DPI QA Document Administrator -1st Shift

NOTICE:
The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates.

DPI QA Document Administrator

Inva Gen Pharmaceuticals, Inc.

Hauppauge, NY location

Full Time

(Base/ Hourly)

$23/hr - $30/hr

In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance – medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) – vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits.

1st Shift 7:00AM - 3:30PM

Must be willing and able to work any assigned shift ranging from first, second, or third shift. Work schedule may be Monday to Friday, Tuesday to Saturday, or some combination thereof based on business needs.

• Responsible for the printing and issuance of controlled documents to all departments as requested by departments in support of the day to day activities.
• Tracking the printing and issuance of documents control.
• To control the printing and issuance of documents needed daily for manufacturing, packaging, warehousing etc.
• Receive fulfil requests for documents from the Master Control System.
• Keep logbook updated for reconciliation of documents (How may printed vs. how many used) and confirm destruction of any document not issued or otherwise used.
• In the event of an inspection or department review, the logbook will be submitted as evidence of control.
• Training will be provided with regards to any SOPs or WI to be followed.
  
  Instruction on the process will be given as hands on training.
• Will need to interact with various departments as necessary for control of documents
• Other duties may be assigned as necessary to the role

• High School Diploma

• 1-2 years experience in an automated work environment preferred.

• Must have good organizational and record keeping skills.
• Must be able to use a computer to access the Master Control Program
• Must have the ability to use MS Excel, MS word, understanding of general filing principles.
• Must be able to read and write English since all documentation is in English.

Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India’s pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.

Driven by the purpose ‘Caring for Life’, Cipla’s focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy.

Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.

Inva Gen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of…