About this opportunity
Hartmann Young lists this Quality Control Compliance Lead opportunity in city of albany, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Hartmann Young is partnered with a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotechnology companies to support the development, manufacture, and delivery of therapies for patients. We are looking for a QC Compliance Lead to join the team in Albany, New York.
The Role
In this role, you will support laboratory compliance, investigations and continuous improvement within a pharmaceutical manufacturing environment. You will also lead root cause investigations, oversee QC compliance activities and ensure laboratory quality systems remain inspection-ready. You’ll work across laboratories, testing raw materials, chemical intermediates, APIs and stability samples, applying your expertise in analytical chemistry and quality systems.
You’ll also:
Collaborate across teams to establish effective investigation approaches that support customer expectations and business priorities;
Communicate investigation progress, findings and outcomes to key stakeholders and senior management;
Analyse and trend QC laboratory data and performance metrics to identify recurring issues and areas for improvement;
Work closely with QC leadership to address emerging themes and systemic risks, implementing sustainable improvements where required;
Review and enhance analytical methods, procedures and training materials to support consistent laboratory performance;
Identify opportunities to challenge and improve existing processes, introducing more efficient and effective ways of working.
The Person
Bachelor’s Degree in Chemistry or related field;
Minimum of 6 years’ experience in a QC laboratory environment OR equivalent combination of relevant education and experience may be substituted as appropriate;
Investigations experience including root cause analysis, writing, and CAPA identification;
Strong knowledge of cGMP, FDA and international regulations, quality systems and applicable API pharmaceutical requirements, including relevant ICH guidelines.
We're looking for someone with a good understanding of pharmaceutical manufacturing processes and laboratory operations, with excellent communication, influencing and stakeholder management skills. Ideally, you'll be highly organised, with strong time management and prioritisation skills, and the ability to manage multiple projects and deadlines independently. You'll be comfortable interpreting technical procedures, regulatory guidance and scientific literature, and translating requirements into clear actions and documentation.
Please note - relocation support is available for this position.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.