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Piramal Jobs (NOW HIRING)

Be the First to Apply 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 ...

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing ...

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How much do piramal jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for piramal in the United States is $28.14, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $29.57 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a professional at Piramal?

To thrive at Piramal, you generally need a relevant academic background in fields like pharmaceuticals, chemistry, or business, along with experience in your specific domain. Familiarity with industry-specific tools such as ERP systems, laboratory information management systems (LIMS), and certifications like GMP or Six Sigma is often required. Strong analytical thinking, teamwork, and effective communication are crucial soft skills for excelling in a collaborative and innovative environment. These competencies are essential for ensuring quality, compliance, and driving growth in the dynamic pharmaceutical and healthcare sectors where Piramal operates.

What is the difference between Piramal vs Pharmacist?

AspectPiramalPharmacist
Required CredentialsGraduate degree in pharmacy, pharmaceutical sciences, or related fieldDiploma or degree in pharmacy (D Pharm, B Pharm)
Work EnvironmentPharmaceutical manufacturing, research, or corporate rolesDispensing medicines, patient counseling, retail or hospital pharmacy
Industry UsagePharmaceutical companies, research organizations, healthcare firmsCommunity pharmacies, hospitals, retail drug stores

While Piramal primarily refers to a pharmaceutical company involved in manufacturing and research, a Pharmacist is a healthcare professional responsible for dispensing medicines and advising patients. The roles differ in scope: Piramal employees may work in R&D or corporate settings, whereas Pharmacists work directly with patients in pharmacy settings. Both require pharmaceutical knowledge, but their daily tasks and work environments vary significantly.

What types of projects and teams can new hires expect to work with at Piramal?

At Piramal, new hires often join multidisciplinary teams that focus on projects ranging from pharmaceutical research and development to manufacturing and quality assurance. Depending on the department, you may collaborate closely with scientists, engineers, regulatory specialists, and business development professionals. The environment encourages cross-functional collaboration, exposing employees to various aspects of the pharmaceutical industry and offering opportunities to contribute to impactful projects. This structure not only broadens your experience but also supports professional growth within the organization.

What is Piramal?

Piramal is a global business conglomerate with interests in pharmaceuticals, financial services, real estate, and healthcare analytics. The company is known for its innovative products and solutions in healthcare and life sciences, serving clients worldwide. Piramal Group operates through various subsidiaries, including Piramal Pharma Limited and Piramal Realty. The organization focuses on sustainable growth and has a strong presence both in India and internationally.
What cities are hiring for Piramal jobs? Cities with the most Piramal job openings:
What states have the most Piramal jobs? States with the most job openings for Piramal jobs include:
Infographic showing various Piramal job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution, with an average salary of $58,531 per year, or $28.1 per hour.

Senior Quality Assurance Compliance Specialist

Piramal Pharma Limited

Bethlehem, PA โ€ข On-site

$81K - $112K/yr

Full-time

Re-posted 4 days ago


Job description

Be the First to Apply

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.

For more details, please visit https://www.piramalcriticalcare.com/global/

Job Title

Senior Quality Assurance Compliance Specialist

Job Description

Provides continuous oversight of daily Quality activities to ensure compliance with internal procedures and regulatory requirements. Responsible for documentation control, review, and management to maintain GMP and regulatory compliance.

Essential Duties and Responsibilities

  • Review, approve, and disposition finished products and provide final Certificate of Analysis (CoA) approval

  • Facilitate client project management to ensure quality deliverables are completed on time and in full

  • Coordinate investigation and closure of non-conformances, ensuring CAPA and change controls are initiated and completed

  • Lead or participate in cross-functional deviation investigations and improvement projects

  • Review and approve laboratory investigations, ensuring root cause identification

  • Support QA team members and assist in departmental training

  • Provide support during regulatory audits

  • Review BOMs, inspection plans, pallet patterns, calibration records, and SOPs

  • Perform internal audits and assist in audit report preparation

  • Maintain and revise QA procedures

  • Support Annual Product Review (APR) through data collection and database management

  • Manage vendor complaint processes

  • Monitor and trend deviations, laboratory investigations (LIs), CAPAs, customer complaints, and change controls

  • Perform special projects as assigned by Quality Management

  • Oversee and review obsolete material destruction processes

  • Conduct quality inspections on packaging lines as required

  • Maintain supplier approval programs

  • Support and maintain site Document Control System

  • Review, approve, and close Document Change Requests

  • Track document changes using DCC tools and ensure closure of associated actions

  • Maintain document archives, including offsite storage

  • Print and issue controlled documents, forms, and logbooks

  • Review documentation in eDMS for formatting and accuracy

  • Upload and manage documents in the electronic Document Management System (eDMS)

  • Route documents for approval within eDMS workflows

  • Retrieve documentation for audits in a timely manner

  • Maintain and revise document control procedures

Key Competencies(knowledge, skills, and abilities every person mustpossessto be successful)

  • Strong critical thinking and problem-solving skills

  • Excellent customer service and professional communication skills

  • Strong verbal and written communication abilities

  • Energetic, motivated, and detail-oriented approach

  • Strong organizational skills with attention to detail

  • Ability toanalyzedata,identifytrends, and make regulatory decisions

  • Ability to explain issues, propose solutions, and manage urgent requests effectively

  • Capability to drive projects and implement process/system improvements

Education/Experience

  • Bachelor's degree in a scientific, quality assurance, or technical field

  • Minimum5+ years of relevant experience

  • Strong understanding of pharmaceutical cGMP, industry standards, and regulations

  • Strong cross-functional communication skills acrossdifferent levelsof the organization

  • Expertisein Quality systems and tools

  • Proficiencyin Microsoft Outlook, Excel, Word, and other web-based systems

  • Strong understanding of computer system validation and GAMP requirements