GROVE, NYPosted 24 days ago

Job summary

• Job post source

  This job is directly from Pharmavise Corporation

• Job overview

  The GMP Professionals role at Pharmavise Corporation focuses on ensuring compliance with Good Manufacturing Practice regulations to support pharmaceutical, medical device, and biotechnology clients in maintaining quality and regulatory standards.

• Responsibilities and impact

  The role involves ensuring GMP compliance in manufacturing and distribution, reviewing regulatory requirements, developing quality systems, conducting internal audits, collaborating with cross-functional teams, providing GMP training, supporting regulatory inspections, and staying updated on GMP regulations.

• Compensation and benefits

  Competitive compensation packages are offered, though specific salary and benefits details are not provided.

• Experience and skills

  Candidates need a bachelor's degree in a relevant field and at least 5 years of GMP compliance experience in pharmaceutical, biotech, or medical device industries, with strong knowledge of GMP regulations and quality systems; certifications like RAC or ASQ CQA are preferred but not required.

• Work environment and culture

  Pharmavise values excellence through quality and promotes equal opportunity employment with a commitment to diversity and inclusion.

• Company information

  Pharmavise Corporation is a regulatory compliance consulting firm partnering with pharmaceutical, medical device, and biotechnology clients to solve complex compliance issues and improve patient health and safety.

• Application process

  Applicants are encouraged to visit the company website and contact info@pharmavise.com for accommodations or further information.

• Unique job features

  This role offers the critical opportunity to impact pharmaceutical product quality and compliance through expert GMP oversight and collaboration with diverse teams.

Company overview

Pharmavise Corporation is a strategic partner for pharmaceutical, medical device, and biotechnology companies, offering expertise in quality, regulatory, and compliance services. Headquartered in Florida, the company supports clients from development to commercialization, ensuring adherence to industry standards. Founded by Ricardo Joseph, Pharmavise employs a team of professionals specializing in drug safety, GMP, and clinical subject matter expertise. The company's commitment to excellence is reflected in its diverse service offerings and its role as a trusted advisor in the life sciences and healthcare sectors.

How to land this job

• Position your resume to highlight your expertise in GMP compliance, emphasizing your experience with pharmaceutical manufacturing, packaging, and distribution processes to align with Pharmavise's core needs.

• Focus on showcasing your knowledge of regulatory requirements such as FDA, EMA, ICH Q7, and EU GMP, along with your skills in quality systems like documentation control, change control, deviations, and CAPA.

• Apply through multiple platforms including Pharmavise Corporation's official corporate website and LinkedIn to maximize your application visibility and increase your chances of being noticed.

• Connect with GMP, Quality Assurance, or Regulatory Compliance professionals at Pharmavise on LinkedIn; open conversations with ice breakers like asking about recent regulatory challenges they've faced or commenting on Pharmavise’s commitment to quality and patient safety.

• Optimize your resume for ATS by incorporating keywords from the job description such as 'GMP compliance,' 'quality systems,' 'regulatory audits,' 'CAPA,' and 'pharmaceutical manufacturing' to ensure it passes automated screening effectively.

• Leverage Jennie Johnson's Power Apply feature to automate tailoring your resume, applying through multiple channels, and finding relevant LinkedIn contacts, allowing you to dedicate more time to preparing for interviews and networking effectively.