Principal Analytical Specialist

The Principal Specialist - Quality Control Analytical (QC Analytical) Lead, will serve as the Lead for the Microbiology side of the QC unit at a large molecule manufacturing plant. This role is critical to ensuring that QC Analytical functions are aligned with regulatory requirements, company objectives, and industry’s best practices. The incumbent will be accountable for overseeing the QC Analytical team, working under the Head of Quality Control or Head of Quality in Baltimore. The incumbent will lead the QC Analytical strategy for the site, interface with client counterparts, and partner cross-functionally with Manufacturing, Quality Assurance, Regulatory Affairs, and Supply Chain to ensure timely analysis and inspection readiness. This role is a working Lead Specialist role, and will include hands-on QC work, including sampling and testing, as well as being the lead of the other analysts and specialists within QC Analytical group., * Responsible for Quality Control (QC) Analytical operations, including product support for stability studies, raw material, microbiology lab and packing material testing, ensuring compliance with Good Laboratory Practices (GLP) and applicable regulatory requirements.

• Manage routine analytical tests on raw materials, on intermediate and finished products, and for facility utilities, such as water, gas, and environmental sampling.
• Operate as the lead 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.
• Ensure all QC test methods, protocols, and technical reports related to Analytical operations comply with current pharmacopeial and regulatory requirements.
• 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.
• Establish functional working teams for self-assessment of compliance to SOPs and data integrity standards.
• Ensure preparation and timely closure of audit action plans and escalate concerns appropriately.
• Lead investigations and ensure 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.
• Manage, coach, and develop the QC Analytical team and contribute to their professional growth.
• Proactively monitor QC analytical trends, complaints, failures, deviations, and changes to identify opportunities for process, system, and product improvements.

• Education: Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, or a related scientific discipline is required; Master’s degree is desired.
• Experience: 8-12 years of progressively responsible experience 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: Proven experience supporting regulatory inspections and third-party audits.
• Technical Expertise: Strong working knowledge of biologic analytical techniques and validation of methods.
• Leadership Skills: Demonstrated ability to lead cross-functional teams, build relationships across departments, and foster a culture of quality, compliance, and accountability.
• Training & Development: Skilled in implementing robust 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.

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., Syngene is a contract research, development and manufacturing organization (CRDMO) that provides integrated discovery, development, and manufacturing services to pharmaceutical, biotechnology, animal healthcare, consumer goods and agrochemical companies. Syngene’s clients are world leaders in their fields, ranging from leading global multinationals to small and medium-sized start-ups, non-profit institutions, academic institutes and government organizations.