to SPOR / IDMP.</li><li>
Quality review of ICSRs.</li><li>
Ensures all relevant documents are submitted to the Trial Master File (TMF) as per company SOP/Sponsor requirements for clinical trials and the Pharmacovigilance System Master File for post-marketing programs as appropriate.</li><li>
Maintains understanding and compliance with SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCP, ICH guidelines, GVP, project/program plans and the drug development process.</li><li>
Fosters constructive and professional working relationships with all project team members, internal and external.</li><li>
Participates in audits as required/appropriate.</li><li>
Applies safety reporting regulatory intelligence maintained by Syneos Health to all safety reporting activities.</li></ul><p></p><p>
Qualifications:</p><p></p><ul><li>
Bachelor&rsquo;s Degree in life science, registered nurse, pharmacist or an equivalent combination of education and experience that gives the individual the necessary knowledge, skills, and abilities to perform the job.</li><li>
Safety Database systems and knowledge of medical terminology required.</li><li>
Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations related to Safety and Pharmacovigilance.</li><li>
Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint), Visio, email (Outlook), Team Share (or another management/shared content/workspace) and internet.</li><li>
Ability to work independently and in a team environment.</li><li>
Excellent communication and interpersonal skills, both written and spoken.</li><li>
Good organizational skills with proven ability to prioritize and work on multiple tasks and projects.</li><li>
Detail oriented with a high degree of accuracy and ability to meet deadlines.</li></ul><p></p><p><b>
Get to know Syneos Health</b></p><p><br>
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.</p><p></p><p>
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.</p><p></p><p>
http://www.syneoshealth.com</p><p></p><p><b>
Additional Information</b></p><p><br>
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.</p><p><b>
Summary</b>
</p>Roles within Pharmacovigilance &amp; Safety job family are responsible for providing expertise on pharmacovigilance services. This includes participating in all aspects of the medical safety team's involvement in assigned trials, such as performing medical review and clarification of trial-related Adverse Events, providing aggregate reviews of safety information, and serving as an internal consultant to pharmacovigilance case processing teams. Provides and contributes trends and safety signal detection and risk management assessment and provides safety support to the clinical development teams.Impact and ContributionIndividual contributors with responsibility in a professional or technical discipline or specialty, but may manage two or fewer employees. May direct the work of lower level professionals or manage processes and programs. The majority of time is spent contributing to the design, implementation or delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education. Entry to developing individual contributor. Delivers work of limited scope, typically smaller, less complex projects. Requires theoretical knowledge of a professional area, typically obtained through education and/or prior experience.</div>

Safety & PV Specialist I

Qatar Airways

<div><div><div><div><div><div><div><div>Job title
</div><div>Compliance &amp; Safety Engineer Level 2
</div></div><div><div>Ref #
</div><div>230118
</div></div><div><div>Location
</div><div>Qatar - Doha
</div></div><div><div>Job family
</div><div>Not Specified
</div></div><div><div><ul><li>Closing date: 06-Jan-2026</li></ul><br>
</div></div></div></div></div><div><div><div><div><div><div>Qatar Airways are pleased to announce an incredibly exciting opportunity to join our <b>Group Risk, Safety &amp; Security (GRS&amp;S) </b>team as a <b>Safety - Technical Engineer Level 2</b> to be based in Doha, Qatar.<br>
<br>
As a <b>Safety - Technical Engineer Level 2,</b> you will responsible to associate Technical - Safety Management and other team members in operation of company Safety Management Systems and ensure that constant maintenance standards applied to QTR and Customer aircraft are satisfied to the requirements to Parts 145, M and CAMO.<br>
<br>
<b>Specific responsibilities for the role include:</b><br>
<ul><li>Aircraft Technical Investigations within CAMO/MRO operations</li><li>Human Factor related investigations within CAMO/MRO operations</li><li>Technical Occurrence assessments within CAMO/MRO operations</li><li>Safety Management System functions within MRO/CAMO operations</li><li>Utilizing of Safety Risk management tools and Techniques operations</li><li>Involvement in the Risk Assessments/Management of Changes .</li><li>Health and Safety processes in CAMO/MRO</li><li>Support the review and follow up of mitigation actions submitted by various departments</li><li>Assist in updating current company technical procedures and manuals in to maintain compliance to acceptable levels</li><li>Support the preparation of Safety - Technical Notices and Safety Bulletins .</li><li>Communicate effectively with internal and external stakeholders.</li></ul><br>
<b>
Be part of an extraordinary story</b><br>
Your skills. Your imagination. Your ambition. Here, there are no boundaries to your potential and the impact you can make. You&rsquo;ll find infinite opportunities to grow and work on the biggest, most rewarding challenges that will build your skills and experience. You have the chance to be a part of our future, and build the life you want while being part of an international community. Our best is here and still to come. To us, impossible is only a challenge. Join us as we dare to achieve what&rsquo;s never been done before.<br>
<br>
Together, everything is possible.</div>
</div></div></div></div></div><div><div><div><h3 class="jobSectionHeader"><b>Qualifications
</b></h3></div></div><div><div><div><div><div><b>About you</b><br>
The successful candidate will have the following skills and qualifications:<br>
<ul><li>Relevant tertiary qualification with a minimum of 4 years of job-related experience within aviation safety or a related field, ideally within the aviation sector.</li><li>Degree (B. Eng., BSc in Mechanical, Electrical, Electronics, Mechatronics or Aeronautical Engineering), or Diploma in Aircraft Maintenance Engineering .</li><li>Experience in Compliance &amp; Safety/Quality assurance/maintenance/continued airworthiness environment.</li><li>Experience in incident/accident investigation and root cause analysis</li><li>4+ years' experience in aircraft technical investigations and human factor related investigations within CAMO/MRO.</li><li>Experience in Safety Management section of CAMO and MRO. Experience in Occupational Health and Safety will be considered as an additional skill.</li><li>Good understanding of Safety Risk Management Tools and Techniques.</li><li>Experience in Risk Assessments/Management of Changes.</li><li>Detailed knowledge of air legislation, particularly ICAO, EASA &amp; FAA Regulations.</li><li>Detailed Knowledge of Compliance &amp; Safety/Quality &amp; Safety systems, continued airworthiness and aircraft maintenance fundamentals.</li><li>Excellent problem-solving abilities with analytical skills.</li><li>Proficiency in the use of computers and industry software;</li><li>Good English communication skills both written and verbal.</li></ul><br>
<b>
About Qatar Airways Group</b><br>
Our story started with four aircraft. Today, we deliver excellence across 12 different businesses coming together as one. We&rsquo;ve grown fast, broken records and set trends that others follow. We don&rsquo;t slow down by the fear of failure. Instead, we dare to achieve what&rsquo;s never been done before. So, whether you&rsquo;re creating a unique experience for our customers or innovating behind the scenes, every person contributes to our proud story. A story of spectacular growth and determination. Now is the time to bring your best ideas and passion to a place where your ambition will know no boundaries, and be part of a truly global community.</div><p><b>
How to apply</b><br>
If you&rsquo;re ready to join a progressive team and have a challenging and rewarding career, then apply now by uploading your CV and completing our quick application form.</p><br>
</div></div><div></div><div><div><br>
<div><b>About Qatar Airways Group
</b></div><br>
Our story started with four aircraft. Today, we deliver excellence across 12 different businesses coming together as one. We&rsquo;ve grown fast, broken records and set trends that others follow. We don&rsquo;t slow down by the fear of failure. Instead, we dare to achieve what&rsquo;s never been done before.<br>
<br>
So whether you&rsquo;re creating a unique experience for our customers or innovating behind the scenes, every person contributes to our proud story. A story of spectacular growth and determination. Now is the time to bring your best ideas and passion to a place where your ambition will know no boundaries, and be part of a truly global community.<br>
</div></div><div><div>https://aa115.taleo.net/careersection/QA_External_CS/jobapply.ftl?lang=en&amp;job=230118</div></div></div></div></div></div></div></div>

Compliance & Safety Engineer Level 2

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