Quality Control Associate - Temporary Assignment

Responsibilities:

Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines.

• Apply and develop QC knowledge while participating in procedures and projects under guidance from senior staff.
• Ensure all tasks comply with GMP, quality standards, and legal regulations, escalating issues when needed.
• Reviews work generated by the team as required ensuring all procedures are followed.
• Plan and execute method development, transfer, validation, and reporting activities accurately and on time.
• Resolve analytical issues collaboratively and escalate unresolved problems per defined procedures.
• Maintain clear, proactive communication with internal and external stakeholders, representing the team when required.
• Propose new methodologies and suggest optimizations to improve processes and performance.
• Support onboarding of new team members and ensure high professional standards across the lab.
• Maintain laboratory records, logbooks, and data systems in accordance with GLP and internal procedures.
• Conduct instrument maintenance, calibration, and qualification, while adhering to HSE and GMP guidelines.
• Work effectively in cross-functional teams, support audits, and contribute to KPI tracking and continuous improvement initiatives.
• Use analytical techniques and instrumentation, such as gas and high-performance liquid chromatography (HPLC) amongst others.

Qualifications:

• University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field (mandatory).
• Requires educational / training experience in a QC laboratory environment.
• Hands-on experience in Analytical Chemistry and QC procedures (desirable).
• Training and experience of GMP and ICH guidelines standards (desirable).
• Knowledge on HPLC and GC, and familiarity with Empower Software (desirable).
• Technical understanding of GMP practices, analytical theory and techniques.
• Documentation skills and attention to detail - Fluency in English is a requirement.
• Computer literate with good working knowledge of the MS Office package.

Hovione is a proud Equal Opportunity Employer

Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

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