Manufacturing Associate Scientist

Piscataway, NJ 08854

Employment Type: Contract Job Category: Chemist/ Lab Job Number: NA1798077410 Compensation: $35-40 / hour

Job Description

Title: Manufacturing Associate Scientist

Location: Piscataway, New Jersey

Hire Type: Contract to Hire

Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S.

As a contract employee of Sterling, you are eligible to receive a Full Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental & vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan.

Job Summary: 
This employee follows the cGMP manufacturing processes and technology transfer. Authors documents (SOPs) to support batch records. Prepares production systems, buffers and media for use in the production area. Maintains production batch records and tracks/orders materials as necessary from the storage warehouse. Trains new operators and revises SOPs as needed. Troubleshoots process changes as well as implements new production procedures. Shall maintain the highest safety standards and quality.

Job Duties:
  • Participate in the development and optimization of manufacturing processes for new and existing products.
  • Writes and reviews SOPs.
  • Assist in opening and closing change controls.
  • Assist in opening and closing CAPAS.
  • Provide support to Quality Assurance and the Validation Group to resolve deviations in manufacturing.
  • Participate in collaboration with other Departments in the pursuit of excellence to achieve the highest level of product quality, compliance, manufacturing efficiency, and product development.
  • Provide support to Quality and Compliance Departments during regulatory audits.
  • Provide contributions on project teams.

  • MS (1-3), BS (3+) years of relevant experience in a Biopharmaceutical organization.
  • Experience and knowledge in drug substance manufacturing (Fermentation and protein purification) and in drug product manufacturing (aseptic processing areas). 
  •  Knowledge in MS Word, MS Excel, MS PowerPoint, Outlook, experimental design, data collection, and statistical analysis.
  • Good communication skills both verbal and written.
  • Quality oriented.
  • Highly negotiation skills.
  • Excellent time management skills.
  • Effective in the set-up of priorities and establishing objectives.

Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information.

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