Bausch Health Companies Inc.

Define and lead the global medical strategy for aesthetic device portfolio, ensuring scientific excellence and regulatory compliance. | Requires MD or PhD with 15+ years in aesthetic medical devices, leadership experience, and expertise in clinical trials and regulatory interactions. | Job Location: AlisoViejo, California, USA | Anaheim, California, USA | Bakersfield, California, USA | BeverlyHills, California, USA | Burbank, California, USA | Carlsbad, California, USA | Chico, California, USA | Cupertino, California, USA | Davis, California, USA | Encinitas, California, USA | Encino, California, USA | FosterCity, California, USA | Fresno, California, USA | Fullerton, California, USA | Hayward, California, USA | HuntingtonBeach, California, USA | Irvine, California, USA | LongBeach, California, USA | LosAngeles, California, USA | Modesto, California, USA | MountainView, California, USA | Napa, California, USA | Novato, California, USA | Oceanside, California, USA | Ontario, California, USA | PalmSprings, California, USA | PaloAlto, California, USA | Pasadena, California, USA | Petaluma, California, USA | Pleasanton, California, USA | RanchoCucamonga, California, USA | RedwoodCity, California, USA | Riverside, California, USA | Sacramento, California, USA | SacramentoSouth, California, USA | SanBernandino, California, USA | SanDiego, California, USA | SanDimas, California, USA | SanFrancisco, California, USA | SanJose, California, USA | SantaAna, California, USA | SantaBarbara, California, USA | SantaClarita, California, USA | SantaMonica, California, USA | SantaRosa, California, USA | SealBeach, California, USA | Sonoma, California, USA | Stockton, California, USA | Sunnyvale, California, USA | Temecula, California, USA | ThousandOaks, California, USA | Torrance, California, USA | Tustin, California, USA | Ventura, California, USA | WalnutCreek, California, USA | WestCovina, California, USA | Eugene, Oregon, USA | Portland, Oregon, USA | Bothell, Washington, USA | Redmond, Washington, USA | Renton, Washington, USA | Seattle, Washington, USA | Spokane, Washington, USA | Vancouver, Washington, USA Job Requisition ID: 14396 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Executive Director, Solta Global Medical reports to the Senior Vice President, Head of Global Medical Affairs (GMA) and is the strategic and scientific leader responsible for defining and guiding the global medical and clinical development strategy for Solta’s aesthetic device portfolio. This role ensures scientific excellence, compliant communication, and cross-functional alignment across Medical Affairs, Clinical Development, Biomedical, Regulatory, and Commercial teams globally. Responsibilities: • Define and lead the global medical strategy for Solta’s aesthetics device portfolio. • Serve as the Global Medical Lead providing scientific direction across product lifecycle stages. • Represent Medical Affairs in executive committees, due diligence evaluations, and governance boards. • Set strategic direction for clinical development priorities and evidence generation in support to the Clinical Development Lead who retains full responsibility for clinical trial execution, CRO management, investigator engagement, and operational delivery. • Support the Clinical Development Lead to ensure trial designs align with regulatory and commercial goals. Review and endorse clinical development plans and pivotal study strategies. • Ensure that clinical development activities support differentiated claims and global regulatory standards. • Lead the global Medical Affairs function and provide guidance to the medical affairs team, including scientific communications, KOL engagement, and medical information. • Lead the development and implementation of the Global Medical Plan aligned with lifecycle strategy. • Oversee claims substantiation and ensure scientific accuracy in promotional materials. • Guide integrated evidence planning (IEP) across clinical, RWE, and HEOR domains. • Lead publication strategy and global congress participation. • Champion transparency and scientific rigor in medical communications. • Serve as the medical governance authority ensuring adherence to GCP, ICH, and internal SOPs. • Collaborate with Legal, Regulatory, and Compliance to ensure ethical medical activities. • Provide strategic oversight for safety signal detection and benefit-risk assessments. Qualifications: • MD, PhD, or equivalent advanced degree in Medicine, Biomedical Science, or related field preferred. • Board certification or experience in Dermatology, Plastic Surgery, or related field strongly preferred. • Minimum 15 years of experience in the aesthetics medical device industry, or biotechnology required • Proven track record in aesthetic medicine, dermatology, or energy-based device development. • At least 8 years of leadership experience managing cross-functional and global medical/clinical teams. • Demonstrated experience with clinical trials for devices, including regulatory submissions, claims generation, and post-market evidence. • Experience with concepts in one or more of the following areas is preferred: radio-frequency-tissue interaction, laser-tissue interaction, thermally induced tissue damage, laser tissue ablation, ultrasound-assisted liposuction • Strong experience interacting with regulatory authorities and KOLs globally. • Deep understanding of aesthetic device clinical development, claims substantiation, and market access evidence. • Excellent leadership, interpersonal, and communication skills. • Strong scientific writing and data interpretation capabilities. • Business acumen and strategic agility to align scientific goals with commercial objectives. • Ability to thrive in a fast-paced, matrixed, and global organization. The range of starting base pay for this role is 260K – 358K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Lead global medical and clinical strategies for aesthetic devices, ensuring scientific excellence and regulatory compliance. | Requires MD or PhD with 15+ years in aesthetic medical devices, leadership in cross-functional teams, and experience with clinical trials and regulatory interactions. | Job Location: AlisoViejo, California, USA | Anaheim, California, USA | Bakersfield, California, USA | BeverlyHills, California, USA | Burbank, California, USA | Carlsbad, California, USA | Chico, California, USA | Cupertino, California, USA | Davis, California, USA | Encinitas, California, USA | Encino, California, USA | FosterCity, California, USA | Fresno, California, USA | Fullerton, California, USA | Hayward, California, USA | HuntingtonBeach, California, USA | Irvine, California, USA | LongBeach, California, USA | LosAngeles, California, USA | Modesto, California, USA | MountainView, California, USA | Napa, California, USA | Novato, California, USA | Oceanside, California, USA | Ontario, California, USA | PalmSprings, California, USA | PaloAlto, California, USA | Pasadena, California, USA | Petaluma, California, USA | Pleasanton, California, USA | RanchoCucamonga, California, USA | RedwoodCity, California, USA | Riverside, California, USA | Sacramento, California, USA | SacramentoSouth, California, USA | SanBernandino, California, USA | SanDiego, California, USA | SanDimas, California, USA | SanFrancisco, California, USA | SanJose, California, USA | SantaAna, California, USA | SantaBarbara, California, USA | SantaClarita, California, USA | SantaMonica, California, USA | SantaRosa, California, USA | SealBeach, California, USA | Sonoma, California, USA | Stockton, California, USA | Sunnyvale, California, USA | Temecula, California, USA | ThousandOaks, California, USA | Torrance, California, USA | Tustin, California, USA | Ventura, California, USA | WalnutCreek, California, USA | WestCovina, California, USA | Eugene, Oregon, USA | Portland, Oregon, USA | Bothell, Washington, USA | Redmond, Washington, USA | Renton, Washington, USA | Seattle, Washington, USA | Spokane, Washington, USA | Vancouver, Washington, USA Job Requisition ID: 14396 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Executive Director, Solta Global Medical reports to the Senior Vice President, Head of Global Medical Affairs (GMA) and is the strategic and scientific leader responsible for defining and guiding the global medical and clinical development strategy for Solta’s aesthetic device portfolio. This role ensures scientific excellence, compliant communication, and cross-functional alignment across Medical Affairs, Clinical Development, Biomedical, Regulatory, and Commercial teams globally. Responsibilities: • Define and lead the global medical strategy for Solta’s aesthetics device portfolio. • Serve as the Global Medical Lead providing scientific direction across product lifecycle stages. • Represent Medical Affairs in executive committees, due diligence evaluations, and governance boards. • Set strategic direction for clinical development priorities and evidence generation in support to the Clinical Development Lead who retains full responsibility for clinical trial execution, CRO management, investigator engagement, and operational delivery. • Support the Clinical Development Lead to ensure trial designs align with regulatory and commercial goals. Review and endorse clinical development plans and pivotal study strategies. • Ensure that clinical development activities support differentiated claims and global regulatory standards. • Lead the global Medical Affairs function and provide guidance to the medical affairs team, including scientific communications, KOL engagement, and medical information. • Lead the development and implementation of the Global Medical Plan aligned with lifecycle strategy. • Oversee claims substantiation and ensure scientific accuracy in promotional materials. • Guide integrated evidence planning (IEP) across clinical, RWE, and HEOR domains. • Lead publication strategy and global congress participation. • Champion transparency and scientific rigor in medical communications. • Serve as the medical governance authority ensuring adherence to GCP, ICH, and internal SOPs. • Collaborate with Legal, Regulatory, and Compliance to ensure ethical medical activities. • Provide strategic oversight for safety signal detection and benefit-risk assessments. Qualifications: • MD, PhD, or equivalent advanced degree in Medicine, Biomedical Science, or related field preferred. • Board certification or experience in Dermatology, Plastic Surgery, or related field strongly preferred. • Minimum 15 years of experience in the aesthetics medical device industry, or biotechnology required • Proven track record in aesthetic medicine, dermatology, or energy-based device development. • At least 8 years of leadership experience managing cross-functional and global medical/clinical teams. • Demonstrated experience with clinical trials for devices, including regulatory submissions, claims generation, and post-market evidence. • Experience with concepts in one or more of the following areas is preferred: radio-frequency-tissue interaction, laser-tissue interaction, thermally induced tissue damage, laser tissue ablation, ultrasound-assisted liposuction • Strong experience interacting with regulatory authorities and KOLs globally. • Deep understanding of aesthetic device clinical development, claims substantiation, and market access evidence. • Excellent leadership, interpersonal, and communication skills. • Strong scientific writing and data interpretation capabilities. • Business acumen and strategic agility to align scientific goals with commercial objectives. • Ability to thrive in a fast-paced, matrixed, and global organization. The range of starting base pay for this role is 260K – 358K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Selling and managing the sale of aesthetic medical equipment, providing product training, and developing customer relationships. | Experience in selling capital medical equipment, knowledge of FDA GMPs, clinical procedures, and strong communication skills. | Job Location: Akron, Ohio, USA | Amherst, Ohio, USA | Cincinnati, Ohio, USA | Cleveland, Ohio, USA | Columbus, Ohio, USA | Dayton, Ohio, USA | Delaware, Ohio, USA | Dublin, Ohio, USA | NewAlbany, Ohio, USA | Portsmouth, Ohio, USA | Toledo, Ohio, USA | Youngstown, Ohio, USA | Zanesville, Ohio, USA Job Requisition ID: 14536 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. We’re Expanding Our Sales Team! Solta Medical, a division of Bausch Health Companies Inc. (NYSE/TSX: BHC), is committed to improving patients’ quality of life through sophisticated technology and elegant design, providing true aesthetic and therapeutic benefits. For more than a decade, Solta has developed innovative treatment technologies that deliver proven and effective aesthetic care options to physicians and consumers worldwide. The Capital Equipment Specialist has general responsibilities for selling, planning, organizing, and implementing all account management activities related to the sale and distribution of Solta’s capital equipment in a given territory. The Capital Equipment Specialist has high accountability for achieving the territory sales quotas and objectives. The Capital Equipment Specialist has primary responsibilities for: • Achieving sales quota results in the assigned territory. • Performing effective territory penetration coverage and account identification to drive sales and increase the customer base for Solta devices. • Providing training presentations and demonstrations to the customer on application and use of the company’s products using effective communication and sales techniques. • Educating the customer regarding the indications contraindications and safety of Solta products and how they fulfill the needs of the customer. • Supporting and helping to facilitate the execution of regional training workshops and tradeshows within the territory and area. • Pre-planning sales calls and maintaining efficient time management skills to ensure maximum customer contact and highest level of customer service. • Developing and maintaining up-to-date account files. • Preparing sales contracts quotes price and terms per company guidelines. • Completing administrative responsibilities including quarterly business plans weekly expense reports up-to-date account profiles and Solta’s computer customer database. • Maintaining updated knowledge of the industry and competitive products. • Developing and maintaining supportive productive and effective relationships at all levels within the organization. • Maintaining compliance with all applicable quality and regulatory guidelines as an integral part of business operations. • Maintaining consistent communication with Director of Sales and Sales Consultant(s) on all matters related to the territory and area including accurate forecasting. • Demonstrating a strong work ethic and represent Solta with high integrity ethics honesty loyalty and professionalism. Qualifications: • Bachelors degree preferred along with experience selling capital equipment in the Aesthetics or Dermatology space. • Ability to communicate effectively orally and in writing with all levels of employees. • Ability to make effective and persuasive communications and technical presentations to physicians, management and/or large groups. Ability to thoroughly understand and communicate the attributes and qualities of Solta products using professional selling and closing skills. • Ability to use word processing and database applications and various software programs such as Excel and PowerPoint. • Knowledge of FDA GMPs. Ability to function in a controlled environment regulated by FDA GMPs. • Knowledge of clinical surgical techniques and procedures and medical terminology. • Excellent planning and organizational skills. Skill in managing time effectively. Ability to be flexible in changing daily workload priorities as directed. • Ability to travel adequately to cover territory including overnight stays, attend tradeshows and corporate and training meetings. • Candidates should also demonstrate strong interpersonal, teamwork and workload planning skills • Ability to maintain suitable work station (including inventory) remotely. • Ability to transport of up to 60 pounds of equipment within territory and have valid driver’s license with clean driving record. Other requirements include; • Valid driver’s license with a clean driving record. • Ability to travel 75% of the time and cover territory appropriately. This may include overnights based on the territory or may pertain to training or corporate meetings. Occasional weekends to support tradeshows or local events. • Ability to transport up to 60 pounds of equipment within territory. • Technical acumen to use various software programs and various hardware such as a keyboard and mouse. The range of starting base pay for this role is 80K-100K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, stock purchase plan, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Define and lead the global medical strategy for aesthetic devices, ensuring scientific excellence and regulatory compliance. | Requires an advanced degree in Medicine or Biomedical Science, 15+ years in aesthetic medical devices, and extensive leadership experience managing global teams. | Job Location: AlisoViejo, California, USA | Anaheim, California, USA | Bakersfield, California, USA | BeverlyHills, California, USA | Burbank, California, USA | Carlsbad, California, USA | Chico, California, USA | Cupertino, California, USA | Davis, California, USA | Encinitas, California, USA | Encino, California, USA | FosterCity, California, USA | Fresno, California, USA | Fullerton, California, USA | Hayward, California, USA | HuntingtonBeach, California, USA | Irvine, California, USA | LongBeach, California, USA | LosAngeles, California, USA | Modesto, California, USA | MountainView, California, USA | Napa, California, USA | Novato, California, USA | Oceanside, California, USA | Ontario, California, USA | PalmSprings, California, USA | PaloAlto, California, USA | Pasadena, California, USA | Petaluma, California, USA | Pleasanton, California, USA | RanchoCucamonga, California, USA | RedwoodCity, California, USA | Riverside, California, USA | Sacramento, California, USA | SacramentoSouth, California, USA | SanBernandino, California, USA | SanDiego, California, USA | SanDimas, California, USA | SanFrancisco, California, USA | SanJose, California, USA | SantaAna, California, USA | SantaBarbara, California, USA | SantaClarita, California, USA | SantaMonica, California, USA | SantaRosa, California, USA | SealBeach, California, USA | Sonoma, California, USA | Stockton, California, USA | Sunnyvale, California, USA | Temecula, California, USA | ThousandOaks, California, USA | Torrance, California, USA | Tustin, California, USA | Ventura, California, USA | WalnutCreek, California, USA | WestCovina, California, USA | Eugene, Oregon, USA | Portland, Oregon, USA | Bothell, Washington, USA | Redmond, Washington, USA | Renton, Washington, USA | Seattle, Washington, USA | Spokane, Washington, USA | Vancouver, Washington, USA Job Requisition ID: 14396 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Executive Director, Solta Global Medical reports to the Senior Vice President, Head of Global Medical Affairs (GMA) and is the strategic and scientific leader responsible for defining and guiding the global medical and clinical development strategy for Solta’s aesthetic device portfolio. This role ensures scientific excellence, compliant communication, and cross-functional alignment across Medical Affairs, Clinical Development, Biomedical, Regulatory, and Commercial teams globally. Responsibilities: • Define and lead the global medical strategy for Solta’s aesthetics device portfolio. • Serve as the Global Medical Lead providing scientific direction across product lifecycle stages. • Represent Medical Affairs in executive committees, due diligence evaluations, and governance boards. • Set strategic direction for clinical development priorities and evidence generation in support to the Clinical Development Lead who retains full responsibility for clinical trial execution, CRO management, investigator engagement, and operational delivery. • Support the Clinical Development Lead to ensure trial designs align with regulatory and commercial goals. Review and endorse clinical development plans and pivotal study strategies. • Ensure that clinical development activities support differentiated claims and global regulatory standards. • Lead the global Medical Affairs function and provide guidance to the medical affairs team, including scientific communications, KOL engagement, and medical information. • Lead the development and implementation of the Global Medical Plan aligned with lifecycle strategy. • Oversee claims substantiation and ensure scientific accuracy in promotional materials. • Guide integrated evidence planning (IEP) across clinical, RWE, and HEOR domains. • Lead publication strategy and global congress participation. • Champion transparency and scientific rigor in medical communications. • Serve as the medical governance authority ensuring adherence to GCP, ICH, and internal SOPs. • Collaborate with Legal, Regulatory, and Compliance to ensure ethical medical activities. • Provide strategic oversight for safety signal detection and benefit-risk assessments. Qualifications: • MD, PhD, or equivalent advanced degree in Medicine, Biomedical Science, or related field preferred. • Board certification or experience in Dermatology, Plastic Surgery, or related field strongly preferred. • Minimum 15 years of experience in the aesthetics medical device industry, or biotechnology required • Proven track record in aesthetic medicine, dermatology, or energy-based device development. • At least 8 years of leadership experience managing cross-functional and global medical/clinical teams. • Demonstrated experience with clinical trials for devices, including regulatory submissions, claims generation, and post-market evidence. • Experience with concepts in one or more of the following areas is preferred: radio-frequency-tissue interaction, laser-tissue interaction, thermally induced tissue damage, laser tissue ablation, ultrasound-assisted liposuction • Strong experience interacting with regulatory authorities and KOLs globally. • Deep understanding of aesthetic device clinical development, claims substantiation, and market access evidence. • Excellent leadership, interpersonal, and communication skills. • Strong scientific writing and data interpretation capabilities. • Business acumen and strategic agility to align scientific goals with commercial objectives. • Ability to thrive in a fast-paced, matrixed, and global organization. The range of starting base pay for this role is 260K – 358K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Lead and define the global medical and clinical development strategy for Solta’s aesthetic device portfolio, ensuring scientific excellence and regulatory compliance. | Extensive experience in aesthetic medical devices, clinical research, and leadership in a global medical affairs environment, with advanced medical or scientific degrees. | Job Location: AlisoViejo, California, USA | Anaheim, California, USA | Bakersfield, California, USA | BeverlyHills, California, USA | Burbank, California, USA | Carlsbad, California, USA | Chico, California, USA | Cupertino, California, USA | Davis, California, USA | Encinitas, California, USA | Encino, California, USA | FosterCity, California, USA | Fresno, California, USA | Fullerton, California, USA | Hayward, California, USA | HuntingtonBeach, California, USA | Irvine, California, USA | LongBeach, California, USA | LosAngeles, California, USA | Modesto, California, USA | MountainView, California, USA | Napa, California, USA | Novato, California, USA | Oceanside, California, USA | Ontario, California, USA | PalmSprings, California, USA | PaloAlto, California, USA | Pasadena, California, USA | Petaluma, California, USA | Pleasanton, California, USA | RanchoCucamonga, California, USA | RedwoodCity, California, USA | Riverside, California, USA | Sacramento, California, USA | SacramentoSouth, California, USA | SanBernandino, California, USA | SanDiego, California, USA | SanDimas, California, USA | SanFrancisco, California, USA | SanJose, California, USA | SantaAna, California, USA | SantaBarbara, California, USA | SantaClarita, California, USA | SantaMonica, California, USA | SantaRosa, California, USA | SealBeach, California, USA | Sonoma, California, USA | Stockton, California, USA | Sunnyvale, California, USA | Temecula, California, USA | ThousandOaks, California, USA | Torrance, California, USA | Tustin, California, USA | Ventura, California, USA | WalnutCreek, California, USA | WestCovina, California, USA | Eugene, Oregon, USA | Portland, Oregon, USA | Bothell, Washington, USA | Redmond, Washington, USA | Renton, Washington, USA | Seattle, Washington, USA | Spokane, Washington, USA | Vancouver, Washington, USA Job Requisition ID: 14396 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Executive Director, Solta Global Medical reports to the Senior Vice President, Head of Global Medical Affairs (GMA) and is the strategic and scientific leader responsible for defining and guiding the global medical and clinical development strategy for Solta’s aesthetic device portfolio. This role ensures scientific excellence, compliant communication, and cross-functional alignment across Medical Affairs, Clinical Development, Biomedical, Regulatory, and Commercial teams globally. Responsibilities: • Define and lead the global medical strategy for Solta’s aesthetics device portfolio. • Serve as the Global Medical Lead providing scientific direction across product lifecycle stages. • Represent Medical Affairs in executive committees, due diligence evaluations, and governance boards. • Set strategic direction for clinical development priorities and evidence generation in support to the Clinical Development Lead who retains full responsibility for clinical trial execution, CRO management, investigator engagement, and operational delivery. • Support the Clinical Development Lead to ensure trial designs align with regulatory and commercial goals. Review and endorse clinical development plans and pivotal study strategies. • Ensure that clinical development activities support differentiated claims and global regulatory standards. • Lead the global Medical Affairs function and provide guidance to the medical affairs team, including scientific communications, KOL engagement, and medical information. • Lead the development and implementation of the Global Medical Plan aligned with lifecycle strategy. • Oversee claims substantiation and ensure scientific accuracy in promotional materials. • Guide integrated evidence planning (IEP) across clinical, RWE, and HEOR domains. • Lead publication strategy and global congress participation. • Champion transparency and scientific rigor in medical communications. • Serve as the medical governance authority ensuring adherence to GCP, ICH, and internal SOPs. • Collaborate with Legal, Regulatory, and Compliance to ensure ethical medical activities. • Provide strategic oversight for safety signal detection and benefit-risk assessments. Qualifications: • MD, PhD, or equivalent advanced degree in Medicine, Biomedical Science, or related field preferred. • Board certification or experience in Dermatology, Plastic Surgery, or related field strongly preferred. • Minimum 15 years of experience in the aesthetics medical device industry, or biotechnology required • Proven track record in aesthetic medicine, dermatology, or energy-based device development. • At least 8 years of leadership experience managing cross-functional and global medical/clinical teams. • Demonstrated experience with clinical trials for devices, including regulatory submissions, claims generation, and post-market evidence. • Experience with concepts in one or more of the following areas is preferred: radio-frequency-tissue interaction, laser-tissue interaction, thermally induced tissue damage, laser tissue ablation, ultrasound-assisted liposuction • Strong experience interacting with regulatory authorities and KOLs globally. • Deep understanding of aesthetic device clinical development, claims substantiation, and market access evidence. • Excellent leadership, interpersonal, and communication skills. • Strong scientific writing and data interpretation capabilities. • Business acumen and strategic agility to align scientific goals with commercial objectives. • Ability to thrive in a fast-paced, matrixed, and global organization. The range of starting base pay for this role is 260K – 358K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Define and lead the global medical strategy for aesthetic devices, ensuring scientific excellence, regulatory compliance, and cross-functional alignment. | Extensive experience in medical device clinical development, leadership in aesthetic medicine or dermatology, and proven ability to manage global medical teams. | Job Location: AlisoViejo, California, USA | Anaheim, California, USA | Bakersfield, California, USA | BeverlyHills, California, USA | Burbank, California, USA | Carlsbad, California, USA | Chico, California, USA | Cupertino, California, USA | Davis, California, USA | Encinitas, California, USA | Encino, California, USA | FosterCity, California, USA | Fresno, California, USA | Fullerton, California, USA | Hayward, California, USA | HuntingtonBeach, California, USA | Irvine, California, USA | LongBeach, California, USA | LosAngeles, California, USA | Modesto, California, USA | MountainView, California, USA | Napa, California, USA | Novato, California, USA | Oceanside, California, USA | Ontario, California, USA | PalmSprings, California, USA | PaloAlto, California, USA | Pasadena, California, USA | Petaluma, California, USA | Pleasanton, California, USA | RanchoCucamonga, California, USA | RedwoodCity, California, USA | Riverside, California, USA | Sacramento, California, USA | SacramentoSouth, California, USA | SanBernandino, California, USA | SanDiego, California, USA | SanDimas, California, USA | SanFrancisco, California, USA | SanJose, California, USA | SantaAna, California, USA | SantaBarbara, California, USA | SantaClarita, California, USA | SantaMonica, California, USA | SantaRosa, California, USA | SealBeach, California, USA | Sonoma, California, USA | Stockton, California, USA | Sunnyvale, California, USA | Temecula, California, USA | ThousandOaks, California, USA | Torrance, California, USA | Tustin, California, USA | Ventura, California, USA | WalnutCreek, California, USA | WestCovina, California, USA | Eugene, Oregon, USA | Portland, Oregon, USA | Bothell, Washington, USA | Redmond, Washington, USA | Renton, Washington, USA | Seattle, Washington, USA | Spokane, Washington, USA | Vancouver, Washington, USA Job Requisition ID: 14396 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Executive Director, Solta Global Medical reports to the Senior Vice President, Head of Global Medical Affairs (GMA) and is the strategic and scientific leader responsible for defining and guiding the global medical and clinical development strategy for Solta’s aesthetic device portfolio. This role ensures scientific excellence, compliant communication, and cross-functional alignment across Medical Affairs, Clinical Development, Biomedical, Regulatory, and Commercial teams globally. Responsibilities: • Define and lead the global medical strategy for Solta’s aesthetics device portfolio. • Serve as the Global Medical Lead providing scientific direction across product lifecycle stages. • Represent Medical Affairs in executive committees, due diligence evaluations, and governance boards. • Set strategic direction for clinical development priorities and evidence generation in support to the Clinical Development Lead who retains full responsibility for clinical trial execution, CRO management, investigator engagement, and operational delivery. • Support the Clinical Development Lead to ensure trial designs align with regulatory and commercial goals. Review and endorse clinical development plans and pivotal study strategies. • Ensure that clinical development activities support differentiated claims and global regulatory standards. • Lead the global Medical Affairs function and provide guidance to the medical affairs team, including scientific communications, KOL engagement, and medical information. • Lead the development and implementation of the Global Medical Plan aligned with lifecycle strategy. • Oversee claims substantiation and ensure scientific accuracy in promotional materials. • Guide integrated evidence planning (IEP) across clinical, RWE, and HEOR domains. • Lead publication strategy and global congress participation. • Champion transparency and scientific rigor in medical communications. • Serve as the medical governance authority ensuring adherence to GCP, ICH, and internal SOPs. • Collaborate with Legal, Regulatory, and Compliance to ensure ethical medical activities. • Provide strategic oversight for safety signal detection and benefit-risk assessments. Qualifications: • MD, PhD, or equivalent advanced degree in Medicine, Biomedical Science, or related field preferred. • Board certification or experience in Dermatology, Plastic Surgery, or related field strongly preferred. • Minimum 15 years of experience in the aesthetics medical device industry, or biotechnology required • Proven track record in aesthetic medicine, dermatology, or energy-based device development. • At least 8 years of leadership experience managing cross-functional and global medical/clinical teams. • Demonstrated experience with clinical trials for devices, including regulatory submissions, claims generation, and post-market evidence. • Experience with concepts in one or more of the following areas is preferred: radio-frequency-tissue interaction, laser-tissue interaction, thermally induced tissue damage, laser tissue ablation, ultrasound-assisted liposuction • Strong experience interacting with regulatory authorities and KOLs globally. • Deep understanding of aesthetic device clinical development, claims substantiation, and market access evidence. • Excellent leadership, interpersonal, and communication skills. • Strong scientific writing and data interpretation capabilities. • Business acumen and strategic agility to align scientific goals with commercial objectives. • Ability to thrive in a fast-paced, matrixed, and global organization. The range of starting base pay for this role is 260K – 358K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Define and lead the global medical and clinical development strategy for aesthetic devices, ensuring scientific excellence and regulatory compliance. | Extensive experience in medical device industry, leadership in medical affairs or clinical development, advanced medical degree, and experience with clinical trials and regulatory interactions. | Job Location: AlisoViejo, California, USA | Anaheim, California, USA | Bakersfield, California, USA | BeverlyHills, California, USA | Burbank, California, USA | Carlsbad, California, USA | Chico, California, USA | Cupertino, California, USA | Davis, California, USA | Encinitas, California, USA | Encino, California, USA | FosterCity, California, USA | Fresno, California, USA | Fullerton, California, USA | Hayward, California, USA | HuntingtonBeach, California, USA | Irvine, California, USA | LongBeach, California, USA | LosAngeles, California, USA | Modesto, California, USA | MountainView, California, USA | Napa, California, USA | Novato, California, USA | Oceanside, California, USA | Ontario, California, USA | PalmSprings, California, USA | PaloAlto, California, USA | Pasadena, California, USA | Petaluma, California, USA | Pleasanton, California, USA | RanchoCucamonga, California, USA | RedwoodCity, California, USA | Riverside, California, USA | Sacramento, California, USA | SacramentoSouth, California, USA | SanBernandino, California, USA | SanDiego, California, USA | SanDimas, California, USA | SanFrancisco, California, USA | SanJose, California, USA | SantaAna, California, USA | SantaBarbara, California, USA | SantaClarita, California, USA | SantaMonica, California, USA | SantaRosa, California, USA | SealBeach, California, USA | Sonoma, California, USA | Stockton, California, USA | Sunnyvale, California, USA | Temecula, California, USA | ThousandOaks, California, USA | Torrance, California, USA | Tustin, California, USA | Ventura, California, USA | WalnutCreek, California, USA | WestCovina, California, USA | Eugene, Oregon, USA | Portland, Oregon, USA | Bothell, Washington, USA | Redmond, Washington, USA | Renton, Washington, USA | Seattle, Washington, USA | Spokane, Washington, USA | Vancouver, Washington, USA Job Requisition ID: 14396 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Executive Director, Solta Global Medical reports to the Senior Vice President, Head of Global Medical Affairs (GMA) and is the strategic and scientific leader responsible for defining and guiding the global medical and clinical development strategy for Solta’s aesthetic device portfolio. This role ensures scientific excellence, compliant communication, and cross-functional alignment across Medical Affairs, Clinical Development, Biomedical, Regulatory, and Commercial teams globally. Responsibilities: • Define and lead the global medical strategy for Solta’s aesthetics device portfolio. • Serve as the Global Medical Lead providing scientific direction across product lifecycle stages. • Represent Medical Affairs in executive committees, due diligence evaluations, and governance boards. • Set strategic direction for clinical development priorities and evidence generation in support to the Clinical Development Lead who retains full responsibility for clinical trial execution, CRO management, investigator engagement, and operational delivery. • Support the Clinical Development Lead to ensure trial designs align with regulatory and commercial goals. Review and endorse clinical development plans and pivotal study strategies. • Ensure that clinical development activities support differentiated claims and global regulatory standards. • Lead the global Medical Affairs function and provide guidance to the medical affairs team, including scientific communications, KOL engagement, and medical information. • Lead the development and implementation of the Global Medical Plan aligned with lifecycle strategy. • Oversee claims substantiation and ensure scientific accuracy in promotional materials. • Guide integrated evidence planning (IEP) across clinical, RWE, and HEOR domains. • Lead publication strategy and global congress participation. • Champion transparency and scientific rigor in medical communications. • Serve as the medical governance authority ensuring adherence to GCP, ICH, and internal SOPs. • Collaborate with Legal, Regulatory, and Compliance to ensure ethical medical activities. • Provide strategic oversight for safety signal detection and benefit-risk assessments. Qualifications: • MD, PhD, or equivalent advanced degree in Medicine, Biomedical Science, or related field preferred. • Board certification or experience in Dermatology, Plastic Surgery, or related field strongly preferred. • Minimum 15 years of experience in the aesthetics medical device industry, or biotechnology required • Proven track record in aesthetic medicine, dermatology, or energy-based device development. • At least 8 years of leadership experience managing cross-functional and global medical/clinical teams. • Demonstrated experience with clinical trials for devices, including regulatory submissions, claims generation, and post-market evidence. • Experience with concepts in one or more of the following areas is preferred: radio-frequency-tissue interaction, laser-tissue interaction, thermally induced tissue damage, laser tissue ablation, ultrasound-assisted liposuction • Strong experience interacting with regulatory authorities and KOLs globally. • Deep understanding of aesthetic device clinical development, claims substantiation, and market access evidence. • Excellent leadership, interpersonal, and communication skills. • Strong scientific writing and data interpretation capabilities. • Business acumen and strategic agility to align scientific goals with commercial objectives. • Ability to thrive in a fast-paced, matrixed, and global organization. The range of starting base pay for this role is 260K – 358K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

Define and lead the global medical and clinical development strategy for aesthetic devices, ensuring scientific excellence and regulatory compliance. | Requires an advanced degree (MD, PhD), 15+ years in aesthetic medical devices or biotech, and extensive leadership experience in clinical and medical affairs. | Job Location: AlisoViejo, California, USA | Anaheim, California, USA | Bakersfield, California, USA | BeverlyHills, California, USA | Burbank, California, USA | Carlsbad, California, USA | Chico, California, USA | Cupertino, California, USA | Davis, California, USA | Encinitas, California, USA | Encino, California, USA | FosterCity, California, USA | Fresno, California, USA | Fullerton, California, USA | Hayward, California, USA | HuntingtonBeach, California, USA | Irvine, California, USA | LongBeach, California, USA | LosAngeles, California, USA | Modesto, California, USA | MountainView, California, USA | Napa, California, USA | Novato, California, USA | Oceanside, California, USA | Ontario, California, USA | PalmSprings, California, USA | PaloAlto, California, USA | Pasadena, California, USA | Petaluma, California, USA | Pleasanton, California, USA | RanchoCucamonga, California, USA | RedwoodCity, California, USA | Riverside, California, USA | Sacramento, California, USA | SacramentoSouth, California, USA | SanBernandino, California, USA | SanDiego, California, USA | SanDimas, California, USA | SanFrancisco, California, USA | SanJose, California, USA | SantaAna, California, USA | SantaBarbara, California, USA | SantaClarita, California, USA | SantaMonica, California, USA | SantaRosa, California, USA | SealBeach, California, USA | Sonoma, California, USA | Stockton, California, USA | Sunnyvale, California, USA | Temecula, California, USA | ThousandOaks, California, USA | Torrance, California, USA | Tustin, California, USA | Ventura, California, USA | WalnutCreek, California, USA | WestCovina, California, USA | Eugene, Oregon, USA | Portland, Oregon, USA | Bothell, Washington, USA | Redmond, Washington, USA | Renton, Washington, USA | Seattle, Washington, USA | Spokane, Washington, USA | Vancouver, Washington, USA Job Requisition ID: 14396 Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact. The Executive Director, Solta Global Medical reports to the Senior Vice President, Head of Global Medical Affairs (GMA) and is the strategic and scientific leader responsible for defining and guiding the global medical and clinical development strategy for Solta’s aesthetic device portfolio. This role ensures scientific excellence, compliant communication, and cross-functional alignment across Medical Affairs, Clinical Development, Biomedical, Regulatory, and Commercial teams globally. Responsibilities: • Define and lead the global medical strategy for Solta’s aesthetics device portfolio. • Serve as the Global Medical Lead providing scientific direction across product lifecycle stages. • Represent Medical Affairs in executive committees, due diligence evaluations, and governance boards. • Set strategic direction for clinical development priorities and evidence generation in support to the Clinical Development Lead who retains full responsibility for clinical trial execution, CRO management, investigator engagement, and operational delivery. • Support the Clinical Development Lead to ensure trial designs align with regulatory and commercial goals. Review and endorse clinical development plans and pivotal study strategies. • Ensure that clinical development activities support differentiated claims and global regulatory standards. • Lead the global Medical Affairs function and provide guidance to the medical affairs team, including scientific communications, KOL engagement, and medical information. • Lead the development and implementation of the Global Medical Plan aligned with lifecycle strategy. • Oversee claims substantiation and ensure scientific accuracy in promotional materials. • Guide integrated evidence planning (IEP) across clinical, RWE, and HEOR domains. • Lead publication strategy and global congress participation. • Champion transparency and scientific rigor in medical communications. • Serve as the medical governance authority ensuring adherence to GCP, ICH, and internal SOPs. • Collaborate with Legal, Regulatory, and Compliance to ensure ethical medical activities. • Provide strategic oversight for safety signal detection and benefit-risk assessments. Qualifications: • MD, PhD, or equivalent advanced degree in Medicine, Biomedical Science, or related field preferred. • Board certification or experience in Dermatology, Plastic Surgery, or related field strongly preferred. • Minimum 15 years of experience in the aesthetics medical device industry, or biotechnology required • Proven track record in aesthetic medicine, dermatology, or energy-based device development. • At least 8 years of leadership experience managing cross-functional and global medical/clinical teams. • Demonstrated experience with clinical trials for devices, including regulatory submissions, claims generation, and post-market evidence. • Experience with concepts in one or more of the following areas is preferred: radio-frequency-tissue interaction, laser-tissue interaction, thermally induced tissue damage, laser tissue ablation, ultrasound-assisted liposuction • Strong experience interacting with regulatory authorities and KOLs globally. • Deep understanding of aesthetic device clinical development, claims substantiation, and market access evidence. • Excellent leadership, interpersonal, and communication skills. • Strong scientific writing and data interpretation capabilities. • Business acumen and strategic agility to align scientific goals with commercial objectives. • Ability to thrive in a fast-paced, matrixed, and global organization. The range of starting base pay for this role is 260K – 358K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan. Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts. We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.