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Placements24 is seeking a meticulous Remote Quality Assurance Inspector focused on sanitation to support remote operations. You will review sanitation data, photos, and walkthroughs to ensure compliance with health and hygiene standards, providing precise feedback to drive improvements.
The role demands strong attention to detail, experience in QA and a solid grasp of sanitation principles, with the flexibility to work fully remotely from anywhere in South Africa.
Our client is seeking a highly observant and technically proficient Remote Quality Assurance Inspector specializing in sanitation to join their virtual operations team. In this fully remote position, you will play a critical role in ensuring that sanitation standards and quality control measures are met across various client sites by analyzing submitted data, photographic evidence, and virtual walkthroughs. You will meticulously review reports and provide expert feedback to ensure compliance with stringent health and hygiene protocols. This role is ideal for an individual with a keen eye for detail and a deep understanding of sanitation best practices, capable of performing thorough assessments from a distance.
Our client is seeking a highly observant and technically proficient Remote Quality Assurance Inspector specializing in sanitation to join their virtual operations team. In this fully remote position, you will play a critical role in ensuring that sanitation standards and quality control measures are met across various client sites by analyzing submitted data, photographic evidence, and virtual walkthroughs. You will meticulously review reports and provide expert feedback to ensure compliance with stringent health and hygiene protocols. This role is ideal for an individual with a keen eye for detail and a deep understanding of sanitation best practices, capable of performing thorough assessments from a distance.
Remote ThermoFisher Scientific
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'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 - now and in the future.
We are currently seeking a **Principal Regulatory Affairs Specialist** to join our global Regulatory Affairs department, Reg Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.
In this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials, studies and projects.
You will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance.
You will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients.
You will act as a representative of the regulatory department with other departments, supporting business development, working on initiatives, and contributing to quality improvement. You will also arrange, lead, and report on client and regulatory agency meetings.
**The following skills are required to be successful in this position:**
+ preparation and assembly of global regulatory submissions (CTA)
+ interacting with sponsors,
+ review and assess clinical trial regulatory documents,
+ review and assess scientific literature.
+ manages project teams and preparation
+ participate in launch meetings, review meetings and project team meetings.
+ Experience with bid defense meetings
**Qualifications**
What the role requires you to have:
+ Bachelor's degree or advanced degree preferred, or equivalent and relevant formal academic / vocational qualification
+ Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 8+ years
+ Knowledge of the global clinical trials landscape
**Knowledge, Skills and Abilities:**
+ Excellent command of the English language (written and oral) as well as local language where applicable
+ **Experience with Bid Defense meetings**
+ **Experience in leading global regulatory projects for Clinical Trial Applications**
+ Excellent attention to detail and quality as well as excellent editorial/proofreading skills
+ Exceptional interpersonal skills to work effectively in a team environment and act as a liaison with other departments
+ Advanced computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies
+ Strong organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects
+ Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables
+ Excellent understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization; expert knowledge of ICH and other global regulatory guidelines
+ Excellent analytical, investigative and problem-solving skills
**What we offer:**
At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - **_Integrity, Intensity, Innovation and Involvement_** - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Our client is seeking a meticulous and detail-oriented Remote Quality Assurance Inspector to join their dynamic team, supporting operations from anywhere in South Africa . In this crucial role, you will be responsible for conducting remote inspections and verifications of manufactured goods, ensuring they meet stringent quality standards and specifications before they reach the customer. You will utilize advanced digital tools and communication platforms to collaborate with manufacturing sites and clients, providing critical feedback and driving quality improvements. This position offers the unique advantage of contributing to product excellence without the need for physical presence at a specific site.
Our client is seeking a meticulous and detail-oriented Remote Quality Assurance Inspector to join their dynamic team, supporting operations from anywhere in South Africa . In this crucial role, you will be responsible for conducting remote inspections and verifications of manufactured goods, ensuring they meet stringent quality standards and specifications before they reach the customer. You will utilize advanced digital tools and communication platforms to collaborate with manufacturing sites and clients, providing critical feedback and driving quality improvements. This position offers the unique advantage of contributing to product excellence without the need for physical presence at a specific site.
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