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Pharma and life sciences jobs at the forefront of innovation

A Positive Impact For Patients And Their Families

We work closely with our partners to understand their unique requirements, create the right approach to market, and offer expert advice.

With excellent networks in academia, the financial community and the industry, we can support organizations that need high-level consultancy during critical times. We also have the flexibility and industry knowledge to offer specialist human capital solutions in the form of contract staff, project teams and interim cover.

We recruit across all levels of seniority, from research associates to global product managers. Our specialisms include:

  • regulatory affairs;

  • biometrics and biostatistics;

  • medical and regulatory writing;

  • quality assurance and quality control;

  • market access and HEOR;

  • clinical development and clinical operations;

  • technical operations and CMC;

  • process development;

  • supply chain and procurement;

  • R&D,

  • discovery and translational;

  • medical affairs; and manufacturing.

If you’d like to talk to us about finding the right talent for your business, please contact us.

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what's available

Latest roles in Life Sciences Recruitment

  • Director Regulatory Affairs and Quality Assurance

    Irvine | US$160000 - US$180000 per annum + bonus, benefits, equity

    Director, Regulatory Affairs and Quality Assurance Irvine, CA (1x onsite/week) POSITION PURPOSE: The Director of Quality Assurance and Regulatory Affairs is responsible for working with all levels of employees within the organization in providing strategies that include the development and continuous improvement of a sustainable and compliant Quality System; U.S....

  • Quality Assurance Manager

    Cleveland | US$85000 - US$100000 per annum

    Quality Assurance Manager Responsibilities: Responsible for maintaining and continuously improving the Quality Management System (QMS) to 21 CFR 820. Responsible for risk management documentation for products and processes; identifies and updates failure modes and related process/product improvements by facilitating teams and implementing required changes. Handle received complaints and subsequent root...

  • Staff Regulatory Affairs Specialist (hybrid)

    Carlsbad | US$120000 - US$140000 per annum + bonus, benefits, RSU

    The Staff Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to product design teams, change control, and regulatory product submissions. Essential Duties and Responsibilities Collaborates as a core team member on new product...

  • Senior Regulatory Affairs Specialist (hybrid)

    Carlsbad | US$110000 - US$130000 per annum + bonus, RSU, benefits

    *Hybrid on-site/remote position in Carlsbad, CA The Regulatory Affairs Specialist will support the development of submissions for domestic and international clearances for spine surgery products, including Software technologies; as well as the support of daily activities related to product design teams, change control, and regulatory product submissions. Essential Duties and...

  • Product Manager

    Carlsbad | US$88000 - US$115000 per annum + Healthcare Insurance, PTO, 401k

    Product Manager Description: Under minimal supervision, identifies and implements product strategies, marketing plans, promotional and advertising programs, as well as oversees all aspects of product management, including: market launch and surveillance, release to sales and forecasting for assigned product line to ensure that existing and new products meet Company goals...

  • Associate Product Manager

    Carlsbad | US$60000 - US$90000 per annum + Healthcare Insurance, PTO, 401k

    Associate Product Manager Description: Responsible for supporting the development and execution of product strategies, marketing plans, promotional and advertising programs, as well as oversees all aspects of product management, including: requirements definition, surgeon customer feedback, product messaging, product launch, sales force and customer engagement, and product forecasting to ensure that...

  • Vice President, Regulatory Affairs

    Del Mar | US$280000 - US$300000 per annum + bonus, equity

    The Vice President, Global Regulatory Affairs is responsible for leading the development and execution of worldwide regulatory strategy and compliance initiatives. The RA leader is also responsible for maintaining all product registrations throughout the product lifecycle and working collaboratively with external partners and suppliers, while building and scaling a team...

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Your feedback

  • My experience working with Investigo was fantastic and unlike any previous experience I’ve had with a recruitment/placement firm! Investigo did an incredible job of identifying a opportunity as a proper fit, providing valuable information pertaining to the job and organization, preparing me for interviews, following-up post interviews, and continuing to check-in with me 2 months following my start date!

    Account Group Supervisor
  • Investigo will get results for you! Investigo will ensure that they understand your needs then can be relied upon to find great candidates.

    Managing Director
  • Investigo understand how we are trying to grow as a business and the type of organization we are, and that is reflected in the candidates Investigo team brings. They completely understands the need for on paper qualifications as well as the soft-skills we need and doesn’t waste our time with people who won’t fit in with our team values.

    Managing Director - Vue Health

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