Executive-qa

**Job Overview**:
The Quality Assurance professional ensures compliance with regulatory standards, Good Manufacturing Practices (GMP), and company policies to maintain the highest quality of pharmaceutical products. The role involves documentation, audits, validations, and continuous improvement of quality systems.

**Key Stakeholders**:All Department, Customers & Clients on need basis.

**Reporting Structure**:Sr. Manager-QA

**Experience**:02- 04 Years

**Role & Responsibilities**:

- Issuance, archival and retrieval of documents
- Issuance of Control copies to respective dept
- Destruction of the GMP documents once the retention term has passed and controlled copies of the obsolete GMP documents.
- Tracking of all QA documents.
- Maintaining of backup of QA softcopies.
- Maintaining SOP/s with proper indexing.
- Preparation and review of SOPs.
- Management of QA stationary (controlled copies and logbooks)
- Dispatch and line clearance activities.
- Review of BMR/BECR
- Involving in handling of deviations, change control and related CAPAs
- To ensure data integrity compliances while performing activities.

**Competencies**:

- Quick learner with excellent communication skills
- Punctual with proven track record of dedication & reliability
- A team player who is equally capable of working alone
- Fluent in both written and spoken English
- Knowledge /Experience in peptides

In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.

Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.

**Equal employment opportunity**

Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.

We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.

**Piramal Pharma Solutions (PPS)**is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.