Process Engineer


Job Location:

Bethlehem, GA - USA

Monthly Salary: Not Disclosed
Posted on: 8 hours ago
Vacancies: 1 Vacancy

Job Summary

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Division

Piramal Critical Care

Piramal Critical Care (PCC) a business unit of Piramal Pharma is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders.

PCC maintains a wide presence across the US Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane Isoflurane and Halothane as well as Intrathecal Baclofen therapy for spasticity management.

PCC has a strong manufacturing and process development experience with wholly-owned state-of-the-art manufacturing facilities in the United States and India inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world timely at optimal costs.

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Process Engineer

Job Description

Process Engineer responsible for leading hands-on troubleshooting process optimization and continuous improvement of GMP API manufacturing operations

Essential Duties and Responsibilities

  • Acts as SME for API manufacturing processes utility systems and unit operations including distillation reactors scrubbers absorbers and condensers.
  • Accountable for process performance and drives improvements in yield throughput reliability cost and cycle time.
  • Leads troubleshooting and root cause investigations for deviations batch failures and process upsets using data-driven and structured problem-solving methods.
  • Develops and maintains mass and energy balances to support optimization and debottlenecking efforts.
  • Applies Statistical Techniques (SPC DOE etc) to monitor capability reduce variation and improve process stability.
  • Tunes and optimizes process control systems including PID loops to improve operational performance.
  • Leads Lean and Six Sigma initiatives focused on measurable process improvement.
  • Supports capital projects through design implementation commissioning and startup activities.
  • Drafts and reviews URSs SOPs Change Controls validation documents technical reports and investigations.
  • Leads or supports PHA/HAZOPs MOC and incident investigations.
  • Partners closely with Operations Maintenance and Automation to implement practical field-based solutions.
  • Maintains strong plant presence and responds to plant upsets with urgency and sound engineering judgment.
  • Mentors junior engineers and provides technical leadership across manufacturing issues.
  • Drives execution with a bias toward action and measurable results.
  • Other duties as assigned.

Key Competencies (knowledge skills and abilities every person must possess to be successful)

  • Strong analytical and systems-thinking capability with ability to synthesize complex multi-variable process data into clear technical conclusions and actionable decisions.
  • Deep understanding of chemical engineering principles (thermodynamics mass transfer reaction engineering fluid flow heat transfer) applied to real manufacturing systems.
  • Advanced problem-solving and critical thinking skills with demonstrated ability to independently resolve complex process issues in batch or continuous API manufacturing environments.
  • Strong capability to interpret manufacturing data including historian data batch records process trends and deviation histories to identify true drivers of performance.
  • Working knowledge of Statistical Process Control (SPC) and statistical reasoning to assess process stability variation and capability.
  • Strong understanding of pharmaceutical and chemical manufacturing systems including distillation reactors separations heat transfer systems and supporting utility networks.
  • Working knowledge of Process Safety Management (PSM) including safe operation of high-hazard processes operating envelopes and risk-based controls.
  • Experience working with or around highly hazardous chemical systems including toxic corrosive and reactive materials such as chlorine and anhydrous HF with strong safety awareness.
  • Strong understanding of cGMP environments including validation change control deviation management and regulatory compliance expectations.
  • Ability to develop interpret and review technical documentation including URSs SOPs investigations validation protocols and engineering design packages.
  • Strong leadership and influence capability with ability to align cross-functional teams and drive execution without direct authority.
  • High bias toward action and decision-making balancing technical rigor with urgency to ensure safe and reliable production performance.

Education/Experience

  • Bachelor of Science in Chemical Engineering required.
  • 8 years of experience in chemical or pharmaceutical API manufacturing required; 10 years preferred.
  • Demonstrated expertise in troubleshooting and optimizing batch and/or continuous chemical processes in a cGMP manufacturing environment.
  • Strong track record of driving measurable process improvements in yield reliability throughput cost or cycle time using data-driven methods.
  • Lean Six Sigma Green Belt required; Black Belt strongly preferred with practical application in manufacturing environments.
  • Experience with TrackWise Aspen SAP and AutoCAD strongly preferred.

Physical Demands:

Physical Effort (Occurrence frequency for each activity)

Activity

N/A

Occasionally

Frequently

Continuously

Sitting/Standing/Walking: Continuously

Balancing/ Kneeling/Crouching/Stooping: Occasionally

Crawling/Climbing: Occasionally

Reaching/Working Overhead: Frequently

Keyboard Use/Repetitive Hand Motion: Continuously

Pushing/Pulling (up to 50 pounds): Occasionally

Lifting/Carrying (up to 50 pounds): Occasionally

Reporting to this position: N/A Individual Contributor

General Oversight and Direction:

Receives moderate to limited supervision working from objectives set by Manager. Employee organizes and carries out most assignments in accordance with standard practices instructions or previous training. Employee handles some situations independently.

Equal Employment Opportunity

Piramal Critical Care is committed to Equal Employment Opportunity. It is the policy of the Company to encourage and support equal employment opportunity for all associates and applicants without regard to age sex race color ancestry religious creed national origin pregnancy physical or mental disability medical condition marital status political affiliation sexual orientation disabled veteran or Vietnam Era Veteran Status.

Americans with Disabilities Act

Applicants as well as employees who are or become disabled must be able to perform the essential job functions either unaided or with reasonable accommodation. The organization shall determine reasonable accommodation on a case-by-case basis in accordance with applicable law.

Employee Job Responsibilities

You are expected to follow all policies procedures and guidelines conducting yourself in ways that protect the interests and safety of all employees and the company.

The above statements reflect the general duties and responsibilities considered necessary to perform the essential functions of the job. This document should not be considered a fully detailed description of all the work requirements of the position. Piramal Critical Care may change the specific job duties with or without prior notice based on the needs of the organization.


Required Experience:

IC

Be the First to Apply DivisionPiramal Critical CarePiramal Critical Care (PCC) a business unit of Piramal Pharma is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for pati...

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Piramal Pharma Solutions offers complete drug discovery, development, and manufacturing support as a global CDMO, cutting-edge solutions in drug substance and drug product.

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