Lead Production Technician - Bloomsbury, United States - QuVa Pharma

QuVa Pharma
QuVa Pharma
Verified Company
Bloomsbury, United States

3 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter


Description

Our Lead Inspection, Labeling and Packaging (ILP) Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products.

The role oversees planning, scheduling, staffing and daily execution for the inspection, labeling and packaging of compounded sterile products (CSPs), bulk bags and non
  • sterile solutions
. Your attention to detail and adherence to precise procedures will guarantee that our medications reach patients accurately and securely. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.


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What the Lead ILP Technician Does Each Day:
  • Oversees inspection, labeling and packaging operations, including scheduling, processing, and completion of finishing activities in support of CSPs, bulk bags and non
  • sterile solutions
  • Serve as a knowledgeable resource for any team member who needs assistance with products or procedures as well as SME for cross functional project teams
  • Works with label printing teams to ensure appropriate inventory of labels is maintained to support production, including escalation as needed to meet production targets
  • Supports development of weekly ILP plans and schedules
  • Ensures timely communication and coordination of activities to ensure materials are transported and processed in accordance with internal procedures to meet established timelines for delivery and internal processing
  • Resolves and escalates nonroutine incidents immediately
  • Ensures proper cleaning of the processing rooms in accordance with procedures
  • Conducts initial and ongoing training of new operators, demonstrates proper techniques, provides coaching, tracks development, completes required documentation, and advises management of progress; regularly attends training meetings
  • Ensures the proper operation of process equipment in accordance with internal policy and procedure
  • Escalates to supervision information related to individual who call in or arrive late to line

Our Most Successful Lead ILP Technicians:

  • Understand and adhere to all company policies and procedures
  • Recognize priorities and take appropriate followup action
  • Have strong written and verbal communication skills
  • Successfully interact with coworkers on various teams and at various levels to achieve desired outcomes
  • Continually strive to improve efficiency without compromising quality
  • Create / revise training plans to meet a specific objective, including milestones, consideration of resources
  • Have good decisionmaking skills

Minimum Requirements for this Role:


  • High school Diploma or GED from recognized institution or organization
  • At least 1year pharmaceutical manufacturing experience or labeling and/or packaging experience
  • Must be currently authorized to work in the United States on a fulltime basis; QuVa will not sponsor applicants for work visas

Any of the Following Will Give You an Edge:

  • BA degree
  • Proficient with MS Office inclusive of Word, Excel and PowerPoint
  • Familiarity with basic operation of ERP systems

Benefits of Working at QuVa:


  • Set, fulltime, consistent work schedule
  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 17 paid days off plus 8 paid holidays per year
  • Occasional weekend and overtime opportunities with advance notice
  • National, industryleading high growth company with future career advancement opportunities

About QuVa:


QuVa Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care.

We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide.

As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.


As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.


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