With a strong partnership history with various clients in the life sciences industry, our success stems from the collective talents of our dedicated team, making us a leading consulting firm in this field.

With your expertise and dedication, you can help shape a brighter future for the industry. Don’t miss this chance to be a part of an organization that is committed to making the life sciences industry better.

Apply now and join the Pharmavise team!

Career Opportunities

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com   

We are currently seeking talented and experienced professionals with previous experience at the FDA (Food and Drug Administration) to join our team as Former FDA Experts. Below is a detailed job description outlining the responsibilities, qualifications, and expectations for this role: 

Responsibilities: 

  1. Provide expert regulatory guidance and strategic advice to clients on FDA regulations, policies, and procedures related to drug, biologic, and medical device development and approval. 
  2. Review and interpret FDA guidance documents, regulations, and policies to ensure compliance and facilitate successful regulatory submissions. 
  3. Support clients in preparing and submitting regulatory applications, including INDs, BLAs, NDAs, 510(k)s, and PMA submissions, and provide guidance on regulatory strategy and submission content. 
  4. Conduct regulatory assessments and gap analyses to identify potential issues and risks in regulatory submissions and provide recommendations for resolution. 
  5. Assist clients in preparing for FDA meetings, including pre-IND, pre-IDE, pre-NDA/BLA, and pre-PMA meetings, and participate in meetings as a regulatory representative. 
  6. Monitor regulatory trends, changes, and updates from the FDA and provide insights and recommendations to clients on potential impacts on their products and programs. 
  7. Collaborate with cross-functional teams, including regulatory affairs, clinical development, quality assurance, and medical affairs, to ensure alignment on regulatory strategy and objectives. 
  8. Serve as a liaison between clients and regulatory agencies, including facilitating communications, responding to inquiries, and addressing regulatory challenges and issues. 

Qualifications: 

  1. Bachelor’s degree in pharmacy, biology, chemistry, or related field; advanced degree preferred. 
  2. Minimum of 5 years of experience working at the FDA in a regulatory role, with expertise in drug, biologic, or medical device regulation. 
  3. Deep understanding of FDA regulations, guidance documents, and regulatory processes related to drug, biologic, and medical device development and approval. 
  4. Proven track record of successful interactions with the FDA, including experience in preparing and submitting regulatory applications and participating in FDA meetings. 
  5. Excellent communication and interpersonal skills, with the ability to effectively convey complex regulatory concepts and requirements to clients and internal stakeholders. 
  6. Strong analytical and problem-solving abilities, with the ability to assess regulatory risks and develop strategies for mitigation. 
  7. Regulatory affairs certification (RAC) or relevant professional certification (e.g., Regulatory Affairs Certification Board) preferred but not required. 
  8. Ability to work independently and collaboratively as part of a multidisciplinary team, with a commitment to delivering high-quality regulatory support and guidance to clients 

This is a unique opportunity for former FDA professionals to leverage their regulatory expertise and make a meaningful impact in the pharmaceutical and medical device industries. Competitive compensation packages are available. 

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com.  

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality. 

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com    

We are actively seeking skilled and knowledgeable professionals to join our team as Regulatory Affairs Biosimilars Per Diem Consultants. Below, you’ll find a comprehensive job description detailing the responsibilities, qualifications, and expectations for this role: 

Responsibilities: 

  1. Provide expert regulatory affairs guidance and support for biosimilars development projects. 
  2. Review and analyze regulatory requirements and guidelines related to biosimilars in various regions. 
  3. Assist in the preparation, submission, and maintenance of regulatory submissions for biosimilars, including INDs, BLAs, and variations. 
  4. Collaborate with cross-functional teams to ensure alignment on regulatory strategy and objectives. 
  5. Stay updated on regulatory developments and trends impacting biosimilars globally. 
  6. Participate in meetings with regulatory authorities as needed. 
  7. Provide regulatory support and expertise during regulatory agency inspections and audits. 

Qualifications: 

  1. Bachelor’s degree in a scientific or related field; advanced degree preferred. 
  2. Minimum of 8 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry, with specific expertise in biosimilars preferred. 
  3. Strong understanding of regulatory requirements and guidelines governing biosimilars development and approval processes. 
  4. Experience with regulatory submissions for biosimilars, including INDs, BLAs, and variations. 
  5. Excellent communication and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders. 
  6. Proven ability to work independently and manage multiple projects simultaneously. 
  7. Regulatory affairs certification (RAC) preferred but not required. 

This is a unique opportunity for biosimilars consultant professionals to leverage their regulatory expertise on biologic medical products and make a meaningful impact in the pharmaceutical and medical device industries. Competitive compensation packages are available. 

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.  

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com  

We are actively seeking skilled and knowledgeable professionals to join our team as Medical Device Quality and Compliance Experts. Below, you’ll find a comprehensive job description detailing the responsibilities, qualifications, and expectations for this role: 

Responsibilities: 

  1. Lead and oversee quality management system (QMS) activities for medical device products throughout the product lifecycle. 
  2. Develop and implement quality and compliance strategies to ensure adherence to regulatory requirements, standards, and guidelines (e.g., ISO 13485, FDA QSR, MDR). 
  3. Conduct risk assessments and mitigation activities to identify and address potential quality and compliance issues. 
  4. Provide guidance and support on regulatory submissions and interactions with regulatory agencies (e.g., FDA, notified bodies). 
  5. Lead and support internal and external audits, including supplier audits and regulatory inspections. 
  6. Collaborate cross-functionally with R&D, manufacturing, regulatory affairs, and other teams to ensure quality and compliance objectives are met. 
  7. Stay abreast of emerging regulatory trends and changes affecting the medical device industry and proactively implement necessary updates to QMS processes and procedures. 

Qualifications: 

  1. Bachelor’s degree in engineering, life sciences, or related field; advanced degree preferred. 
  2. Minimum of 8 years of experience in quality assurance and regulatory compliance within the medical device industry. 
  3. In-depth knowledge of relevant quality standards and regulations, including ISO 13485, FDA QSR, and EU MDR. 
  4. Experience leading quality management system implementations and maintaining compliance in a regulated environment. 
  5. Strong understanding of risk management principles and methodologies (e.g., ISO 14971). 
  6. Excellent communication and interpersonal skills, with the ability to effectively communicate complex regulatory requirements and concepts. 
  7. Proven ability to lead and influence cross-functional teams and drive quality and compliance initiatives to completion. 
  8. Quality and regulatory certifications (e.g., ASQ CQE, RAC) preferred but not required. 

This is a challenging and rewarding opportunity for individuals passionate about ensuring the safety, efficacy, and quality of medical devices. Competitive compensation and benefits packages are available. 

 

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.  

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com    

We are actively seeking skilled and knowledgeable professionals to join our team as Gene Therapy Experts – Full Time & Per Diem. Below, you’ll find a comprehensive job description detailing the responsibilities, qualifications, and expectations for this role: 

Responsibilities: 

  1. Lead and contribute to gene therapy research and development projects from early discovery through to clinical development. 
  2. Design and execute experiments to optimize gene therapy vectors, transgene expression, and delivery systems. 
  3. Develop and implement innovative strategies to address challenges related to gene therapy vector design, manufacturing, and scalability. 
  4. Collaborate cross-functionally with research, preclinical, clinical, and regulatory teams to advance gene therapy programs. 
  5. Stay abreast of emerging technologies, scientific advancements, and regulatory requirements in the field of gene therapy. 
  6. Contribute to the preparation and review of regulatory submissions, including INDs, BLAs, and orphan drug applications. 
  7. Mentor and provide guidance to junior staff members and collaborators working on gene therapy projects. 

Qualifications: 

  1. PhD or equivalent degree in molecular biology, genetics, biotechnology, or related field. 
  2. Minimum of 5 years of experience in gene therapy research and development within the biotechnology or pharmaceutical industry. 
  3. Strong expertise in gene therapy vector design, optimization, and characterization. 
  4. Experience with gene editing technologies (e.g., CRISPR/Cas9) and viral vector platforms (e.g., AAV, lentivirus). 
  5. Knowledge of regulatory requirements and guidelines governing gene therapy product development (e.g., FDA, EMA). 
  6. Excellent analytical and problem-solving skills, with the ability to design and interpret complex experiments. 
  7. Effective communication and collaboration skills, with the ability to work in a fast-paced, team-oriented environment. 
  8. Leadership experience and a track record of successfully leading gene therapy projects preferred but not required. 

We offer competitive compensation packages, including comprehensive benefits for full-time positions, and flexible scheduling options for per diem roles. 

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.  

 

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com   

Responsibilities: 

  1. Provide expert consultation and guidance on homeopathic treatments and remedies to clients/patients. 
  2. Conduct thorough assessments of clients’ health conditions, medical histories, and treatment goals. 
  3. Develop personalized homeopathic treatment plans tailored to individual clients’ needs and preferences. 
  4. Monitor and evaluate clients’ progress throughout the course of homeopathic treatment and make necessary adjustments to treatment plans as needed. 
  5. Educate clients on the principles of homeopathy, including the holistic approach to health and wellness. 
  6. Collaborate with other healthcare professionals, including conventional medical practitioners, to ensure integrated and comprehensive care for clients. 
  7. Stay updated on developments and advancements in the field of homeopathy, including new remedies and treatment modalities. 
  8. Maintain accurate and detailed records of client consultations, treatment plans, and outcomes. 

Qualifications: 

  1. Certification or licensure in homeopathy from a recognized accrediting body. 
  2. Minimum of 5 years of experience practicing homeopathy in a clinical setting. 
  3. Deep understanding of homeopathic principles, remedies, and treatment protocols. 
  4. Excellent interpersonal and communication skills, with the ability to establish rapport with clients and effectively convey complex information. 
  5. Strong analytical and problem-solving abilities, with a holistic approach to health and wellness. 
  6. Empathy, compassion, and a genuine desire to help others achieve optimal health and well-being. 
  7. Ability to work independently and collaboratively as part of a multidisciplinary team. 
  8. Willingness to maintain confidentiality and adhere to ethical standards of practice. 

This is a per diem consultant position, offering flexible scheduling arrangements based on consultant availability and client demand. 

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.  

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com    

Responsibilities: 

  1. Lead and contribute to cell therapy research and development projects aimed at advancing novel cellular therapies for various diseases and conditions. 
  2. Design and optimize cell therapy manufacturing processes, including cell isolation, expansion, differentiation, and characterization. 
  3. Develop innovative strategies to enhance the efficacy, safety, and scalability of cell therapy products. 
  4. Collaborate cross-functionally with research, translational, clinical, and regulatory teams to advance cell therapy programs from preclinical development through to clinical trials and commercialization. 
  5. Stay abreast of emerging technologies, scientific advancements, and regulatory requirements in the field of cell therapy. 
  6. Contribute to the preparation and review of regulatory submissions, including INDs, BLAs, and marketing authorization applications. 
  7. Mentor and provide guidance to junior staff members and collaborators working on cell therapy projects. 

Qualifications: 

  1. PhD or equivalent degree in cell biology, immunology, regenerative medicine, or related field. 
  2. Minimum of 5 years of experience in cell therapy research and development within the biotechnology or pharmaceutical industry. 
  3. Strong expertise in cell culture techniques, cell engineering, and cell-based assays. 
  4. Experience with cell therapy manufacturing processes, including GMP requirements and quality control/assurance. 
  5. Knowledge of regulatory requirements and guidelines governing cell therapy product development (e.g., FDA, EMA). 
  6. Excellent analytical and problem-solving skills, with the ability to design and interpret complex experiments. 
  7. Effective communication and collaboration skills, with the ability to work in a fast-paced, team-oriented environment. 
  8. Leadership experience and a track record of successfully leading cell therapy projects preferred but not required. 

We offer competitive compensation packages, including comprehensive benefits for full-time positions, and flexible scheduling options for per diem roles.

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.  

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com    

Responsibilities: 

  1. Provide expert consultation and support in drug safety and pharmacovigilance to pharmaceutical companies and regulatory agencies. 
  2. Review and evaluate adverse event reports and safety data for investigational and marketed drugs, ensuring compliance with regulatory requirements and guidelines. 
  3. Conduct signal detection activities to identify potential safety concerns associated with drug products and collaborate with cross-functional teams to mitigate risks. 
  4. Develop and implement risk management plans (RMPs) and risk minimization strategies to optimize the benefit-risk profile of drugs. 
  5. Provide guidance on safety-related labeling updates, including drafting and review of product labels, package inserts, and risk communication materials. 
  6. Support regulatory submissions and interactions with health authorities related to drug safety, including responses to safety-related inquiries and requests for information. 
  7. Contribute to the development and implementation of pharmacovigilance processes and systems to ensure compliance with global regulatory requirements (e.g., FDA, EMA, ICH). 
  8. Stay abreast of emerging safety issues, pharmacovigilance trends, and regulatory developments in the pharmaceutical industry. 

Qualifications: 

  1. Advanced degree in pharmacy, pharmacology, life sciences, or related field. 
  2. Minimum of 5 years of experience in drug safety and pharmacovigilance within the pharmaceutical industry, CRO, or regulatory agency. 
  3. In-depth knowledge of global pharmacovigilance regulations and guidelines (e.g., FDA, EMA, ICH), including experience with safety reporting requirements (e.g., ICSR, SUSAR). 
  4. Strong understanding of pharmacovigilance processes, risk management methodologies, and signal detection techniques. 
  5. Experience with safety database systems (e.g., ARGUS, ARISg) and adverse event case processing. 
  6. Excellent analytical and problem-solving skills, with the ability to interpret and communicate complex safety data and risk assessments. 
  7. Effective communication and collaboration skills, with the ability to interact with internal and external stakeholders, including health authorities. 
  8. Regulatory affairs certification (RAC) or drug safety certification (e.g., CSPV, RPhS) preferred but not required. 

This is a challenging and rewarding opportunity for individuals passionate about drug safety and patient well-being. Competitive compensation packages are available. 

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.  

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com    

Responsibilities: 

  1. Provide expert consultation and support in bioequivalence study design, conduct, analysis, and interpretation to pharmaceutical companies and contract research organizations (CROs). 
  2. Review study protocols, statistical analysis plans (SAPs), and study reports to ensure compliance with regulatory requirements and guidelines (e.g., FDA, EMA, ICH). 
  3. Design and oversee bioequivalence studies for generic drug products, including selection of appropriate study designs, endpoints, and statistical methods. 
  4. Conduct pharmacokinetic (PK) and statistical analyses of bioequivalence data using software such as WinNonlin or SAS. 
  5. Prepare and review bioequivalence sections of regulatory submissions, including abbreviated new drug applications (ANDAs), bioequivalence study reports, and responses to regulatory inquiries. 
  6. Provide guidance on bioanalytical method development and validation for bioequivalence studies. 
  7. Stay abreast of emerging regulatory requirements, scientific advancements, and best practices in bioequivalence and generic drug development. 
  8. Collaborate with cross-functional teams, including regulatory affairs, clinical development, and quality assurance, to ensure successful execution of bioequivalence programs. 

Qualifications: 

  1. Advanced degree (PhD, PharmD, or equivalent) in pharmaceutical sciences, pharmacokinetics, or related field. 
  2. Minimum of 5 years of experience in bioequivalence study design and conduct within the pharmaceutical industry, CRO, or regulatory agency. 
  3. Deep understanding of bioequivalence principles, study methodologies, and regulatory requirements in major markets (e.g., US, EU). 
  4. Proficiency in pharmacokinetic/pharmacodynamic (PK/PD) modeling and simulation techniques. 
  5. Experience with bioanalytical method development and validation for PK studies. 
  6. Strong analytical and problem-solving skills, with the ability to interpret complex PK data and statistical analyses. 
  7. Excellent communication and presentation skills, with the ability to effectively convey technical information to diverse audiences. 
  8. Regulatory affairs certification (RAC) or relevant professional certification (e.g., DABT, CCRP) preferred but not required. 

This is a challenging and rewarding opportunity for individuals passionate about bioequivalence and generic drug development. Competitive compensation packages are available. 

 

EEO Employer:   

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality. 

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