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Job Description


Manager Operations, Final Packaging 2nd shift

View: 29

Company: Roche
Contract: PERM
Location: New Jersey - Branchburg, United States


Manager Operations, Final Packaging 2nd shift 3:00pm-11:30pm

This position is eligible for a Shift Differential. 

Responsibilities:

  • Plans, schedules and supervises an overall 2nd shift staff ranging up to 50 people in Packaging operations.  Motivates team and oversees resource deployment to meet production demands across often shifting priorities and deadlines. Capable of using good judgment and assertive decision making to adjust to changing demand and competing priorities.   
  • Performs supervisory functions including performance management, career development guidance, and training and development opportunities for staff.
  • Achieves financial objectives by preparing, managing operating and capital budgets; scheduling expenditures; analyzing variances; initiating corrective actions.  Maintains control of work group expenses within limits of DOA.
  • Ensures that work group performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA, FDA, ISO).
  • Ensures compliance with applicable corporate policies and procedures, regulatory and quality requirements, and adherence to Standard Operating Procedures (SOPs) and production batch records.  Responsible for the oversight of the creation and maintenance of area SOPs and batch records including the progression towards digital solutions (e.g., electronic batch records). 
  • Represents as applicable Packaging area and leads and/or participates in product based project activities such as new product transfers and validations.  Recommends, drives and implements process improvements and leads projects to successful achievement.
  • Resolves problems/issues encountered in the logistics and planning processes for production.
  • Produces reports and statistics to depict key performance metrics. Comfortable and capable with basic office software (i.e., Word, Excel, PowerPoint, etc.).
  • Participates as applicable in area audits and ensures nonconformance reports and CAPA’s are drafted and completed in appropriate timeframes. Documents operations, planning, and logistics activities accurately and appropriately, and according to established formats. Writes and/or revises documents (e.g., SOPs, Variances, Rework Orders, Change Requests) timely and in compliance with cGMP/ QSR practices
  • Communicates with other departments, staff groups and customers and keeps senior management informed on area issues and topics and seeks to play a strategic role in dealing with planning, coordinating, administration and general management issues.

Education:

  • Minimum required: Bachelor’s Degree in Biological/Life Sciences, Chemistry, Biochemistry or related field. or equivalent combination of education and work experience.Preferred: Ph.D.

Job-related Experience:

  • Minimum required: At least 8 years of relevant industry experience.
  •  Preferred: Proven leadership with team management experience. Demonstrated ability to generate and implement process improvement initiatives. Familiar with LEAN concepts.

Knowledge, Skill or Ability

  • Required: Experience in assay optimization, experimental design, versatile laboratory practice, data analysis, and data and concept presentation. FDA experience desired. Experience in quality systems regulations. Demonstrates basic understanding of other scientific disciplines       
  • Preferred:  Proficient use of automated and computerized systems including familiarity with SAP or Trackwise.
 
 
 
 
 
 
 





More Info / Apply

(external link to recruiter web page)








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