QuVa Pharma-posted 2 months ago
$98,891 - $135,975/Yr
Full-time • Manager
Bloomsbury, NJ
1,001-5,000 employees
Chemical Manufacturing

Our Manager, Manufacturing Operations plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include managing the manufacturing of sterile pharmaceuticals within the facility. The primary function is to oversee all operations, and personnel, of Inspection, Labeling and Packaging Operations where multiple requirements and challenges will exist requiring a good knowledge base and ability to apply operational, quality, and regulatory skill sets. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

  • Manages staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements
  • Manages operations to assure all products are visually inspected, labeled and packed into their finished containers as per applicable standard operating procedure
  • Prepares and submits weekly/monthly reports, prepares metrics and trends data to identify and prioritize continuous improvement opportunities
  • Establishes & maintains cooperative cross-functional relationships with peers in Quality, and other manufacturing operations colleagues to meet plant objectives
  • Leads in development & maintenance of a safe manufacturing environment. Participates in safety meetings, investigates accidents, and takes appropriate corrective action to eliminate hazardous conditions
  • Counsels, trains, & develops front line leaders for efficient performance and assists in their career development; creates an atmosphere of team effort & open communication
  • Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on-time closure
  • Bachelor's Degree in Life Science or another related field
  • 3 years of supervisory or management experience
  • Hands-on direct shop floor involvement: Troubleshooting
  • Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas
  • 3 years prior experience in cGMP / FDA regulated industry
  • Understanding of process flows, gap assessments and analysis of data to drive improvement
  • Proficiency with computerized tracking tools
  • Comprehensive knowledge of adult learning techniques
  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 22 paid days off plus 8 paid holidays per year
  • Occasional weekend and overtime opportunities with advance notice
  • National, industry-leading high growth company with future career advancement opportunities
  • The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions
  • Range: $98,891-$135,975
  • This role is also eligible for an annual incentive bonus, subject to program terms and guidelines
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