Pharmaceutical Manufacturing Specialists with Engineering Background
NEW YORK, NYPosted 22 days ago
Job summary
Job post source
This job is directly from Pharmavise Corporation
Job overview
The Pharmaceutical Manufacturing Specialist with an engineering background at Pharmavise Corporation supports pharmaceutical manufacturing operations by applying engineering expertise to optimize processes and ensure compliance, contributing to client success and patient safety.
Responsibilities and impact
The role involves optimizing manufacturing processes and equipment, collaborating with cross-functional teams, leading process improvements, conducting risk assessments, troubleshooting manufacturing issues, supporting equipment validation, maintaining documentation, and staying updated on industry trends.
Compensation and benefits
Competitive compensation packages are available; specific details on salary, bonuses, or benefits are not provided.
Experience and skills
Candidates must have a bachelor's degree in engineering with at least 5 years of pharmaceutical manufacturing experience, knowledge of manufacturing processes and regulatory requirements, proficiency in engineering tools, and strong communication and project management skills.
Work environment and culture
Pharmavise values excellence through quality and is an equal opportunity employer committed to diversity and inclusion, providing accommodations for applicants as needed.
Company information
Pharmavise Consulting Corp. is a regulatory compliance consulting firm partnering with Pharmaceutical, Medical Device, and Biotechnology clients to address complex compliance issues and improve patient health and safety.
Job location and travel
This is a remote position, allowing work from any location.
Unique job features
The job offers the opportunity to work on continuous improvement initiatives and apply engineering principles in pharmaceutical manufacturing within a consulting environment.
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
Tailor your resume to emphasize your engineering expertise in pharmaceutical manufacturing, highlighting skills in process optimization, equipment design, and facility management as outlined by Pharmavise Corporation's job description.
Focus on showcasing experience with cross-functional collaboration, process improvement initiatives such as Lean Six Sigma, and regulatory compliance knowledge including cGMP, FDA, and EMA guidelines.
Apply to the Pharmaceutical Manufacturing Specialist position through Pharmavise Corporation's official corporate website, LinkedIn, and other job portals to maximize your application visibility.
Connect with current employees or team members in the pharmaceutical manufacturing or engineering divisions at Pharmavise on LinkedIn; initiate conversations by referencing recent company updates, industry trends, or asking about their experience working on process improvements or regulatory challenges.
Optimize your resume for ATS by incorporating keywords from the job posting such as 'process optimization,' 'risk mitigation,' 'CAPA,' 'equipment qualification,' 'Lean Six Sigma,' and 'regulatory compliance' to increase the chances of passing automated screenings.
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