Specialist – Quality Control Analytical

Job Title: Specialist Quality Control Analytical

Reporting to: Head of Quality Control Analytical

Department: Quality Control

Location: Baltimore Maryland

About Syngene

Incorporated in 1993 Syngene International Ltd. is an innovation-focused global discovery development and manufacturing organization providing integrated scientific services to the pharmaceutical biotechnology nutrition animal health consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb Baxter Amgen GSK and Merck KGaA. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems improve R&D productivity speed up time to market and lower the cost of innovation.

At Syngene safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability including following safety guidelines procedures and SOPs in letter and spirit.

Job Summary

The Specialist Quality Control Analytical (QC Analytical) will serve as an analyst/specialist for the Microbiology side of the QC unit at a large molecule manufacturing plant. The incumbent will work within the QC Analytical group for the site and partner cross-functionally with QC Micro Manufacturing Quality Assurance Regulatory Affairs and Supply Chain to ensure timely analysis and inspection readiness. This role is a working Specialist role and will include hands-on QC work including sampling and testing as well as working with analysts and specialists within QC Analytical group to develop qualify/validate and transfer methods.

Primary Responsibilities

• Responsible for working in Quality Control (QC) Analytical operations including product support for stability studies raw material ensuring compliance with Good Laboratory Practices (GLP) and applicable regulatory requirements.
• Operate as the specialist in performing routine sampling and testing for all analytical tests including for utility raw material in-process and product and stability.
• Coordinate with Quality Assurance (QA) and other departments to ensure development and transfer of analytical tests and methods.
• Ensure qualification validation performance and transfer of analytical methods within the QC department.
• Interact with clients and project teams to ensure seamless execution of project-related activities.
• Collaborate with the Biologics Process Development team to plan and execute testing activities in support of drug substance development and manufacturing.
• Ensure that laboratory incidents out-of-specifications (OOS) deviations out-of-trend (OOT) results and client complaints related to QC testing are thoroughly investigated root causes identified and corrective and preventive actions (CAPA) implemented in a timely manner.
• Ensure all documentation including SOPs IOPs EOPs and STPs is periodically reviewed updated and maintained as per the documentation control system.
• Ensure timely completion of QC activities as per project timelines. Update work plans periodically to accommodate changes in project scope priorities or timelines.
• Adhere to ALCOA principles of data integrity for self and ensure compliance by team members.
• Participate in functional working teams for self-assessment of compliance to SOPs and data integrity standards.
• Support preparation and timely closure of audit action plans and escalate concerns appropriately.
• Support investigations and closure of client and regulatory audit observations related to QC Analytical.
• Ensure lab safety protocols are followed at all times and resolve technical issues in the QC Analytical lab effectively.
• Support QC Analytical documentation in regulatory filings including Prior Approval Submissions renewals updates and supplements as required.
• Support monitoring of QC analytical trends complaints failures deviations and changes to identify opportunities for process system and product improvements.

Education & Qualifications

• Education: Bachelors degree in Chemistry Biochemistry Chemical Engineering or a related scientific discipline is required;
• Subject Matter Expert in Quality Control within biologics or pharmaceutical manufacturing environments specifically for large molecule products.
• Regulatory Knowledge: Understanding of USDA and USFDA ICH EU and Health Canada regulations as well as USP and other pharmacopeial standards relevant to biologics manufacturing.
• Audit Experience: Experience supporting regulatory inspections and third-party audits.
• Technical Expertise: Working knowledge of biologic analytical techniques and validation of methods.
• Leadership Skills: Ability to lead cross-functional teams build relationships across departments and foster a culture of quality compliance and accountability.
• Training & Development: Experience working within quality systems qualifications and validations and product lifecycle quality management.
• Continuous Improvement: A track record of driving successful continuous improvement projects to enhance efficiency reduce deviations and increase product quality.

Additional Competencies:

• Experience in bioanalytical and bioassay methods for monoclonal antibodies and other biologic molecules.
• Plan and manage resources for smooth operations in the QC analytical lab.

Equal Opportunity Employer:

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age colour national origin citizenship status physical or mental disability race religion creed gender sex sexual orientation gender identity and/or expression genetic information marital status status with regard to public assistance veteran status or any other characteristic protected by applicable legislation or local addition Syngene will provide reasonable accommodations for qualified individuals with disabilities.