Sr Formulation Technician (12hr days, 2-2-3 rotation)
On-siteGreenville, North Carolina, United States
Job Summary
Operate and monitor advanced equipment on vial line 9 while ensuring compliance with cGMP regulations and company SOPs. Collaborate with cross-functional teams to optimize production processes, troubleshoot technical issues, and implement solutions. Maintain accurate documentation and work in a clean room environment, adhering to strict environmental conditions regarding personal items and attire. This role supports the Pharma Services Group's mission to develop solutions for global health challenges, including drug development and production. Shift hours are 12 hours daily on a 2-2-3 rotating schedule, with a requirement for a high school diploma and minimum two years of experience in pharmaceutical manufacturing or related fields.
Required Qualifications
- High school diploma or equivalent
- Minimum of 2 years of work experience in a pharmaceutical manufacturing, operations, production, lab setting or related field
- Must be able to stand for extended periods
- Must be able to lift up to 25 pounds
- Must be able to work in a clean room environment
- Must be able to wear personal protective equipment (PPE) for extended periods
- Must be available for 12 hr shift/days
- Must be available for a 2-2-3 rotating schedule
- Must be available for 6am-6pm shift hours
- Must be able to comply with cGMP regulations
- Must be able to follow SOPs
- Must be able to maintain accurate documentation
- Must have strong attention to detail
- Must be able to work in a highly regulated environment
- Must have strong problem-solving skills
- Must have strong communication skills
- Must be able to operate and monitor advanced equipment
- Must be able to troubleshoot technical issues
- Must be able to implement solutions
- Must be able to collaborate with cross-functional teams
- Must be able to optimize production processes
- Must be able to ensure quality and efficiency of pharmaceutical manufacturing processes
- Must be able to contribute to the production of life-saving medications and therapies
Desired Qualifications
- Experience in a cGMP environment
- Experience working in a clean room environment
- Experience with aseptic processing and sterile drug manufacturing
- Strong understanding of pharmaceutical manufacturing processes
- Proficiency in following SOPs and maintaining accurate documentation
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