• Job Description

  Req#: 543864

  JOB SUMMARY:

  The DSCSA analyst is responsible for reviewing how PAI functions conduct activities in handling serialized products, in compliance with internal policies /procedures, that affect DSCSA data integrity.

  The Analyst has to work with one or more functions and create weekly report on observations, that can be leveraged for improving the processes at PAI. The role is onsite, based in Greenville, SC.

  ESSENTIAL DUTIES AND RESPONSIBILITIES:

  1. The main responsibilities are to measure compliance in handling serialized products, and help to improve processes through training, procedures, and feedback.
  2. Work with PM – DSCSA to track customer DSCSA scorecards and internal DSCSA issues
  3. Create / maintain a process to conduct audits with a checklist of issues
  4. Create / update a tracker to document issues, in which a process was not adhered to
  5. Conduct joint meetings with department and VP of IT, to confirm the findings with the department
  6. Work with the department in creating action plan for repeat issues
  7. Provide weekly report to PM-DSCSA and VP of IT

  1. Make recommendations on process and technology that will help to identify and eliminate DSCSA issues

  1. Identify time consuming mistakes, and identify how different functions can improve their process to minimize effort spent in corrections
  2. Ensure that processes and process updates are reflected in SOPs of the related functions
  3. Determine training needs and conduct periodic refreshers to help users who impact DSCSA data
  4. Partner with other IT resources on integration with serialization, EDI, contracts software, quality systems, and other systems to consider technology options that support this role.

  1. Perform other duties as assigned.

  EDUCATION AND/OR EXPERIENCE:

  A Bachelors’ degree in Information Systems or Computer Science field(s) and 5+ years of work experience. Or an equivalent combination of education and experience. Experience in working in warehouse, shopfloor (production), quality control is highly desirable. Desirable experience of 1-2 years of experience in pharmaceuticals, and 1-2 years of SAP experience (using one or more modules in operations, quality, warehouse, master data, sales and distribution). Knowledge of IT systems, Six Sigma tools, root cause analysis and process improvement methodologies is desirable.

  KNOWLEDGE, SKILLS & ABILITIES:

  This position requires the individual be organized, detail-oriented, and self-motivated. Standard office equipment is used.

  PHYSICAL REQUIREMENTS/WORKING CONDITIONS:

  The physical requirements and working conditions listed for this job are representative of those required on the job. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties and responsibilities. Computer keyboarding, computer monitor and mouse use including reaching forward, grasping, finger and wrist manipulations, and neck bending and turning: near vision is necessary for computer monitor use. Periodic visits to cGMP manufacturing, packaging and warehouse areas.

  PAI is an Equal Opportunity Employer. PAI uses E-Verify.

  EEO Employer / Veteran / Disabled.

• About the company

  Pharmaceutical Associates, Inc. (PAI) has been at the forefront of producing generic liquid pharmaceuticals for nearly 50 years.

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