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Operations Investigator - DPI

Job in Hauppauge, Suffolk County, New York, 11788, USA
Listing for: Cipla USA
Full Time position
Listed on 2025-12-19
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Data Analyst
Job Description & How to Apply Below

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.

Job Title: Operations Investigator (Manufacturing and Packaging)

Organization: Inva Gen Pharmaceuticals, Inc.

Location: Hauppauge, Long Island

Employment Type: Full Time

Hourly Rate: $21 - $30

Benefits: 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.

Work Hours / Shift / Remote: 9:00am - 5:30pm, OT as required

Responsibilities / Accountabilities
  • Investigation of manufacturing and packaging deviations and non‑conformances to determine root cause and implementation of Corrective and Preventative Actions (CAPAs) to prevent recurrence.
  • Work with cross‑functional teams to gather data, lead, and perform Root Cause Analysis to determine the likely root cause of the event.
  • Preparing investigation reports that include recommendations on investigation findings for medium/high severity non‑conformances and communicating findings and recommendations at group meetings.
  • Ability to conduct in‑depth interviews and gather pertinent information to drive root cause conclusions, product impact analyses, and initiations of CAPA actions.
  • Reviewing completed Batch Manufacturing Records (BMR) and logbooks following cGMP standards in support of investigations.
  • Reviewing, editing, and revising controlled documents (batch records, logbooks, SOPs, etc.) following cGMP standards to ensure compliance with written procedures.
  • Monitoring production processes to acquire vital data in support of investigations and track the efficiency of changes.
  • Gathering, trending, and analyzing process‑related data to drive consistency and timeliness.
  • Training new employees in investigative processes and techniques and documenting all training.
  • Coordinating and/or leading cross‑functional meetings with multiple departments.
  • Prepare product complaint investigations, assist in investigating quality issues, OOS, and OOT, and prepare reports for the same.
  • Evaluating, developing, and qualifying manufacturing equipment (IQ, OQ, and PQ) and preparing necessary PQ protocols.
  • Risk assessment and risk mitigation by performing FMECA (Failure modes, effects, and criticality analysis).
Education Qualifications
  • A bachelor's or advanced degree in pharmaceutical sciences, chemistry, or a related field is typically required.
Experience
  • 2-5+ years' experience.
Skills / Competencies
  • Proficiency with Microsoft Office, SAP, Track wise.
  • Strong analytical skills and proven organizational ability and attention to detail.
  • Strong verbal and written communication skills.
  • Ability to multitask and work in a fast‑paced environment under tight deadlines.
  • Ability to think analytically, apply sound judgement, and solve problems.
  • Strong command over written and verbal English is required.
  • Interpersonal skills.
  • Maintains knowledge of current good manufacturing practices.
  • General understanding of equipment, instruments, and systems involved in the manufacturing process.
  • Excellent verbal and written communication skills, detail‑oriented personality, and ability to work collaboratively across functions.
  • Experience interacting with regulatory health authorities if needed.
  • Knowledge of global regulations and standards.
  • Ability to follow gowning procedure and work in a production environment.
About Cipla

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,…

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