Who We Are
Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$6 billion. Supported by more than 40 manufacturing facilities and more than 40.000 employees around the globe, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe.
Over the last two decades, Sun Pharma has established itself as a leading player in the generics market, and are rapidly ramping up their presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology.
Values
At Sun Pharma our core values—Humility, Integrity, Passion, and Innovation—are part of our unique culture, known as Sunology.
We are empowering our employees to create their “Own Sunshine”. We believe in being Better Everyday by investing on lifelong learning, Taking Charge by owning our impact, and Thriving Together in a workplace where collaboration is encouraged. We are committed to being an inclusive and equitable employer, valuing diverse perspectives and creating an environment where all individuals feel respected, heard, and inspired to bring their best selves to work.
SUN Pharma is seeking a dynamic QA Specialist Biologics. As the QA Specialist Biologics, the selected candidate will play a pivotal role in ensuring the batch release and certification of our Biologics product.Taking the helm of the Pharma Branded team, they will foster a culture of excellence in quality management.
Overall Job Purpose
The QA Specialist Biologics is responsible for ensuring compliance in Sun Pharma’s Biological products manufactured externally, worldwide. This includes supporting the Sr. QP/QA CMO Manager Biologics on product development and commercial operations, in addition to ensure on-time release of product under release responsibility of Biological group plus appropriate maintenance of local quality systems. He/she ensures that activities at Contract Manufacturing Organizations are conducted according to the relevant Standard Operating Procedures aligned with the Quality Assurance Agreement and Regulatory expectations. Supports the QMS that consolidates Health Authority Regulations into Sun Quality requirements for Biologic products
Major Responsibilities:
- Management of weekly QA batch release planning of Biologics products
- Review of batch documentation of Biologics products (Drug Substance, Drugh Product and/or Finished Product) as preparation of batch certification by QP to ensure compliance with GMP and with the marketing authorizations as well applicable and correct documentation for release (CoA, CoC etc.)
- Management ( of key quality systems including deviations, change controls, CAPAs, complaints, etc. associated with Biologics products, by liaising with CMOs, QA Manager/QP , Operational staff, QC and other Sun stakeholders associated with Drug Substance , Drug Products or Finished Product appropriately and in a timely fashion.
- Prepare of annual product reviews (APR/PQR) of Biologics products together QA staff.
- Manage and maintain product specification in accordance with current marketing authorizations and ensure timely updated of applicable associated documentation in support for batch release.
- Review, prepare batch document for QP Batch release of clinical trial batches, and ensures proper maintenance of product specification files to ensure compliance with INDs and IMPDs. (ocassionally)
- Responsible for receiving, managing, and tracking CMO change notification; performing timely communication with both internal and external internal stakeholders according to the requirements of Quality Agreements.
- Ensures the comprehensive use of risk management tools in aspects across the quality management system, and product related elements to assess impact on product quality, and overall compliance with regulatory expectations and with the marketing authorizations.
- Support the timely implementation of global standards and procedures by execution of associated GAP assessments against local procedures.
- Support the maintenance and update of Quality Management System.
- Support planning and inspection readiness for external audits (from partners, Corporate Quality Systems and regulatory authorities
Qualifications, Knowledge, Experience & Skills
Education Qualifications (Graduate- Post Graduate)
Mandatory
- HBO or Bachelor Degree in (Bio-) Chemistry, Pharmacy, Biotechnology or similar education.
- 5 years of relevant experience in (bio) pharmaceutical Drug Substance and/or Drug Product manufacturing.
- Strong knowledge of EU GMP, US CFRs.
- Well versed in Microsoft Excel.
- Fluent in English
Work experience
Mandatory
- Tenure: minimum 5 years
- Industry: (Bio) pharmaceutical, sterile manufacturing
- Content areas: Manufacturing, QA /QC, QA manufacturing operation.
Technical Competencies
- Experience on preparation of batch release, including batch documentation review and preparation for batch certification.
- Strong cGMP experience and knowledge, QA/QC and regulatory compliance (US, EU and other international agencies)
- Advanced knowledge and experience in DS/DP biopharmaceutical operations, QA/QC processes and contract manufacturing.
- Good understanding of complex change control processes and interaction with regulatory affair processes.
- Understanding of regulatory submission processes.
- Capable of reviewing and assessing manufacturing and analytical technical documents and provide sound quality assessments on change controls, deviations and complaints.
- Experience working with electronic Document Management, electronic Training systems and Trackwise
- Understanding of risk assessment and risk management fundamentals/tools
- Experience interacting with external parties.
- Good knowledge of MS office and Windows based computer applications.
Behavioral Skills/Competencies (e.g. excellent communication skills, strong collaborator, Problem solving etc.)
- Strong interpersonal skills, excellent communication skills, good presentation, negotiations and influencing skills
- Ability to effectively manage multiple, complex priorities and quick shifting of those.
- Team player, task oriented and keen on working in a cross-cultural working environment.
- People oriented with tendency to help others and go beyond her/his area of responsibility.
What we offer
- Flexible working scheme
- Competitive salary
- International environment
- 25 holidays + 1 extra day off on your birthday
