{"@context":"https://schema.org","@type":"JobPosting","title":"Sr. Chemist - GLP& Documentation (ARD)","description":"

Role & responsibilities

The Sr. Chemist will oversee GLP-compliant laboratory operations, ensuring that all experimental work, testing, and analytical activities meet internal and regulatory standards. Responsibilities include planning and executing experiments, maintaining accurate laboratory records, preparing and reviewing technical documents, and supporting validation and stability studies. The role will involve reviewing and updating standard operating procedures (SOPs), test methods, and batch records, as well as ensuring timely and complete documentation for audits and regulatory submissions.

The Sr. Chemist will collaborate with Quality Control, Quality Assurance, and R&D teams to troubleshoot issues, support investigations, and drive continuous improvement in laboratory practices and documentation quality.

Preferred candidate profile

Strong Laboratory Skills with hands-on experience in routine analytical testing, method execution, instrument handling, and GLP-compliant lab practices.
Proven Quality Control experience, including documentation review, data integrity, deviation handling support, and compliance with regulatory and internal standards.
Excellent Analytical Skills for preparing validation protocols, MOA, COA & ROA.
Bachelors or Masters degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
Sound knowledge of GLP and relevant regulatory guidelines and associated documentation requirements.
Experience in pharmaceutical APIs or intermediates manufacturing environments is preferred.
Knowledge of ALCOA & ALCOA++.

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