Creation and ongoing update of product regulatory information in standardized information packs. Support of customer, regulatory, and 3rd party audits. Supporting the regional Pharma division Sales Te...

Creation and ongoing update of product regulatory information in standardized information packs. Support of customer, regulatory, and 3rd party audits. Supporting the regional Pharma division Sales Te...

Regulatory Affairs Specialist - Valencia, CA. Kelly® Science & Clinical is seeking a Regulatory Specialist for a temporary, long-term position (approx. The role ensures high-quality products are consi...

Regulatory Affairs Specialist - Valencia, CA. The Regulatory Specialist will also act as a back-up for Radioassay. Kelly® Science & Clinical is seeking a Regulatory Specialist for a temporary, lo...

Job Title: Regulatory Affairs Specialist. Regulatory Affairs Certification (RAC) or equivalent credential (preferred). Life Sciences, Engineering, Regulatory Affairs, or a related field.

Job Title: Regulatory Affairs Specialist. Life Sciences, Engineering, Regulatory Affairs, or a related field. Regulatory Affairs Certification (RAC) or equivalent credential (preferred).

Job Title: Regulatory Affairs Specialist. Life Sciences, Engineering, Regulatory Affairs, or a related field. Regulatory Affairs Certification (RAC) or equivalent credential (preferred).

Job Title: Regulatory Affairs Specialist. Regulatory Affairs Certification (RAC) or equivalent credential (preferred). Life Sciences, Engineering, Regulatory Affairs, or a related field.

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. VP of Quality & Regulatory Affai...

The Regulatory Affairs Specialist is a key partner within Regulatory Affairs and will have responsibility of the direct execution of some corporate regulatory filings. VP of Quality & Regulatory Affai...

Senior Regulatory Affairs Specialist. Master’s Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Certification is a plus (such as RAC from the Regulatory Affairs Pr...

Senior Regulatory Affairs Specialist. Master’s Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Certification is a plus (such as RAC from the Regulatory Affairs Pr...

Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Minimum five ...

Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP development, and GMP audits and inspections). Minimum five ...

Master’s Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Senior Regulatory Affairs Specialist. Acts as a regulatory representative on core product development tea...

Master’s Degree in Regulatory Affairs and may be used in lieu of direct regulatory experience. Senior Regulatory Affairs Specialist. Acts as a regulatory representative on core product development tea...

Regulatory Affairs Specialist/Manager will oversee medical device development and market introduction, ensuring compliance with regulatory standards for Class I, II, and III devices. A minimum of 5 ye...

The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for SkinMedica products. Prepares and submits regulatory documents for cosmetic registra...

The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for SkinMedica products. Prepares and submits regulatory documents for cosmetic registra...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society). Acts as a regulatory representative on core product development teams, communicates regulatory requirements and...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society). Acts as a regulatory representative on core product development teams, communicates regulatory requirements and...

He/She has responsibility for compliance with US and EU regulatory requirements and partners with the international regulatory affairs group to support regulatory submissions. Minimum of 7 years of ex...

Minimum of 7 years of experience medical device regulatory affairs Or advanced degree with a minimum of 5 years of experience medical device regulatory affairs. He/She has responsibility for complianc...

A minimum of a bachelor’s degree and 1-3 years’ work experience in regulatory affairs. RA certification (by Regulatory Affairs Professional Society). Support the regulatory submission activities to ob...

Seeking a Senior Regulatory Affairs Specialist with expertise in US and EU regulatory requirements, EU MDR regulation, and medical device regulatory submissions to sustain the current product portfoli...

The role of the Regulatory Affairs Specialist will be to support the global regulatory affairs of the business with a specialized focus on the United States. This position will be primarily responsibl...

The role of the Regulatory Affairs Specialist will be to support the global regulatory affairs of the business with a specialized focus on the United States. This position will be primarily responsibl...

In this dynamic role as a Senior Regulatory Affairs Specialist, you will be responsible for informing both local and global regulatory partners of sustaining changes through the Medtronic Agile system...

In this dynamic role as a Senior Regulatory Affairs Specialist, you will be responsible for informing both local and global regulatory partners of sustaining changes through the Medtronic Agile system...

Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and ...

Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and ...

As a Specialist, Regulatory Affairs for TMTT, you will complete and maintain clinical and commercial regulatory approvals of Class III implantable products in the US and EU, focusing on the paradigm s...

As a Specialist, Regulatory Affairs for TMTT, you will complete and maintain clinical and commercial regulatory approvals of Class III implantable products in the US and EU, focusing on the paradigm s...

Participate in representing the OUS regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regula...

Minimum five (5) years of experience in Regulatory Affairs. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP...

Minimum five (5) years of experience in Regulatory Affairs. Demonstrated knowledge of Regulatory Affairs regulations, guidance, and procedures (Good Mfg Practice, Good Practices training programs, SOP...

Bachelor’s degree in Engineering, Physical or Biological Sciences, Regulatory, other technical disciplines, or equivalent.

Bachelor’s degree in Engineering, Physical or Biological Sciences, Regulatory, other technical disciplines, or equivalent.

Minimum two years of experience in Regulatory Affairs or Quality Assurance in the medical device industry.

Minimum two years of experience in Regulatory Affairs or Quality Assurance in the medical device industry.