Regulatory Affairs and Quality Manager

Location: St. Paul, MN - remote to start, but will transition to a hybrid model in the coming months Contract: 3-12 month contract to likely hire Pay: $20-22.50/hr Openings: 1 Must-haves - Bachelors Degree in chemistry, biology, or other scientific/technical discipline - Database management skills - Very detail oriented - Excellent written and verbal...

Location: St. Paul, MN - remote to start, but will transition to a hybrid model in the coming monthsContract: 3-12 month contract to likely hirePay: $20-22.50/hrOpenings: 1Must-haves - Bachelors Degree in chemistry, biology, or other scientific/technical discipline- Database management skills- Very detail oriented- Excellent written and verbal communication...

Location: St. Paul, MN - remote to start, but will transition to a hybrid model in the coming monthsContract: 3-12 month contract to likely hirePay: $20-22.50/hrOpenings: 1Must-haves - Bachelors Degree in chemistry, biology, or other scientific/technical discipline- Database management skills- Very detail oriented- Excellent written and verbal communication...

Title - Regulatory Affairs Specialist Hybrid in St Paul, Entry level- new grads encouraged to applyPay - 22-24/hourContract- Conversion Potential (W2)Day-to-DayInsight Global is seeking a Regulatory Affairs Specialist to join one of our largest chemical and water clients in the Eagan area. This person will be working within the Regulatory Affairs division...

Job Description Job Description · Perform assigned regulatory activities including submissions/responses to country authorities. Daily Responsibilities - Job Description suppliers should use: · Plan and prepare documents for EU MDR Technical File original submissions or responses to Notified Body for existing Technical Files under review. · Assist in...

Responsibilities:Manage submissions and projects as assigned by Regulatory leadership, ensuring compliance, planning, and execution.Represent regulatory interests on cross-functional teams.Process, interpret, and provide recommendations for complex regulatory strategies.Offer regulatory and technical expertise to cross-functional teams.Critically review...

Responsibilities:Manage submissions and projects as assigned by Regulatory leadership, ensuring compliance, planning, and execution.Represent regulatory interests on cross-functional teams.Process, interpret, and provide recommendations for complex regulatory strategies.Offer regulatory and technical expertise to cross-functional teams.Critically review...

Location: St. Paul, MN - remote to start, but will transition to a hybrid model in the coming monthsContract: 3-12 month contract to likely hirePay: $ /hrOpenings: 1Must-haves Bachelors Degree in chemistry, biology, or other scientific/technical disciplineDatabase management skillsVery detail orientedExcellent written and verbal communication...

Location: St. Paul, MN - remote to start, but will transition to a hybrid model in the coming monthsContract: 3-12 month contract to likely hirePay: $20-22.50/hrOpenings: 1Must-haves - Bachelors Degree in chemistry, biology, or other scientific/technical discipline- Database management skills- Very detail oriented- Excellent written and verbal communication...

Title - Regulatory Affairs Specialist Hybrid in St Paul, Entry level- new grads encouraged to applyPay - 22-24/hourContract- Conversion Potential (W2)Day-to-DayInsight Global is seeking a Regulatory Affairs Specialist to join one of our largest chemical and water clients in the Eagan area. This person will be working within the Regulatory Affairs division...

Job DescriptionJob Description·         Perform assigned regulatory activities including submissions/responses to country authorities. Daily Responsibilities - Job Description suppliers should use:·         Plan and prepare documents for EU MDR Technical File original submissions or responses to Notified Body for existing Technical Files...

The Vice President of Quality and Compliance is a critical leadership role responsible for setting and enforcing the highest standards of quality and compliance throughout all aspects of our manufacturing operations. This executive will lead our efforts to ensure that all products meet or exceed regulatory standards and customer expectations, driving...

The Vice President of Quality and Compliance is a critical leadership role responsible for setting and enforcing the highest standards of quality and compliance throughout all aspects of our manufacturing operations. This executive will lead our efforts to ensure that all products meet or exceed regulatory standards and customer expectations, driving...

Recruiter: Lukas Daniel Richardson About the role: At Boston Scientific, you'll discover a place where you can have meaningful purpose, improving lives through your life's work. In Rhythm Management (RM) we offer solutions for treating irregular heart rhythms and heart failure and protecting against sudden cardiac arrest. We continue to innovate in key areas...

Our client is one of the largest dairy producers in the US, their business supports a network of local cooperatives, independent dealers, and other large retailers serving producers, and animal owners throughout the United States. Through industry-leading R&D and committed partnerships, they innovate nutrition products and practices. As they continue...

SUMMARY The Quality Management Representative is responsible for the quality operations function of the quality system and compliance aspects related to this function. The individual initiates and/or supports innovative activities associated to product quality, quality systems and compliance, establishes priorities and facilitates resource allocation....

Summary Works with senior leadership to plan, direct and coordinate the overall quality plan of the organization which includes the collaboration and integration of active working committees and/or individual service areas. Position collaborates with colleagues on management team to improve productivity, processes and patient/resident/customer outcomes....

Description Summary The Director of Clinical Affairs is responsible for all clinical aspects of medical device development projects at all stages of the product life cycle, for clinical affairs activities, and for special projects. This full-time role reports to the Senior Vice President of Regulatory Affairs and Quality Assurance and is located in the...

Job Summary The VP Government Affairs and Chief of Staff is responsible for the government relations activities on behalf of Johns Hopkins All Children’s Hospital with a focus on issues involving pediatric advocacy, research, treatment, education healthcare, higher education, corporate relations and private business development in the state of Florida and...

Job SummaryThe VP Government Affairs and Chief of Staff is responsible for the government relations activities on behalf of Johns Hopkins All Children's Hospital with a focus on issues involving pediatric advocacy, research, treatment, education healthcare, higher education, corporate relations and private business development in the state of Florida and...