Key Skills

Job Description

QA CMO Biologics Specialist 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. About SUN Pharma 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 products for commercial use in Europe. Taking the helm of the Pharma Branded team, they will foster a culture of excellence in quality management. Additionally, the selected candidate will be responsible for overseeing the quality assurance and compliance activities of Investigational Medicinal Products (IMPs) for European clinical trials. 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 Biologic products Review of batch documentation of Biologics and APIs 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 (Initiates, investigates and ensures timely closures) of key quality systems including deviations, change controls, CAPAs, complaints associated with the products, by liaising with CMOs, QA Manager/QP , operations, QC and other Sun stakeholders associated with Drug Substance/API , Drug Products or Medical Devices appropriately and in a timely fashion. Prepare of annual product reviews (APR/PQR) of Biologics products 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. 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 API/DP biopharmaceutical operations, QA/QC processes and contract manufacturing. Good understanding of complex change control processes and interaction with regulatory affair processes. Good 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

Core Responsibilities

Oversee quality assurance and compliance for biologics manufactured by external partners, including batch release preparation, documentation review, and support for QP certification. Manage quality systems and CMO interactions, maintain product specifications and quality documentation, and support audits, inspections, and regulatory compliance.

Requirements

Requires a bachelor's degree in biochemistry, chemistry, pharmacy, biotechnology, or a related field, plus at least five years of relevant biopharmaceutical manufacturing experience. Candidates should have strong GMP and regulatory knowledge, experience with biologics and contract manufacturing, batch release and quality systems, and fluent English.

Benefits

• Flexible Working Scheme
• Competitive Salary
• International Environment
• 25 Holidays
• Birthday Day Off