Pharmaceutical Glatt Operator

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Irfa******

  • United States 
  • Last Update: 03.05.2019 at 12:00

Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Greenville, North Carolina
Country
United States

Category


Research Positions

Description


Key Responsibility Areas
  • Quality:  Ensures the quality of work, products and services as a first priority; complies or exceeds all regulatory and cGMP compliance standards as well as ensure accuracy of analyses as it relates to right first time measures
  • Safety: Adheres to all workplace safety laws, regulations, standards, and practices and actively advances a culture of safety within their team and organization
Specific Responsibilities Responsibilities include, but are not limited to:
  • With minimal supervision, assist in the manufacture of scale-up, biobatch and full commercial scale batches and development and CTM batches
  • With minimal supervision, assemble, disassemble, clean and store manufacturing equipment
  • Ensure that all work is accurate, precise, properly documented, compliant with SOPs and FDA cGMP guidelines
  • With supervision, document batch manufacturing in batch records accurately and completely as required
  • Perform and witness manufacturing steps
Qualifications
  • Glatt fluid bed dryer experience required
  • High school diploma or equivalent with at least six years of pharmaceutical industry experience
  • Associate degree in Applied Science degree with four years of equivalent pharmaceutical industry experience
Key Competencies/Requirements
  • Accountability: Assume responsibility for successfully accomplishing work objectives and delivering business results; setting high standards of performance for self and others
  • Agility: Respond positively to change, embracing and using new practices or values to accomplish goals and solve problems
  • Creativity: Explore and advances opportunities to develop novel solutions and approaches to the improvement of processes and services
  • Empowerment: Find opportunities to improve and extend their contribution to the organization and their teammates
  • Integrity: Demonstrate the highest commitment to integrity and showing respect for and value all individuals for their diverse backgrounds, experiences, styles, approaches and ideas
  • Passion: Evidence passion for the organization, our people, and the difference we make daily in improving the lives and health of people
  • Attention to Detail: Ensure information is complete and accurate; follow up with others to ensure that agreements and commitments have been fulfilled
  • Task Management: Plan work well, maintain flexibility and facilitate change when needed while optimizing quality and productivity
General Statement Mayne Pharma is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

Seniority Level

Mid-Senior level

Industry

  • Pharmaceuticals

Employment Type

Full-time

Job Functions

  • Manufacturing

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