STAAR® Surgical Co jobs in Monrovia, CA - 31 jobs

MAIN JOB RESPONSIBILITIES / COMPETENCIES 1. Follow all applicable SOPs including Production Control, Environmental Control, Good Documentation Practice and Work Instruction procedures. Legibly document process records on Device History Record Forms. 2. Perform highly technical tasks in support of manufacturing including equipment set-up and manufacturing of product, tool changes, sterilization processes, and filtration of material and calibration activities as assigned. 3. Consistently meets quality and productivity targets. 4. Troubleshoot issues on equipment and assist with preventative maintenance. 5. Assist in revising procedures related to operation and preventative maintenance. 6. Support qualification activities and edit equipment programs (as required). 7. Other duties as assigned. REQUIREMENTS EDUCATION & TRAINING * Must possess a high school diploma/general education diploma (GED) or equivalent combination of education/experience. * Certification required to operate sterilizers (as required). * Basic CNC training. EXPERIENCE * Previous experience in using a microscope and other measurement equipment is recommended. * Experience with an ISO or GMP manufacturing environment. * Previous experience performing setup or operation of CNC machinery is recommended. SKILLS * Must be able to read, write, and speak English. * Needs to be able to communicate with co-workers at all levels. * Must possess good manual dexterity, technical aptitude and an ability to troubleshoot problems * Ability to take direction from lead/supervisor and other management and contribute to departmental goals. * Should possess adequate organizational skills to handle heavy workloads. * Basic computer skills strongly preferred. Pay range: $23 - $28 per hour - Final compensation/salary will be depend on experience STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.

MAIN JOB RESPONSIBILITIES / COMPETENCIES 1. Manage and coordinate the activities associated with various manufacturing processes in a cGMP-compliant manufacturing operation, including, but not limited to, assembly, sterilization, packaging, Clean Room operations, machining and material processing. 2. Manage and coordinate shelf life, qualification, and validation production runs between 3. Responsible and accountable for production schedule adherence, productivity and product quality 4. Ensure that Manufacturing personnel have been trained in required SOPs, in accordance with the established Training SOP. 5. Accountable for departmental compliance with production procedures, manufacturing specifications and regulatory requirements. 6. Review production operations and make recommendations for cost reduction and quality/productivity improvements. 7. Ensure that production activities are documented and records are maintained in accordance with applicable SOPs. 8. Maximize department, equipment and manpower utilization. 9. Ensure adherence to Company safety policies and procedures. 10. Provide employee development opportunities through coaching, delegating and cross-training. 11. Provide the leadership necessary to maximize the productivity of each employee, including active listening, ongoing feedback, meaningful development and growth opportunities as well as an effective documented review process. 12. Other duties as assigned. REQUIREMENTS EDUCATION & TRAINING * A Bachelor's degree, science or engineering preferred or equivalent combination of education/experience. * Graduate business degree a plus EXPERIENCE * 3 years manufacturing experience in medical device, pharmaceutical or other FDA-regulated industry * Leadership experience * Clean room operations experience a strong plus SKILLS * Demonstrated understanding of, and ability to practically implement, cGMP/QSR/ISO requirements * Excellent team building and interpersonal skills * Excellent prioritization, multi-tasking and organization skills Pay range is $140k-$180k - Final compensation will depend on experience. STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.

* Support silicone and materials-based manufacturing operations, including material preparation, lot traceability, and process monitoring. * Execute daily production plans to meet safety, quality, delivery, and efficiency targets. * Supervise production personnel engaged in extrusion, molding, curing, trimming, and related secondary operations within the assigned area or shift. * Partner with Quality, Engineering, Maintenance, and Supply Chain departments to resolve production issues and support improvement activities. * Ensure accurate and timely entry of production, labor, and training data in applicable systems (e.g., ERP, timekeeping). * Support shift-specific operations, 24/7 manufacturing facility with primary shift hours (7:00am - 3:30pm, Mon - Fri) Qualificationsarrow_right * High school diploma or GED; bachelor's degree in engineering or related field degree preferred. * Experience in Lean Manufacturing is advantageous * Minimum 3 years of experience in a manufacturing environment, preferably extrusion, molding, or materials-based operations. * LSR/Medical Molding experience preferred * Proficient in Microsoft Office Suite, including ERP experience (SAP preferred) * Excellent interpersonal and communication skills, with the ability to work effectively across cross-functional teams * Proven people management experience, including coaching, performance management, and team development. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. #LI-MEDICAL

MAIN JOB RESPONSIBILITIES / COMPETENCIES 1. Act as consolidation point for receiving, processing, investigating and reporting product complaints. 2. Coordinate and/or perform the evaluation, investigation, follow-up and documentation of all STAAR product complaints. Maintain complaint files. 3. Coordinate complaint investigations according to complaint handling procedures, which includes but is not limited to: a. Interface with physicians and/or health care professionals regarding information relevant to the product complaint. b. Interface and coordinate with Regulatory, Quality, Clinical Affairs and Medical Affairs to conduct investigations, risk assessments and determine reporting requirements. 4. Perform prompt handling of complaints, including identification and evaluation of device product complaints for potential reportable adverse event according to procedures. 5. Inform management responsible for complaint handling when information in a complaint suggests that action may be required to prevent unreasonable risk of substantial harm to the public, that there is an indication of a trend or that there are unusual adverse events. 6. Ensure incident reports (e.g. Medical Device Reports, Health Canada Reports, Vigilance reports, etc.) are submitted in compliance with respective regulations (e.g. U.S. FDA Regulations, Canadian Medical Device Regulations, MDD/MDR, MDSAP, etc.) 7. Ensure accuracy, integrity, completeness and consistent content of product complaint reports, investigations, incident reports, in the complaint files and electronic complaint database. 8. Support external (e.g. FDA, DEKRA, etc.) and internal audits as required 9. Provide support, as required for other aspects of the post-market surveillance system (i.e., data analysis of complaint reports, files and adverse event reporting logs). 10. Provide support for medical affairs activities, as requested. 11. Other duties as assigned. REQUIREMENTS EDUCATION & TRAINING * High School graduate or equivalent required. Associate's Degree or higher desired. EXPERIENCE * 1 year's ophthalmic experience, or equivalent combination of education and experience, preferred. * 3 years' experience in FDA regulated industry preferred; experience handling complaints and medical device reporting is highly desirable. * Demonstrated understanding of, and ability to interpret, regulations and guidelines governing medical device manufacturing, including but not limited to, CFRs, ISO 13485, MDD, CMDR, MDSAP, MDR SKILLS * Proficiency in MS Word and Excel. * Ability to work well within a team and interdepartmentally. * Special competencies: timely and quality decision making; well-developed organizational ability, time management reasoning and problem solving skills. * Good communication skills, written and verbal. Pay range: $25 - $32 per hour - Final compensation/salary will be depend on experience STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.

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. This position is located in Los Angeles, CA. The Senior Field Service Engineering Technician provides advanced technical support for Solta Medical systems through on-site service and remote troubleshooting. This remote role ensures optimal system performance and customer satisfaction by performing installations, maintenance, and repairs, while also supporting escalations and field analysis. The position partners closely with Product Support, Depot, and Engineering teams to drive service quality and continuous improvement. Principle Responsibilities and Duties: Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title. Core Technical Functions o Follow documented Field Service Procedures o Use diagnostic tools, service aids, service documents and log files to troubleshoot, test and repair medical equipment (laser, RF and ultrasound). o Provide technical expertise for servicing Solta Medical equipment. o Provide on-site field service including product installation, maintenance, upgrades, and repairs. o Use proprietary software tools to review system log files for error evaluation, system troubleshooting, and field analysis. o Use escalation process to inform Service Manager of unresolved issues and suggest performance improvements. Customer & Partner Interaction o Assist with service calls and email from customers, distributors, and internal personnel. o Provide customer, distributor, and/or third-party training as necessary. o Draft, maintain and train to service procedures and process documentation to support consistent field execution and compliance. o Conduct technical and procedural training for third-party repair personnel and distributors to ensure proper service and maintenance of Solta systems. Logistics & Territory Management o Manage parts and scheduling in the territory for timely service parts shipments. o Maintain trunk stock parts inventory and replenishment to comply with established operating standards. o Work with third-party service consultants for territory coverage of service repairs. Documentation & Case Management o Utilize Salesforce and ServiceMax to accurately record service activity, field actions, and case updates. o Manage Salesforce / ServiceMax case workflows to ensure timely and complete case closure and communication with customers and internal teams. Leadership & Collaboration o Acts as a mentor to members of the Product Support and Service organization. o Be prepared to lead team meetings and act as interim manager when needed. o Contribute to product specific meetings when asked with practical insight and detail as needed. Other Experience, Training or Certifications Required: * Minimum HS degree or GED, preferred AA Degree in Electronics, Biomedical Engineering, or equivalent experience * Minimum 7+ years of previous field service * Medical Device: Experience with medical devices a plus * Regulatory: Working knowledge of FDA and/or QSR and/or experience in a regulated industry a plus * Risk Management: General knowledge of risk management for medical devices a plus * Design Control: General knowledge of design control process a plus * ESD: General knowledge of ESD environment * Self-starter, detail oriented, demonstrated ability to support customers with minimal supervision * Ability to use diagnostic test equipment * Ability and willingness to work with various teams including sales, marketing, engineering and manufacturing in the support of company products * Ability to produce results while working with multiple projects under tight deadlines * Excellent customer service and support skills * Ability to maintain inventory / service records and paperwork in a timely manner * Valid driver's license and acceptable driving record required * Approximately 50% travel on average required, mostly domestically but occasionally internationally * Advanced Ability to use Microsoft Windows software including Word, Excel, PowerPoint, Teams and Outlook Language and Verbal Skills Individual must have excellent verbal and written communication skills and a demonstrated ability to communicate clearly and professionally. Math Skills Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Analytical and Reading Skills Ability to read and understand company procedures. Ability to define problems, collect data, establish facts, draw valid conclusions and report on findings. Physical Requirements While performing the duties of this job, the employee may be required to perform lifting tasks of up to 70 pounds for short durations. Duties of this job may involve standing and/or walking for extended periods of time. Duties also involve daily keyboard data entry. Specific vision abilities required by this job include close vision. Work Environment Most work will be performed in an office environment or at a customer's site (typically a private medical practice). The noise level in the work environment is usually low to moderate. Some work may entail incidental exposure to bio-hazardous materials (repair product in doctor's offices) where the employee must employ standard techniques to protect against chemical and biological hazards Safety Solta Medical is committed to the health and safety of our employees. We expect that all employees will perform their responsibilities while maintaining a safe, cooperative, and productive work environment, thus ensuring the health and safety of themselves and others. The range of starting base pay for this role is $34.00 to $45.00 per hour. 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.

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.

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 Regional Manager (Neuroscience Sales) will be responsible for the daily supervision of one geographical region, including coaching for improved performance and monitoring the sales activity within the region. The RSM will be accountable for a group of Territory Managers who make product presentations to achieve product awareness, educate the market and generate prescriptions. Region includes California, Oregon, Washington, Utah, Colorado, Nevada, & Arizona Major Duties & responsibilities: * Provide leadership and direction while meeting sales goals and managing the sales activities and development of sales representatives. * Develop and implement strategic business plans to meet Regional, area and Company goals. * Implement and uphold all company compliance policies and procedures for self and region. * Recruit and select qualified candidates to fill open sales positions within the Region. * Assume accountability and responsibility for own personal career growth and development. * Be a leader and manager - creating long and short-term development objectives. * Attend National & Regional conferences when necessary. * Build a strong regional team through evaluation of the activities and effectiveness of sales representatives on a consistent basis, providing guidance, coaching and support to increase competence. * Drive adoption of best practices throughout region to increase Territory Manager performance and regional success * Monitor data analytics information to ensure full utilization for maximum impact on prescribing physicians. * Plan and conduct effective sales meetings, ensuring compliance of Company policies and regional expectations. * Collaborate and communicate with Marketing and Sales Administration on literature requests, supplies, relevant data maintenance, support issues and fleet management issues. * Coordinate administrative demands and field day objectives. Qualifications: * We seek a candidate with a Bachelor's Degree in a related discipline. * 3+ years of successful pharmaceutical sales experience is required with management or training experience in a pharmaceutical environment preferred. Experience in the Psychiatry field is strongly desired. * Proven success managing sales representatives across diverse geography desired. * Strong interpersonal, teamwork, organizational, follow-up and workload planning skills. * Ability to deliver presentations at all levels of the organization * Ability to perform all job duties which necessitates: * Driving in a geographically large territory for long periods of time each day. * Traveling by airplane and car within the US. * Performing other job-related duties and responsibilities as may be assigned from time to time. The Regional Sales Manager should have a travel expectation of 50-75%. The range of starting base pay for this role is 140K-180K. 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.

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the worldfrom the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. **Position Objective** Bausch + Lombs Pharmaceutical and Consumer R&D organization is seeking hands-on _in vitro_ scientist to contribute to our research efforts to develop therapies for sight-threatening disease. The Scientist II, Biological Research will be responsible for developing _in vitro_ cell-based disease models to investigate novel, research-stage therapeutics and to support formulation screening for clinical-stage programs across all segments of the eye. He/She/They will conduct hands-on experiments to differentiate, characterize, and assess drug effects in various cell culture model systems. The ideal candidate will have demonstrated expertise working with complex cell-based disease model systems to test hypotheses related to pharmacological mechanism of action. Additional experience in the design and oversight of follow-on _in vivo_ pharmacology experiments is a plus. This role will be lab-based, and the candidate will work with a highly collaborative team to support multiple projects. He/She/They will share our passion for bringing innovative medicines to patients. **Responsibilities** + Research, design and execute strategic experiments to establish gold-standard and novel _in vitro_ cell-based model systems to support ophthalmic drug research and development + Independently conduct cell culture techniques and develop cell-based assays + Independently utilize multiple experimental methods to characterize cell-based systems and evaluate the pharmacological action of novel therapeutics + Generate and document high-quality experimental results + Present data and results to multiple cross-functional stakeholders within the organization as well as external collaborators + Effectively collaborate and communicate with peers and teams to support multiple projects **Qualifications/Requirements** + Title commensurate with experience + Masters degree in molecular biology, cell biology, immunology, biological science, or other related discipline with at least 2 years of industry experience, or + Bachelors degree in molecular biology, cell biology, immunology, biological science, or other related discipline with at least 4 years of industry experience + Previous experience conducting ophthalmology research, in academia and/or industry, is a major plus + Demonstrated hands-on experience in cell culture, as well as cell and molecular biology techniques, including viability assays, PCR, gel electrophoresis, immunohistochemistry, and microscopy + Previous experience conducting electrophysiological assessments is a plus + Knowledgeable of _in vivo_ approaches to test disease hypotheses and assess drug action + Strong written and verbal communication skills + Highly motivated person who can work both independently and as part of a team in a fast-paced environment **We offer competitive salary & excellent benefits including:** + Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date + 401K Plan with company match and ongoing company contribution + Paid time off vacation (3 weeks - prorated upon hire), floating holidays and sick time + Employee Stock Purchase Plan with company match + Employee Incentive Bonus + Tuition Reimbursement (select degrees) + Ongoing performance feedback and annual compensation review This position may be available in the following location(s): [[location_obj]] All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. For U.S. locations that require disclosure of compensation, the starting pay for this role is between $95,000.00 and $120,000.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including location. U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement (******************************************************************************************************** . Our Benefit Programs:Employee Benefits: Bausch + Lomb (***************************************** Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Working at Freudenberg: We will wow your world! Responsibilities: Fabricate mechanical parts using CNC & Manual mill, CNC & manual lathe, and other metal working equipment. Rework of parts tooling, molds, and fixturing. Knowledge in measurement equipment (calipers, micrometers, etc.). Design, build, and machine prototype molds, new production molds, extrusion dies and mandrels, cutting tools, pad printing, guiding, and holding fixtures to meet production requirements and work order requests. Prioritize, track, and report the status of all jobs and work orders in a timely fashion. Keep mold maintenance logs, tooling inventory, and equipment maintenance records updated and current. Coordinate outsourcing of machining job that require outside expertise, equipment, or capacity. Qualifications: High school or GED equivalent degree or equivalent experience in related field, trade school is preferred. Math skills, with good knowledge in algebra and trigonometry. Minimum 3 years of experience in providing tool repair, support, and maintenance to a manufacturing environment, specializing in medical grade silicone extrusion and molding processes preferred. Ability to design simple mechanical components from concepts and documents. Working knowledge of SolidWorks, MasterCAM, CNC equipment, conventional mills, lathes, and surface grinding. Strong technical ability in reading and interpreting blueprints, drawings, and 3D CAD files is required. Demonstrated ability to troubleshoot and resolve problems in an organized manner. Mechanically inclined, close attention to detail, adapts to change easily, and high level of motivation to complete tasks promptly. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg Medical LLC

MAIN JOB RESPONSIBILITIES / COMPETENCIES 1. Thorough knowledge and appropriate implementation of intermediate production functions such as Manufacture of In-process Materials (HEMA, Collagen Solution) 2. Maintain all equipment (including glassware) used for In-process Materials production 3. Perform other manufacturing processes, such as: * Collamer Rod Grinding * Collamer Button Inspection * Collamer Material Test Sample Preparation * Collamer Drying Process 4. Sample Water Systems 5. Completes required production documentation accurately. 6. Consistently meets quality and productivity targets. 7. Appropriately follows company policies, rules, and regulations. 8. Maintain work area environment in a clean and orderly manner. 9. Work independently in the areas assigned. 10. Other duties as assigned. REQUIREMENTS EDUCATION & TRAINING * High school diploma, GED or equivalent combination of education/experience. EXPERIENCE * Minimum 2yrs laboratory experience; or work experience SKILLS * Ability to understand and implement general GMP concepts. * Ability to take direction from lead/supervisor and other management * Capable of learning and performing duties with minimum supervision. * Ability to read, write and speak English. * Ability to lift up to 25 pounds. Pay range: $22 to 24/ per hour - Final compensation will depend on experience. STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.

MAIN JOB RESPONSIBILITIES / COMPETENCIES 1. Support Manufacturing Engineers with process development and optimization, process validation and trouble-shooting manufacturing and engineering issues. 2. Provide engineering support to Manufacturing lines. 3. Execute product and process qualification protocols and summarize results in report format. 4. Review Manufacturing and Quality Control Standard Operating Procedures and Drawings to ensure adequacy. Recommend revisions to existing procedures and drawings when needed. 5. Train Manufacturing and Quality personnel in protocol execution, special test procedures, etc., as required. 6. Set-up and qualify manufacturing equipment as needed and required. 7. Other duties as assigned by Director of Manufacturing Engineering. REQUIREMENTS EDUCATION & TRAINING * B.S. in Mechanical Engineering or equivalent industry experience required. EXPERIENCE * Knowledge of precision machinery and machining techniques required. * Experience in intraocular lens manufacturing desirable. * Experience in the medical device industry desirable. SKILLS * Good verbal and written communication skills. * Good analytical and problem-solving skills. * Basic computer knowledge (Excel, Word) Pay range is $75K to $100K - Final compensation will depend on experience. STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.

Working at Freudenberg: We will wow your world! Responsibilities: Leads silicone and materials-based manufacturing operations and efficiencies by establishing priorities and sequences for manufacturing products. Drives progress and status in attaining objectives in operations and plans accordingly with current conditions by review of activity reports and financial statements. Ensures daily production plans meet safety, quality, delivery, and efficiency targets. Oversee and develop production personnel engaged in extrusion, molding, and related secondary operations. Partner with Quality, Engineering, Maintenance, and Supply Chain departments to resolve production issues and support improvement activities. Support operations, 24/7 manufacturing facility with primary shift hours (7:00am - 4:00pm, Mon - Fri) Qualifications: Associate's, bachelor's degree or equivalent experience in engineering or related field degree Experience in Lean Manufacturing is advantageous Minimum 5 years of experience in a manufacturing environment, preferably extrusion, molding, or materials-based operations. LSR/Medical Molding experience preferred Proficient in Microsoft Office Suite, including ERP experience (SAP preferred) Excellent interpersonal and communication skills, with the ability to work effectively across cross-functional teams Proven people management experience, including coaching, performance management, and team development. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg Medical LLC

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.

Join our high-impact manufacturing team as a Manufacturing Associate III at Endologix! WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training-supported by industry-leading clinical evidence. At Endologix, we're driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health. What sets us apart is not just our technology, but our culture. At Endologix, we foster a collaborative, mission-driven environment where every team member plays a vital role in advancing patient care. We value integrity, tenacity, and innovation-and we support our people with the tools, trust, and training they need to grow and continuously learn. If you're passionate about making a meaningful impact in healthcare, you'll find purpose and belonging here. ABOUT THE ROLE: We're looking for a talented Manufacturing Associate III to join our high-impact manufacturing team. In this role, you'll be responsible for the efficient and accurate assembly of high-quality medical devices in compliance with approved Manufacturing Process Instructions (MPIs), Standard Operating Procedures (SOPs), and quality standards. This role requires a strong understanding of medical device manufacturing processes and a commitment to continuous improvement. The Associate III serves as a technical resource on the production floor, assisting in troubleshooting line issues, identifying root causes, and recommending corrective actions. In addition, this individual actively contributes to process improvement initiatives, supports training of junior team members, and collaborates cross-functionally with Engineering, Quality, and other support functions to ensure smooth production flow and compliance with regulatory requirements. Responsibilities WHAT YOU'LL DO: Assemble medical device products using small hand tools, calibrated instruments, microscopes, measurement devices, and test fixtures. Ensure full compliance with Endologix policies, procedures, and quality standards, including safety regulations, environmental protocols, and required stretching exercises. Maintain cleanroom and controlled environment integrity through proper attire and adherence to controlled environment practices. Perform in-process quality checks and promptly report any safety, quality, or process-related concerns. Identify and escalate unacceptable materials and sub-assemblies to Engineering and/or the Supervisor. Ensure complete compliance with Endologix Quality and Regulatory policies and Core Values. Take ownership of product quality by strictly following manufacturing instructions and completing quality records accurately. Adhere to Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Collaborate with supervisors, engineers, and technicians to troubleshoot line issues and implement process improvements. Understand and use production terminology and demonstrate awareness of common manufacturing defects and their impact. Exhibit flexibility by performing effectively across multiple assembly stations with minimal errors. Participate actively in Lean Manufacturing and 5S initiatives to enhance efficiency and workplace organization. Demonstrate knowledge of Lean principles and apply them to daily operations. Proactively engage cross-functional resources to resolve production issues. Read and interpret engineering drawings, specifications, and method sheets accurately. Enter data into electronic systems as required for documentation and tracking. Serve as a certified trainer for manufacturing processes; train and mentor other production employees. Provide coaching and guidance to peers on standard operating procedures and assembly techniques. Support supervisors as needed, including participating in leadership tasks and line coordination. Perform other duties as assigned by supervisor. Qualifications WHAT YOU'LL BRING: Education: High school diploma or equivalent required; associate or technical degree preferred. Experience: 3-5 years of experience in a regulated manufacturing environment, preferably in the medical device industry. Experience working within a clean room environment. Lean & 5S experience desired. Skills/Competencies: Strong attention to detail and ability to follow complex instructions and procedures. Demonstrated ability to troubleshoot line issues and work independently with minimal supervision. Effective communication skills and the ability to collaborate within a team environment. Familiarity with lean manufacturing principles and continuous improvement methodologies is a plus. HOW YOU'LL SHOW UP: All In: Bring full commitment to everything you do. Support one another, hold yourself accountable, and take ownership of your work. Move with urgency, deliver on your promises, and lead with boldness and passion. Act with Integrity: Prioritize ethics and transparency in every decision. Earn trust by being honest, respectful, and dependable - working diligently to uphold the confidence of your colleagues, customers, and communities. Tenacious: Meet challenges head-on with resilience and resolve. Stay focused, push through obstacles, and consistently look for solutions, not excuses. Pioneering: Challenge the status quo and embrace innovation. Develop new ideas, test bold solutions, and pave the way for others - driving progress through curiosity and creativity. WHAT WE OFFER: At Endologix, we know that great work starts with great people - and people do their best when they feel valued and supported. That's why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You'll be part of a team that's making a real impact on patients' lives. When you join us, you're not just taking a job, you're building a meaningful career with a team that's invested in your success. The compensation package includes: Hourly rate of $25.00/hr-$30.00/hr Discretionary bonus Equity participation as approved by Board of Directors (4-year vesting schedule) Comprehensive health, dental, and vision insurance plans Generous PTO and holiday schedule 401(k) retirement plan with company match Plus: Employee wellness initiatives and mental health support Collaborative and inclusive company culture focused on impact and innovation Opportunities for career growth and internal mobility OUR COMMITMENT TO DIVERSITY & INCUSION: Endologix LLC. is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. Position Objective Bausch + Lomb's Pharmaceutical and Consumer R&D organization is seeking hands-on in vitro scientist to contribute to our research efforts to develop therapies for sight-threatening disease. The Scientist II, Biological Research will be responsible for developing in vitro cell-based disease models to investigate novel, research-stage therapeutics and to support formulation screening for clinical-stage programs across all segments of the eye. He/She/They will conduct hands-on experiments to differentiate, characterize, and assess drug effects in various cell culture model systems. The ideal candidate will have demonstrated expertise working with complex cell-based disease model systems to test hypotheses related to pharmacological mechanism of action. Additional experience in the design and oversight of follow-on in vivo pharmacology experiments is a plus. This role will be lab-based, and the candidate will work with a highly collaborative team to support multiple projects. He/She/They will share our passion for bringing innovative medicines to patients. Responsibilities * Research, design and execute strategic experiments to establish gold-standard and novel in vitro cell-based model systems to support ophthalmic drug research and development * Independently conduct cell culture techniques and develop cell-based assays * Independently utilize multiple experimental methods to characterize cell-based systems and evaluate the pharmacological action of novel therapeutics * Generate and document high-quality experimental results * Present data and results to multiple cross-functional stakeholders within the organization as well as external collaborators * Effectively collaborate and communicate with peers and teams to support multiple projects Qualifications/Requirements * Title commensurate with experience * Master's degree in molecular biology, cell biology, immunology, biological science, or other related discipline with at least 2 years of industry experience, or * Bachelor's degree in molecular biology, cell biology, immunology, biological science, or other related discipline with at least 4 years of industry experience * Previous experience conducting ophthalmology research, in academia and/or industry, is a major plus * Demonstrated hands-on experience in cell culture, as well as cell and molecular biology techniques, including viability assays, PCR, gel electrophoresis, immunohistochemistry, and microscopy * Previous experience conducting electrophysiological assessments is a plus * Knowledgeable of in vivo approaches to test disease hypotheses and assess drug action * Strong written and verbal communication skills * Highly motivated person who can work both independently and as part of a team in a fast-paced environment We offer competitive salary & excellent benefits including: * Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date * 401K Plan with company match and ongoing company contribution * Paid time off - vacation (3 weeks - prorated upon hire), floating holidays and sick time * Employee Stock Purchase Plan with company match * Employee Incentive Bonus * Tuition Reimbursement (select degrees) * Ongoing performance feedback and annual compensation review This position may be available in the following location(s): US - Irvine, CA (Westcoast Hub) All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. For U.S. locations that require disclosure of compensation, the starting pay for this role is between $95,000.00 and $120,000.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including location. U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation. Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms. To learn more please read Bausch + Lomb's Job Offer Fraud Statement. Our Benefit Programs: Employee Benefits: Bausch + Lomb Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

* Support silicone and materials-based manufacturing operations, including material preparation, lot traceability, and process monitoring. * Execute daily production plans to meet safety, quality, delivery, and efficiency targets. * Supervise production personnel engaged in extrusion, molding, curing, trimming, and related secondary operations within the assigned area or shift. * Partner with Quality, Engineering, Maintenance, and Supply Chain departments to resolve production issues and support improvement activities. * Ensure accurate and timely entry of production, labor, and training data in applicable systems (e.g., ERP, timekeeping). * Support shift-specific operations, 24/7 manufacturing facility with primary shift hours (11:00pm - 7:30am, Mon - Fri) Qualificationsarrow_right * High school diploma or GED; bachelor's degree in engineering or related field degree preferred. * Experience in Lean Manufacturing is advantageous * Minimum 3 years of experience in a manufacturing environment, preferably extrusion, molding, or materials-based operations. * LSR/Medical Molding experience preferred * Proficient in Microsoft Office Suite, including ERP experience (SAP preferred) * Excellent interpersonal and communication skills, with the ability to work effectively across cross-functional teams * Proven people management experience, including coaching, performance management, and team development. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. #LI-MEDICAL

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.

Working at Freudenberg: We will wow your world! Responsibilities: Support silicone and materials-based manufacturing operations, including material preparation, lot traceability, and process monitoring. Execute daily production plans to meet safety, quality, delivery, and efficiency targets. Supervise production personnel engaged in extrusion, molding, curing, trimming, and related secondary operations within the assigned area or shift. Partner with Quality, Engineering, Maintenance, and Supply Chain departments to resolve production issues and support improvement activities. Ensure accurate and timely entry of production, labor, and training data in applicable systems (e.g., ERP, timekeeping). Support shift-specific operations, 24/7 manufacturing facility with primary shift hours (7:00am - 3:30pm, Mon - Fri) Qualifications: High school diploma or GED; bachelor's degree in engineering or related field degree preferred. Experience in Lean Manufacturing is advantageous Minimum 3 years of experience in a manufacturing environment, preferably extrusion, molding, or materials-based operations. LSR/Medical Molding experience preferred Proficient in Microsoft Office Suite, including ERP experience (SAP preferred) Excellent interpersonal and communication skills, with the ability to work effectively across cross-functional teams Proven people management experience, including coaching, performance management, and team development. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg Medical LLC

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.