Job summary
Job post source
This job is directly from Fagron
Job overview
The Production Specialist at Fagron supports production projects and change controls to ensure timely completion and compliance in a GMP manufacturing environment.
Responsibilities and impact
The role involves managing production projects, coordinating cross-functional teams, maintaining planning tools, supporting manufacturing and ERP systems, updating production documents, and ensuring compliance with SOPs and training.
Compensation and benefits
The position offers a competitive salary, health, vision, and dental insurance, company-paid life insurance, generous paid holidays and time off, company matching 401K, employee assistance program, and flexible working arrangements.
Experience and skills
Requires a BA/BS in a science field or equivalent experience, at least one year in an FDA regulated GMP environment, strong organizational and critical thinking skills, advanced writing skills, proficiency in MS Office, AX, and MasterControl, and strong communication skills.
Work environment and culture
Fagron fosters a supportive environment focused on performance development and long-term career success, with a modern facility in Canton, MA offering amenities like ample parking and a well-equipped breakroom.
Company information
Fagron is a global leader in personalized medicine founded in 1990 in the Netherlands, employing over 3,000 people worldwide and committed to innovative pharmaceutical solutions.
Job location and travel
The job is located at Fagron's state-of-the-art compounding facility in Canton, Massachusetts, featuring ample parking and employee amenities.
Application process
Applicants are instructed to apply online through careers.fagron.com.
Unique job features
The role is distinguished by its involvement in personalized medicine production projects within a GMP environment and offers flexible working arrangements and a modern facility.
Company overview
Fagron is a global leader in pharmaceutical compounding, providing personalized medication solutions to improve patient care. They generate revenue by offering a broad range of products and services, including raw materials, equipment, and innovative formulations to pharmacies and hospitals worldwide. Founded in 1990 in Rotterdam, the Netherlands, Fagron has expanded significantly through strategic acquisitions and a strong focus on research and development, positioning itself as a key player in the healthcare industry.
How to land this job
Position your resume to highlight your experience supporting production projects within FDA regulated, GMP manufacturing environments, emphasizing your ability to manage projects from initiation to completion with minimal supervision.
Focus on showcasing your proficiency in change controls, technical writing, and your strong organizational and critical thinking skills, as these are crucial for driving production tasks and maintaining compliance at Fagron.
Apply through multiple channels including Fagron's corporate careers site at careers.fagron.com and LinkedIn to maximize your application's visibility.
Connect with current employees in Fagron's production or manufacturing divisions on LinkedIn; use ice breakers like commenting on the company's leadership in personalized medicine or asking about their experience working on production projects at the Canton facility.
Optimize your resume for ATS by incorporating keywords from the job description such as 'change controls,' 'GMP manufacturing,' 'production projects,' 'technical writing,' and 'AX and MasterControl software' to ensure it passes initial screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications through multiple platforms and identify relevant LinkedIn contacts for networking, allowing you to focus your time on preparing for interviews and skill development.
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